Progenitor Cell Line (hPheo1) Derived from a Human Pheochromocytoma Tumor

BACKGROUND: Pheochromocytomas are rare tumors generally arising in the medullary region of the adrenal gland. These tumors release excessive epinephrine and norepinephrine resulting in hypertension and cardiovascular crises for which surgery is the only definitive treatment. Molecular mechanisms tha...

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Main Authors:	Ghayee, Hans K., Bhagwandin, Vikash J., Stastny, Victor, Click, Arielle, Ding, Liang-Hao, Mizrachi, Dario, Zou, Ying S., Chari, Raj, Lam, Wan L., Bachoo, Robert M., Smith, Alice L., Story, Michael D., Sidhu, Stan, Robinson, Bruce G., Nwariaku, Fiemu E., Gazdar, Adi F., Auchus, Richard J., Shay, Jerry W.
Format:	Artigo
Sprog:	Inglês
Udgivet:	Public Library of Science 2013
Fag:	Research Article
Online adgang:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3681983/ https://ncbi.nlm.nih.gov/pubmed/23785438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0065624
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Progenitor Cell Line (hPheo1) Derived from a Human Pheochromocytoma Tumor

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