Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia
about
Absence of sperm RNA elements correlates with idiopathic male infertilityThe role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutationsA genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermiaA genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermiaGenome-wide association study implicates testis-sperm specific FKBP6 as a susceptibility locus for impaired acrosome reaction in stallions.The "omics" of human male infertility: integrating big data in a systems biology approach.Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.Strong association of SLC1A1 and DPF3 gene variants with idiopathic male infertility in Han Chinese.Evaluation of 172 candidate polymorphisms for association with oligozoospermia or azoospermia in a large cohort of men of European descent.Cumulative alkylating agent exposure and semen parameters in adult survivors of childhood cancer: a report from the St Jude Lifetime Cohort StudyGenetic susceptibility to male infertility: news from genome-wide association studies.High resolution X chromosome-specific array-CGH detects new CNVs in infertile malesExome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family.Environmentally induced epigenetic transgenerational inheritance of male infertility.Lack of association of KATNAL1 gene sequence variants and azoospermia in humansEvaluation of five candidate genes from GWAS for association with oligozoospermia in a Han Chinese population.Excess of rare variants in genes that are key epigenetic regulators of spermatogenesis in the patients with non-obstructive azoospermia.MTHFR 677C>T polymorphism increases the male infertility risk: a meta-analysis involving 26 studiesThe puzzles of the prokineticin 2 pathway in human reproductionSusceptibility to male infertility: replication study in Japanese men looking for an association with four GWAS-derived loci identified in European men.Yeast model identifies ENTPD6 as a potential non-obstructive azoospermia pathogenic gene.Failure of homologous synapsis and sex-specific reproduction problems.Association of polymorphisms of A260G and A386G in DAZL gene with male infertility: a meta-analysis and systemic review.The use of genomics, proteomics, and metabolomics in identifying biomarkers of male infertilityRecent advances in the genetics of testicular failure.Genetic causes of spermatogenic failure.The Genetics of Infertility: Current Status of the Field.The human sperm epigenome and its potential role in embryonic development.The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility.Emerging evidence for the role of genomic instability in male factor infertility.Initiative for standardization of reporting genetics of male infertility.Single gene defects leading to sperm quantitative anomalies.Association and meta-analysis of HLA and non-obstructive azoospermia in the Han Chinese population.Genome-wide association study for sperm concentration in Holstein-Friesian bulls.Genomewide association study of HLA alloimmunization in previously pregnant blood donors.Taste receptor polymorphisms and male infertility.Genetic intersection of male infertility and cancer.Association of TUSC1 and DPF3 gene polymorphisms with male infertility.Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men.Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.
P2860
Q28384677-474F293A-583E-4D03-BE77-809A7967CCE0Q28385113-484AB717-D8F9-4791-991F-444C9A1F7327Q28943316-C66A20A3-2EFF-46EE-964F-9ED08AC6C862Q28943544-646154B4-3C91-4563-BE6A-35FC525F1207Q30425447-3FED6046-4ADD-47A3-BB9E-227E4AB01B71Q31031878-8E09F8C4-4758-410F-8252-2BC88DF121FFQ33894894-C3AFB99C-B054-4D3F-BF5D-ECD5797609F6Q33897310-788DC740-6BC4-4BCE-B42C-3A2894C640E5Q34109272-634E18AC-B8F5-4B42-A6B1-11812F7197B5Q34317913-AB10AB57-5FB8-4953-9CEB-4567D8713CFBQ34407128-12466C72-C07D-4B82-BA04-CF149C3A057BQ34440842-ED682B89-4380-4732-AE6B-9013A84FBF62Q34486302-FA432707-B8F4-4982-BFE0-18DDC72A2A48Q34615540-891DCD68-CABA-41E1-8F1C-55D8BED3FCC2Q34662333-150119BA-025D-4C14-A94C-A205C106085AQ35058492-EAC6966D-3F3E-4154-B198-E27756903D43Q35148746-241D91A6-F4A0-4855-A61A-D22A8F504326Q35203125-3864B319-B4E5-4AEA-AA80-E322F654498DQ35551224-21372EDB-4EAA-4F0B-B0C8-EF730D2789E7Q35816210-2A6D4A1B-AA03-4EBC-A4FB-C211BCF69BA2Q35830164-AD87FE18-4472-4CE9-BC56-EDC3BD1213ACQ36036342-2A959643-A3B0-4CD4-8E08-4FE958DF44A1Q36530272-E072DCEE-C1F0-4EE5-91BC-DEBCBC55B501Q36839432-73DDADDF-5D0E-45AA-BA02-64B41550F80EQ36861520-8983F96B-1101-4DD0-A96B-3F36D9F7C3B5Q37074590-B6F6491B-1FFE-4D48-BA3C-8C53BABE3508Q37450892-495F964B-3434-41FE-AF92-4EE6439B921AQ37631298-2EE93662-1178-4D62-9C36-71C3055BC9CBQ37826198-D1FC81B4-9A29-4F2F-981C-872D547CB577Q37964747-12EC7389-714C-4578-992B-47B98E7E24DBQ38440120-B16D5F37-A804-46DD-8116-CD630D21B948Q38806004-EE61E8DA-C92A-42C3-8167-7EC1718EFF57Q38824115-602D7D49-E29D-4DAE-B9D3-CBD4503E1DE5Q42685527-A0F2D1D5-4EBC-47B2-9351-BC4C3BB51275Q46702086-85A742C9-CA9B-422D-90A9-7221EE6FE19AQ47241166-E7376403-B384-442D-93D9-D6520EED372AQ47747812-6F7FEEFE-1E47-4602-88C9-3F4EAF268A60Q48248875-B2CD6519-BFAD-4741-A85C-021D0F274230Q49915022-F1EFB98D-CB87-4670-BE9C-7FC754E5E1DBQ52661766-642CAD12-1EA3-4A2D-80E8-D20488456843
P2860
Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia
description
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2009
@ast
im November 2009 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2009/11/01)
@nl
наукова стаття, опублікована в листопаді 2009
@uk
مقالة علمية (نشرت في نوفمبر 2009)
@ar
name
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@ast
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@en
type
label
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@ast
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@en
prefLabel
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@ast
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@en
P3181
P1433
P1476
Genome-wide study of single-nu ...... mia and severe oligozoospermia
@en
P2093
Douglas T. Carrell
P304
P3181
P356
10.2164/JANDROL.109.007971
P577
2009-11-01T00:00:00Z