Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma

Pheochromocytomas are rare neoplasias of neural crest origin arising from chromaffin cells of the adrenal medulla and sympathetic ganglia (extra-adrenal pheochromocytoma). Pheochromocytoma that develop in rats homozygous for a loss-of-function mutation in p27Kip1 (MENX syndrome) show a clear progres...

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Main Authors: Molatore, Sara, Liyanarachchi, Sandya, Irmler, Martin, Perren, Aurel, Mannelli, Massimo, Ercolino, Tonino, Beuschlein, Felix, Jarzab, Barbara, Wloch, Jan, Ziaja, Jacek, Zoubaa, Saida, Neff, Frauke, Beckers, Johannes, Höfler, Heinz, Atkinson, Michael J., Pellegata, Natalia S.
格式: Artigo
語言:Inglês
出版: National Academy of Sciences 2010
主題:
Biological Sciences
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2972990/
https://ncbi.nlm.nih.gov/pubmed/20937862
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1003956107
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