Detalhe da pesquisa
1.
Regulation of CaV3.2 channels by the receptor for activated C kinase 1 (Rack-1).
Pflugers Arch
; 474(4): 447-454, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34623515
2.
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Am J Hum Genet
; 103(5): 666-678, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30343943
3.
Synthesis and cytotoxic effects of 2-thio-3,4-dihydroquinazoline derivatives as novel T-type calcium channel blockers.
Bioorg Med Chem
; 28(11): 115491, 2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32327350
4.
Discovery of Michael acceptor containing 1,4-dihydropyridines as first covalent inhibitors of L-/T-type calcium channels.
Bioorg Chem
; 91: 103187, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31419643
5.
Correction to: Regulation of CaV3.2 channels by the receptor for activated C kinase 1 (Rack-1).
Pflugers Arch
; 474(4): 455, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34674025
6.
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Am J Hum Genet
; 104(3): 562, 2019 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30849329
7.
RIM1/2-Mediated Facilitation of Cav1.4 Channel Opening Is Required for Ca2+-Stimulated Release in Mouse Rod Photoreceptors.
J Neurosci
; 35(38): 13133-47, 2015 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-26400943
8.
Two heterozygous Cav3.2 channel mutations in a pediatric chronic pain patient: recording condition-dependent biophysical effects.
Pflugers Arch
; 468(4): 635-42, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26706850
9.
CaV2.2 channel cell surface expression is regulated by the light chain 1 (LC1) of the microtubule-associated protein B (MAP1B) via UBE2L3-mediated ubiquitination and degradation.
Pflugers Arch
; 466(11): 2113-26, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24566975
10.
Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?
Cell Rep Med
; 5(2): 101425, 2024 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38382469
11.
A next generation peripherally restricted Cavα2δ-1 ligand with inhibitory action on Cav2.2 channels and utility in neuropathic pain.
Biomed Pharmacother
; 174: 116472, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38531121
12.
Functional interactions between voltage-gated Ca(2+) channels and Rab3-interacting molecules (RIMs): new insights into stimulus-secretion coupling.
Biochim Biophys Acta
; 1818(3): 551-8, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22198390
13.
Familial hemiplegic migraine type 1 mutations W1684R and V1696I alter G protein-mediated regulation of Ca(V)2.1 voltage-gated calcium channels.
Biochim Biophys Acta
; 1822(8): 1238-46, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22549042
14.
The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation of neuronal P/Q-type Ca2+ channels.
Cephalalgia
; 33(6): 398-407, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23430985
15.
Differential regulation of Cav 3.2 and Cav 2.2 calcium channels by CB1 receptors and cannabidiol.
Br J Pharmacol
; 180(12): 1616-1633, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36647671
16.
Functional coupling of Rab3-interacting molecule 1 (RIM1) and L-type Ca2+ channels in insulin release.
J Biol Chem
; 286(18): 15757-65, 2011 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-21402706
17.
Voltage-gated calcium channel nanodomains: molecular composition and function.
FEBS J
; 289(3): 614-633, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576127
18.
Ca V 3.2 calcium channels contribute to trigeminal neuralgia.
Pain
; 163(12): 2315-2325, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35467587
19.
Splice-variant specific effects of a CACNA1H mutation associated with writer's cramp.
Mol Brain
; 14(1): 145, 2021 09 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34544471
20.
The de novo CACNA1A pathogenic variant Y1384C associated with hemiplegic migraine, early onset cerebellar atrophy and developmental delay leads to a loss of Cav2.1 channel function.
Mol Brain
; 14(1): 27, 2021 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33557884