Menin represses malignant phenotypes of melanoma through regulating multiple pathways

Substantial genetic evidence suggests that chromosome 11q is involved in regulating initiation and progression of malignant melanomas. Mutations of the MEN1 gene, located in chromosome 11q13, predispose individuals to the multiple endocrine neoplasia type 1 (MEN1) familial syndrome. MEN1 patients de...

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Detalles Bibliográficos
Autores principales: Gao, Shu-Bin, Feng, Zi-Jie, Xu, Bin, Chen, Yan, Zheng, Hong-Hua, Yin, Ping, Hua, Xianxin, Jin, Guang-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822947/
https://www.ncbi.nlm.nih.gov/pubmed/21129151
http://dx.doi.org/10.1111/j.1582-4934.2010.01222.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822947/
https://www.ncbi.nlm.nih.gov/pubmed/21129151
http://dx.doi.org/10.1111/j.1582-4934.2010.01222.x

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