RecQ family helicases: Roles as tumor suppressor proteins

Oncogene

Volumn 21, Issue 58 REV. ISS. 8, 2002, Pages 9008-9021

  Nakayama, Hiroaki ^a,b  

^a KYUSHU UNIVERSITY   (Japan)

^b NONE   (Japan)

Author keywords

Bloom's syndrome; Cancer predisposition; Hyper recombination; RecQ helicase; Rothmund Thomson syndrome; Werner's syndrome

Indexed keywords

HELICASE; RECQ HELICASE; TUMOR SUPPRESSOR PROTEIN; UNCLASSIFIED DRUG;

BLOOM SYNDROME; CANCER SUSCEPTIBILITY; CHROMOSOME ABERRATION; ESCHERICHIA COLI; GENETIC RECOMBINATION; GENETIC STABILITY; HETEROZYGOSITY LOSS; HUMAN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FAMILY; REVIEW; ROTHMUND THOMSON SYNDROME; TUMOR SUPPRESSOR GENE; WERNER SYNDROME;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; APOPTOSIS; DNA; DNA HELICASES; DNA REPAIR; DNA REPLICATION; ESCHERICHIA COLI PROTEINS; GENES, TUMOR SUPPRESSOR; HUMANS; MOLECULAR SEQUENCE DATA; RECOMBINATION, GENETIC; RECQ HELICASES; SEQUENCE HOMOLOGY, AMINO ACID;

ESCHERICHIA COLI; PYRONIA TITHONUS;

EID: 0037115947     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1205959     Document Type: Review

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