Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair
about
Genetics of primary ovarian insufficiency: new developments and opportunitiesA molecular model for the role of SYCP3 in meiotic chromosome organisationSUMO localizes to the central element of synaptonemal complex and is required for the full synapsis of meiotic chromosomes in budding yeast.MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instabilityMeiosis in mice without a synaptonemal complexIdentification of heat shock factor 1 molecular and cellular targets during embryonic and adult female meiosisA novel mouse synaptonemal complex protein is essential for loading of central element proteins, recombination, and fertilityMeiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanismsC14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertilityMouse 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 cellsMeiosis I arrest abnormalities lead to severe oligozoospermia in meiosis 1 arresting protein (M1ap)-deficient miceAccelerated reproductive aging in females lacking a novel centromere protein SYCP2L.Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1.Alignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) ProteinDnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissuesInterplay between synaptonemal complex, homologous recombination, and centromeres during mammalian meiosis.Structural insight into the central element assembly of the synaptonemal complexGenomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.NEK1 Facilitates Cohesin Removal during Mammalian SpermatogenesisOrganization of the synaptonemal complex during meiosis in Caenorhabditis elegans.Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia.Structural analysis of the human SYCE2-TEX12 complex provides molecular insights into synaptonemal complex assemblySpermatogenesis associated 22 is required for DNA repair and synapsis of homologous chromosomes in mouse germ cells.A Screen for Genomic Disorders of Infertility Identifies MAST2 Duplications Associated with Nonobstructive Azoospermia in Humans.Mouse models in male fertility researchThe DNA damage checkpoint protein RAD9A is essential for male meiosis in the mouse.Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure casesDynamic localization of SMC5/6 complex proteins during mammalian meiosis and mitosis suggests functions in distinct chromosome processesPhylogenies of central element proteins reveal the dynamic evolutionary history of the mammalian synaptonemal complex: ancient and recent components.A yeast two-hybrid screen for SYP-3 interactors identifies SYP-4, a component required for synaptonemal complex assembly and chiasma formation in Caenorhabditis elegans meiosis.Clamping down on mammalian meiosis.The Genetics of Infertility: Current Status of the Field.Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation.Premature ovarian failure: a critical condition in the reproductive potential with various genetic causes.Single-molecule observation of DNA compaction by meiotic protein SYCP3.Sister chromatid cohesion control and aneuploidy.Resolving complex chromosome structures during meiosis: versatile deployment of Smc5/6.Superresolution expansion microscopy reveals the three-dimensional organization of the Drosophila synaptonemal complex.Tex19.1 promotes Spo11-dependent meiotic recombination in mouse spermatocytes
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P2860
Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repair
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2009 nî lūn-bûn
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2009 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի փետրվարին հրատարակված գիտական հոդված
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2009年の論文
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2009年論文
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2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
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2009年论文
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name
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@ast
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@en
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@nl
type
label
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@ast
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@en
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@nl
prefLabel
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@ast
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@en
Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@nl
P2093
P2860
P3181
P1433
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Mutation of the mouse Syce1 ge ...... ural components and DNA repair
@en
P2093
Ewelina Bolcun-Filas
Howard J Cooke
Mary Taggart
Ricardo Benavente
Robert Speed
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1000393
P407
P577
2009-02-01T00:00:00Z