검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
HERG K+ channel blockade by the antipsychotic drug thioridazine: An obligatory role for the S6 helix residue F656 Milnes JT, Witchel HJ, Leaney JL, Leishman DJ, Hancox JC Biochemical and Biophysical Research Communications, 351(1), 273, 2006 |
| 2 |
The N588K-HERG K+ channel mutation in the'short QT syndrome': Mechanism of gain-in-function determined at 37 degrees C McPate MJ, Duncan RS, Milnes JT, Witchel HJ, Hancox JC Biochemical and Biophysical Research Communications, 334(2), 441, 2005 |
| 3 |
Potent inhibition of human cardiac potassium (HERG) channels by the anti-estrogen agent clomiphene - without QT interval prolongation Yuill KH, Borg JJ, Ridley JM, Milnes JT, Witchel HJ, Paul AA, Kozlowski RZ, Hancox JC Biochemical and Biophysical Research Communications, 318(2), 556, 2004 |
| 4 |
High affinity HERG K+ channel blockade by the antiarrhythmic agent dronedarone: resistance to mutations of the S6 residues Y652 and F656 Ridley JM, Milnes JT, Witchel HJ, Hancox JC Biochemical and Biophysical Research Communications, 325(3), 883, 2004 |
| 5 |
Characterisation of recombinant HERG K+ channel blockade by the Class Ia antiarrhythmic drug procainamide Ridley JM, Milnes JT, Benest AV, Masters JD, Witchel HJ, Hancox JC Biochemical and Biophysical Research Communications, 306(2), 388, 2003 |