X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
about
Experimental methods to preserve male fertility and treat male factor infertilityRecent advances in understanding & managing male infertilityThe human RHOX gene cluster: target genes and functional analysis of gene variants in infertile menMale Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.The genetics of human infertility by functional interrogation of SNPs in mice.FSHB -211G>T stratification for follicle-stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism.Single gene defects leading to sperm quantitative anomalies.A PLK4 mutation causing azoospermia in a man with Sertoli cell-only syndrome.Genetics of Male Infertility.Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.SPINK2 deficiency causes infertility by inducing sperm defects in heterozygotes and azoospermia in homozygotes.Relationship of genetic causes and inhibin B in non obstructive azoospermia spermatogenic failure.Human male infertility and its genetic causes.Functional study of a novel missense single-nucleotide variant of NUP107 in two daughters of Mexican origin with premature ovarian insufficiency.Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.Next-generation sequencing for patients with non-obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations.A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure.Distinct prophase arrest mechanisms in human male meiosis.A novel TEX11 mutation induces azoospermia: a case report of infertile brothers and literature review.Quantitative proteomic profiling of the human ovary from early to mid-gestation reveals protein expression dynamics of oogenesis and folliculogenesis.Disorders of spermatogenesis: Perspectives for novel genetic diagnostics after 20 years of unchanged routine.[Rational diagnosis and treatment of male infertility].CUL4B mutations are uncommon in Japanese patients with Sertoli-cell-only syndrome and azoospermia.Recent developments in genetics and medically assisted reproduction: from research to clinical applicationsEvolutionarily-conserved MZIP2 is essential for crossover formation in mammalian meiosisX-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
P2860
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P2860
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@ast
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@en
type
label
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@ast
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@en
prefLabel
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@ast
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.
@en
P2093
P2860
P356
P1476
X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men
@en
P2093
Albrecht Röpke
Aleksandar Rajkovic
Alexander N Yatsenko
Andrea J Berman
Andrew P Georgiadis
Birgit Westernströer
Frank Tüttelmann
Joseph Sanfilippo
Sabine Kliesch
Stefan Schlatt
P2860
P304
P356
10.1056/NEJMOA1406192
P407
P577
2015-05-13T00:00:00Z