Nalaganje...
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....
Shranjeno v:
| izdano v: | Cancer Biol Ther |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Taylor & Francis
2015
|
| Teme: | |
| Online dostop: | 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 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|