Salk Institute for Biological Studies;The University of Sydney
发明人:
申请号：
EP14787709.6
公开号：
EP2988752A4
申请日:
2014.04.24
申请国别(地区):
EP
年份:
2017
代理人:
摘要：
The present disclosure provides compositions that include a nanoparticle and a compound that increases the biological activity of the vitamin D receptor (VDR) (e.g., a VDR agonist), and methods of using such compounds to increase retention or storage of vitamin A, vitamin D, and/or lipids by a cell, such as an epithelial or stellate cell. Such methods can be used to treat or prevent fibrosis.
