Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage.
about
ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomesA high incidence of meiotic silencing of unsynapsed chromatin is not associated with substantial pachytene loss in heterozygous male mice carrying multiple simple robertsonian translocationsRAD21L, a novel cohesin subunit implicated in linking homologous chromosomes in mammalian meiosisDouble-strand break repair on sex chromosomes: challenges during male meiotic prophaseMeiotic pairing and segregation of achiasmate sex chromosomes in eutherian mammals: the role of SYCP3 proteinVariation in genome-wide levels of meiotic recombination is established at the onset of prophase in mammalian malesMouse BAZ1A (ACF1) is dispensable for double-strand break repair but is essential for averting improper gene expression during spermatogenesisSPO11-independent DNA repair foci and their role in meiotic silencingRegulation of DNA double-strand break repair pathway choiceReversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathwayZIP4H (TEX11) deficiency in the mouse impairs meiotic double strand break repair and the regulation of crossing overAGO4 regulates entry into meiosis and influences silencing of sex chromosomes in the male mouse germlineThe cohesin subunit RAD21L functions in meiotic synapsis and exhibits sexual dimorphism in fertilityPolycomb 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 meiosisMeiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanismsFunctional conservation of Mei4 for meiotic DNA double-strand break formation from yeasts to miceMouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPaseSpata22, a novel vertebrate-specific gene, is required for meiotic progress in mouse germ cellsMouse pachytene checkpoint 2 (trip13) is required for completing meiotic recombination but not synapsisMeiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in miceHORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activityMouse TRIP13/PCH2 is required for recombination and normal higher-order chromosome structure during meiosisMeiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1.HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytesATM controls meiotic double-strand-break formationAlignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) ProteinA dominant, recombination-defective allele of Dmc1 causing male-specific sterility.DNA polymerase beta is critical for mouse meiotic synapsis.Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytesDifferential expression and sex chromosome association of CHD3/4 and CHD5 during spermatogenesisBRCA1 establishes DNA damage signaling and pericentric heterochromatin of the X chromosome in male meiosis.p53 and TAp63 participate in the recombination-dependent pachytene arrest in mouse spermatocytes.Evolutionary conservation of meiotic DSB proteins: more than just Spo11The expression profile of the major mouse SPO11 isoforms indicates that SPO11beta introduces double strand breaks and suggests that SPO11alpha has an additional role in prophase in both spermatocytes and oocytes.Phosphorylation of chromosome core components may serve as axis marks for the status of chromosomal events during mammalian meiosisCul4A is essential for spermatogenesis and male fertility.The meiotic checkpoint network: step-by-step through meiotic prophaseEssential developmental, genomic stability, and tumour suppressor functions of the mouse orthologue of hSSB1/NABP2.Molecular basis for enhancement of the meiotic DMC1 recombinase by RAD51 associated protein 1 (RAD51AP1)
P2860
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P2860
Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage.
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Surveillance of different reco ...... identical developmental stage
@nl
Surveillance of different reco ...... identical developmental stage.
@ast
Surveillance of different reco ...... identical developmental stage.
@en
Surveillance of different reco ...... identical developmental stage.
@en-gb
type
label
Surveillance of different reco ...... identical developmental stage
@nl
Surveillance of different reco ...... identical developmental stage.
@ast
Surveillance of different reco ...... identical developmental stage.
@en
Surveillance of different reco ...... identical developmental stage.
@en-gb
prefLabel
Surveillance of different reco ...... identical developmental stage
@nl
Surveillance of different reco ...... identical developmental stage.
@ast
Surveillance of different reco ...... identical developmental stage.
@en
Surveillance of different reco ...... identical developmental stage.
@en-gb
P2093
P2860
P50
P3181
P1476
Surveillance of different reco ...... identical developmental stage.
@en
P2093
Maria Jasin
Paul S Burgoyne
Scott Keeney
Shantha Mahadevaiah
P2860
P304
P3181
P356
10.1128/MCB.25.16.7203-7215.2005
P407
P577
2005-08-01T00:00:00Z