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Leader 00000nz a2200037n 45 0
001 WKP|Q60572593 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000209.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q60572593‏
035 ‎‡a (OCoLC)Q60572593‏
100 0 ‎‡a Graeme I. Bell‏ ‎‡c American molecular genetics researcher‏ ‎‡9 en‏
375 ‎‡a 1‏ ‎‡2 iso5218‏
670 ‎‡a Author's 5-amino-imidazole carboxamide riboside acutely potentiates glucose-stimulated insulin secretion from mouse pancreatic islets by KATP channel-dependent and -independent pathways‏
670 ‎‡a Author's A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin‏
670 ‎‡a Author's A brief perspective on insulin production‏
670 ‎‡a Author's A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance‏
670 ‎‡a Author's A case of hepatocyte nuclear factor-1 alpha diabetes/MODY3 masquerading as type 1 diabetes in a Mexican-American adolescent and responsive to a low dose of sulfonylurea‏
670 ‎‡a Author's A genome-wide search for human non-insulin-dependent‏
670 ‎‡a Author's A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.‏
670 ‎‡a Author's A KpnI polymorphism for the human insulin-responsive glucose transporter gene (GLUT4) on chromosome 17.‏
670 ‎‡a Author's A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes‏
670 ‎‡a Author's A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk‏
670 ‎‡a Author's A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus‏
670 ‎‡a Author's A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young‏
670 ‎‡a Author's A molecular inventory of human pancreatic islets: sequence analysis of 1000 cDNA clones‏
670 ‎‡a Author's A novel syndrome of diabetes mellitus, renal dysfunction and genital malformation associated with a partial deletion of the pseudo-POU domain of hepatocyte nuclear factor-1beta‏
670 ‎‡a Author's A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus‏
670 ‎‡a Author's A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus‏
670 ‎‡a Author's A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus‏
670 ‎‡a Author's A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene‏
670 ‎‡a Author's A single residue, aspartic acid 95, in the delta opioid receptor specifies selective high affinity agonist binding.‏
670 ‎‡a Author's A Tyrosine Phosphatase is Associated with the Somatostatin Receptor‏
670 ‎‡a Author's A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene‏
670 ‎‡a Author's Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.‏
670 ‎‡a Author's Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta‏
670 ‎‡a Author's Adaptation to hyperglycemia enhances insulin secretion in glucokinase mutant mice‏
670 ‎‡a Author's Agonists and antagonists bind to different domains of the cloned kappa opioid receptor‏
670 ‎‡a Author's Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism‏
670 ‎‡a Author's Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.‏
670 ‎‡a Author's Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.‏
670 ‎‡a Author's Alternative splicing of human insulin receptor messenger RNA.‏
670 ‎‡a Author's Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA‏
670 ‎‡a Author's An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.‏
670 ‎‡a Author's An in vivo cis-regulatory screen at the type 2 diabetes associated TCF7L2 locus identifies multiple tissue-specific enhancers‏
670 ‎‡a Author's Analysis of the regions flanking the human insulin gene and sequence of an Alu family member‏
670 ‎‡a Author's Anti-diabetic effect of ginsenoside Re in ob/ob mice‏
670 ‎‡a Author's Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.‏
670 ‎‡a Author's Appalachian spring: variations on ancient gastro-entero-pancreatic themes in New World mammals‏
670 ‎‡a Author's Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1‏
670 ‎‡a Author's Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization‏
670 ‎‡a Author's Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization‏
670 ‎‡a Author's Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3.‏
670 ‎‡a Author's Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3‏
670 ‎‡a Author's Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population‏
670 ‎‡a Author's Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate‏
670 ‎‡a Author's Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome‏
670 ‎‡a Author's Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses‏
670 ‎‡a Author's Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population‏
670 ‎‡a Author's Association of the KCNJ11 variant E23K with type 2 diabetes in Indo-Trinidadians‏
670 ‎‡a Author's BamHI RFLP at the GLUT3 locus‏
670 ‎‡a Author's BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11‏
670 ‎‡a Author's Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese‏
670 ‎‡a Author's beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4‏
670 ‎‡a Author's beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.‏
670 ‎‡a Author's Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene‏
670 ‎‡a Author's Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young‏
670 ‎‡a Author's Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas‏
670 ‎‡a Author's Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.‏
670 ‎‡a Author's Calpain-10 is a component of the obesity-related quantitative trait locus Adip1.‏
670 ‎‡a Author's Calpain system regulates muscle mass and glucose transporter GLUT4 turnover‏
670 ‎‡a Author's Calpains play a role in insulin secretion and action‏
670 ‎‡a Author's Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase‏
670 ‎‡a Author's cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young‏
670 ‎‡a Author's cDNA sequence coding for human kidney catalase‏
670 ‎‡a Author's Changes in endothelial nitric oxide synthase mRNA during vasospasm after subarachnoid hemorrhage in monkeys‏
670 ‎‡a Author's Changes in Pancreatic Islet Glucokinase and Hexokinase Activities With Increasing Age, Obesity, and the Onset of Diabetes‏
670 ‎‡a Author's Chapter 1. Isolation and Assay of Eukaryotic DNA-Dependent RNA Polymerases‏
670 ‎‡a Author's Characterization and expression of human HepG2/erythrocyte glucose-transporter gene‏
670 ‎‡a Author's Characterization of a third human thyroid hormone receptor coexpressed with other thyroid hormone receptors in several tissues‏
670 ‎‡a Author's Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene‏
670 ‎‡a Author's Characterization of a thyroid hormone receptor expressed in human kidney and other tissues‏
670 ‎‡a Author's Characterization of cloned somatostatin receptors SSTR4 and SSTR5.‏
670 ‎‡a Author's Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2): different glucokinase defects lead to a common phenotype‏
670 ‎‡a Author's Characterization of Japanese families with early-onset type 2‏
670 ‎‡a Author's Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes‏
670 ‎‡a Author's Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library‏
670 ‎‡a Author's Chromosomal assignments of genes for trypsin, chymotrypsin B, and elastase in mouse‏
670 ‎‡a Author's Chromosomal assignments of human genes for serine proteases trypsin, chymotrypsin B, and elastase‏
670 ‎‡a Author's Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor‏
670 ‎‡a Author's Chromosome assignment of mouse insulin, colony stimulating factor 1, and low-density lipoprotein receptors‏
670 ‎‡a Author's Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin‏
670 ‎‡a Author's Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene‏
670 ‎‡a Author's Clinical characteristics of subjects with a missense mutation in glucokinase.‏
670 ‎‡a Author's Cloned somatostatin receptors: identification of subtype-selective peptides and demonstration of high affinity binding of linear peptides‏
670 ‎‡a Author's Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney‏
670 ‎‡a Author's Cloning and functional comparison of kappa and delta opioid receptors from mouse brain‏
670 ‎‡a Author's Cloning of a novel somatostatin receptor, SSTR3, coupled to adenylylcyclase‏
670 ‎‡a Author's Cloning of cDNAs for human phosphoribosylpyrophosphate synthetases 1 and 2 and X chromosome localization of PRPS1 and PRPS2 genes‏
670 ‎‡a Author's Cloning of rat and mouse P2Y purinoceptors‏
670 ‎‡a Author's Cloning of rat KATP-2 channel and decreased expression in pancreatic islets of male Zucker diabetic fatty rats‏
670 ‎‡a Author's Cloning of the alpha 1 subunit of a voltage-dependent calcium channel expressed in pancreatic beta cells‏
670 ‎‡a Author's Cloning of two distinct copies of human phosphoribosylpyrophosphate synthetase cDNA.‏
670 ‎‡a Author's Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes‏
670 ‎‡a Author's Compensation in pancreatic beta-cell function in subjects with glucokinase mutations‏
670 ‎‡a Author's Confirmed Locus on Chromosome 11p and Candidate Loci on 6q and 8p for the Triglyceride and Cholesterol Traits of Combined Hyperlipidemia‏
670 ‎‡a Author's Congenital insulin resistance associated with a conformational alteration in a conserved beta-sheet in the insulin receptor L1 domain‏
670 ‎‡a Author's Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism‏
670 ‎‡a Author's Control of pancreas and liver gene expression by HNF transcription factors‏
670 ‎‡a Author's Core transcriptional regulatory circuitry in human hepatocytes‏
670 ‎‡a Author's Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications.‏
670 ‎‡a Author's Creation of an inositol 1,4,5-trisphosphate-sensitive Ca2+ store in secretory granules of insulin-producing cells‏
670 ‎‡a Author's Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice‏
670 ‎‡a Author's Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice‏
670 ‎‡a Author's Diabetes, dependence, asymptotics, selection and significance‏
670 ‎‡a Author's Diabetes mellitus and genetically programmed defects in beta-cell function‏
670 ‎‡a Author's Diagnosis and treatment of neonatal diabetes: a United States experience‏
670 ‎‡a Author's Differential effects of overexpressed glucokinase and hexokinase I in isolated islets. Evidence for functional segregation of the high and low Km enzymes‏
670 ‎‡a Author's Differential expression of messenger RNAs for somatostatin receptor subtypes SSTR1, SSTR2 and SSTR3 in adult rat brain: analysis by RNA blotting and in situ hybridization histochemistry‏
670 ‎‡a Author's Differential expression of somatostatin receptor subtypes in brain‏
670 ‎‡a Author's Diminished insulin and glucagon secretory responses to arginine in nondiabetic subjects with a mutation in the hepatocyte nuclear factor-4alpha/MODY1 gene‏
670 ‎‡a Author's Dinucleotide repeat polymorphism at D9S328E‏
670 ‎‡a Author's Dinucleotide repeat polymorphism at D9S328E (EST hbc220).‏
670 ‎‡a Author's Dinucleotide repeat polymorphism at the human GLUT2 locus‏
670 ‎‡a Author's Dinucleotide repeat polymorphism at the human ribophorin II locus‏
670 ‎‡a Author's Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in a gene on chromosome 20 encoding a G-protein coupled receptor (D20S32e).‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in D20S17 (CRI-L127)‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in Gs-alpha subunit gene (GNAS1) on chromosome 20.‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3.‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in the human glucagon gene (GCG).‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in the human SRC gene on chromosome 20‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in the human thyroid hormone receptor alpha gene (THRA1) on chromosome 17‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in the human thyroid hormone receptor α gene (THRA1) on chromosome 17‏
670 ‎‡a Author's Dinucleotide repeat polymorphism in the NEC2 gene‏
670 ‎‡a Author's Disease associations. Chance, artifact, or susceptibility genes?‏
670 ‎‡a Author's Distribution of kappa opioid receptor mRNA in adult mouse brain: an in situ hybridization histochemistry study‏
670 ‎‡a Author's Donald F. Steiner MD, 1930-2014: discoverer of proinsulin‏
670 ‎‡a Author's Dual promoter structure of ZFP106: regulation by myogenin and nuclear respiratory factor-1.‏
