Research Project
Grant-in-Aid for Challenging Exploratory Research
1.We identified UBA5 as a causative gene for a hereditary developmental disease. 2.We generated knock-in mice harboring the disease-related Uba5 mutation. 3.We developed an experiment system that we can easily detect Ufm1-conjugated proteins, and we identified several novel targets for Ufm1 using this system.
All 2016 2015 2014 Other
All Int'l Joint Research (3 results) Journal Article (2 results) (of which Int'l Joint Research: 1 results, Peer Reviewed: 2 results, Open Access: 1 results, Acknowledgement Compliant: 1 results) Presentation (1 results) Remarks (3 results)
J Biol Chem.
Volume: - Issue: 17 Pages: 9025-9041
10.1074/jbc.m116.715474
Mol. Cell
Volume: 56 Issue: 2 Pages: 261-274
10.1016/j.molcel.2014.08.007
http://www.med.niigata-u.ac.jp/bc1/welcome.html
http://www.helsinki.fi/neurosci/groups/lehesjoki_group.html