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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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Detalhes bibliográficos
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.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2010
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Acesso em linha: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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