화학공학소재연구정보센터
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