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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...

詳細記述

保存先:
書誌詳細
主要な著者: Gao, Shu-Bin, Feng, Zi-Jie, Xu, Bin, Chen, Yan, Zheng, Hong-Hua, Yin, Ping, Hua, Xianxin, Jin, Guang-Hui
フォーマット: Artigo
言語:Inglês
出版事項: Blackwell Publishing Ltd 2011
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3822947/
https://ncbi.nlm.nih.gov/pubmed/21129151
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2010.01222.x
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