670 ‎‡a Author's Effect of genetic variation in a Drosophila model of diabetes-associated misfolded human proinsulin.‏
670 ‎‡a Author's Enhanced levels of insulin-like growth factor messenger RNA in human colon carcinomas and liposarcomas‏
670 ‎‡a Author's Enhancing pancreatic Beta-cell regeneration in vivo with pioglitazone and alogliptin‏
670 ‎‡a Author's Epilepsy in the United Kingdom: seizure frequency and severity, anti-epileptic drug utilization and impact on life in 1652 people with epilepsy‏
670 ‎‡a Author's Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls‏
670 ‎‡a Author's Erratum to: Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene‏
670 ‎‡a Author's Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees‏
670 ‎‡a Author's Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues‏
670 ‎‡a Author's Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice‏
670 ‎‡a Author's Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat‏
670 ‎‡a Author's Evolution of β-Cell Dysfunction in the Male Zucker Diabetic Fatty Rat‏
670 ‎‡a Author's Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus‏
670 ‎‡a Author's Exome sequencing and genetic testing for MODY.‏
670 ‎‡a Author's Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls‏
670 ‎‡a Author's Exon-intron organization, expression, and chromosomal localization of the human motilin gene‏
670 ‎‡a Author's Expression and regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice‏
670 ‎‡a Author's Expression of Calcium Channel mRNAs in Rat Pancreatic Islets and Downregulation After Glucose Infusion‏
670 ‎‡a Author's Expression of human epidermal growth factor precursor cDNA in transfected mouse NIH 3T3 cells‏
670 ‎‡a Author's Expression of multiple growth factors in a human lung cancer cell line‏
670 ‎‡a Author's Expression of the human insulin gene in an alternate mammalian cell and in cell extracts‏
670 ‎‡a Author's Facilitative glucose transport proteins: structure and regulation of expression in adipose tissue‏
670 ‎‡a Author's Factor VIII:C synthesis in the kidney‏
670 ‎‡a Author's Femtosecond laser desorption ionization mass spectrometry imaging and multivariate analysis of lipids in pancreatic tissue‏
670 ‎‡a Author's Frameshift mutation, A263fsinsGG, in the hepatocyte nuclear factor-1beta gene associated with diabetes and renal dysfunction‏
670 ‎‡a Author's From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation‏
670 ‎‡a Author's Fructose transporter in human spermatozoa and small intestine is GLUT5‏
670 ‎‡a Author's Functional properties of the R154X HNF-4alpha protein generated by a mutation associated with maturity-onset diabetes of the young, type 1.‏
670 ‎‡a Author's Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample‏
670 ‎‡a Author's G protein-activated inwardly rectifying potassium channel (GIRK1/KGA) mRNA in adult rat heart and brain by in situ hybridization histochemistry‏
670 ‎‡a Author's Gastric Inhibitory Polypeptide: Structure and Chromosomal Localization of the Human Gene‏
670 ‎‡a Author's Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q‏
670 ‎‡a Author's Gene symbol: IPF1. Disease: MODY 4‏
670 ‎‡a Author's Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta‏
670 ‎‡a Author's Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1‏
670 ‎‡a Author's Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans‏
670 ‎‡a Author's Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin.‏
670 ‎‡a Author's Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2‏
670 ‎‡a Author's Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2 (non-insulin-dependent) diabetes mellitus in different populations‏
670 ‎‡a Author's Genetic Testing in Diabetes Mellitus‏
670 ‎‡a Author's Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population‏
670 ‎‡a Author's Genetic variants of hepatocyte nuclear factor-1beta in Chinese young-onset diabetic patients with nephropathy‏
670 ‎‡a Author's Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus‏
670 ‎‡a Author's Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.‏
670 ‎‡a Author's Genetic variation in the hepatocyte nuclear factor-3beta gene‏
670 ‎‡a Author's Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians‏
670 ‎‡a Author's Genetics and pathophysiology of neonatal diabetes mellitus‏
670 ‎‡a Author's Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals‏
670 ‎‡a Author's Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas‏
670 ‎‡a Author's Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.‏
670 ‎‡a Author's Genome-wide Scan for Type 2 Diabetes Loci in Hong Kong Chinese and Confirmation of a Susceptibility Locus on Chromosome 1q21-q25‏
670 ‎‡a Author's Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility‏
670 ‎‡a Author's Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus‏
670 ‎‡a Author's Gi alpha 1 selectively couples somatostatin receptor subtype 3 to adenylyl cyclase: identification of the functional domains of this alpha subunit necessary for mediating the inhibition by somatostatin of cAMP formation‏
670 ‎‡a Author's Gi alpha 3 and G‏
670 ‎‡a Author's Gi alpha 3 and G(o) alpha selectively associate with the cloned somatostatin receptor subtype SSTR2‏
670 ‎‡a Author's Glucokinase mutations, insulin secretion, and diabetes mellitus‏
670 ‎‡a Author's Glucokinase: structural analysis of a protein involved in susceptibility to diabetes‏
670 ‎‡a Author's Glucose transporter expression in brain. cDNA sequence of mouse GLUT3, the brain facilitative glucose transporter isoform, and identification of sites of expression by in situ hybridization‏
670 ‎‡a Author's Glucose transporter gene and non-insulin-dependent diabetes‏
670 ‎‡a Author's Glycemic control promotes pancreatic beta-cell regeneration in streptozotocin-induced diabetic mice‏
670 ‎‡a Author's Hamster preproglucagon contains the sequence of glucagon and two related peptides‏
670 ‎‡a Author's Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene‏
670 ‎‡a Author's High-level expression of human insulin receptor cDNA in mouse NIH 3T3 cells‏
670 ‎‡a Author's High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization‏
670 ‎‡a Author's HincII RFLP at the human hexokinase I (HK1) locus on chromosome 10‏
670 ‎‡a Author's HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes‏
670 ‎‡a Author's Human alpha 2-macroglobulin gene is located on chromosome 12‏
670 ‎‡a Author's Human antithrombin II (AT3) gene length polymorphism revealed by the polymerase chain reaction‏
670 ‎‡a Author's Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification‏
670 ‎‡a Author's Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogen‏
670 ‎‡a Author's Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency‏
670 ‎‡a Author's Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism‏
670 ‎‡a Author's Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively‏
670 ‎‡a Author's Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6‏
670 ‎‡a Author's Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation‏
670 ‎‡a Author's Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity‏
670 ‎‡a Author's Human hexokinase II: localization of the polymorphic gene to chromosome 2.‏
670 ‎‡a Author's Human hexokinase: sequences of amino- and carboxyl-terminal halves are homologous‏
670 ‎‡a Author's Human insulin-like growth factor I and II messenger RNA: isolation of complementary DNA and analysis of expression‏
670 ‎‡a Author's Human insulin-receptor gene‏
670 ‎‡a Author's Human insulin-receptor gene. Partial sequence and amplification of exons by polymerase chain reaction‏
670 ‎‡a Author's Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism‏
670 ‎‡a Author's Human intestinal glucose transporter expression and localization of GLUT5.‏
670 ‎‡a Author's Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history‏
670 ‎‡a Author's Human Oct3 gene family: cDNA sequences, alternative splicing, gene organization, chromosomal location, and expression at low levels in adult tissues‏
670 ‎‡a Author's Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13‏
670 ‎‡a Author's Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2‏
670 ‎‡a Author's Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms‏
670 ‎‡a Author's Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7.‏
670 ‎‡a Author's Hyperexcitability to sulphonylurea in MODY3.‏
670 ‎‡a Author's Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus‏
670 ‎‡a Author's Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families‏
670 ‎‡a Author's Identification of a ligand-binding region of the human insulin receptor encoded by the second exon of the gene‏
670 ‎‡a Author's Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas‏
670 ‎‡a Author's Identification of gestationally regulated genes in rat myometrium by use of messenger ribonucleic acid differential display‏
670 ‎‡a Author's Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese‏
670 ‎‡a Author's Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs‏
670 ‎‡a Author's Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young‏
670 ‎‡a Author's Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)‏
670 ‎‡a Author's Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young‏
670 ‎‡a Author's Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies‏
670 ‎‡a Author's Imaging Beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic Beta cells‏
670 ‎‡a Author's Immunological detection of isoforms of the somatostatin receptor subtype, SSTR2.‏
670 ‎‡a Author's Impaired insulin secretion in transgenic mice over-expressing calpastatin in pancreatic β-cells‏
670 ‎‡a Author's In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes‏
670 ‎‡a Author's In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q‏
670 ‎‡a Author's In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q (GlnB22-insulin).‏
670 ‎‡a Author's Increase in serum leptin and uterine leptin receptor messenger RNA levels during pregnancy in rats‏
670 ‎‡a Author's Increase in Serum Leptin and Uterine Leptin Receptor Messenger RNA Levels during Pregnancy in Rats1‏
670 ‎‡a Author's Increased expression of endothelin B receptor mRNA following subarachnoid hemorrhage in monkeys‏
670 ‎‡a Author's Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR2 and SSTR5 through different mechanisms‏
670 ‎‡a Author's Inositol 1,4,5-trisphosphate receptors, secretory granules and secretion in endocrine and neuroendocrine cells‏
670 ‎‡a Author's Insulin gene mutations as a cause of permanent neonatal diabetes‏
670 ‎‡a Author's Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.‏
670 ‎‡a Author's Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood‏
670 ‎‡a Author's Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family‏
670 ‎‡a Author's Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans‏
670 ‎‡a Author's Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing‏
670 ‎‡a Author's Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations‏
670 ‎‡a Author's Integrative cross tissue analysis of gene expression identifies novel type 2 diabetes genes‏
670 ‎‡a Author's Is islet amyloid polypeptide a significant factor in pathogenesis or pathophysiology of diabetes?‏
670 ‎‡a Author's Islet amyloid polypeptide (amylin): no evidence of an abnormal precursor sequence in 25 type 2 (non-insulin-dependent) diabetic patients‏
670 ‎‡a Author's Isolation and assay of eukaryotic DNA-dependent RNA polymerases‏
670 ‎‡a Author's Isolation and characterization of a cloned rat insulin gene‏
670 ‎‡a Author's Isolation and nucleotide sequence of a cDNA encoding the precursor of mouse nerve growth factor‏
670 ‎‡a Author's Isolation and sequence of a rat chymotrypsin B gene‏
670 ‎‡a Author's Isolation of a cDNA Clone Encoding a KATP Channel-Like Protein Expressed in Insulin-Secreting Cells, Localization of the Human Gene to Chromosome Band 21q22.1, and Linkage Studies With NIDDM‏
670 ‎‡a Author's Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance‏
670 ‎‡a Author's Lack of association of the polymorphic locus in the 5'-flanking region of the human insulin gene and diabetes in American blacks‏
