Identification of recurrent USP48 and BRAF mutations in Cushing’s disease
In this study the authors report USP48 and BRAF are frequently mutated in USP8 wild-type corticotroph adenomas, and cause Cushing’s disease mainly through promoting the promoter activity of POMC. Inhibition of BRAF may be a promising therapeutic strategy for the treatment of patients with BRAF-mutat...
Saved in:
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2018
|
Subjects: | |
Online Access: | https://doaj.org/article/2b3bf5b0c1aa40f1ad4cc48e49ee5bed |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Be the first to leave a comment!