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.
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
4.
Identification of interleukin-1 beta as a key mediator in the upregulation of Cav3.2-USP5 interactions in the pain pathway.
Mol Pain
; 13: 1744806917724698, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28741432
5.
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
6.
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
7.
The Cav1.2 N terminus contains a CaM kinase site that modulates channel trafficking and function.
Pflugers Arch
; 467(4): 677-86, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24862738
8.
Elimination of the vesicular acetylcholine transporter in the striatum reveals regulation of behaviour by cholinergic-glutamatergic co-transmission.
PLoS Biol
; 9(11): e1001194, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22087075
9.
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
10.
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
11.
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
12.
Electrophysiological and computational analysis of Cav3.2 channel variants associated with familial trigeminal neuralgia.
Mol Brain
; 15(1): 91, 2022 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36397158
13.
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
14.
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
15.
A CACNA1A variant associated with trigeminal neuralgia alters the gating of Cav2.1 channels.
Mol Brain
; 14(1): 4, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33413531
16.
De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.
Mol Brain
; 14(1): 126, 2021 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34399820
17.
Rare functional missense variants in CACNA1H: What can we learn from Writer's cramp?
Mol Brain
; 14(1): 18, 2021 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33478561
18.
Functional identification of potential non-canonical N-glycosylation sites within Cav3.2 T-type calcium channels.
Mol Brain
; 13(1): 149, 2020 11 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33176830
19.
A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Cav3.2 T-type channel activity.
Mol Brain
; 13(1): 33, 2020 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32143681
20.
Differential regulation of Cav2.2 channel exon 37 variants by alternatively spliced µ-opioid receptors.
Mol Brain
; 12(1): 98, 2019 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31775826