670 ‎‡a Author's Leptin, the obese gene product, rapidly modulates synaptic transmission in the hypothalamus.‏
670 ‎‡a Author's Letters‏
670 ‎‡a Author's Linkage Analysis of Maturity-Onset Diabetes of the Young With Microsatellite Polymorphisms: No Linkage to ADA or GLUT2 Genes in Two Families‏
670 ‎‡a Author's Linkage and association between insulin-dependent diabetes mellitus‏
670 ‎‡a Author's Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7‏
670 ‎‡a Author's Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus‏
670 ‎‡a Author's Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.‏
670 ‎‡a Author's Linkage of calpain 10 to type 2 diabetes: the biological rationale‏
670 ‎‡a Author's Linkage studies in NIDDM with markers near the sulphonylurea receptor gene‏
670 ‎‡a Author's Linkage studies of maturity onset diabetes of the young--R.W. pedigree‏
670 ‎‡a Author's Localization of hepatocyte nuclear factor-4α in the nucleolus and nucleus is regulated by its C-terminus‏
670 ‎‡a Author's Localization of human somatostatin receptor 5 gene‏
670 ‎‡a Author's Localization of human somatostatin receptor 5 gene (SSTR5) to chromosome band 16p13.3 by fluorescence in situ hybridization‏
670 ‎‡a Author's Localization of inositol trisphosphate receptor subtype 3 to insulin and somatostatin secretory granules and regulation of expression in islets and insulinoma cells‏
670 ‎‡a Author's Localization of insulin-like growth factor genes to human chromosomes 11 and 12‏
670 ‎‡a Author's Localization of the Gene Encoding a Neutral Amino Acid Transporter-like Protein to Human Chromosome Band 19q13.3 and Characterization of a Simple Sequence Repeat DNA Polymorphism‏
670 ‎‡a Author's Localization of the Genes Encoding Two Transcription Factors, LMX1 and CDX3, Regulating Insulin Gene Expression to Human Chromosomes 1 and 13‏
670 ‎‡a Author's Localization of the glucagon receptor gene to human chromosome band 17q25‏
670 ‎‡a Author's Localization of the kappa opioid receptor gene to human chromosome band 8q11.2.‏
670 ‎‡a Author's Loci on chromosomes 2‏
670 ‎‡a Author's Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans‏
670 ‎‡a Author's Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia‏
670 ‎‡a Author's Macrosomia and neonatal hypoglycaemia in RW pedigree subjects with a mutation (Q268X) in the gene encoding hepatocyte nuclear factor 4alpha (HNF4A)‏
670 ‎‡a Author's Mapping Diabetes-Susceptibility Genes: Lessons Learned From Search for DNA Marker for Maturity-Onset Diabetes of the Young‏
670 ‎‡a Author's Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects‏
670 ‎‡a Author's Mapping polypeptide hormone genes in the mouse: somatostatin, glucagon, calcitonin, and parathyroid hormone‏
670 ‎‡a Author's Maturity-onset diabetes of the young‏
670 ‎‡a Author's Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene‏
670 ‎‡a Author's Maturity-Onset Diabetes of the Young Due to a Mutation in the Hepatocyte Nuclear Factor-4α Binding Site in the Promoter of the Hepatocyte Nuclear Factor-1α Gene‏
670 ‎‡a Author's Maturity onset diabetes of the young (MODY).‏
670 ‎‡a Author's Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibility‏
670 ‎‡a Author's Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder‏
670 ‎‡a Author's Microsatellite polymorphism in human insulin receptor gene (INSR) on chromosome 19.‏
670 ‎‡a Author's Microsatellite polymorphism in the human platelet glycoprotein IIIa gene (GP3A) on chromosome 17‏
670 ‎‡a Author's Missense glucokinase mutation in maturity-onset diabetes of the young and mutation screening in late-onset diabetes‏
670 ‎‡a Author's MODY: a model for the study of the molecular genetics of NIDDM.‏
670 ‎‡a Author's MODY: history, genetics, pathophysiology, and clinical decision making‏
670 ‎‡a Author's Molecular analysis of the fructose transporter gene‏
670 ‎‡a Author's Molecular analysis of the fructose transporter gene (GLUT5) in isolated fructose malabsorption‏
670 ‎‡a Author's Molecular biology of islet amyloid polypeptide‏
670 ‎‡a Author's Molecular biology of mammalian glucose transporters‏
670 ‎‡a Author's Molecular biology of somatostatin receptors‏
670 ‎‡a Author's Molecular genetics of diabetes mellitus in Chinese subjects: identification of mutations in glucokinase and hepatocyte nuclear factor-1alpha genes in patients with early-onset type 2 diabetes mellitus/MODY.‏
670 ‎‡a Author's Molecular genetics of MODY in Germany‏
670 ‎‡a Author's Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20‏
670 ‎‡a Author's Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young‏
670 ‎‡a Author's Molecular mechanisms of agonist-induced desensitization of the cloned mouse kappa opioid receptor.‏
670 ‎‡a Author's Molecular model of human beta-cell glucokinase built by analogy to the crystal structure of yeast hexokinase B.‏
670 ‎‡a Author's Mouse prepro-epidermal growth factor synthesis by the kidney and other tissues‏
670 ‎‡a Author's Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.‏
670 ‎‡a Author's Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6.‏
670 ‎‡a Author's Mutant proinsulin proteins associated with neonatal diabetes are retained in the endoplasmic reticulum and not efficiently secreted‏
670 ‎‡a Author's Mutation in hepatocyte nuclear factor-1 beta gene‏
670 ‎‡a Author's Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.‏
670 ‎‡a Author's Mutation of an aspartate at residue 89 in somatostatin receptor subtype 2 prevents Na+ regulation of agonist binding but does not alter receptor-G protein association‏
670 ‎‡a Author's Mutations in hepatocyte nuclear factor 1beta are not a common cause of maturity-onset diabetes of the young in the U.K.‏
670 ‎‡a Author's Mutations in the coding region of the insulin promoter factor 1 gene are not a common cause of maturity-onset diabetes of the young in Japanese subjects‏
670 ‎‡a Author's Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects‏
670 ‎‡a Author's Mutations in the glucokinase gene are not a major cause of late-onset type 2‏
670 ‎‡a Author's Mutations in the glucokinase gene are not a major cause of late-onset type 2 (non-insulin-dependent) diabetes mellitus in Japanese subjects‏
670 ‎‡a Author's Mutations in the guinea pig preproglucagon gene are restricted to a specific portion of the prohormone sequence‏
670 ‎‡a Author's Mutations in the Hepatocyte Nuclear Factor-1 Gene Are a Common Cause of Maturity-Onset Diabetes of the Young in the U.K‏
670 ‎‡a Author's Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young‏
670 ‎‡a Author's Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)‏
670 ‎‡a Author's Mutations in the hepatocyte nuclear factor-1alpha gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4.‏
670 ‎‡a Author's Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.‏
670 ‎‡a Author's Mutations in the Hepatocyte Nuclear Factor-1α/MODY3 Gene in Japanese Subjects With Early- and Late-Onset NIDDM‏
670 ‎‡a Author's Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)‏
670 ‎‡a Author's Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes‏
670 ‎‡a Author's Mutations of the human glucokinase gene and diabetes mellitus‏
670 ‎‡a Author's Nature or nurture: an insightful illustration from a Chinese family with hepatocyte nuclear factor-1 alpha diabetes‏
670 ‎‡a Author's Nature or nurture: an insightful illustration from a Chinese family with hepatocyte nuclear factor-1 alpha diabetes (MODY3)‏
670 ‎‡a Author's Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment‏
670 ‎‡a Author's Neonatal diabetes mellitus: a model for personalized medicine‏
670 ‎‡a Author's Neonatal diabetes mellitus due to complete glucokinase deficiency‏
670 ‎‡a Author's NHS services for epilepsy from the patient's perspective: a survey of primary, secondary and tertiary care access throughout the UK.‏
670 ‎‡a Author's NIDDM is associated with loss of pancreatic beta-cell L-type Ca2+ channel activity‏
670 ‎‡a Author's No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene‏
670 ‎‡a Author's No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY‏
670 ‎‡a Author's No evidence for mutations in a putative beta-cell ATP-sensitive K+ channel subunit in MODY, NIDDM, or GDM.‏
670 ‎‡a Author's Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitators.‏
670 ‎‡a Author's [Non-insulin dependent diabetes in children and adolescents]‏
670 ‎‡a Author's Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus‏
670 ‎‡a Author's Novel MODY3 Mutations in the Hepatocyte Nuclear Factor-1 Gene: Evidence for a Hyperexcitability of Pancreatic -cells to Intravenous Secretagogues in a Glucose-Tolerant Carrier of a P447L Mutation‏
670 ‎‡a Author's Nuclear translocation of SHP and visualization of interaction with HNF-4alpha in living cells‏
670 ‎‡a Author's Nucleotide sequence of a cDNA clone encoding human preproinsulin‏
670 ‎‡a Author's Nucleotide sequence of the yeast 5S ribosomal RNA gene and adjacent putative control regions‏
670 ‎‡a Author's Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60.‏
670 ‎‡a Author's Onset features and subsequent clinical evolution of childhood diabetes over several years.‏
670 ‎‡a Author's Optical imaging of pancreatic beta cells in living mice expressing a mouse insulin I promoter-firefly luciferase transgene‏
670 ‎‡a Author's Organ alchemy: producing insulin in the liver‏
670 ‎‡a Author's Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY‏
670 ‎‡a Author's Organization and Partial Sequence of the Hepatocyte Nuclear Factor-4α/MODY1 Gene and Identification of a Missense Mutation, R127W, in a Japanese Family With MODY‏
670 ‎‡a Author's Organization of the human GLUT2‏
670 ‎‡a Author's Organization of the human GLUT2 (pancreatic beta-cell and hepatocyte) glucose transporter gene‏
670 ‎‡a Author's Parasexual analysis of human pepsinogen molecular heterogeneity‏
670 ‎‡a Author's Patients’ perspectives on services for epilepsy: a survey of patient satisfaction, preferences and information provision in 2394 people with epilepsy‏
670 ‎‡a Author's Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10.‏
670 ‎‡a Author's Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy‏
670 ‎‡a Author's Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors.‏
670 ‎‡a Author's Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees‏
670 ‎‡a Author's Phosphorylation of yeast DNA-dependent RNA polymerases in vivo and in vitro. Isolation of enzymes and identification of phosphorylated subunits‏
670 ‎‡a Author's Phosphorylation of yeast RNA polymerases‏
670 ‎‡a Author's Polymorphic DNA region adjacent to the 5' end of the human insulin gene‏
670 ‎‡a Author's Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35‏
670 ‎‡a Author's Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13‏
670 ‎‡a Author's Polymorphic human somatostatin gene is located on chromosome 3‏
670 ‎‡a Author's Polymorphism in exon 4a of the human GLUT4/ muscle-fat facilitative glucose transporter gene detected by SSCP.‏
670 ‎‡a Author's Prevalence of insulin-gene mutations in non-insulin-dependent diabetes mellitus‏
670 ‎‡a Author's Properties of a polymorphic DNA segment in the 5' flanking region of the human insulin gene‏
670 ‎‡a Author's PvuII polymorphic sites in the human insulin receptor gene INSR‏
670 ‎‡a Author's Rat inwardly rectifying potassium channel Kir6.2: cloning electrophysiological characterization, and decreased expression in pancreatic islets of male Zucker diabetic fatty rats‏
670 ‎‡a Author's Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4alpha/MODY1 gene‏
670 ‎‡a Author's Reduced skeletal muscle calpain-10 transcript level is due to a cumulative decrease in major isoforms‏
670 ‎‡a Author's Regulation of glucose transporter messenger RNA levels in rat adipose tissue by insulin.‏
670 ‎‡a Author's Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome‏
670 ‎‡a Author's Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome‏
670 ‎‡a Author's Resting beta-cells - A functional reserve?‏
670 ‎‡a Author's RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.‏
