Fanconi anemia group J mutation abolishes its DNA repair function by uncoupling DNA translocation from helicase activity or disruption of protein-DNA complexes

Blood

Volumn 116, Issue 19, 2010, Pages 3780-3791

  Wu, Yuliang ^a   Sommers, Joshua A ^a   Suhasini, Avvaru N ^a   Leonard, Thomas ^b   Deakyne, Julianna S ^c   Mazin, Alexander V ^c   Shin ya, Kazuo ^d   Kitao, Hiroyuki ^e   Brosh Jr , Robert M ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

^d NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^e KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CISPLATIN; CYSTEINE; FANCONI ANEMIA GROUP J PROTEIN; FANCONI ANEMIA PROTEIN; HELICASE; IRON SULFUR PROTEIN; RECOMBINANT PROTEIN; TELOMESTATIN; UNCLASSIFIED DRUG;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CELL FUNCTION; CELL SURVIVAL; DNA METABOLISM; DNA PROTEIN COMPLEX; DNA REPAIR; ENZYME ACTIVITY; FANCONI ANEMIA; GENE TRANSLOCATION; GENETIC LINKAGE; HYDROLYSIS; MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PURIFICATION;

EID: 77958512174     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2009-11-256016     Document Type: Article

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