Role of the TEL-AML1 fusion gene in the molecular pathogenesis of childhood acute lymphoblastic leukaemia

Oncogene

Volumn 23, Issue 24, 2004, Pages 4275-4283

  Zelent, Arthur ^a   Greaves, Mel ^a   Enver, Tariq ^b  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Co repressor; Histone deacetylase; Prenatal; Translocation

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX 1; UNCLASSIFIED DRUG; ONCOPROTEIN; TEL AML1 FUSION PROTEIN; TEL-AML1 FUSION PROTEIN; TRANSCRIPTION FACTOR RUNX1;

ACUTE LYMPHOBLASTIC LEUKEMIA; B CELL LYMPHOMA; BLAST TRANSFORMATION; CHIMERA; CHROMOSOME TRANSLOCATION; DISEASE MARKER; FUSION GENE; GENE EXPRESSION; GENE FREQUENCY; GENE FUNCTION; GENE LOCUS; GENE REARRANGEMENT; GENETIC ASSOCIATION; GENETIC CODE; HEMATOLOGIC MALIGNANCY; HUMAN; LEUKEMOGENESIS; PRIORITY JOURNAL; PROGNOSIS; PROTEIN STABILITY; REVIEW; TRANSCRIPTION INITIATION; ACUTE LYMPHOCYTIC LEUKEMIA; ANIMAL; DISEASE MODEL; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; METABOLISM;

ANIMALS; CORE BINDING FACTOR ALPHA 2 SUBUNIT; DISEASE MODELS, ANIMAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; ONCOGENE PROTEINS, FUSION; SEQUENCE ANALYSIS, DNA;

EID: 2942682886     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1207672     Document Type: Review

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