Detalhe da pesquisa
1.
Putative malignant hyperthermia mutation CaV1.1-R174W is insufficient to trigger a fulminant response to halothane or confer heat stress intolerance.
J Biol Chem;
299(8): 104992, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37392848
2.
Voltage sensor movements of CaV1.1 during an action potential in skeletal muscle fibers.
Proc Natl Acad Sci U S A;
118(40)2021 10 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34583989
3.
A skeletal muscle L-type Ca2+ channel with a mutation in the selectivity filter (CaV1.1 E1014K) conducts K.
J Biol Chem;
293(9): 3126-3133, 2018 03 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29326166
4.
Distinct Components of Retrograde Ca(V)1.1-RyR1 Coupling Revealed by a Lethal Mutation in RyR1.
Biophys J;
110(4): 912-21, 2016 Feb 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26910427
5.
Bridging the myoplasmic gap II: more recent advances in skeletal muscle excitation-contraction coupling.
J Exp Biol;
219(Pt 2): 175-82, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26792328
6.
Depressed pacemaker activity of sinoatrial node myocytes contributes to the age-dependent decline in maximum heart rate.
Proc Natl Acad Sci U S A;
110(44): 18011-6, 2013 Oct 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24128759
7.
Functional assessment of three Rem residues identified as critical for interactions with Ca(2+) channel ß subunits.
Pflugers Arch;
467(11): 2299-306, 2015 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25771954
8.
Triclosan impairs excitation-contraction coupling and Ca2+ dynamics in striated muscle.
Proc Natl Acad Sci U S A;
109(35): 14158-63, 2012 Aug 28.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22891308
9.
Malignant hyperthermia susceptibility arising from altered resting coupling between the skeletal muscle L-type Ca2+ channel and the type 1 ryanodine receptor.
Proc Natl Acad Sci U S A;
109(20): 7923-8, 2012 May 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22547813
10.
Ca(V)1.1: The atypical prototypical voltage-gated Ca²âº channel.
Biochim Biophys Acta;
1828(7): 1587-97, 2013 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22982493
11.
Impaired gating of an L-Type Ca(2+) channel carrying a mutation linked to malignant hyperthermia.
Biophys J;
104(9): 1917-22, 2013 May 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23663834
12.
Advances in CaV1.1 gating: New insights into permeation and voltage-sensing mechanisms.
Channels (Austin);
17(1): 2167569, 2023 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36642864
13.
A neurodevelopmental disorder caused by a dysfunctional CACNA1A allele.
eNeurologicalSci;
31: 100456, 2023 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36938367
14.
Complex effects on CaV2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder.
Sci Rep;
12(1): 9186, 2022 06 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35655070
15.
The role of action potential changes in depolarization-induced failure of excitation contraction coupling in mouse skeletal muscle.
Elife;
112022 01 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34985413
16.
Selective posttranslational inhibition of CaVß1-associated voltage-dependent calcium channels with a functionalized nanobody.
Nat Commun;
13(1): 7556, 2022 Dec 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36494348
17.
Into the spotlight: RGK proteins in skeletal muscle.
Cell Calcium;
98: 102439, 2021 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34261001
18.
Zebrafish as a Model System for the Study of Severe CaV2.1 (α1A) Channelopathies.
Front Mol Neurosci;
12: 329, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32116539
19.
A mutation in CaV2.1 linked to a severe neurodevelopmental disorder impairs channel gating.
J Gen Physiol;
151(6): 850-859, 2019 06 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31015257
20.
Semi-automated Analysis of Mouse Skeletal Muscle Morphology and Fiber-type Composition.
J Vis Exp;
(126)2017 08 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28892032