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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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Detaylı Bibliyografya
Asıl Yazarlar: Andreasson, Adam, Kiss, Nimrod B, Caramuta, Stefano, Sulaiman, Luqman, Svahn, Fredrika, Bäckdahl, Martin, Höög, Anders, Juhlin, C Christofer, Larsson, Catharina
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Landes Bioscience 2013
Konular:
Online Erişim: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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