The Ret(C620R) Mutation Affects Renal and Enteric Development in a Mouse Model of Hirschsprung’s Disease

In rare families RET tyrosine kinase receptor substitutions located in exon 10 (especially at positions 609, 618, and 620) can concomitantly cause the MEN 2A (multiple endocrine neoplasia type 2A) or FMTC (familial medullary thyroid carcinoma) cancer syndromes, and Hirschsprung’s disease (HSCR). No...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Carniti, Cristiana, Belluco, Sara, Riccardi, Elena, Cranston, Aaron N., Mondellini, Piera, Ponder, Bruce A.J., Scanziani, Eugenio, Pierotti, Marco A., Bongarzone, Italia
Format: Artigo
Idioma:Inglês
Publicat: American Society for Investigative Pathology 2006
Matèries:
Original Research Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1606559/
https://ncbi.nlm.nih.gov/pubmed/16565500
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2006.050607
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars