Isoforms of c-KIT differ in activation of signalling pathways and transformation of NIH3T3 fibroblasts

Oncogene

Volumn 18, Issue 40, 1999, Pages 5573-5581

  Caruana, Georgina ^a,b   Cambareri, Antony C ^a   Ashman, Leonie K ^a  

^a INSTITUTE OF MEDICAL AND VETERINARY SCIENCE   (Australia)

^b MOUNT SINAI HOSPITAL   (Canada)

Author keywords

c KIT; Isoforms; Ligand binding; Signal transduction; Transformation

Indexed keywords

MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHATIDYLINOSITOL 3 KINASE; STEEL FACTOR; STEM CELL FACTOR;

ALTERNATIVE RNA SPLICING; ANCHORAGE INDEPENDENT GROWTH; ANIMAL CELL; ARTICLE; AUTOPHOSPHORYLATION; CARCINOGENICITY; CELL STRAIN 3T3; CELL TRANSFORMATION; COLONY FORMATION; CONTACT INHIBITION; CONTROLLED STUDY; ENDOCYTOSIS; ENZYME ACTIVATION; INTERNALIZATION; LIGAND BINDING; MOUSE; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION;

1-PHOSPHATIDYLINOSITOL 3-KINASE; 3T3 CELLS; AMINO ACID SEQUENCE; ANIMALS; CELL ADHESION; CELL TRANSFORMATION, NEOPLASTIC; DNA, COMPLEMENTARY; HUMANS; MICE; MICE, NUDE; PROTEIN ISOFORMS; PROTO-ONCOGENE PROTEINS C-KIT; RECOMBINANT FUSION PROTEINS; RNA SPLICING; SIGNAL TRANSDUCTION; STEM CELL FACTOR; TRANSFECTION; TUMOR STEM CELL ASSAY;

ANIMALIA; MUS MUSCULUS;

EID: 0033619144     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1202939     Document Type: Article

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