about
Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney diseaseDemethylation of CpG islands in the 5' upstream regions mediates the expression of the human testis-specific gene MAGEB16 and its mouse homolog Mageb16.The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertilityIdentical twins:one with anti-glomerular basement membrane glomerulonephritis,the other with systemic lupus erythematosus.Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum.Microarray profiling of microRNAs expressed in testis tissues of developing primates.Epigenetic modifications promote the expression of the orphan nuclear receptor NR0B1 in human lung adenocarcinoma cells.Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation.[Nested coamplification polymerase chain reaction].A novel large deletion of the DOCK8 gene in a Chinese family with autosomal-recessive hyper-IgE syndrome.Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T>C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy.Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy.[Identification and functional analysis of a testis-specific E3 ubiquitin ligase gene Rnf148 in mouse].A single nucleotide polymorphism in a miR-1302 binding site in CGA increases the risk of idiopathic male infertility.Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.A new mutant transcript generated in Znf230 exon 2 knockout mice reveals a potential exon structure in the targeting vector sequence.[Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].Absence of the H2AX mutations in idiopathic infertile men with spermatogenic impairment.[Study on the distribution of Y chromosome haplogroups in Sichuan Han population].[Study on DAZ gene copy deletion in severe oligozoospermia sperm donor for ICSI].Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.Single-nucleotide polymorphism rs2290692 in the 3'UTR of ITPKC associated with susceptibility to Kawasaki disease in a Han Chinese population.Mutation screening and association study of the TSSK4 Gene in Chinese infertile men with impaired spermatogenesis.Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.Testis-specific protein, Y-linked 1 activates PI3K/AKT and RAS signaling pathways through suppressing IGFBP3 expression during tumor progression[Fluorescence probe two-hybridization technique and its application in medical genechips][Studies on molecular epidemiology of Y chromosome azoospermia factor microdeletions in Chinese patients with idiopathic azoospermia or severe oligozoospermia]Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermiaHigh risk genetic factor in Chinese patients with idiopathic male infertility: deletion of DAZ gene copy on Y chromosomeEvidence for the association of Y-chromosome haplogroups with susceptibility to spermatogenic failure in a Chinese Han populationMassive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/or maturation arrestY chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairmentDAZ1/DAZ2 cluster deletion mediated by gr/gr recombination per se may not be sufficient for spermatogenesis impairment: a study of Chinese normozoospermic menPreliminary study of the relationship between DAZ gene copy deletions and spermatogenic impairment in Chinese men[Y chromosome variations and male infertility]
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P50
description
researcher ORCID ID=0000-0002-9206-0312
@en
name
Yuan Yang
@en
Yuan Yang
@nl
type
label
Yuan Yang
@en
Yuan Yang
@nl
prefLabel
Yuan Yang
@en
Yuan Yang
@nl
P106
P31
P496
0000-0002-9206-0312