670 ‎‡a Author's Ribosomal RNA genes of Saccharomyces cerevisiae. I. Physical map of the repeating unit and location of the regions coding for 5 S, 5.8 S, 18 S, and 25 S ribosomal RNAs‏
670 ‎‡a Author's Ribosomal RNA genes of Saccharomyces cerevisiae. II. Physical map and nucleotide sequence of the 5 S ribosomal RNA gene and adjacent intergenic regions‏
670 ‎‡a Author's Role of BH3-only molecules Bim and Puma in β-cell death in Pdx1 deficiency‏
670 ‎‡a Author's RyR2 and calpain-10 delineate a novel apoptosis pathway in pancreatic islets‏
670 ‎‡a Author's SCOPE: SCUBA-2 Continuum Observations of Pre-protostellar Evolution - survey description and compact source catalogue‏
670 ‎‡a Author's Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle‏
670 ‎‡a Author's Seeing is believing: how the MIP-luc mouse can advance the field of islet transplantation and β-cell regeneration‏
670 ‎‡a Author's Selective interaction of 5'-bromodeoxyuridine substituted DNA with different chromosomal proteins‏
670 ‎‡a Author's Seminars in Medicine of the Beth Israel Hospital, Boston. Non-insulin-dependent diabetes mellitus - a genetically programmed failure of the beta cell to compensate for insulin resistance‏
670 ‎‡a Author's Sequence and functional characterization of a third inositol trisphosphate receptor subtype, IP3R-3, expressed in pancreatic islets, kidney, gastrointestinal tract, and other tissues‏
670 ‎‡a Author's Sequence data and association statistics from 12,940 type 2 diabetes cases and controls‏
670 ‎‡a Author's Sequence of a cDNA clone encoding human preproinsulin-like growth factor II.‏
670 ‎‡a Author's Sequence of a cDNA coding for mouse manganese superoxide dismutase‏
670 ‎‡a Author's Sequence of a cDNA encoding guinea pig IGF-I.‏
670 ‎‡a Author's Sequence of a human fetal skeletal muscle potassium channel cDNA related to RCK4‏
670 ‎‡a Author's Sequence of a New World primate insulin having low biological potency and immunoreactivity‏
670 ‎‡a Author's Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene‏
670 ‎‡a Author's Sequence of human hexokinase III cDNA and assignment of the human hexokinase III gene (HK3) to chromosome band 5q35.2 by fluorescence in situ hybridization‏
670 ‎‡a Author's Sequence of the human insulin gene‏
670 ‎‡a Author's Sequence of the variant thyroxine-binding globulin of Australian aborigines. Only one of two amino acid replacements is responsible for its altered properties‏
670 ‎‡a Author's Sequence, tissue distribution, and chromosomal localization of mRNA encoding a human glucose transporter-like protein‏
670 ‎‡a Author's Sequence, tissue distribution, and functional characterization of the rat fructose transporter GLUT5‏
670 ‎‡a Author's Sequences of islet amyloid polypeptide precursors of an old world monkey, the pig-tailed macaque (Macaca nemestrina), and the dog (Canis familiaris)‏
670 ‎‡a Author's Somatostatin receptors, an expanding gene family: cloning and functional characterization of human SSTR3, a protein coupled to adenylyl cyclase‏
670 ‎‡a Author's Specific gene transcription in yeast nuclei and chromatin by added homologous RNA polymerases I and II‏
670 ‎‡a Author's Splice variant of the somatostatin receptor 2 subtype, somatostatin receptor 2B, couples to adenylyl cyclase‏
670 ‎‡a Author's Stimulation of tyrosine phosphatase and inhibition of cell proliferation by somatostatin analogues: mediation by human somatostatin receptor subtypes SSTR1 and SSTR2.‏
670 ‎‡a Author's Structure and function of ASP, the human homolog of the mouse agouti gene‏
670 ‎‡a Author's Structure and function of mammalian facilitative sugar transporters.‏
670 ‎‡a Author's Structure and transcription of the human m3 muscarinic receptor gene‏
670 ‎‡a Author's Structure of a mouse submaxillary messenger RNA encoding epidermal growth factor and seven related proteins‏
670 ‎‡a Author's Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom‏
670 ‎‡a Author's Subcellular recruitment by TSG118 and TSPYL implicates a role for zinc finger protein 106 in a novel developmental pathway‏
670 ‎‡a Author's Sustained expression of hepatocyte nuclear factor-6 leads to loss of pancreatic beta-cells by apoptosis‏
670 ‎‡a Author's Systemic alterations in the metabolome of diabetic NOD mice delineate increased oxidative stress accompanied by reduced inflammation and hypertriglyceremia‏
670 ‎‡a Author's T-cell receptor alpha-chain gene is split in a human T-cell leukemia cell line with a t‏
670 ‎‡a Author's T-cell receptor alpha-chain gene is split in a human T-cell leukemia cell line with a t(11;14)(p15;q11).‏
670 ‎‡a Author's TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action.‏
670 ‎‡a Author's The 24,000 dalton subunit and the activity of yeast RNA polymerases‏
670 ‎‡a Author's The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships‏
670 ‎‡a Author's The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families‏
670 ‎‡a Author's [The association of non-insulin-dependent diabetes mellitus with the genes responsible for carbohydrate and lipid metabolism in the Chinese]‏
670 ‎‡a Author's The cost-effectiveness of personalized genetic medicine: the case of genetic testing in neonatal diabetes‏
670 ‎‡a Author's The effect of pH on the structure and activity of yeast RNA polymerase I‏
670 ‎‡a Author's The genetic architecture of type 2 diabetes‏
670 ‎‡a Author's The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences‏
670 ‎‡a Author's The human glucagon gene is located on chromosome 2‏
670 ‎‡a Author's The insulin gene is located on chromosome 11 in humans‏
670 ‎‡a Author's The insulin gene is located on the short arm of chromosome 11 in humans‏
670 ‎‡a Author's The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population‏
670 ‎‡a Author's The molecular genetics of diabetes mellitus‏
670 ‎‡a Author's The population association of glucokinase gene with type 2‏
670 ‎‡a Author's The population association of glucokinase gene with type 2 (noninsulin-dependent) diabetes mellitus in Chinese‏
670 ‎‡a Author's Three Strikes and You're Cured‏
670 ‎‡a Author's Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms‏
670 ‎‡a Author's Transgenic mice with green fluorescent protein-labeled pancreatic beta -cells.‏
670 ‎‡a Author's Treatment of hyperglycemia in a 7-year-old child diagnosed with neonatal diabetes‏
670 ‎‡a Author's Tumor hypoglycemia: relationship to high molecular weight insulin-like growth factor-II.‏
670 ‎‡a Author's Two EcoRI RFLPs at the GLUT2 locus‏
670 ‎‡a Author's Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family‏
670 ‎‡a Author's Update in neonatal diabetes‏
670 ‎‡a Author's Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphism‏
670 ‎‡a Author's Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians‏
670 ‎‡a Author's Variation in the calpain-10 gene affects blood glucose levels in the British population‏
670 ‎‡a Author's Variation in the perilipin gene‏
670 ‎‡a Author's Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome‏
670 ‎‡a Author's Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease‏
670 ‎‡a Author's Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome‏
670 ‎‡a Author's Yeast DNA-dependent RNA polymerase I. A rapid procedure for the large scale purification of homogeneous enzyme‏
670 ‎‡a Author's Yeast DNA dependent RNA polymerases I, II and III. The existence of subunits common to the three enzymes‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/ISNI|0000000038911804‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/viaf/58562916‏
670 ‎‡a wikidata authority control‏ ‎‡u https://viaf.org/processed/LC|n 2008181940‏
912 ‎‡a identificationandfunctionalcharacterizationofg6pc2codingvariantsinfluencingglycemictraitsdefineaneffectortranscriptattheg6pc2abcb11locus‏ ‎‡A Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus‏ ‎‡9 1‏
912 ‎‡a erratumsequencedataandassociationstatisticsfrom12940type2diabetescasesandcontrols‏ ‎‡A Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls‏ ‎‡9 1‏
912 ‎‡a letters‏ ‎‡A Letters‏ ‎‡9 1‏
919 ‎‡a gialpha1selectivelycouplessomatostatinreceptorsubtype3toadenylylcyclaseidentificationofthefunctionaldomainsofthisalphasubunitnecessaryformediatingtheinhibitionbysomatostatinofcampformation‏ ‎‡A Gi alpha 1 selectively couples somatostatin receptor subtype 3 to adenylyl cyclase: identification of the functional domains of this alpha subunit necessary for mediating the inhibition by somatostatin of cAMP formation‏ ‎‡9 1‏
919 ‎‡a gialpha3andg‏ ‎‡A Gi alpha 3 and G‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphismatd9s328eesthbc220‏ ‎‡A Dinucleotide repeat polymorphism at D9S328E (EST hbc220).‏ ‎‡9 1‏
919 ‎‡a gialpha3andgoalphaselectivelyassociatewiththeclonedsomatostatinreceptorsubtypesstr2‏ ‎‡A Gi alpha 3 and G(o) alpha selectively associate with the cloned somatostatin receptor subtype SSTR2‏ ‎‡9 1‏
919 ‎‡a glucokinasemutationsinsulinsecretionanddiabetesmellitus‏ ‎‡A Glucokinase mutations, insulin secretion, and diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a glucokinasestructuralanalysisofaproteininvolvedinsusceptibilitytodiabetes‏ ‎‡A Glucokinase: structural analysis of a protein involved in susceptibility to diabetes‏ ‎‡9 1‏
919 ‎‡a glucosetransporterexpressioninbraincdnasequenceofmouseglut3thebrainfacilitativeglucosetransporterisoformandidentificationofsitesofexpressionbyinsituhybridization‏ ‎‡A Glucose transporter expression in brain. cDNA sequence of mouse GLUT3, the brain facilitative glucose transporter isoform, and identification of sites of expression by in situ hybridization‏ ‎‡9 1‏
919 ‎‡a glucosetransportergeneandnoninsulindependentdiabetes‏ ‎‡A Glucose transporter gene and non-insulin-dependent diabetes‏ ‎‡9 1‏
919 ‎‡a glycemiccontrolpromotespancreaticbetacellregenerationinstreptozotocininduceddiabeticmice‏ ‎‡A Glycemic control promotes pancreatic beta-cell regeneration in streptozotocin-induced diabetic mice‏ ‎‡9 1‏
919 ‎‡a hamsterpreproglucagoncontainsthesequenceofglucagonand2relatedpeptides‏ ‎‡A Hamster preproglucagon contains the sequence of glucagon and two related peptides‏ ‎‡9 1‏
919 ‎‡a hepaticfunctioninafamilywithanonsensemutationr154xinthehepatocytenuclearfactor4alphamody1gene‏ ‎‡A Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene‏ ‎‡9 1‏
919 ‎‡a highlevelexpressionofhumaninsulinreceptorcdnainmousenih3t3cells‏ ‎‡A High-level expression of human insulin receptor cDNA in mouse NIH 3T3 cells‏ ‎‡9 1‏
919 ‎‡a highresolutionchromosomallocalizationofhumangenesforamylaseproopiomelanocortinsomatostatinandadnafragmentd3s1byinsituhybridization‏ ‎‡A High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization‏ ‎‡9 1‏
919 ‎‡a hinciirflpatthehumanhexokinase1hk1locusonchromosome10‏ ‎‡A HincII RFLP at the human hexokinase I (HK1) locus on chromosome 10‏ ‎‡9 1‏
919 ‎‡a polymorphiclocusnearthehumaninsulingeneisassociatedwithinsulindependentdiabetesmelliitus‏ ‎‡A A Polymorphic Locus Near the Human Insulin Gene Is Associated with Insulin-dependent Diabetes Melliitus‏ ‎‡9 1‏
919 ‎‡a sequenceandfunctionalcharacterizationofa3inositoltrisphosphatereceptorsubtypeip3r3expressedinpancreaticisletskidneygastrointestinaltractandothertissues‏ ‎‡A Sequence and functional characterization of a third inositol trisphosphate receptor subtype, IP3R-3, expressed in pancreatic islets, kidney, gastrointestinal tract, and other tissues‏ ‎‡9 1‏
919 ‎‡a polymorphiclocusnearthehumaninsulingeneisassociatedwithinsulindependentdiabetesmellitus‏ ‎‡A A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a 2generationscreenofthehumangenomeforsusceptibilitytoinsulindependentdiabetesmellitus‏ ‎‡A A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a simpletestforthehighfrequencyp291fsinscmutationinthehnf1alphamody3gene‏ ‎‡A A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene‏ ‎‡9 1‏
919 ‎‡a hladqhaplotypesdifferbyethnicityinpatientswithchildhoodonsetdiabetes‏ ‎‡A HLA-DQ haplotypes differ by ethnicity in patients with childhood-onset diabetes‏ ‎‡9 1‏
919 ‎‡a geneticcontributionofpolymorphismoftheglut1andglut4genestothesusceptibilitytotype2‏ ‎‡A Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2‏ ‎‡9 1‏
