Detalhe da pesquisa
1.
Apocalmodulin itself promotes ion channel opening and Ca(2+) regulation.
Cell
; 159(3): 608-22, 2014 Oct 23.
Artigo
Inglês
| MEDLINE | ID: mdl-25417111
2.
Mechanism of local and global Ca2+ sensing by calmodulin in complex with a Ca2+ channel.
Cell
; 133(7): 1228-40, 2008 Jun 27.
Artigo
Inglês
| MEDLINE | ID: mdl-18585356
3.
CACNA1C-Related Channelopathies.
Handb Exp Pharmacol
; 279: 159-181, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36598608
4.
Impaired CaV1.2 inactivation reduces the efficacy of calcium channel blockers in the treatment of LQT8.
J Mol Cell Cardiol
; 173: 92-100, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36272554
5.
The molecular basis of the inhibition of CaV1 calcium-dependent inactivation by the distal carboxy tail.
J Biol Chem
; 296: 100502, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-33667546
6.
Infanticide vs. inherited cardiac arrhythmias.
Europace
; 23(3): 441-450, 2021 03 08.
Artigo
Inglês
| MEDLINE | ID: mdl-33200177
7.
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome.
Circ Res
; 120(1): 39-48, 2017 Jan 06.
Artigo
Inglês
| MEDLINE | ID: mdl-27765793
8.
Following Optogenetic Dimerizers and Quantitative Prospects.
Biophys J
; 111(6): 1132-1140, 2016 Sep 20.
Artigo
Inglês
| MEDLINE | ID: mdl-27542508
9.
Novel fluorescence resonance energy transfer-based reporter reveals differential calcineurin activation in neonatal and adult cardiomyocytes.
J Physiol
; 593(17): 3865-84, 2015 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-26096996
10.
Calmodulin mutations associated with long QT syndrome prevent inactivation of cardiac L-type Ca(2+) currents and promote proarrhythmic behavior in ventricular myocytes.
J Mol Cell Cardiol
; 74: 115-24, 2014 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-24816216
11.
A modular switch for spatial Ca2+ selectivity in the calmodulin regulation of CaV channels.
Nature
; 451(7180): 830-4, 2008 Feb 14.
Artigo
Inglês
| MEDLINE | ID: mdl-18235447
12.
Structural and functional plasticity in long-term cultures of adult ventricular myocytes.
J Mol Cell Cardiol
; 65: 76-87, 2013 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-24076394
13.
Calmodulin Mutations in Human Disease.
Channels (Austin)
; 17(1): 2165278, 2023 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36629534
14.
Rapid modeling of an ultra-rare epilepsy variant in wild-type mice by in utero prime editing.
bioRxiv
; 2023 Dec 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38106154
15.
CaV1.2 channelopathic mutations evoke diverse pathophysiological mechanisms.
J Gen Physiol
; 154(11)2022 11 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36167061
16.
Fibroblast growth factor homologous factors serve as a molecular rheostat in tuning arrhythmogenic cardiac late sodium current.
Nat Cardiovasc Res
; 1(5): 1-13, 2022 May.
Artigo
Inglês
| MEDLINE | ID: mdl-35662881
17.
A bilobal model of Ca2+-dependent inactivation to probe the physiology of L-type Ca2+ channels.
J Gen Physiol
; 150(12): 1688-1701, 2018 12 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30470716
18.
Allosteric regulators selectively prevent Ca2+-feedback of CaV and NaV channels.
Elife
; 72018 09 10.
Artigo
Inglês
| MEDLINE | ID: mdl-30198845
19.
Sodium channel blockade may contribute to the analgesic efficacy of antidepressants.
J Pain
; 8(4): 315-24, 2007 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-17175203
20.
A high-capacity membrane potential FRET-based assay for NaV1.8 channels.
Assay Drug Dev Technol
; 4(1): 37-48, 2006 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-16506887