Tyrosine kinase receptors as molecular targets In pheochromocytomas and paragangliomas

Pheochromocytomas and paragangliomas are neuroendocrine tumors shown to be responsive to multi-targeted tyrosine kinase inhibitor treatment. Despite growing knowledge regarding their genetic basis, the ability to predict behavior in these tumors remains challenging. There is also limited knowledge o...

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Detalles Bibliográficos
Autores principales: Cassol, Clarissa A., Winer, Daniel, Liu, Wei, Guo, Miao, Ezzat, Shereen, Asa, Sylvia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977182/
https://www.ncbi.nlm.nih.gov/pubmed/24390213
http://dx.doi.org/10.1038/modpathol.2013.233

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977182/
https://www.ncbi.nlm.nih.gov/pubmed/24390213
http://dx.doi.org/10.1038/modpathol.2013.233

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