Wordt geladen...
The same pocket in menin binds both MLL and JunD, but oppositely regulates transcription
Menin is a tumor suppressor protein whose loss or inactivation causes multiple endocrine neoplasia type 1 (MEN1), a hereditary autosomal dominant tumor syndrome characterized by tumorigenesis in multiple endocrine organs(1). Menin interacts with a multitude of proteins and involves in a variety of c...
Bewaard in:
| Hoofdauteurs: | , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2012
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3983792/ https://ncbi.nlm.nih.gov/pubmed/22327296 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature10806 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|