Differential activity of c-KIT splice forms is controlled by extracellular peptide insert length

Cellular Signalling

Volumn 25, Issue 11, 2013, Pages 2231-2238

  Phung, Bengt ^a,b   Steingrímsson, Eiríkur ^b   Rönnstrand, Lars ^a  

^a LUND UNIVERSITY   (Sweden)

^b UNIVERSITY OF ICELAND   (Iceland)

Author keywords

Growth factor receptor; Melanoma survival; Pigment synthesis; Receptor kinase rotation; Splice form; Stem cell factor

Indexed keywords

MELANIN; MITOGEN ACTIVATED PROTEIN KINASE; STEM CELL FACTOR RECEPTOR; TETRAPEPTIDE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CELL SURVIVAL; CONTROLLED STUDY; INTERNALIZATION; MELANOGENESIS; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN PHOSPHORYLATION; UBIQUITINATION;

GROWTH FACTOR RECEPTOR; MELANOMA SURVIVAL; PIGMENT SYNTHESIS; RECEPTOR KINASE ROTATION; SPLICE FORM; STEM CELL FACTOR;

ALTERNATIVE SPLICING; ANIMALS; CELL LINE, TUMOR; CELL SURVIVAL; GENE EXPRESSION REGULATION, NEOPLASTIC; HUMANS; MICE; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; PHOSPHORYLATION; PROTEIN ISOFORMS; PROTEIN STRUCTURE, TERTIARY; PROTO-ONCOGENE PROTEINS C-KIT; SIGNAL TRANSDUCTION; UBIQUITINATION;

EID: 84882652190     PISSN: 08986568     EISSN: 18733913     Source Type: Journal    
DOI: 10.1016/j.cellsig.2013.07.011     Document Type: Article

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