검색결과 : 4건
| No. | Article |
|---|---|
| 1 |
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 |
| 2 |
The C-terminal HCN4 variant P883R alters channel properties and acts as genetic modifier of atrial fibrillation and structural heart disease Weigl I, Geschwill P, Reiss M, Bruehl C, Draguhn A, Koenen M, Sedaghat-Hamedani F, Meder B, Thomas D, Katus HA, Schweizer PA Biochemical and Biophysical Research Communications, 519(1), 141, 2019 |
| 3 |
Vernakalant activates human cardiac K(2P)17.1 background K+ channels Seyler C, Schweizer PA, Zitron E, Katus HA, Thomas D Biochemical and Biophysical Research Communications, 451(3), 415, 2014 |
| 4 |
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 |