MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
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MutS homologue hMSH4: interaction with eIF3f and a role in NHEJ-mediated DSB repairExtreme heterogeneity in the molecular events leading to the establishment of chiasmata during meiosis i in human oocytes.Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese menhMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machineryDNA mismatch repair: molecular mechanism, cancer, and ageingTwo single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrestRole for Msh5 in the regulation of Ig class switch recombinationMolecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesisManipulation of DNA Repair Proficiency in Mouse Models of Colorectal CancerGenetics of the ovarian reserveGenetics of primary ovarian insufficiency: new developments and opportunitiesConditional inactivation of the DNA damage response gene Hus1 in mouse testis reveals separable roles for components of the RAD9-RAD1-HUS1 complex in meiotic chromosome maintenanceMammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesisPostreplicative mismatch repair.The budding yeast Msh4 protein functions in chromosome synapsis and the regulation of crossover distribution.Genetic analysis of mlh3 mutations reveals interactions between crossover promoting factors during meiosis in baker's yeast.Impact of DNA mismatch repair system alterations on human fertility and related treatmentsInactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterilityVariation in crossover frequencies perturb crossover assurance without affecting meiotic chromosome segregation in Saccharomyces cerevisiaeDelineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvaseThe Saccharomyces cerevisiae Mlh1-Mlh3 heterodimer is an endonuclease that preferentially binds to Holliday junctions.Mutation of the mouse Syce1 gene disrupts synapsis and suggests a link between synaptonemal complex structural components and DNA repairStructural and functional divergence of MutS2 from bacterial MutS1 and eukaryotic MSH4-MSH5 homologs.Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase IRegulated CPEB phosphorylation during meiotic progression suggests a mechanism for temporal control of maternal mRNA translationMeiotic failure in male mice lacking an X-linked factorRNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosisMouse HFM1/Mer3 is required for crossover formation and complete synapsis of homologous chromosomes during meiosisPositional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in miceDeletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell lossFancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in miceC14ORF39/SIX6OS1 is a constituent of the synaptonemal complex and is essential for mouse fertilityMouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formationMammalian CNTD1 is critical for meiotic crossover maturation and deselection of excess precrossover sitesA novel testis-enriched gene Spata33 is expressed during spermatogenesisOvol1 regulates meiotic pachytene progression during spermatogenesis by repressing Id2 expressionMEIOB exhibits single-stranded DNA-binding and exonuclease activities and is essential for meiotic recombinationMutation in mouse hei10, an e3 ubiquitin ligase, disrupts meiotic crossing overAlignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) ProteinA meiotic chromosomal core consisting of cohesin complex proteins recruits DNA recombination proteins and promotes synapsis in the absence of an axial element in mammalian meiotic cells.
P2860
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P248
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P2860
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
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2000 nî lūn-bûn
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2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2000 թվականի մայիսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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MutS homolog 4 localization to ...... eiosis in male and female mice
@ast
MutS homolog 4 localization to ...... eiosis in male and female mice
@en
MutS homolog 4 localization to ...... eiosis in male and female mice
@nl
type
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MutS homolog 4 localization to ...... eiosis in male and female mice
@ast
MutS homolog 4 localization to ...... eiosis in male and female mice
@en
MutS homolog 4 localization to ...... eiosis in male and female mice
@nl
prefLabel
MutS homolog 4 localization to ...... eiosis in male and female mice
@ast
MutS homolog 4 localization to ...... eiosis in male and female mice
@en
MutS homolog 4 localization to ...... eiosis in male and female mice
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P2093
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MutS homolog 4 localization to ...... eiosis in male and female mice
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P2093
E Avdievich
J W Pollard
R D Kolodner
R Kucherlapati
W Edelmann
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2000-05-01T00:00:00Z