919 ‎‡a geneticcomplexityinadrosophilamodelofdiabetesassociatedmisfoldedhumanproinsulin‏ ‎‡A Genetic complexity in a Drosophila model of diabetes-associated misfolded human proinsulin.‏ ‎‡9 1‏
919 ‎‡a humanalpha2macroglobulingeneislocatedonchromosome12‏ ‎‡A Human alpha 2-macroglobulin gene is located on chromosome 12‏ ‎‡9 1‏
919 ‎‡a humanantithrombin2at3genelengthpolymorphismrevealedbythepolymerasechainreaction‏ ‎‡A Human antithrombin II (AT3) gene length polymorphism revealed by the polymerase chain reaction‏ ‎‡9 1‏
919 ‎‡a humancollagentype2alpha1col2a1genevntrpolymorphismdetectedbygeneamplification‏ ‎‡A Human collagen, type II, alpha 1, (COL2A1) gene: VNTR polymorphism detected by gene amplification‏ ‎‡9 1‏
919 ‎‡a humanfacilitativeglucosetransportersisolationfunctionalcharacterizationandgenelocalizationofcdnasencodinganisoformglut5expressedinsmallintestinekidneymuscleandadiposetissueandanunusualglucosetransporterpseudogen‏ ‎‡A Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogen‏ ‎‡9 1‏
919 ‎‡a humanfructose16bisphosphatasegenefbp1exonintronorganizationlocalizationtochromosomebands9q222q223andmutationscreeninginsubjectswithfructose16bisphosphatasedeficiency‏ ‎‡A Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphismatd9s328e‏ ‎‡A Dinucleotide repeat polymorphism at D9S328E‏ ‎‡9 1‏
919 ‎‡a diminishedinsulinandglucagonsecretoryresponsestoarginineinnondiabeticsubjectswithamutationinthehepatocytenuclearfactor4alphamody1gene‏ ‎‡A Diminished insulin and glucagon secretory responses to arginine in nondiabetic subjects with a mutation in the hepatocyte nuclear factor-4alpha/MODY1 gene‏ ‎‡9 1‏
919 ‎‡a effectofphonthestructureandactivityofyeastrnapolymerase1‏ ‎‡A The effect of pH on the structure and activity of yeast RNA polymerase I‏ ‎‡9 1‏
919 ‎‡a differentialexpressionofsomatostatinreceptorsubtypesinbrain‏ ‎‡A Differential expression of somatostatin receptor subtypes in brain‏ ‎‡9 1‏
919 ‎‡a singleresidueasparticacid95inthedeltaopioidreceptorspecifiesselectivehighaffinityagonistbinding‏ ‎‡A A single residue, aspartic acid 95, in the delta opioid receptor specifies selective high affinity agonist binding.‏ ‎‡9 1‏
919 ‎‡a tyrosinephosphataseisassociatedwiththesomatostatinreceptor‏ ‎‡A A Tyrosine Phosphatase is Associated with the Somatostatin Receptor‏ ‎‡9 1‏
919 ‎‡a differentialexpressionofmessengerrnasforsomatostatinreceptorsubtypessstr1sstr2andsstr3inadultratbrainanalysisbyrnablottingandinsituhybridizationhistochemistry‏ ‎‡A Differential expression of messenger RNAs for somatostatin receptor subtypes SSTR1, SSTR2 and SSTR3 in adult rat brain: analysis by RNA blotting and in situ hybridization histochemistry‏ ‎‡9 1‏
919 ‎‡a geneticassociationswithobstructivesleepapneatraitsinhispaniclatinoamericans‏ ‎‡A Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans‏ ‎‡9 1‏
919 ‎‡a differentialeffectsofoverexpressedglucokinaseandhexokinase1inisolatedisletsevidenceforfunctionalsegregationofthehighandlowkmenzymes‏ ‎‡A Differential effects of overexpressed glucokinase and hexokinase I in isolated islets. Evidence for functional segregation of the high and low Km enzymes‏ ‎‡9 1‏
919 ‎‡a diagnosisandtreatmentofneonataldiabetesaunitedstatesexperience‏ ‎‡A Diagnosis and treatment of neonatal diabetes: a United States experience‏ ‎‡9 1‏
919 ‎‡a diabetesmellitusandgeneticallyprogrammeddefectsinbetacellfunction‏ ‎‡A Diabetes mellitus and genetically programmed defects in beta-cell function‏ ‎‡9 1‏
919 ‎‡a genomewidescanfortype2diabeteslociinhongkongchineseandconfirmationofasusceptibilitylocusonchromosome1q21q25‏ ‎‡A Genome-wide Scan for Type 2 Diabetes Loci in Hong Kong Chinese and Confirmation of a Susceptibility Locus on Chromosome 1q21-q25‏ ‎‡9 1‏
919 ‎‡a diabetesdependenceasymptoticsselectionandsignificance‏ ‎‡A Diabetes, dependence, asymptotics, selection and significance‏ ‎‡9 1‏
919 ‎‡a defectivepancreaticbetacellglycolyticsignalinginhepatocytenuclearfactor1alphadeficientmice‏ ‎‡A Defective pancreatic beta-cell glycolytic signaling in hepatocyte nuclear factor-1alpha-deficient mice‏ ‎‡9 1‏
919 ‎‡a defectiveinsulinsecretioninhepatocytenuclearfactor1alphadeficientmice‏ ‎‡A Defective insulin secretion in hepatocyte nuclear factor 1alpha-deficient mice‏ ‎‡9 1‏
919 ‎‡a genesforinsulin1and2parathyroidhormoneandcalcitoninareonratchromosome1‏ ‎‡A Genes for insulin I and II, parathyroid hormone, and calcitonin are on rat chromosome 1‏ ‎‡9 1‏
919 ‎‡a evolutionofbetacelldysfunctioninthemalezuckerdiabeticfattyrat‏ ‎‡A Evolution of beta-cell dysfunction in the male Zucker diabetic fatty rat‏ ‎‡9 1‏
919 ‎‡a seminarsinmedicineofthebethisraelhospitalbostonnoninsulindependentdiabetesmellitusageneticallyprogrammedfailureofthebetacelltocompensateforinsulinresistance‏ ‎‡A Seminars in Medicine of the Beth Israel Hospital, Boston. Non-insulin-dependent diabetes mellitus - a genetically programmed failure of the beta cell to compensate for insulin resistance‏ ‎‡9 1‏
919 ‎‡a generalizedresistancetothyroidhormoneassociatedwithamutationintheligandbindingdomainofthehumanthyroidhormonereceptorbeta‏ ‎‡A Generalized resistance to thyroid hormone associated with a mutation in the ligand-binding domain of the human thyroid hormone receptor beta‏ ‎‡9 1‏
919 ‎‡a selectiveinteractionof5bromodeoxyuridinesubstituteddnawithdifferentchromosomalproteins‏ ‎‡A Selective interaction of 5'-bromodeoxyuridine substituted DNA with different chromosomal proteins‏ ‎‡9 1‏
919 ‎‡a seeingisbelievinghowthemiplucmousecanadvancethefieldofislettransplantationandβcellregeneration‏ ‎‡A Seeing is believing: how the MIP-luc mouse can advance the field of islet transplantation and β-cell regeneration‏ ‎‡9 1‏
919 ‎‡a genesymbolipf1diseasemody4‏ ‎‡A Gene symbol: IPF1. Disease: MODY 4‏ ‎‡9 1‏
919 ‎‡a genefornoninsulindependentdiabetesmellitusmaturityonsetdiabetesoftheyoungsubtypeislinkedtodnapolymorphismonhumanchromosome20q‏ ‎‡A Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q‏ ‎‡9 1‏
919 ‎‡a searchingforniddmsusceptibilitygenesstudiesofgeneswithtripletrepeatsexpressedinskeletalmuscle‏ ‎‡A Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle‏ ‎‡9 1‏
919 ‎‡a genomewidescanformetabolicsyndromeandrelatedquantitativetraitsinhongkongchineseandconfirmationofasusceptibilitylocusonchromosome1q21q25‏ ‎‡A Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25.‏ ‎‡9 1‏
919 ‎‡a scopescuba2continuumobservationsofpreprotostellarevolutionsurveydescriptionandcompactsourcecatalogue‏ ‎‡A SCOPE: SCUBA-2 Continuum Observations of Pre-protostellar Evolution - survey description and compact source catalogue‏ ‎‡9 1‏
919 ‎‡a ryr2andcalpain10delineateanovelapoptosispathwayinpancreaticislets‏ ‎‡A RyR2 and calpain-10 delineate a novel apoptosis pathway in pancreatic islets‏ ‎‡9 1‏
919 ‎‡a creationofaninositol145trisphosphatesensitiveca2+storeinsecretorygranulesofinsulinproducingcells‏ ‎‡A Creation of an inositol 1,4,5-trisphosphate-sensitive Ca2+ store in secretory granules of insulin-producing cells‏ ‎‡9 1‏
919 ‎‡a humangproteincoupledinwardlyrectifyingpotassiumchannelgirk1genekcnj3localizationtochromosome2andidentificationofasimpletandemrepeatpolymorphism‏ ‎‡A Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism‏ ‎‡9 1‏
919 ‎‡a evolutionofβcelldysfunctioninthemalezuckerdiabeticfattyrat‏ ‎‡A Evolution of β-Cell Dysfunction in the Male Zucker Diabetic Fatty Rat‏ ‎‡9 1‏
919 ‎‡a gastricinhibitorypolypeptidestructureandchromosomallocalizationofthehumangene‏ ‎‡A Gastric Inhibitory Polypeptide: Structure and Chromosomal Localization of the Human Gene‏ ‎‡9 1‏
919 ‎‡a associationofnoninsulindependentdiabetesmellituswiththegenesresponsibleforcarbohydrateandlipidmetabolisminthechinese‏ ‎‡A [The association of non-insulin-dependent diabetes mellitus with the genes responsible for carbohydrate and lipid metabolism in the Chinese]‏ ‎‡9 1‏
919 ‎‡a humangenesforinsulinlikegrowthfactors1and2andepidermalgrowthfactorarelocatedon12q22q24111p15and4q25q27respectively‏ ‎‡A Human genes for insulin-like growth factors I and II and epidermal growth factor are located on 12q22----q24.1, 11p15, and 4q25----q27, respectively‏ ‎‡9 1‏
919 ‎‡a yeastartificialchromosomebasedmapoftheregionofchromosome20containingthediabetessusceptibilitygenemody1andamyeloidleukemiarelatedgene‏ ‎‡A A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene‏ ‎‡9 1‏
919 ‎‡a abnormalinsulinsecretionnotinsulinresistanceisthegeneticorprimarydefectofmodyintherwpedigree‏ ‎‡A Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree.‏ ‎‡9 1‏
919 ‎‡a exclusionofepidermalgrowthfactorandhighresolutionphysicalmappingacrosstheriegersyndromelocus‏ ‎‡A Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus‏ ‎‡9 1‏
919 ‎‡a humanglucagonlikepeptide1receptorgenelocalizationtochromosomeband6p21byfluorescenceinsituhybridizationandlinkageofahighlypolymorphicsimpletandemrepeatdnapolymorphismtoothermarkersonchromosome6‏ ‎‡A Human glucagon-like peptide-1 receptor gene. Localization to chromosome band 6p21 by fluorescence in situ hybridization and linkage of a highly polymorphic simple tandem repeat DNA polymorphism to other markers on chromosome 6‏ ‎‡9 1‏
919 ‎‡a roleofbh3onlymoleculesbimandpumainβcelldeathinpdx1deficiency‏ ‎‡A Role of BH3-only molecules Bim and Puma in β-cell death in Pdx1 deficiency‏ ‎‡9 1‏
919 ‎‡a ribosomalrnagenesofsaccharomycescerevisiae2physicalmapandnucleotidesequenceofthe5sribosomalrnageneandadjacentintergenicregions‏ ‎‡A Ribosomal RNA genes of Saccharomyces cerevisiae. II. Physical map and nucleotide sequence of the 5 S ribosomal RNA gene and adjacent intergenic regions‏ ‎‡9 1‏
919 ‎‡a humanglut4musclefatglucosetransportergenecharacterizationandgeneticvariation‏ ‎‡A Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation‏ ‎‡9 1‏
919 ‎‡a abnormalnephrondevelopmentassociatedwithaframeshiftmutationinthetranscriptionfactorhepatocytenuclearfactor1beta‏ ‎‡A Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta‏ ‎‡9 1‏
919 ‎‡a adaptationtohyperglycemiaenhancesinsulinsecretioninglucokinasemutantmice‏ ‎‡A Adaptation to hyperglycemia enhances insulin secretion in glucokinase mutant mice‏ ‎‡9 1‏
919 ‎‡a humanhexokinase2geneexonintronorganizationmutationscreeninginniddmanditsrelationshiptomusclehexokinaseactivity‏ ‎‡A Human hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activity‏ ‎‡9 1‏
919 ‎‡a agonistsandantagonistsbindtodifferentdomainsoftheclonedkappaopioidreceptor‏ ‎‡A Agonists and antagonists bind to different domains of the cloned kappa opioid receptor‏ ‎‡9 1‏
919 ‎‡a humanhexokinase2localizationofthepolymorphicgenetochromosome2‏ ‎‡A Human hexokinase II: localization of the polymorphic gene to chromosome 2.‏ ‎‡9 1‏
919 ‎‡a humanhexokinasesequencesofaminoandcarboxylterminalhalvesarehomologous‏ ‎‡A Human hexokinase: sequences of amino- and carboxyl-terminal halves are homologous‏ ‎‡9 1‏
919 ‎‡a humaninsulinlikegrowthfactor1and2messengerrnaisolationofcomplementarydnaandanalysisofexpression‏ ‎‡A Human insulin-like growth factor I and II messenger RNA: isolation of complementary DNA and analysis of expression‏ ‎‡9 1‏
919 ‎‡a humaninsulinreceptorgene‏ ‎‡A Human insulin-receptor gene‏ ‎‡9 1‏
919 ‎‡a alterationsintcf7l2expressiondefineitsroleasakeyregulatorofglucosemetabolism‏ ‎‡A Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism‏ ‎‡9 1‏
919 ‎‡a ribosomalrnagenesofsaccharomycescerevisiae1physicalmapoftherepeatingunitandlocationoftheregionscodingfor5s58s18sand25sribosomalrnas‏ ‎‡A Ribosomal RNA genes of Saccharomyces cerevisiae. I. Physical map of the repeating unit and location of the regions coding for 5 S, 5.8 S, 18 S, and 25 S ribosomal RNAs‏ ‎‡9 1‏
919 ‎‡a rflpforthehumantransforminggrowthfactorbeta1genetgfbonchromosome19‏ ‎‡A RFLP for the human transforming growth factor beta-1 gene (TGFB) on chromosome 19.‏ ‎‡9 1‏
919 ‎‡a exomesequencingandgenetictestingformody‏ ‎‡A Exome sequencing and genetic testing for MODY.‏ ‎‡9 1‏
919 ‎‡a aggregationofthe5insulingenepolymorphismininsulindependenttype1diabetesmellitusfamilies‏ ‎‡A The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families‏ ‎‡9 1‏
919 ‎‡a gproteinactivatedinwardlyrectifyingpotassiumchannelgirk1kgamrnainadultratheartandbrainbyinsituhybridizationhistochemistry‏ ‎‡A G protein-activated inwardly rectifying potassium channel (GIRK1/KGA) mRNA in adult rat heart and brain by in situ hybridization histochemistry‏ ‎‡9 1‏
919 ‎‡a alteredinsulinsecretoryresponsestoglucoseindiabeticandnondiabeticsubjectswithmutationsinthediabetessusceptibilitygenemody3onchromosome12‏ ‎‡A Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12.‏ ‎‡9 1‏
919 ‎‡a alteredinsulinsecretoryresponsestoglucoseinsubjectswithamutationinthemody1geneonchromosome20‏ ‎‡A Altered insulin secretory responses to glucose in subjects with a mutation in the MODY1 gene on chromosome 20.‏ ‎‡9 1‏
919 ‎‡a alternativesplicingofhumaninsulinreceptormessengerrna‏ ‎‡A Alternative splicing of human insulin receptor messenger RNA.‏ ‎‡9 1‏
919 ‎‡a alternativesplicingofhumaninwardlyrectifyingk+channelromk1mrna‏ ‎‡A Alternative splicing of human inwardly rectifying K+ channel ROMK1 mRNA‏ ‎‡9 1‏
919 ‎‡a approachforidentifyingsimplesequencerepeatdnapolymorphismsnearclonedcdnasandgeneslinkagestudiesoftheisletamyloidpolypeptideamylinandliverglycogensynthasegenesandniddm‏ ‎‡A An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.‏ ‎‡9 1‏
919 ‎‡a invivocisregulatoryscreenatthetype2diabetesassociatedtcf7l2locusidentifiesmultipletissuespecificenhancers‏ ‎‡A An in vivo cis-regulatory screen at the type 2 diabetes associated TCF7L2 locus identifies multiple tissue-specific enhancers‏ ‎‡9 1‏
919 ‎‡a analysisoftheregionsflankingthehumaninsulingeneandsequenceofanalufamilymember‏ ‎‡A Analysis of the regions flanking the human insulin gene and sequence of an Alu family member‏ ‎‡9 1‏
919 ‎‡a antidiabeticeffectofginsenosidereinobobmice‏ ‎‡A Anti-diabetic effect of ginsenoside Re in ob/ob mice‏ ‎‡9 1‏
919 ‎‡a apa1andsst1rflpsattheinsulinlikegrowthfactor2igf2locusonchromosome11‏ ‎‡A Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11.‏ ‎‡9 1‏
919 ‎‡a appalachianspringvariationsonancientgastroenteropancreaticthemesinnewworldmammals‏ ‎‡A Appalachian spring: variations on ancient gastro-entero-pancreatic themes in New World mammals‏ ‎‡9 1‏
919 ‎‡a humaninsulinreceptorgenepartialsequenceandamplificationofexonsbypolymerasechainreaction‏ ‎‡A Human insulin-receptor gene. Partial sequence and amplification of exons by polymerase chain reaction‏ ‎‡9 1‏
919 ‎‡a humaninsulinreceptorsubstrate1geneirs1chromosomallocalizationto2q35q361andidentificationofasimpletandemrepeatdnapolymorphism‏ ‎‡A Human insulin receptor substrate-1 gene (IRS1): chromosomal localization to 2q35-q36.1 and identification of a simple tandem repeat DNA polymorphism‏ ‎‡9 1‏
919 ‎‡a assignmentofhumanpotassiumchannelgenekcna4kv14pcn2tochromosome11q134q141‏ ‎‡A Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1‏ ‎‡9 1‏
919 ‎‡a humanintestinalglucosetransporterexpressionandlocalizationofglut5‏ ‎‡A Human intestinal glucose transporter expression and localization of GLUT5.‏ ‎‡9 1‏
919 ‎‡a humanisletamyloidpolypeptidegenecompletenucleotidesequencechromosomallocalizationandevolutionaryhistory‏ ‎‡A Human islet amyloid polypeptide gene: complete nucleotide sequence, chromosomal localization, and evolutionary history‏ ‎‡9 1‏
919 ‎‡a costeffectivenessofmodygenetictestingtranslatinggenomicadvancesintopracticalhealthapplications‏ ‎‡A Cost-effectiveness of MODY genetic testing: translating genomic advances into practical health applications.‏ ‎‡9 1‏
919 ‎‡a humanoct3genefamilycdnasequencesalternativesplicinggeneorganizationchromosomallocationandexpressionatlowlevelsinadulttissues‏ ‎‡A Human Oct3 gene family: cDNA sequences, alternative splicing, gene organization, chromosomal location, and expression at low levels in adult tissues‏ ‎‡9 1‏
919 ‎‡a assignmentofslc6a9tohumanchromosomeband1p33byinsituhybridization‏ ‎‡A Assignment of SLC6A9 to human chromosome band 1p33 by in situ hybridization‏ ‎‡9 1‏
919 ‎‡a humanpancreaticbetacellglucokinasecdnasequenceandlocalizationofthepolymorphicgenetochromosome7bandp13‏ ‎‡A Human pancreatic beta-cell glucokinase: cDNA sequence and localization of the polymorphic gene to chromosome 7, band p 13‏ ‎‡9 1‏
919 ‎‡a humansomatostatinreceptorgeneslocalizationofsstr5tohumanchromosome20p112‏ ‎‡A Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2‏ ‎‡9 1‏
919 ‎‡a humansomatostatinreceptorgeneslocalizationtohumanchromosomes1417and22andidentificationofsimpletandemrepeatpolymorphisms‏ ‎‡A Human somatostatin receptor genes: localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms‏ ‎‡9 1‏
919 ‎‡a humantype1pituitaryadenylatecyclaseactivatingpolypeptidereceptoradcyap1rlocalizationtochromosomeband7p14andintegrationintothecytogeneticphysicalandgeneticmapofchromosome7‏ ‎‡A Human type I pituitary adenylate cyclase activating polypeptide receptor (ADCYAP1R): localization to chromosome band 7p14 and integration into the cytogenetic, physical, and genetic map of chromosome 7.‏ ‎‡9 1‏
919 ‎‡a hyperexcitabilitytosulphonylureainmody3‏ ‎‡A Hyperexcitability to sulphonylurea in MODY3.‏ ‎‡9 1‏
919 ‎‡a assignmentofthegastricinhibitorypolypeptidereceptorgenegiprtochromosomebands19q132q133byfluorescenceinsituhybridization‏ ‎‡A Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization‏ ‎‡9 1‏
919 ‎‡a identificationof14newglucokinasemutationsanddescriptionoftheclinicalprofileof42mody2families‏ ‎‡A Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families‏ ‎‡9 1‏
919 ‎‡a identificationofaligandbindingregionofthehumaninsulinreceptorencodedbythe2exonofthegene‏ ‎‡A Identification of a ligand-binding region of the human insulin receptor encoded by the second exon of the gene‏ ‎‡9 1‏
919 ‎‡a identificationofdiabeticretinopathygenesthroughagenomewideassociationstudyamongmexicanamericansfromstarrcountytexas‏ ‎‡A Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas‏ ‎‡9 1‏
919 ‎‡a identificationofgestationallyregulatedgenesinratmyometriumbyuseofmessengerribonucleicaciddifferentialdisplay‏ ‎‡A Identification of gestationally regulated genes in rat myometrium by use of messenger ribonucleic acid differential display‏ ‎‡9 1‏
919 ‎‡a restingbetacellsafunctionalreserve‏ ‎‡A Resting beta-cells - A functional reserve?‏ ‎‡9 1‏
919 ‎‡a identificationofmicrosatellitemarkersnearthehumangenesencodingthebetacellatpsensitivek+channelandlinkagestudieswithniddminjapanese‏ ‎‡A Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese‏ ‎‡9 1‏
919 ‎‡a relationshipofinsulinreceptorsubstrate1and2genotypestophenotypicfeaturesofpolycysticovarysyndrome‏ ‎‡A Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome‏ ‎‡9 1‏
919 ‎‡a relationshipofcalpain10genotypetophenotypicfeaturesofpolycysticovarysyndrome‏ ‎‡A Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome‏ ‎‡9 1‏
919 ‎‡a regulationofglucosetransportermessengerrnalevelsinratadiposetissuebyinsulin‏ ‎‡A Regulation of glucose transporter messenger RNA levels in rat adipose tissue by insulin.‏ ‎‡9 1‏
919 ‎‡a assignmentofthegeneencodingglycogensynthasegystohumanchromosome19bandq133‏ ‎‡A Assignment of the gene encoding glycogen synthase (GYS) to human chromosome 19, band q13.3.‏ ‎‡9 1‏
919 ‎‡a assignmentofthegeneencodingthealpha1subunitoftheneuroendocrinebraintypecalciumchannelcacnl1a2tohumanchromosome3bandp143‏ ‎‡A Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3‏ ‎‡9 1‏
919 ‎‡a identificationofmicrosatellitemarkersnearthehumanobgeneandlinkagestudiesinniddmaffectedsibpairs‏ ‎‡A Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs‏ ‎‡9 1‏
919 ‎‡a associationofalowfrequencyvariantinhnf1awithtype2diabetesinalatinopopulation‏ ‎‡A Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population‏ ‎‡9 1‏
919 ‎‡a identificationof9novelmutationsinthehepatocytenuclearfactor1alphageneassociatedwithmaturityonsetdiabetesoftheyoung‏ ‎‡A Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young‏ ‎‡9 1‏
919 ‎‡a identificationof9novelmutationsinthehepatocytenuclearfactor1alphageneassociatedwithmaturityonsetdiabetesoftheyoungmody3‏ ‎‡A Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)‏ ‎‡9 1‏
919 ‎‡a identificationof3missensemutationsintheperoxisomeproliferatoractivatedreceptoralphageneinjapanesesubjectswithmaturityonsetdiabetesoftheyoung‏ ‎‡A Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young‏ ‎‡9 1‏
919 ‎‡a identificationoftype2diabetesgenesinmexicanamericansthroughgenomewideassociationstudies‏ ‎‡A Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies‏ ‎‡9 1‏
919 ‎‡a imagingbetacelldevelopmentinrealtimeusingpancreaticexplantsfrommicewithgreenfluorescentproteinlabeledpancreaticbetacells‏ ‎‡A Imaging Beta cell development in real-time using pancreatic explants from mice with green fluorescent protein-labeled pancreatic Beta cells‏ ‎‡9 1‏
919 ‎‡a immunologicaldetectionofisoformsofthesomatostatinreceptorsubtypesstr2‏ ‎‡A Immunological detection of isoforms of the somatostatin receptor subtype, SSTR2.‏ ‎‡9 1‏
919 ‎‡a impairedinsulinsecretionintransgenicmiceoverexpressingcalpastatininpancreaticβcells‏ ‎‡A Impaired insulin secretion in transgenic mice over-expressing calpastatin in pancreatic β-cells‏ ‎‡9 1‏
919 ‎‡a invitroprocessingandsecretionofmutantinsulinproteinsthatcausepermanentneonataldiabetes‏ ‎‡A In vitro processing and secretion of mutant insulin proteins that cause permanent neonatal diabetes‏ ‎‡9 1‏
919 ‎‡a associationofgeneticvariationofthetransforminggrowthfactoralphagenewithcleftlipandpalate‏ ‎‡A Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate‏ ‎‡9 1‏
919 ‎‡a associationoftheauatrichelementpolymorphisminppp1r3withhormonalandmetabolicfeaturesofpolycysticovarysyndrome‏ ‎‡A Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome‏ ‎‡9 1‏
919 ‎‡a associationofthecalpain10genewithtype2diabetesineuropeansresultsofpooledandmetaanalyses‏ ‎‡A Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphismatthehumanglut2locus‏ ‎‡A Dinucleotide repeat polymorphism at the human GLUT2 locus‏ ‎‡9 1‏
919 ‎‡a associationofthecalpain10genewithtype2diabetesmellitusinamexicanpopulation‏ ‎‡A Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population‏ ‎‡9 1‏
919 ‎‡a associationofthekcnj11variante23kwithtype2diabetesinindotrinidadians‏ ‎‡A Association of the KCNJ11 variant E23K with type 2 diabetes in Indo-Trinidadians‏ ‎‡9 1‏
919 ‎‡a reducedskeletalmusclecalpain10transcriptlevelisduetoacumulativedecreaseinmajorisoforms‏ ‎‡A Reduced skeletal muscle calpain-10 transcript level is due to a cumulative decrease in major isoforms‏ ‎‡9 1‏
919 ‎‡a bamhirflpattheglut3locus‏ ‎‡A BamHI RFLP at the GLUT3 locus‏ ‎‡9 1‏
919 ‎‡a bamhirflpattheinsulinlikegrowthfactor2igf2locusonchromosome11‏ ‎‡A BamHI RFLP at the insulin-like growth factor II (IGF2) locus on chromosome 11‏ ‎‡9 1‏
919 ‎‡a invivomeasurementandbiologicalcharacterisationofthediabetesassociatedmutantinsulinpr46q‏ ‎‡A In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q‏ ‎‡9 1‏
919 ‎‡a evidenceofnonpancreaticbetacelldependentrolesoftcf7l2intheregulationofglucosemetabolisminmice‏ ‎‡A Evidence of non-pancreatic beta cell-dependent roles of Tcf7l2 in the regulation of glucose metabolism in mice‏ ‎‡9 1‏
919 ‎‡a betacelltranscriptionfactorsanddiabetesmutationsinthecodingregionofthebeta2neurod1neurod1andnkx22nkx2bgenesarenotassociatedwithmaturityonsetdiabetesoftheyounginjapanese‏ ‎‡A Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese‏ ‎‡9 1‏
919 ‎‡a evidenceforafamilyofhumanglucosetransporterlikeproteinssequenceandgenelocalizationofaproteinexpressedinfetalskeletalmuscleandothertissues‏ ‎‡A Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues‏ ‎‡9 1‏
919 ‎‡a reducedpancreaticpolypeptideresponsetohypoglycemiaandamylinresponsetoarginineinsubjectswithamutationinthehnf4alphamody1gene‏ ‎‡A Reduced pancreatic polypeptide response to hypoglycemia and amylin response to arginine in subjects with a mutation in the HNF-4alpha/MODY1 gene‏ ‎‡9 1‏
919 ‎‡a betacelltranscriptionfactorsanddiabetesnoevidencefordiabetesassociatedmutationsinthegeneencodingthebasichelixloophelixtranscriptionfactorneurogenicdifferentiation4‏ ‎‡A beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4‏ ‎‡9 1‏
919 ‎‡a betacelltranscriptionfactorsanddiabetesnoevidencefordiabetesassociatedmutationsinthegeneencodingthebasichelixloophelixtranscriptionfactorneurogenicdifferentiation4neurod4injapanesepatientswithmody‏ ‎‡A beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY.‏ ‎‡9 1‏
