Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 9, 1997, Pages 4538-4542

  Fritz, Eberhard ^a   Elsea, Sarah H ^b   Patel, Pragna I ^b   Meyn, M Stephen ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

DNA repair; genetic recombination; topoisomerase

Indexed keywords

COMPLEMENTARY DNA; DNA TOPOISOMERASE; HELICASE;

ARTICLE; ATAXIA TELANGIECTASIA; AUTOSOMAL RECESSIVE DISORDER; CANCER RISK; DNA DAMAGE; DNA REPAIR; DNA SEQUENCE; GENE EXPRESSION; GENETIC RECOMBINATION; GENETIC STABILITY; HUMAN; HUMAN CELL; IMMUNE DEFICIENCY; MOLECULAR CLONING; PRIORITY JOURNAL; RADIOSENSITIVITY;

EID: 0030940537     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.9.4538     Document Type: Article

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