Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia

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

Volumn 99, Issue 23, 2002, Pages 15101-15106

  Wiemels, Joseph L ^a   Leonard, Brian C ^a   Wang, Yunxia ^a   Segal, Mark R ^a   Hunger, Stephen P ^a   Smith, Martyn T ^a   Crouse, Vonda ^a   Ma, Xiaomei ^a   Buffler, Patricia A ^a   Pine, Sharon R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HYBRID PROTEIN; IMMUNOGLOBULIN HEAVY CHAIN; NUCLEOSIDE; T LYMPHOCYTE RECEPTOR;

ACUTE LYMPHOBLASTIC LEUKEMIA; ADULT; ARTICLE; CHILD; CHROMOSOME 1; CHROMOSOME 19; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; FEMALE; GENE; GENE E2A; GENE FUSION; GENE PBX1; GENETIC SCREENING; HUMAN; HUMAN CELL; INTRON; LEUKEMOGENESIS; MALE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; TUMOR CELL LINE;

ADOLESCENT; ARTIFICIAL GENE FUSION; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; GENE REARRANGEMENT; HOMEODOMAIN PROTEINS; HUMANS; IMMUNOGLOBULIN HEAVY CHAINS; INFANT; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; MALE; MOLECULAR SEQUENCE DATA; ONCOGENE PROTEINS, FUSION; POLYMERASE CHAIN REACTION; RECEPTORS, ANTIGEN, T-CELL; RESTRICTION MAPPING; TRANSLOCATION, GENETIC;

EID: 18744372705     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.222481199     Document Type: Article

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