Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines

Genes Chromosomes and Cancer

Volumn 20, Issue 1, 1997, Pages 16-23

  Ong, S Tiong ^a   Fong, Kwun M ^b   Bader, Scott A ^b   Minna, John D ^b   Le Beau, Michelle M ^a   McKeithan, Timothy W ^a   Rassool, Feyruz V ^a,c  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^c UNIVERSITY OF CHICAGO MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 3P; CONTROLLED STUDY; GENE DELETION; GENE REARRANGEMENT; HUMAN; HUMAN CELL; LUNG CANCER; PRIORITY JOURNAL; TUMOR CELL CULTURE; TUMOR SUPPRESSOR GENE;

ACID ANHYDRIDE HYDROLASES; BASE SEQUENCE; BLOTTING, SOUTHERN; CHROMOSOME DELETION; CHROMOSOME FRAGILE SITES; CHROMOSOME FRAGILITY; CHROMOSOMES, HUMAN, PAIR 3; CLONING, MOLECULAR; DNA PROBES; DNA, NEOPLASM; GENE EXPRESSION REGULATION, NEOPLASTIC; GENOMIC LIBRARY; HUMANS; MOLECULAR SEQUENCE DATA; NEOPLASM PROTEINS; POLYMERASE CHAIN REACTION; PROTEINS; RNA, NEOPLASM; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; TUMOR CELLS, CULTURED;

EID: 0030930174     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199709)20:1<16::AID-GCC3>3.0.CO;2-C     Document Type: Article

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