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Page 1
Molecular heterogeneity of RET loss of function in Hirschsprung's disease.
Carlomagno F, De Vita G, Berlingieri MT, de Franciscis V, Melillo RM, Colantuoni V, Kraus MH, Di Fiore PP, Fusco A, Santoro M. Carlomagno F, et al. Among authors: de vita g, de franciscis v. EMBO J. 1996 Jun 3;15(11):2717-25. EMBO J. 1996. PMID: 8654369 Free PMC article.
A potential pathogenetic mechanism for multiple endocrine neoplasia type 2 syndromes involves ret-induced impairment of terminal differentiation of neuroepithelial cells.
Califano D, D'Alessio A, Colucci-D'Amato GL, De Vita G, Monaco C, Santelli G, Di Fiore PP, Vecchio G, Fusco A, Santoro M, de Franciscis V. Califano D, et al. Among authors: de vita g, de franciscis v. Proc Natl Acad Sci U S A. 1996 Jul 23;93(15):7933-7. doi: 10.1073/pnas.93.15.7933. Proc Natl Acad Sci U S A. 1996. PMID: 8755580 Free PMC article.
Ligand stimulation of a Ret chimeric receptor carrying the activating mutation responsible for the multiple endocrine neoplasia type 2B.
Rizzo C, Califano D, Colucci-D'Amato GL, De Vita G, D'Alessio A, Dathan NA, Fusco A, Monaco C, Santelli G, Vecchio G, Santoro M, de Franciscis V. Rizzo C, et al. Among authors: de vita g, de franciscis v. J Biol Chem. 1996 Nov 15;271(46):29497-501. doi: 10.1074/jbc.271.46.29497. J Biol Chem. 1996. PMID: 8910618 Free article.
105 results