A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity

Human Molecular Genetics

Volumn 20, Issue 4, 2011, Pages 820-826

  Gu, Jian ^a   Ye, Yuanqing ^a   Spitz, Margaret R ^a   Lin, Jie ^a   Kiemeney, Lambertus A ^b   Xing, Jingliang ^a   Hildebrandt, Michelle A T ^a   Ki Hong, Waun ^a   Amos, Christopher I ^a   Wu, Xifeng ^a  

^a UNIVERSITY OF TEXAS MD ANDERSON CANCER CENTER   (United States)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BLEOMYCIN; PROTEIN NOXA;

ADULT; AGED; ARTICLE; CHEMOSENSITIVITY; CHROMOSOME 18Q; CHROMOSOME BREAKAGE; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HOMOZYGOTE; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; MALE; NORMAL HUMAN; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; WILD TYPE;

AGED; AGED, 80 AND OVER; BLEOMYCIN; CASE-CONTROL STUDIES; CHROMATIN; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 18; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MIDDLE AGED; MUTAGENS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS C-BCL-2; TUMOR MARKERS, BIOLOGICAL; YOUNG ADULT;

EID: 78751697971     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddq509     Document Type: Article

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