Deciphering von Hippel-Lindau (VHL/Vhl)-Associated Pancreatic Manifestations by Inactivating Vhl in Specific Pancreatic Cell Populations

The von Hippel-Lindau (VHL) syndrome is a pleomorphic familial disease characterized by the development of highly vascularized tumors, such as hemangioblastomas of the central nervous system, pheochromocytomas, renal cell carcinomas, cysts and neuroendocrine tumors of the pancreas. Up to 75% of VHL...

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Détails bibliographiques
Auteurs principaux: Shen, H.-C. Jennifer, Adem, Asha, Ylaya, Kris, Wilson, Arianne, He, Mei, Lorang, Dominique, Hewitt, Stephen M., Pechhold, Klaus, Harlan, David M., Lubensky, Irina A., Schmidt, Laura S., Linehan, W. Marston, Libutti, Steven K.
Format: Artigo
Langue:Inglês
Publié: Public Library of Science 2009
Sujets:
Research Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2660574/
https://ncbi.nlm.nih.gov/pubmed/19340311
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0004897
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