919 ‎‡a invivomeasurementandbiologicalcharacterisationofthediabetesassociatedmutantinsulinpr46qglnb22insulin‏ ‎‡A In vivo measurement and biological characterisation of the diabetes-associated mutant insulin p.R46Q (GlnB22-insulin).‏ ‎‡9 1‏
919 ‎‡a betacelltranscriptionfactorsanddiabetesnoevidencefordiabetesassociatedmutationsinthehepatocytenuclearfactor3betagene‏ ‎‡A Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene‏ ‎‡9 1‏
919 ‎‡a increaseinserumleptinanduterineleptinreceptormessengerrnalevelsduringpregnancyinrats‏ ‎‡A Increase in serum leptin and uterine leptin receptor messenger RNA levels during pregnancy in rats‏ ‎‡9 1‏
919 ‎‡a yeastdnadependentrnapolymerases12and3theexistenceofsubunitscommontothe3enzymes‏ ‎‡A Yeast DNA dependent RNA polymerases I, II and III. The existence of subunits common to the three enzymes‏ ‎‡9 1‏
919 ‎‡a evaluatingthecontributionofrarevariantstotype2diabetesandrelatedtraitsusingpedigrees‏ ‎‡A Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees‏ ‎‡9 1‏
919 ‎‡a yeastdnadependentrnapolymerase1arapidprocedureforthelargescalepurificationofhomogeneousenzyme‏ ‎‡A Yeast DNA-dependent RNA polymerase I. A rapid procedure for the large scale purification of homogeneous enzyme‏ ‎‡9 1‏
919 ‎‡a variationwithinthetype2diabetessusceptibilitygenecalpain10andpolycysticovarysyndrome‏ ‎‡A Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome‏ ‎‡9 1‏
919 ‎‡a erratumtoclinicalandmoleculargeneticsofneonataldiabetesduetomutationsintheinsulingene‏ ‎‡A Erratum to: Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene‏ ‎‡9 1‏
919 ‎‡a genomewideassociationstudyofstaphylococcusaureuscarriageinacommunitybasedsampleofmexicanamericansinstarrcountytexas‏ ‎‡A Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphismatthehumanribophorin2locus‏ ‎‡A Dinucleotide repeat polymorphism at the human ribophorin II locus‏ ‎‡9 1‏
919 ‎‡a variationofapolipoproteinbgeneisassociatedwithobesityhighbloodcholesterollevelsandincreasedriskofcoronaryheartdisease‏ ‎‡A Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease‏ ‎‡9 1‏
919 ‎‡a ratinwardlyrectifyingpotassiumchannelkir62cloningelectrophysiologicalcharacterizationanddecreasedexpressioninpancreaticisletsofmalezuckerdiabeticfattyrats‏ ‎‡A Rat inwardly rectifying potassium channel Kir6.2: cloning electrophysiological characterization, and decreased expression in pancreatic islets of male Zucker diabetic fatty rats‏ ‎‡9 1‏
919 ‎‡a pvuiipolymorphicsitesinthehumaninsulinreceptorgeneinsr‏ ‎‡A PvuII polymorphic sites in the human insulin receptor gene INSR‏ ‎‡9 1‏
919 ‎‡a betacelltranscriptionfactorsanddiabetesnoevidencefordiabetesassociatedmutationsinthehepatocytenuclearfactor3betagenehnf3binjapanesepatientswithmaturityonsetdiabetesoftheyoung‏ ‎‡A Beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the hepatocyte nuclear factor-3beta gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young‏ ‎‡9 1‏
919 ‎‡a beyondtype2diabetesobesityandhypertensionanaxisincludingsleepapnealeftventricularhypertrophyendothelialdysfunctionandaorticstiffnessamongmexicanamericansinstarrcountytexas‏ ‎‡A Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas‏ ‎‡9 1‏
919 ‎‡a bgl2rflpatthehumanerythrocytehepg2typeglucosetransporterglutlocusonchromosome1‏ ‎‡A Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1.‏ ‎‡9 1‏
919 ‎‡a increaseinserumleptinanduterineleptinreceptormessengerrnalevelsduringpregnancyinrats1‏ ‎‡A Increase in Serum Leptin and Uterine Leptin Receptor Messenger RNA Levels during Pregnancy in Rats1‏ ‎‡9 1‏
919 ‎‡a functionallyorientedanalysisofcardiometabolictraitsinatransethnicsample‏ ‎‡A Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample‏ ‎‡9 1‏
919 ‎‡a calpain10isacomponentoftheobesityrelatedquantitativetraitlocusadip1‏ ‎‡A Calpain-10 is a component of the obesity-related quantitative trait locus Adip1.‏ ‎‡9 1‏
919 ‎‡a increasedexpressionofendothelinbreceptormrnafollowingsubarachnoidhemorrhageinmonkeys‏ ‎‡A Increased expression of endothelin B receptor mRNA following subarachnoid hemorrhage in monkeys‏ ‎‡9 1‏
919 ‎‡a 31900regionofchromosome11includingtheobesitygenetubbyandatpsensitivepotassiumchannelgenessur1andkir62doesnotcontainamajorsusceptibilitylocusforniddmin127nonhispanicwhiteaffectedsibships‏ ‎‡A The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships‏ ‎‡9 1‏
919 ‎‡a 24000daltonsubunitandtheactivityofyeastrnapolymerases‏ ‎‡A The 24,000 dalton subunit and the activity of yeast RNA polymerases‏ ‎‡9 1‏
919 ‎‡a variationintheperilipingeneplinaffectsglucoseandlipidmetabolisminnonhispanicwhitewomenwithandwithoutpolycysticovarysyndrome‏ ‎‡A Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome‏ ‎‡9 1‏
919 ‎‡a variationintheperilipingene‏ ‎‡A Variation in the perilipin gene‏ ‎‡9 1‏
919 ‎‡a epilepsyintheunitedkingdomseizurefrequencyandseverityantiepilepticdrugutilizationandimpactonlifein1652peoplewithepilepsy‏ ‎‡A Epilepsy in the United Kingdom: seizure frequency and severity, anti-epileptic drug utilization and impact on life in 1652 people with epilepsy‏ ‎‡9 1‏
919 ‎‡a variationinthecalpain10geneaffectsbloodglucoselevelsinthebritishpopulation‏ ‎‡A Variation in the calpain-10 gene affects blood glucose levels in the British population‏ ‎‡9 1‏
919 ‎‡a calpainsystemregulatesmusclemassandglucosetransporterglut4turnover‏ ‎‡A Calpain system regulates muscle mass and glucose transporter GLUT4 turnover‏ ‎‡9 1‏
919 ‎‡a calpainsplayaroleininsulinsecretionandaction‏ ‎‡A Calpains play a role in insulin secretion and action‏ ‎‡9 1‏
919 ‎‡a candidategenestudiesinpedigreeswithmaturityonsetdiabetesoftheyoungnotlinkedwithglucokinase‏ ‎‡A Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase‏ ‎‡9 1‏
919 ‎‡a tcf7l2variantrs7903146affectstheriskoftype2diabetesbymodulatingincretinaction‏ ‎‡A TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action.‏ ‎‡9 1‏
919 ‎‡a cdnasequenceandlocalizationofpolymorphichumancytosolicphosphoenolpyruvatecarboxykinasegenepck1tochromosome20bandq1331pck1isnottightlylinkedtomaturityonsetdiabetesoftheyoung‏ ‎‡A cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young‏ ‎‡9 1‏
919 ‎‡a inhibitionofcellproliferationbythesomatostatinanaloguerc160ismediatedbysomatostatinreceptorsubtypessstr2andsstr5throughdifferentmechanisms‏ ‎‡A Inhibition of cell proliferation by the somatostatin analogue RC-160 is mediated by somatostatin receptor subtypes SSTR2 and SSTR5 through different mechanisms‏ ‎‡9 1‏
919 ‎‡a cdnasequencecodingforhumankidneycatalase‏ ‎‡A cDNA sequence coding for human kidney catalase‏ ‎‡9 1‏
919 ‎‡a changesinendothelialnitricoxidesynthasemrnaduringvasospasmaftersubarachnoidhemorrhageinmonkeys‏ ‎‡A Changes in endothelial nitric oxide synthase mRNA during vasospasm after subarachnoid hemorrhage in monkeys‏ ‎‡9 1‏
919 ‎‡a changesinpancreaticisletglucokinaseandhexokinaseactivitieswithincreasingageobesityandtheonsetofdiabetes‏ ‎‡A Changes in Pancreatic Islet Glucokinase and Hexokinase Activities With Increasing Age, Obesity, and the Onset of Diabetes‏ ‎‡9 1‏
919 ‎‡a propertiesofapolymorphicdnasegmentinthe5flankingregionofthehumaninsulingene‏ ‎‡A Properties of a polymorphic DNA segment in the 5' flanking region of the human insulin gene‏ ‎‡9 1‏
919 ‎‡a prevalenceofinsulingenemutationsinnoninsulindependentdiabetesmellitus‏ ‎‡A Prevalence of insulin-gene mutations in non-insulin-dependent diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a polymorphisminexon4aofthehumanglut4musclefatfacilitativeglucosetransportergenedetectedbysscp‏ ‎‡A Polymorphism in exon 4a of the human GLUT4/ muscle-fat facilitative glucose transporter gene detected by SSCP.‏ ‎‡9 1‏
919 ‎‡a polymorphichumansomatostatingeneislocatedonchromosome3‏ ‎‡A Polymorphic human somatostatin gene is located on chromosome 3‏ ‎‡9 1‏
919 ‎‡a inositol145trisphosphatereceptorssecretorygranulesandsecretioninendocrineandneuroendocrinecells‏ ‎‡A Inositol 1,4,5-trisphosphate receptors, secretory granules and secretion in endocrine and neuroendocrine cells‏ ‎‡9 1‏
919 ‎‡a insulingenemutationsasacauseofpermanentneonataldiabetes‏ ‎‡A Insulin gene mutations as a cause of permanent neonatal diabetes‏ ‎‡9 1‏
919 ‎‡a insulinlikegrowthfactor2geneexpressioninwilmstumourandembryonictissues‏ ‎‡A Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.‏ ‎‡9 1‏
919 ‎‡a chapter1isolationandassayofeukaryoticdnadependentrnapolymerases‏ ‎‡A Chapter 1. Isolation and Assay of Eukaryotic DNA-Dependent RNA Polymerases‏ ‎‡9 1‏
919 ‎‡a polymorphichumaninsulinresponsiveglucosetransportergeneonchromosome17p13‏ ‎‡A Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphismatthehumanribophorin2locusrpn2onchromosome20q‏ ‎‡A Dinucleotide repeat polymorphism at the human ribophorin II locus (RPN2) on chromosome 20q‏ ‎‡9 1‏
919 ‎‡a characterizationandexpressionofhumanhepg2erythrocyteglucosetransportergene‏ ‎‡A Characterization and expression of human HepG2/erythrocyte glucose-transporter gene‏ ‎‡9 1‏
919 ‎‡a genomewideassociationandmetaanalysisinpopulationsfromstarrcountytexasandmexicocityidentifytype2diabetessusceptibilitylociandenrichmentforexpressionquantitativetraitlociintopsignals‏ ‎‡A Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals‏ ‎‡9 1‏
919 ‎‡a insulinmutationscreeningin1044patientswithdiabetesmutationsintheinsgeneareacommoncauseofneonataldiabetesbutararecauseofdiabetesdiagnosedinchildhoodoradulthood‏ ‎‡A Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood‏ ‎‡9 1‏
919 ‎‡a characterizationofa3humanthyroidhormonereceptorcoexpressedwithotherthyroidhormonereceptorsinseveraltissues‏ ‎‡A Characterization of a third human thyroid hormone receptor coexpressed with other thyroid hormone receptors in several tissues‏ ‎‡9 1‏
919 ‎‡a variantswithinthecalpain10geneonchromosome2q37niddm1andrelationshipstotype2diabetesinsulinresistanceandimpairedacuteinsulinsecretionamongscandinaviancaucasians‏ ‎‡A Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians‏ ‎‡9 1‏
919 ‎‡a variablenumbersofpepsinogengenesarelocatedinthecentromericregionofhumanchromosome11anddeterminethehighfrequencyelectrophoreticpolymorphism‏ ‎‡A Variable numbers of pepsinogen genes are located in the centromeric region of human chromosome 11 and determine the high-frequency electrophoretic polymorphism‏ ‎‡9 1‏
919 ‎‡a updateinneonataldiabetes‏ ‎‡A Update in neonatal diabetes‏ ‎‡9 1‏
919 ‎‡a geneticsandpathophysiologyofneonataldiabetesmellitus‏ ‎‡A Genetics and pathophysiology of neonatal diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a insulinpromoterfactor1mutationsanddiabetesintrinidadidentificationofanoveldiabetesassociatedmutatione224kinanindotrinidadianfamily‏ ‎‡A Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family‏ ‎‡9 1‏
919 ‎‡a characterizationofa3simpletandemrepeatpolymorphisminthehumanglucokinasegene‏ ‎‡A Characterization of a third simple tandem repeat polymorphism in the human glucokinase gene‏ ‎‡9 1‏
919 ‎‡a polymorphichumanglucosetransportergeneglutisonchromosome1p313p35‏ ‎‡A Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35‏ ‎‡9 1‏
919 ‎‡a insulinreceptorandapolipoproteingenescontributetodevelopmentofniddminchineseamericans‏ ‎‡A Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans‏ ‎‡9 1‏
919 ‎‡a characterizationofathyroidhormonereceptorexpressedinhumankidneyandothertissues‏ ‎‡A Characterization of a thyroid hormone receptor expressed in human kidney and other tissues‏ ‎‡9 1‏
919 ‎‡a characterizationofclonedsomatostatinreceptorssstr4andsstr5‏ ‎‡A Characterization of cloned somatostatin receptors SSTR4 and SSTR5.‏ ‎‡9 1‏
919 ‎‡a characterizationofglucokinasemutationsassociatedwithmaturityonsetdiabetesoftheyoungtype2mody2differentglucokinasedefectsleadtoacommonphenotype‏ ‎‡A Characterization of glucokinase mutations associated with maturity-onset diabetes of the young type 2 (MODY-2): different glucokinase defects lead to a common phenotype‏ ‎‡9 1‏
919 ‎‡a polymorphicdnaregionadjacenttothe5endofthehumaninsulingene‏ ‎‡A Polymorphic DNA region adjacent to the 5' end of the human insulin gene‏ ‎‡9 1‏
919 ‎‡a enhancingpancreaticbetacellregenerationinvivowithpioglitazoneandalogliptin‏ ‎‡A Enhancing pancreatic Beta-cell regeneration in vivo with pioglitazone and alogliptin‏ ‎‡9 1‏
