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The VHL gene is epigenetically inactivated in pheochromocytomas and abdominal paragangliomas

Pheochromocytoma (PCC) and abdominal paraganglioma (PGL) are neuroendocrine tumors that present with clinical symptoms related to increased catecholamine levels. About a third of the cases are associated with constitutional mutations in pre-disposing genes, of which some may also be somatically muta...

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Detalhes bibliográficos
Main Authors: Andreasson, Adam, Kiss, Nimrod B, Caramuta, Stefano, Sulaiman, Luqman, Svahn, Fredrika, Bäckdahl, Martin, Höög, Anders, Juhlin, C Christofer, Larsson, Catharina
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3933494/
https://ncbi.nlm.nih.gov/pubmed/24149047
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/epi.26686
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