검색결과 : 28건
| No. | Article |
|---|---|
| 1 |
Serine mutation of a conserved threonine in the hERG K+ channel S6-pore region leads to loss-of-function through trafficking impairment Al-Moubarak E, Zhang YH, Dempsey CE, Zhang HG, Harmer SC, Hancox JC Biochemical and Biophysical Research Communications, 526(4), 1085, 2020 |
| 2 |
ANK2 functionally interacts with KCNH2 aggravating long QT syndrome in a double mutation carrier Gessner G, Runge S, Koenen M, Heinemann SH, Koenen M, Haas J, Meder B, Thomas D, Katus HA, Schweizer PA Biochemical and Biophysical Research Communications, 512(4), 845, 2019 |
| 3 |
Identification and functional characterization of the novel human ether-a-go-go-related gene (hERG) R744P mutant associated with hereditary long QT syndrome 2 Aidery P, Kisselbach J, Gaspar H, Baldea L, Schweizer PA, Becker R, Katus HA, Thomas D Biochemical and Biophysical Research Communications, 418(4), 830, 2012 |
| 4 |
A422T mutation in HERG potassium channel retained in ER is rescurable by pharmacologic or molecular chaperones Guo J, Zhang XM, Hu ZS, Zhuang Z, Zhu ZH, Chen Z, Chen W, Zhao ZZ, Zhang CY, Zhang Z Biochemical and Biophysical Research Communications, 422(2), 305, 2012 |
| 5 |
Reconstitution of defective protein trafficking rescues Long-QT syndrome in zebrafish Meder B, Scholz EP, Hassel D, Wolff C, Just S, Berger IM, Patzel E, Karle C, Katus HA, Rottbauer W Biochemical and Biophysical Research Communications, 408(2), 218, 2011 |
| 6 |
Expression, purification, detergent screening and solution NMR backbone assignment of the human potassium channel accessory subunit MiRP1 Chen L, Lai CH, Lai JH, Tian CL Protein Expression and Purification, 76(2), 205, 2011 |
| 7 |
A new approach to long QT syndrome mutation detection by Sequenom MassARRAY (R) system Allegue C, Gil R, Sanchez-Diz P, Torres M, Quintela I, Carracedo A, Brion M Electrophoresis, 31(10), 1648, 2010 |
| 8 |
Evaluation of channel function after alteration of amino acid residues at the pore center of KCNQ1 channel Ikrar T, Hanawa H, Watanabe H, Aizawa Y, Ramadan MM, Chinushi M, Horie M, Aizawa Y Biochemical and Biophysical Research Communications, 378(3), 589, 2009 |
| 9 |
Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function Li W, Wang QF, Du R, Xu QM, Ke QM, Wang B, Chen XL, Tian L, Zhang SY, Kang CL, Guan SM, Yang JG, Song ZF Biochemical and Biophysical Research Communications, 380(1), 127, 2009 |
| 10 |
The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes Li W, Du R, Wang QF, Tian L, Yang JG, Song ZF Biochemical and Biophysical Research Communications, 383(2), 206, 2009 |