Search
Leader | 00000nz a2200037n 45 0 | ||
---|---|---|---|
001 | WKP|Q56112043 (VIAF cluster) (Authority/Source Record) | ||
003 | WKP | ||
005 | 20241221010841.0 | ||
008 | 241221nneanz||abbn n and d | ||
035 | ‡a (WKP)Q56112043 | ||
024 | ‡a 0000-0001-9359-8774 ‡2 orcid | ||
024 | ‡a 0000-0001-5329-0986 ‡2 orcid | ||
024 | ‡a 55934387500 ‡2 scopus | ||
035 | ‡a (OCoLC)Q56112043 | ||
100 | 0 | ‡a João Gonçalves ‡9 ast ‡9 es ‡9 sl | |
375 | ‡a 1 ‡2 iso5218 | ||
400 | 0 | ‡a João Gonçalves ‡c researcher 0000-0001-9359-8774 ‡9 en | |
400 | 0 | ‡a João Gonçalves ‡c wetenschapper ‡9 nl | |
670 | ‡a Author's A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface | ||
670 | ‡a Author's A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia | ||
670 | ‡a Author's A systematic proximity map of the centriole-cilia interface. | ||
670 | ‡a Author's Besnoitia besnoiti and Toxoplasma gondii: two apicomplexan strategies to manipulate the host cell centrosome and Golgi apparatus. | ||
670 | ‡a Author's Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers | ||
670 | ‡a Author's Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency. | ||
670 | ‡a Author's CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions | ||
670 | ‡a Author's Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment | ||
670 | ‡a Author's Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male | ||
670 | ‡a Author's Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility? | ||
670 | ‡a Author's Human mtDNA haplogroups and reduced male fertility: real association or hidden population substructuring | ||
670 | ‡a Author's Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. | ||
670 | ‡a Author's Identification of SOX3 as an XX male sex reversal gene in mice and humans | ||
670 | ‡a Author's Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm | ||
670 | ‡a Author's [Late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency: revision of literature and preconception genetic study of five couples] | ||
670 | ‡a Author's Modulation of translation factor's gene expression by histone deacetylase inhibitors in breast cancer cells. | ||
670 | ‡a Author's Mutation C11994T in the mitochondrial ND4 gene is not a cause of low sperm motility in Portugal. | ||
670 | ‡a Author's No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males | ||
670 | ‡a Author's PROS1 novel splice-site variant decreases protein S expression in patients from two families with thrombotic disease | ||
670 | ‡a Author's Revisiting the tubulin folding pathway: new roles in centrosomes and cilia | ||
670 | ‡a Author's [Screening for Y chromosome sequences in patients with Turner syndrome] | ||
670 | ‡a Author's The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility | ||
670 | ‡a Author's The expression of tubulin cofactor A | ||
670 | ‡a Author's The expression of tubulin cofactor A (TBCA) is regulated by a noncoding antisense Tbca RNA during testis maturation. | ||
670 | ‡a Author's The NEMP family supports metazoan fertility and nuclear envelope stiffness | ||
909 | ‡a (scopus) 55934387500 ‡9 1 | ||
909 | ‡a (orcid) 0000000153290986 ‡9 1 | ||
909 | ‡a (orcid) 0000000193598774 ‡9 1 | ||
919 | ‡a nempfamilysupportsmetazoanfertilityandnuclearenvelopestiffness ‡A The NEMP family supports metazoan fertility and nuclear envelope stiffness ‡9 1 | ||
919 | ‡a expressionoftubulincofactoratbcaisregulatedbyanoncodingantisensetbcarnaduringtestismaturation ‡A The expression of tubulin cofactor A (TBCA) is regulated by a noncoding antisense Tbca RNA during testis maturation. ‡9 1 | ||
919 | ‡a expressionoftubulincofactora ‡A The expression of tubulin cofactor A ‡9 1 | ||
919 | ‡a azfcregionoftheychromosomeatthecrossroadsbetweengeneticdiversityandmaleinfertility ‡A The AZFc region of the Y chromosome: at the crossroads between genetic diversity and male infertility ‡9 1 | ||
919 | ‡a screeningforychromosomesequencesinpatientswithturnersyndrome ‡A [Screening for Y chromosome sequences in patients with Turner syndrome] ‡9 1 | ||
919 | ‡a revisitingthetubulinfoldingpathwaynewrolesincentrosomesandcilia ‡A Revisiting the tubulin folding pathway: new roles in centrosomes and cilia ‡9 1 | ||
919 | ‡a pros1novelsplicesitevariantdecreasesproteinsexpressioninpatientsfrom2familieswiththromboticdisease ‡A PROS1 novel splice-site variant decreases protein S expression in patients from two families with thrombotic disease ‡9 1 | ||
919 | ‡a noevidenceforanmtdnaroleinspermmotilitydatafromcompletesequencingofasthenozoospermicmales ‡A No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males ‡9 1 | ||
919 | ‡a mutationc11994tinthemitochondrialnd4geneisnotacauseoflowspermmotilityinportugal ‡A Mutation C11994T in the mitochondrial ND4 gene is not a cause of low sperm motility in Portugal. ‡9 1 | ||
919 | ‡a modulationoftranslationfactorsgeneexpressionbyhistonedeacetylaseinhibitorsinbreastcancercells ‡A Modulation of translation factor's gene expression by histone deacetylase inhibitors in breast cancer cells. ‡9 1 | ||
919 | ‡a lateonsetcongenitaladrenalhyperplasiadueto21hydroxylasedeficiencyrevisionofliteratureandpreconceptiongeneticstudyof5couples ‡A [Late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency: revision of literature and preconception genetic study of five couples] ‡9 1 | ||
919 | ‡a incorrectdnamethylationofthedazlpromotercpgislandassociateswithdefectivehumansperm ‡A Incorrect DNA methylation of the DAZL promoter CpG island associates with defective human sperm ‡9 1 | ||
919 | ‡a identificationofsox3asan20malesexreversalgeneinmiceandhumans ‡A Identification of SOX3 as an XX male sex reversal gene in mice and humans ‡9 1 | ||
919 | ‡a humanspermatogenicfailurepurgesdeleteriousmutationloadfromtheautosomesandbothsexchromosomesincludingthegenedmrt1 ‡A Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. ‡9 1 | ||
919 | ‡a humanmtdnahaplogroupsandreducedmalefertilityrealassociationorhiddenpopulationsubstructuring ‡A Human mtDNA haplogroups and reduced male fertility: real association or hidden population substructuring ‡9 1 | ||
919 | ‡a geneticdissectionoftheazfregionsofthehumanychromosomethrillerorfillerformaleinfertility ‡A Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility? ‡9 1 | ||
919 | ‡a geneticdissectionoftheazfregionsofthehumanychromosomethrillerorfillerformale ‡A Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male ‡9 1 | ||
919 | ‡a evaluationofmalefertilityassociatedlociinaeuropeanpopulationofpatientswithseverespermatogenicimpairment ‡A Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment ‡9 1 | ||
919 | ‡a cyp21a2mutationsinportuguesepatientswithcongenitaladrenalhyperplasiaidentificationof2novelmutationsandcharacterizationof4differentpartialgeneconversions ‡A CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions ‡9 1 | ||
919 | ‡a congenitaladrenalhyperplasiafocusonthemolecularbasisof21hydroxylasedeficiency ‡A Congenital adrenal hyperplasia: focus on the molecular basis of 21-hydroxylase deficiency. ‡9 1 | ||
919 | ‡a characterizingpartialazfcdeletionsoftheychromosomewithampliconspecificsequencemarkers ‡A Characterizing partial AZFc deletions of the Y chromosome with amplicon-specific sequence markers ‡9 1 | ||
919 | ‡a besnoitiabesnoitiandtoxoplasmagondii2apicomplexanstrategiestomanipulatethehostcellcentrosomeandgolgiapparatus ‡A Besnoitia besnoiti and Toxoplasma gondii: two apicomplexan strategies to manipulate the host cell centrosome and Golgi apparatus. ‡9 1 | ||
919 | ‡a systematicproximitymapofthecentrioleciliainterface ‡A A systematic proximity map of the centriole-cilia interface. ‡9 1 | ||
919 | ‡a novelalumediatedmicrodeletionat11p13removeswt1inapatientwithcryptorchidismandazoospermia ‡A A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia ‡9 1 | ||
919 | ‡a dynamicproteininteractionlandscapeofthehumancentrosomeciliuminterface ‡A A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface ‡9 1 | ||
946 | ‡a b ‡9 1 | ||
996 | ‡2 LC|n 2020184073 | ||
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996 | ‡2 PTBNP|1451882 | ||
996 | ‡2 ISNI|0000000070034792 | ||
996 | ‡2 PTBNP|217544 | ||
996 | ‡2 DNB|128712414 | ||
996 | ‡2 LC|n 88207987 | ||
996 | ‡2 PTBNP|1662764 | ||
996 | ‡2 PTBNP|977378 | ||
996 | ‡2 LC|no2021052499 | ||
996 | ‡2 ISNI|000000011143227X | ||
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996 | ‡2 PTBNP|125319 | ||
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996 | ‡2 ISNI|0000000070221221 | ||
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996 | ‡2 BLBNB|001456866 | ||
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996 | ‡2 PTBNP|1797096 | ||
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996 | ‡2 PTBNP|1013494 | ||
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997 | ‡a 0 0 lived 0 0 ‡9 1 |