Mre11p nuclease activity is dispensable for telomeric rapid deletion

DNA Repair

Volumn 4, Issue 9, 2005, Pages 994-1005

  Williams, Bridget ^a   Bhattacharyya, Mrinal K ^a   Lustig, Arthur J ^a  

^a TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Mre11p; MRX complex; Recombination; Telomeres; TRD

Indexed keywords

DNA; MRE11 PROTEIN; NUCLEASE; CELL CYCLE PROTEIN; DEOXYRIBONUCLEASE; DNA BINDING PROTEIN; ENDONUCLEASE; EXODEOXYRIBONUCLEASE; MRE11 PROTEIN, S CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEIN; TELOMERE BINDING PROTEIN;

ALLELE; ARTICLE; BINDING SITE; CONTROLLED STUDY; DNA BINDING; DNA CONFORMATION; DNA STRUCTURE; ENZYME ACTIVITY; ENZYME STRUCTURE; NONHUMAN; NULL ALLELE; PRIORITY JOURNAL; PROTEIN DNA BINDING; PROTEIN DOMAIN; PROTEIN MOTIF; STRUCTURE ANALYSIS; TELOMERE; CHEMISTRY; DNA REPAIR; GENE DELETION; GENETIC RECOMBINATION; GENETICS; METABOLISM; PHYSIOLOGY; POLYACRYLAMIDE GEL ELECTROPHORESIS; SACCHAROMYCES CEREVISIAE; STRUCTURE ACTIVITY RELATION;

CELL CYCLE PROTEINS; DNA REPAIR; DNA-BINDING PROTEINS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; ENDODEOXYRIBONUCLEASES; ENDONUCLEASES; EXODEOXYRIBONUCLEASES; GENE DELETION; RECOMBINATION, GENETIC; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; STRUCTURE-ACTIVITY RELATIONSHIP; TELOMERE; TELOMERE-BINDING PROTEINS;

EID: 22044450040     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2005.04.016     Document Type: Article

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