Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
about
Human MMS21/NSE2 is a SUMO ligase required for DNA repairMethyl methanesulfonate (MMS) produces heat-labile DNA damage but no detectable in vivo DNA double-strand breaks.The products of the yeast MMS2 and two human homologs (hMMS2 and CROC-1) define a structurally and functionally conserved Ubc-like protein familyCloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutantMetabolism of sulfur amino acids in Saccharomyces cerevisiaeSrs2 and RecQ homologs cooperate in mei-3-mediated homologous recombination repair of Neurospora crassa.Genome-wide requirements for resistance to functionally distinct DNA-damaging agents.Requirement of Nse1, a subunit of the Smc5-Smc6 complex, for Rad52-dependent postreplication repair of UV-damaged DNA in Saccharomyces cerevisiae.Cloning and sequence analysis of the Saccharomyces cerevisiae RAD9 gene and further evidence that its product is required for cell cycle arrest induced by DNA damageMMS2, encoding a ubiquitin-conjugating-enzyme-like protein, is a member of the yeast error-free postreplication repair pathwayCloning and expression in Escherichia coli of a gene for an alkylbase DNA glycosylase from Saccharomyces cerevisiae; a homologue to the bacterial alkA gene.A role for MMS4 in the processing of recombination intermediates during meiosis in Saccharomyces cerevisiaeCloning a eukaryotic DNA glycosylase repair gene by the suppression of a DNA repair defect in Escherichia coli.Saccharomyces cerevisiae 3-methyladenine DNA glycosylase has homology to the AlkA glycosylase of E. coli and is induced in response to DNA alkylation damage.A role for ubiquitin in the clearance of nonfunctional rRNAsDNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiaeRole of RAD52 epistasis group genes in homologous recombination and double-strand break repairInteraction with RPA is necessary for Rad52 repair center formation and for its mediator activity.Radiation-sensitive mutants of Caenorhabditis elegans.A mapping method for Saccharomyces cerevisiae using rad52-induced chromosome lossThe RAD24 (= Rs1) gene product of Saccharomyces cerevisiae participates in two different pathways of DNA repair.Saccharomyces cerevisiae RAD52 alleles temperature-sensitive for the repair of DNA double-strand breaks.DNA repair protein Rad55 is a terminal substrate of the DNA damage checkpointsExcision repair is required for genotoxin-induced mutagenesis in mammalian cells.Meiosis in Neurospora crassa. I. The isolation of recessive mutants defective in the production of viable ascospores.The isolation of mms- and histidine-sensitive mutants in Neurospora crassa.HeLa cell variants that differ in sensitivity to monofunctional alkylating agents, with independence of cytotoxic and mutagenic responses.Genomic phenotyping of the essential and non-essential yeast genome detects novel pathways for alkylation resistance.Identification of a protein essential for a major pathway used by human cells to avoid UV- induced DNA damageA genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damageSmc5p promotes faithful chromosome transmission and DNA repair in Saccharomyces cerevisiae.A core activity associated with the N terminus of the yeast RAD52 protein is revealed by RAD51 overexpression suppression of C-terminal rad52 truncation alleles.Analyzing the dose-dependence of the Saccharomyces cerevisiae global transcriptional response to methyl methanesulfonate and ionizing radiation.Functional Validation of Rare Human Genetic Variants Involved in Homologous Recombination Using Saccharomyces cerevisiae.The Mus81 solution to resolution: generating meiotic crossovers without Holliday junctions.Induction of S.cerevisiae MAG 3-methyladenine DNA glycosylase transcript levels in response to DNA damage.Complementation of Yeast Genes with Human Genes as an Experimental Platform for Functional Testing of Human Genetic Variants.Spontaneous mitotic recombination in mms8-1, an allele of the CDC9 gene of Saccharomyces cerevisiaea/alpha-specific effect on the mms3 mutation on ultraviolet mutagenesis in Saccharomyces cerevisiae.Mutations in yeast proliferating cell nuclear antigen define distinct sites for interaction with DNA polymerase delta and DNA polymerase epsilon.
P2860
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P2860
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
description
1977 nî lūn-bûn
@nan
1977 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1977 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1977年の論文
@ja
1977年論文
@yue
1977年論文
@zh-hant
1977年論文
@zh-hk
1977年論文
@zh-mo
1977年論文
@zh-tw
1977年论文
@wuu
name
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@ast
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@en
type
label
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@ast
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@en
prefLabel
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@ast
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@en
P2860
P1433
P1476
Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae.
@en
P2093
P2860
P407
P577
1977-05-01T00:00:00Z