Menin localization in cell membrane compartment

Menin is encoded by the MEN1 gene, which is mutated in an inherited human syndrome, multiple endocrine neoplasia type 1(MEN1). Menin is primarily nuclear protein, acting as a tumor suppressor in endocrine organs, but as an oncogenic factor in the mixed lineage leukemia, in a tissue-specific manner....

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Publicat a:Cancer Biol Ther
Autors principals: He, Xin, Wang, Lei, Yan, Jizhou, Yuan, Chaoxing, Witze, Eric S., Hua, Xianxin
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 2015
Matèries:
Research Paper
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4847924/
https://ncbi.nlm.nih.gov/pubmed/26560942
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15384047.2015.1108497
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