Chl1 and Ctf4 are required for damage-induced recombinations

Biochemical and Biophysical Research Communications

Volumn 354, Issue 1, 2007, Pages 222-226

  Ogiwara, Hideaki ^a   Ui, Ayako ^a   Lai, Mong Sing ^a   Enomoto, Takemi ^a   Seki, Masayuki ^a  

^a TOHOKU UNIVERSITY   (Japan)

Author keywords

Chl1; Ctf4; Genome stability; Recombination; Repair; Sister chromatid cohesion

Indexed keywords

CAMPTOTHECIN; DNA BINDING PROTEIN; HYDROXYUREA; MESYLIC ACID; PHLEOMYCIN; PROTEIN; PROTEIN CHL1; PROTEIN CTF4; RAD52 PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL CYCLE PHASE; CHROMOSOME DAMAGE; CONTROLLED STUDY; DIPLOIDY; DNA DAMAGE; DNA PROTEIN COMPLEX; DNA RECOMBINATION; DNA REPAIR; FUNCTIONAL PROTEOMICS; GENE DELETION; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HAPLOIDY; HOMOLOGOUS RECOMBINATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DNA BINDING; PROTEIN DNA INTERACTION; PROTEIN FUNCTION; SISTER CHROMATID; SISTER CHROMATID COHESION;

CHROMOSOMAL PROTEINS, NON-HISTONE; DNA DAMAGE; DNA REPAIR; DNA, FUNGAL; DNA-BINDING PROTEINS; GENOMIC INSTABILITY; RECOMBINATION, GENETIC; SACCHAROMYCES CEREVISIAE PROTEINS; SISTER CHROMATID EXCHANGE;

EID: 33846323201     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.12.185     Document Type: Article

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