검색결과 : 3건
No. | Article |
---|---|
1 |
A novel Kir7.1 splice variant expressed in various mouse tissues shares organisational and functional properties with human Leber amaurosis-causing mutations of this K+ channel Vera E, Cornejo I, Burgos J, Niemeyer MI, Sepulveda FV, Cid LP Biochemical and Biophysical Research Communications, 514(3), 574, 2019 |
2 |
Negative charge of the glutamic acid 417 residue is crucial for isomerohydrolase activity of RPE65 Nikolaeva O, Takahashi Y, Moiseyev G, Ma JX Biochemical and Biophysical Research Communications, 391(4), 1757, 2010 |
3 |
Abolished interaction of NUB1 with mutant AIPL1 involved in Leber congenital amaurosis Kanaya K, Sohocki MM, Kamitani T Biochemical and Biophysical Research Communications, 317(3), 768, 2004 |