The multiple endocrine neoplasia type 2B point mutation switches the specificity of the Ret tyrosine kinase towards cellular substrates that are susceptible to interact with Crk and Nck

Oncogene

Volumn 15, Issue 19, 1997, Pages 2257-2265

  Bocciardi, Renata ^a   Mograbi, Baharia ^a   Pasini, Barbara ^b   Borrello, Maria Grazia ^b   Pierotti, Marco A ^b   Bourget, Isabelle ^c   Fischer, Siegmund ^d   Romeo, Giovanni ^a,e   Rossi, Bernard ^c  

^a G GASLINI INSTITUTE   (Italy)

^b NATIONAL CANCER INSTITUTE   (Italy)

^c INSERM   (France)

^d Hôpital Cochin ^*  (France)

^e INTERNATIONAL AGENCY FOR RESEARCH ON CANCER   (France)

Author keywords

Crk; Multiple endocrine neoplasia type 2B; Nck; Paxillin; RET

Indexed keywords

CYTOSKELETON PROTEIN; METHIONINE; PROTEIN TYROSINE KINASE; THREONINE;

ANIMAL CELL; ARTICLE; AUTOPHOSPHORYLATION; ENZYME PHOSPHORYLATION; ENZYME SPECIFICITY; NEUROFIBROMATOSIS; NONHUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTO ONCOGENE;

ANIMALIA;

EID: 0030663857     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1201413     Document Type: Article

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