919 ‎‡a phosphorylationofyeastrnapolymerases‏ ‎‡A Phosphorylation of yeast RNA polymerases‏ ‎‡9 1‏
919 ‎‡a phosphorylationofyeastdnadependentrnapolymerasesinvivoandinvitroisolationofenzymesandidentificationofphosphorylatedsubunits‏ ‎‡A Phosphorylation of yeast DNA-dependent RNA polymerases in vivo and in vitro. Isolation of enzymes and identification of phosphorylated subunits‏ ‎‡9 1‏
919 ‎‡a phenotypicheterogeneitybetweendifferentmutationsofmodysubtypesandwithinmodypedigrees‏ ‎‡A Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees‏ ‎‡9 1‏
919 ‎‡a pharmacologicalcharacterizationoftheclonedkappadeltaandmuopioidreceptors‏ ‎‡A Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors.‏ ‎‡9 1‏
919 ‎‡a permanentneonataldiabetesduetomutationsinkcnj11encodingkir62patientcharacteristicsandinitialresponsetosulfonylureatherapy‏ ‎‡A Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy‏ ‎‡9 1‏
919 ‎‡a patternsoflinkagedisequilibriuminthetype2diabetesgenecalpain10‏ ‎‡A Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10.‏ ‎‡9 1‏
919 ‎‡a patientsperspectivesonservicesforepilepsyasurveyofpatientsatisfactionpreferencesandinformationprovisionin2394peoplewithepilepsy‏ ‎‡A Patients’ perspectives on services for epilepsy: a survey of patient satisfaction, preferences and information provision in 2394 people with epilepsy‏ ‎‡9 1‏
919 ‎‡a parasexualanalysisofhumanpepsinogenmolecularheterogeneity‏ ‎‡A Parasexual analysis of human pepsinogen molecular heterogeneity‏ ‎‡9 1‏
919 ‎‡a characterizationofjapanesefamilieswithearlyonsettype2‏ ‎‡A Characterization of Japanese families with early-onset type 2‏ ‎‡9 1‏
919 ‎‡a insulinresistantdiabetesduetoapointmutationthatpreventsinsulinproreceptorprocessing‏ ‎‡A Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing‏ ‎‡9 1‏
919 ‎‡a insulinsecretoryabnormalitiesinsubjectswithhyperglycemiaduetoglucokinasemutations‏ ‎‡A Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations‏ ‎‡9 1‏
919 ‎‡a characterizationofjapanesefamilieswithearlyonsettype2noninsulindependentdiabetesmellitusandscreeningformutationsintheglucokinaseandmitochondrialtrnaleuuurgenes‏ ‎‡A Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes‏ ‎‡9 1‏
919 ‎‡a chromosomalassignmentandtissuedistributionofnovelexpressedsequencetagsfromahumanpancreaticisletcdnalibrary‏ ‎‡A Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library‏ ‎‡9 1‏
919 ‎‡a organizationofthehumanglut2pancreaticbetacellandhepatocyteglucosetransportergene‏ ‎‡A Organization of the human GLUT2 (pancreatic beta-cell and hepatocyte) glucose transporter gene‏ ‎‡9 1‏
919 ‎‡a organizationofthehumanglut2‏ ‎‡A Organization of the human GLUT2‏ ‎‡9 1‏
919 ‎‡a chromosomalassignmentsofgenesfortrypsinchymotrypsinbandelastaseinmouse‏ ‎‡A Chromosomal assignments of genes for trypsin, chymotrypsin B, and elastase in mouse‏ ‎‡9 1‏
919 ‎‡a chromosomalassignmentsofhumangenesforserineproteasestrypsinchymotrypsinbandelastase‏ ‎‡A Chromosomal assignments of human genes for serine proteases trypsin, chymotrypsin B, and elastase‏ ‎‡9 1‏
919 ‎‡a chromosomallocationsofthehumanandmousegenesforprecursorsofepidermalgrowthfactorandthebetasubunitofnervegrowthfactor‏ ‎‡A Chromosomal locations of the human and mouse genes for precursors of epidermal growth factor and the beta subunit of nerve growth factor‏ ‎‡9 1‏
919 ‎‡a integrativecrosstissueanalysisofgeneexpressionidentifiesnoveltype2diabetesgenes‏ ‎‡A Integrative cross tissue analysis of gene expression identifies novel type 2 diabetes genes‏ ‎‡9 1‏
919 ‎‡a isisletamyloidpolypeptideasignificantfactorinpathogenesisorpathophysiologyofdiabetes‏ ‎‡A Is islet amyloid polypeptide a significant factor in pathogenesis or pathophysiology of diabetes?‏ ‎‡9 1‏
919 ‎‡a isletamyloidpolypeptideamylinnoevidenceofanabnormalprecursorsequencein25type2noninsulindependentdiabeticpatients‏ ‎‡A Islet amyloid polypeptide (amylin): no evidence of an abnormal precursor sequence in 25 type 2 (non-insulin-dependent) diabetic patients‏ ‎‡9 1‏
919 ‎‡a geneticvariationinthehepatocytenuclearfactor3betagenehnf3bdoesnotcontributetomaturityonsetdiabetesoftheyounginfrenchcaucasians‏ ‎‡A Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians‏ ‎‡9 1‏
919 ‎‡a isolationandassayofeukaryoticdnadependentrnapolymerases‏ ‎‡A Isolation and assay of eukaryotic DNA-dependent RNA polymerases‏ ‎‡9 1‏
919 ‎‡a isolationandcharacterizationofaclonedratinsulingene‏ ‎‡A Isolation and characterization of a cloned rat insulin gene‏ ‎‡9 1‏
919 ‎‡a isolationandnucleotidesequenceofacdnaencodingtheprecursorofmousenervegrowthfactor‏ ‎‡A Isolation and nucleotide sequence of a cDNA encoding the precursor of mouse nerve growth factor‏ ‎‡9 1‏
919 ‎‡a isolationandsequenceofaratchymotrypsinbgene‏ ‎‡A Isolation and sequence of a rat chymotrypsin B gene‏ ‎‡9 1‏
919 ‎‡a chromosomeassignmentofmouseinsulincolonystimulatingfactor1andlowdensitylipoproteinreceptors‏ ‎‡A Chromosome assignment of mouse insulin, colony stimulating factor 1, and low-density lipoprotein receptors‏ ‎‡9 1‏
919 ‎‡a chromosomemappingofgenesontheshortarmofhumanchromosome11parathyroidhormonegeneisat11p15togetherwiththegenesforinsulin100harveyras1andbetahemoglobin‏ ‎‡A Chromosome mapping of genes on the short arm of human chromosome 11: parathyroid hormone gene is at 11p15 together with the genes for insulin, c-Harvey-ras 1, and beta-hemoglobin‏ ‎‡9 1‏
919 ‎‡a isolationofacdnacloneencodingakatpchannellikeproteinexpressedininsulinsecretingcellslocalizationofthehumangenetochromosomeband21q221andlinkagestudieswithniddm‏ ‎‡A Isolation of a cDNA Clone Encoding a KATP Channel-Like Protein Expressed in Insulin-Secreting Cells, Localization of the Human Gene to Chromosome Band 21q22.1, and Linkage Studies With NIDDM‏ ‎‡9 1‏
919 ‎‡a kir62variante23kincreasesatpsensitivek+channelactivityandisassociatedwithimpairedinsulinreleaseandenhancedinsulinsensitivityinadultswithnormalglucosetolerance‏ ‎‡A Kir6.2 variant E23K increases ATP-sensitive K+ channel activity and is associated with impaired insulin release and enhanced insulin sensitivity in adults with normal glucose tolerance‏ ‎‡9 1‏
919 ‎‡a lackofassociationofthepolymorphiclocusinthe5flankingregionofthehumaninsulingeneanddiabetesinamericanblacks‏ ‎‡A Lack of association of the polymorphic locus in the 5'-flanking region of the human insulin gene and diabetes in American blacks‏ ‎‡9 1‏
919 ‎‡a leptintheobesegeneproductrapidlymodulatessynaptictransmissioninthehypothalamus‏ ‎‡A Leptin, the obese gene product, rapidly modulates synaptic transmission in the hypothalamus.‏ ‎‡9 1‏
919 ‎‡a dinucleotiderepeatpolymorphisminageneonchromosome20encodingagproteincoupledreceptord20s32e‏ ‎‡A Dinucleotide repeat polymorphism in a gene on chromosome 20 encoding a G-protein coupled receptor (D20S32e).‏ ‎‡9 1‏
919 ‎‡a clinicalandmoleculargeneticsofneonataldiabetesduetomutationsintheinsulingene‏ ‎‡A Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene‏ ‎‡9 1‏
919 ‎‡a organizationandpartialsequenceofthehepatocytenuclearfactor4αmody1geneandidentificationofamissensemutationr127winajapanesefamilywithmody‏ ‎‡A Organization and Partial Sequence of the Hepatocyte Nuclear Factor-4α/MODY1 Gene and Identification of a Missense Mutation, R127W, in a Japanese Family With MODY‏ ‎‡9 1‏
919 ‎‡a organizationandpartialsequenceofthehepatocytenuclearfactor4alphamody1geneandidentificationofamissensemutationr127winajapanesefamilywithmody‏ ‎‡A Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY‏ ‎‡9 1‏
919 ‎‡a organalchemyproducinginsulinintheliver‏ ‎‡A Organ alchemy: producing insulin in the liver‏ ‎‡9 1‏
919 ‎‡a linkageanalysisofmaturityonsetdiabetesoftheyoungwithmicrosatellitepolymorphismsnolinkagetoadaorglut2genesin2families‏ ‎‡A Linkage Analysis of Maturity-Onset Diabetes of the Young With Microsatellite Polymorphisms: No Linkage to ADA or GLUT2 Genes in Two Families‏ ‎‡9 1‏
919 ‎‡a linkageandassociationbetweeninsulindependentdiabetesmellitus‏ ‎‡A Linkage and association between insulin-dependent diabetes mellitus‏ ‎‡9 1‏
919 ‎‡a linkageandassociationbetweeninsulindependentdiabetesmellitusiddmsusceptibilityandmarkersneartheglucokinasegeneonchromosome7‏ ‎‡A Linkage and association between insulin–dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7‏ ‎‡9 1‏
919 ‎‡a functionalpropertiesofther154xhnf4alphaproteingeneratedbyamutationassociatedwithmaturityonsetdiabetesoftheyoungtype1‏ ‎‡A Functional properties of the R154X HNF-4alpha protein generated by a mutation associated with maturity-onset diabetes of the young, type 1.‏ ‎‡9 1‏
919 ‎‡a factor8100synthesisinthekidney‏ ‎‡A Factor VIII:C synthesis in the kidney‏ ‎‡9 1‏
919 ‎‡a femtosecondlaserdesorptionionizationmassspectrometryimagingandmultivariateanalysisoflipidsinpancreatictissue‏ ‎‡A Femtosecond laser desorption ionization mass spectrometry imaging and multivariate analysis of lipids in pancreatic tissue‏ ‎‡9 1‏
946 ‎‡a b‏ ‎‡9 1‏
996 ‎‡2 CAOONL|ncf11953344‏
996 ‎‡2 DNB|1127014331‏
996 ‎‡2 ISNI|0000000040383772‏
996 ‎‡2 LC|nb2007025791‏
996 ‎‡2 NYNYRILM|98795‏
996 ‎‡2 LC|n 88290740‏
996 ‎‡2 BIBSYS|90373550‏
996 ‎‡2 LC|n 99051304‏
996 ‎‡2 B2Q|0000095961‏
996 ‎‡2 ISNI|0000000088141449‏
996 ‎‡2 DNB|143407082‏
996 ‎‡2 RERO|A008601940‏
996 ‎‡2 LC|nb2012015083‏
996 ‎‡2 DNB|17044581X‏
996 ‎‡2 LC|no2020119224‏
996 ‎‡2 RERO|A002987083‏
996 ‎‡2 ISNI|0000000116233835‏
996 ‎‡2 LC|n 84002083‏
996 ‎‡2 ISNI|0000000446213706‏
996 ‎‡2 BIBSYS|7041956‏
996 ‎‡2 NUKAT|n 2018154465‏
996 ‎‡2 ISNI|0000000067074590‏
996 ‎‡2 RERO|A002986892‏
996 ‎‡2 LC|nb2001014851‏
996 ‎‡2 LC|nb2007017982‏
996 ‎‡2 BNF|13964855‏
996 ‎‡2 JPG|500028696‏
996 ‎‡2 NDL|00432804‏
996 ‎‡2 LC|n 84154895‏
996 ‎‡2 BNF|15044372‏
996 ‎‡2 LC|n 83209776‏
996 ‎‡2 CAOONL|ncf10415881‏
996 ‎‡2 LC|nb 98027485‏
996 ‎‡2 NLA|000035711911‏
996 ‎‡2 BIBSYS|1542227325548‏
996 ‎‡2 NLA|000035506607‏
996 ‎‡2 LC|n 81102407‏
996 ‎‡2 LC|nb2023005201‏
996 ‎‡2 ISNI|0000000081386064‏
996 ‎‡2 BIBSYS|1081293‏
996 ‎‡2 BNE|XX4874797‏
996 ‎‡2 DNB|134896114‏
996 ‎‡2 SUDOC|116450797‏
996 ‎‡2 NII|DA00362759‏
996 ‎‡2 PLWABN|9810703402605606‏
996 ‎‡2 ISNI|0000000043144822‏
996 ‎‡2 LC|nb2008010606‏
996 ‎‡2 BIBSYS|90223009‏
996 ‎‡2 ISNI|0000000081605829‏
996 ‎‡2 ISNI|000000044883168X‏
996 ‎‡2 CAOONL|ncf11512703‏
996 ‎‡2 BIBSYS|90137959‏
996 ‎‡2 DNB|131768933X‏
996 ‎‡2 ISNI|000000045136914X‏
996 ‎‡2 CAOONL|ncf10501115‏
996 ‎‡2 BIBSYS|4085853‏
996 ‎‡2 J9U|987007364882705171‏
996 ‎‡2 NUKAT|n 2016175653‏
996 ‎‡2 LC|no2022015558‏
996 ‎‡2 LC|no2015022338‏
996 ‎‡2 ISNI|0000000038911804‏
996 ‎‡2 VLACC|000035435‏
996 ‎‡2 NUKAT|n 99001478‏
996 ‎‡2 BIBSYS|3025680‏
996 ‎‡2 LC|nb2010027596‏
996 ‎‡2 LC|no2009112908‏
996 ‎‡2 DNB|143640151‏
996 ‎‡2 BNC|981059745435906706‏
996 ‎‡2 BNF|13746617‏
996 ‎‡2 J9U|987007412343505171‏
996 ‎‡2 LC|n 2008181940‏
996 ‎‡2 BNF|16098107‏
996 ‎‡2 J9U|987012672570405171‏
996 ‎‡2 LC|nb2003041055‏
996 ‎‡2 ISNI|0000000427566266‏
996 ‎‡2 SUDOC|185775713‏
996 ‎‡2 NII|DA02893064‏
996 ‎‡2 ISNI|0000000038629219‏
996 ‎‡2 CAOONL|ncf10797526‏
996 ‎‡2 SUDOC|174229380‏
996 ‎‡2 RERO|A017738490‏
996 ‎‡2 NDL|00884955‏
996 ‎‡2 LC|n 89107556‏
996 ‎‡2 LC|no2020112278‏
996 ‎‡2 ISNI|0000000371430115‏
996 ‎‡2 DNB|17429672X‏
996 ‎‡2 ISNI|0000000384313049‏
996 ‎‡2 DNB|1158227655‏
996 ‎‡2 NKC|xx0220495‏
996 ‎‡2 LC|n 89658841‏
996 ‎‡2 NUKAT|n 2005122005‏
996 ‎‡2 LC|nb2001017018‏
996 ‎‡2 ISNI|0000000116691828‏
996 ‎‡2 SUDOC|265367018‏
996 ‎‡2 SUDOC|066924146‏
996 ‎‡2 DNB|174018568‏
996 ‎‡2 CAOONL|ncf11891103‏
996 ‎‡2 J9U|987007258467505171‏
996 ‎‡2 NSK|000299870‏
996 ‎‡2 ISNI|0000000065761899‏
996 ‎‡2 LC|no2019092894‏
996 ‎‡2 BIBSYS|90791796‏
996 ‎‡2 ISNI|0000000408688073‏
996 ‎‡2 ISNI|0000000063150656‏
996 ‎‡2 NII|DA02928985‏
996 ‎‡2 LC|n 96098396‏
996 ‎‡2 NKC|kup19990000006205‏
996 ‎‡2 ISNI|0000000037688735‏
996 ‎‡2 NTA|068814879‏
996 ‎‡2 SUDOC|185056008‏
996 ‎‡2 BNF|12275663‏
996 ‎‡2 LC|nb2017025660‏
996 ‎‡2 PLWABN|9810699588605606‏
996 ‎‡2 BNF|14022286‏
996 ‎‡2 SUDOC|09503286X‏
996 ‎‡2 DNB|1199860069‏
996 ‎‡2 NTA|134009614‏
997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏
998 ‎‡a Bell, Graeme I.‏ ‎‡2 ISNI|0000000038911804‏ ‎‡3 suggested‏
998 ‎‡a Bell, Graeme I.‏ ‎‡2 J9U|987007364882705171‏ ‎‡3 suggested‏
998 ‎‡a Bell, Graeme I.‏ ‎‡2 LC|n 2008181940‏ ‎‡3 suggested‏