about
Oocyte development, meiosis and aneuploidyMale infertility and the involvement of the X chromosomeMutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repairThe ubiquitin ligase Ubr2, a recognition E3 component of the N-end rule pathway, stabilizes Tex19.1 during spermatogenesisPolycomb protein SCML2 associates with USP7 and counteracts histone H2A ubiquitination in the XY chromatin during male meiosisRNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosisA novel mouse synaptonemal complex protein is essential for loading of central element proteins, recombination, and fertilityMouse MOV10L1 associates with Piwi proteins and is an essential component of the Piwi-interacting RNA (piRNA) pathwayMEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombinationCombining RNA and protein profiling data with network interactions identifies genes associated with spermatogenesis in mouse and human.Identification of transcripts involved in meiosis and follicle formation during ovine ovary development.TEX11 modulates germ cell proliferation by competing with estrogen receptor β for the binding to HPIP.A 1.1-Mb segmental deletion on the X chromosome causes meiotic failure in male miceTOPAZ1, a novel germ cell-specific expressed gene conserved during evolution across vertebratesRegulation of male fertility by X-linked genes.Reproductive isolation in hybrid mice due to spermatogenesis defects at three meiotic stages.Gene targeting study reveals unexpected expression of brain-expressed X-linked 2 in endocrine and tissue stem/progenitor cells in mice.Multiple loci contribute to genome-wide recombination levels in male mice.Six polymorphisms in genes involved in DNA double-strand break repair and chromosome synapsis: association with male infertility.Deletion of an X-inactivation boundary disrupts adjacent gene silencing.Non-synonymous mutations mapped to chromosome X associated with andrological and growth traits in beef cattle.Characterization of the porcine testis-expressed gene 11 (Tex11).X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.Functional significance of the sex chromosomes during spermatogenesis.TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse.Meiosis-specific proteins MEIOB and SPATA22 cooperatively associate with the single-stranded DNA-binding replication protein A complex and DNA double-strand breaks.Sertoli-cell-specific knockout of connexin 43 leads to multiple alterations in testicular gene expression in prepubertal miceInactivation of Nxf2 causes defects in male meiosis and age-dependent depletion of spermatogoniaEvidence for positive selection of taurine genes within a QTL region on chromosome X associated with testicular size in Australian Brahman cattleNetwork cluster analysis of protein-protein interaction network identified biomarker for early onset colorectal cancer.Meiotic Recombination: The Essence of Heredity.RNA immunoprecipitation identifies novel targets of DAZL in human foetal ovary.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.A SUMO-ubiquitin relay recruits proteasomes to chromosome axes to regulate meiotic recombination.Human male infertility and its genetic causes.Polycomb directs timely activation of germline genes in spermatogenesis.MORC2B is essential for meiotic progression and fertility.A meiotic XPF-ERCC1-like complex recognizes joint molecule recombination intermediates to promote crossover formation.A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
P2860
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P248
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P2860
description
2008 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2008
@ast
im März 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/03/01)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/03/01)
@nl
наукова стаття, опублікована в березні 2008
@uk
مقالة علمية (نشرت في مارس 2008)
@ar
name
Meiotic failure in male mice lacking an X-linked factor
@ast
Meiotic failure in male mice lacking an X-linked factor
@en
Meiotic failure in male mice lacking an X-linked factor
@nl
type
label
Meiotic failure in male mice lacking an X-linked factor
@ast
Meiotic failure in male mice lacking an X-linked factor
@en
Meiotic failure in male mice lacking an X-linked factor
@nl
prefLabel
Meiotic failure in male mice lacking an X-linked factor
@ast
Meiotic failure in male mice lacking an X-linked factor
@en
Meiotic failure in male mice lacking an X-linked factor
@nl
P2093
P2860
P921
P356
P1433
P1476
Meiotic failure in male mice lacking an X-linked factor
@en
P2093
Chengtao Her
Christer Höög
David C Page
K John McLaughlin
Katarina Gell
N Adrian Leu
Peijing Jeremy Wang
Ricardo Benavente
Sigrid Eckardt
P2860
P304
P356
10.1101/GAD.1613608
P577
2008-03-01T00:00:00Z