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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Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2009
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Research Article
On-line přístup: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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