| 9th International Congress of Andrology |
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| Alteracions del contingut de nucleoproteïnes de les cèl·lules espermàtiques. Relació amb la infertilitat en l'home |
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| Altered histone retention and epigenetic modifications in the sperm of infertile men |
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| Anàlisi del contingut de RNA i estudi mutacional de gens candidats en infertilitat masculina |
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| Análisis del gen Tau en la enfermedad de Parkinson, en otros parkinsonismos atípicos y en la demencia frontotemporal |
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| Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers |
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| Apolipoprotein E polymorphism in Alzheimer's disease: a comparative study of two research populations from Spain and the United States. |
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| Caracterització del contingut proteic del nucli de l'espermatozoïde humà i el seu potencial epigenètic |
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| Caracterització proteòmica i molecular d'espermatozoides humans en pacients infèrtils i controls = Proteomic and molecular charachterization of human spermatozoa in infertile patients and controls |
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| Cerebrospinal fluid biomarkers in Alzheimer's disease families with PSEN1 mutations. |
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| Characterization of Human Sperm Protamine Proteoforms through a Combination of Top-Down and Bottom-Up Mass Spectrometry Approaches |
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| Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory |
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| The combined human sperm proteome: cellular pathways and implications for basic and clinical science |
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| A common protamine 1 promoter polymorphism (-190 C->A) correlates with abnormal sperm morphology and increased protamine P1/P2 ratio in infertile patients |
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| Conserved elements in the 5' regulatory region of the amyloid precursor protein gene in primates |
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| The contribution of human sperm proteins to the development and epigenome of the preimplantation embryo |
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| Detection of P2 precursors in the sperm cells of infertile patients who have reduced protamine P2 levels |
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| Distribució diferencial de gens en la cromatina espermàtica i detecció de proteïnes presents en una abundància alterada en pacients infèrtils |
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| The effect of tetrabromobisphenol A on protamine content and DNA integrity in mouse spermatozoa. |
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| Estratègies de diagnòstic genètic en fetus amb malformacions congènites: correlació genotip-fenotip |
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| Estudio de la transición nucleohistona - nucleoprotamina in vivo e in vitro clonaje, secuencia y expresión del gen de la protamina galina |
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| Estudios de asociación genética y detección de mutaciones en pacientes con enfermedad de Parkinson comparación genético-clínica entre los casos esporádicos y familiares |
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| Genètica mèdica |
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| El Genoma humano |
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| The genotype 2/2 of the presenilin-1 polymorphism is decreased in Spanish early-onset Alzheimer's disease |
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| Hemocromatosis hereditaria: estudio del gen HFE y de sus mutaciones en la población española |
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| High apolipoprotein E4 allele frequency in FXTAS patients. |
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| High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2. |
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| High-throughput sperm differential proteomics suggests that epigenetic alterations contribute to failed assisted reproduction |
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| Histone H4 hyperacetylation and rapid turnover of its acetyl groups in transcriptionally inactive rooster testis spermatids |
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| Human Proteinpedia enables sharing of human protein data |
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| Human sperm tail proteome suggests new endogenous metabolic pathways |
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| Identification of a complex population of chromatin-associated proteins in the European sea bass (Dicentrarchus labrax) sperm |
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| Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans. |
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| Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammals. |
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| Identification of endogenous metabolites in human sperm cells using proton nuclear magnetic resonance ((1) H-NMR) spectroscopy and gas chromatography-mass spectrometry (GC-MS). |
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| Identification of proteomic differences in asthenozoospermic sperm samples. |
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| Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the α-synuclein gene in early onset patients |
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| Improved direct sequencing of Alzheimer's amyloid precursor protein |
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| Influence of beta-2 adrenergic receptor gene polymorphism on the hemodynamic response to propranolol in patients with cirrhosis |
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| The Iron Regulatory Protein/Iron Responsive Element (IRP/IRE) system: functional studies of new target mRNAs and pathological implications for novel IRE mutations |
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| La Malaltia d'Alzheimer: contribució a les causes genètiques i als factors de risc genètics |
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| Marked correlations in protein expression identified by proteomic analysis of human spermatozoa |
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| Methodological advances in sperm proteomics. |
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| Molecular and cellular mechanisms of fertilization failure after ICSI |
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| Molecular genetic reports in clinical practice: content and nomenclature of mutations |
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| New ubiquitin mRNA expressed during chicken spermiogenesis |
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| No evidence of linkage to 6p markers in spanish families with juvenile myoclonic epilepsy |
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| Nous paradigmes de la contribució paterna al desenvolupament embrionari primerenc mitjançant l’anàlisi de l’espermatozoide humà amb tècniques d'alt rendiment |
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| Nucleosome positioning in the rat protamine 1 gene in vivo and in vitro |
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| The "omics" of human male infertility: integrating big data in a systems biology approach |
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| Papel de los genes de la presenilina 1, presenilina 2, proteína precursora de amiloide y otros factores de riesgo genético en la enfermedad de Alzheimer familiar |
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| Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background. |
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| PICOGEN: five years experience with a genetic counselling program for dementia. |
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| Polymorphisms, haplotypes and mutations in the protamine 1 and 2 genes. |
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| Population screening for hemochromatosis: a study in 5370 Spanish blood donors. |
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| Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls |
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| Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection. |
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| Protamine/DNA ratios and DNA damage in native and density gradient centrifuged sperm from infertile patients |
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| Protein and DNA contents in sperm from an infertile human male possessing protamine defects that vary over time |
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| Proteomics in the study of the sperm cell composition, differentiation and function |
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| Quantitative Analysis of the Seminal Plasma Proteome in Secondary Hypogonadism |
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| Rapid analysis of mammalian sperm nuclear proteins |
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| Recommendations regarding the genetic and immunological study of reproductive dysfunction |
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| Relationships between human sperm protamines, DNA damage and assisted reproduction outcomes |
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| SBiRM: Focus on proteomics and reproduction. Preface |
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| Semen proteomics and male infertility. |
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| Significant Changes in the Tau A0 and A3 Alleles in Progressive Supranuclear Palsy and Improved Genotyping by Silver Detection |
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| The small RNA content of human sperm reveals pseudogene-derived piRNAs complementary to protein-coding genes |
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| Spanish Multicenter Normative Studies (NEURONORMA Project): methods and sample characteristics. |
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| Sperm nuclear proteome and its epigenetic potential |
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| Sperm telomere length in donor samples is not related to ICSI outcome |
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| Stable-protein Pair Analysis as A Novel Strategy to Identify Proteomic Signatures: Application To Seminal Plasma From Infertile Patients |
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| Standards in semen examination: publishing reproducible and reliable data based on high-quality methodology |
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| Tau gene delN296 mutation, Parkinson's disease, and atypical supranuclear palsy. |
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| Uncommon polymorphism in the presenilin genes in human familial Alzheimer's disease: not to be mistaken with a pathogenic mutation. |
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| Zona pellucida-binding protein 2 (ZPBP2) and several proteins containing BX7B motifs in human sperm may have hyaluronic acid binding or recognition properties. |
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