Somatic heterozygous mutations in ETV6 (TEL) and frequent absence of ETV6 protein in acute myeloid leukemia

Oncogene

Volumn 24, Issue 25, 2005, Pages 4129-4137

  Van Waalwijk Van Doorn Khosrovani, Sahar Barjesteh ^a   Spensberger, Dominik ^a   De Knegt, Yvonne ^a   Tang, Michelle ^a   Löwenberg, Bob ^a   Delwel, Ruud ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

AML; ETV6; TEL

Indexed keywords

COMPLEMENTARY DNA; ETS TRANSLOCATION VARIANT 6; LUCIFERASE; MESSENGER RNA; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ACUTE GRANULOCYTIC LEUKEMIA; ARTICLE; BINDING SITE; CONTROLLED STUDY; DIMERIZATION; DNA POLYMORPHISM; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; KARYOTYPE; LEUKEMOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEQUENCE ANALYSIS; SOMATIC MUTATION; TRANSCRIPTION REGULATION; WESTERN BLOTTING;

ACUTE DISEASE; BONE MARROW CELLS; DNA-BINDING PROTEINS; GENE DELETION; GENE FREQUENCY; HETEROZYGOTE; HUMANS; LEUKEMIA, MYELOID; MUTATION; NUCLEAR PROTEINS; PHOSPHOPROTEINS; PROTO-ONCOGENE PROTEINS C-ETS; REPRESSOR PROTEINS; SEQUENCE DELETION; TRANSLOCATION, GENETIC;

EID: 21344448655     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1208588     Document Type: Article

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