Detalhe da pesquisa
1.
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy.
Int J Mol Sci
; 23(22)2022 Nov 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-36430690
2.
RBP2 stabilizes slow Cav1.3 Ca2+ channel inactivation properties of cochlear inner hair cells.
Pflugers Arch
; 472(1): 3-25, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31848688
3.
New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy.
Hum Mol Genet
; 26(15): 2923-2932, 2017 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28472301
4.
Mechanisms Responsible for ω-Pore Currents in Cav Calcium Channel Voltage-Sensing Domains.
Biophys J
; 113(7): 1485-1495, 2017 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28978442
5.
Cav 1.3 (CACNA1D) L-type Ca2+ channel dysfunction in CNS disorders.
J Physiol
; 594(20): 5839-5849, 2016 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26842699
6.
A Polybasic Plasma Membrane Binding Motif in the I-II Linker Stabilizes Voltage-gated CaV1.2 Calcium Channel Function.
J Biol Chem
; 290(34): 21086-21100, 2015 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-26100638
7.
Biology of AMPA receptor interacting proteins - From biogenesis to synaptic plasticity.
Neuropharmacology
; 197: 108709, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34271020
8.
AMPA receptor anchoring at CA1 synapses is determined by N-terminal domain and TARP γ8 interactions.
Nat Commun
; 12(1): 5083, 2021 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-34426577
9.
Allosteric coupling of sub-millisecond clamshell motions in ionotropic glutamate receptor ligand-binding domains.
Commun Biol
; 4(1): 1056, 2021 09 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34504293
10.
Stabilization of negative activation voltages of Cav1.3 L-Type Ca2+-channels by alternative splicing.
Channels (Austin)
; 15(1): 38-52, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33380256
11.
Gating defects of disease-causing de novo mutations in Cav1.3 Ca2+ channels.
Channels (Austin)
; 12(1): 388-402, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30465465
12.
Aldosterone-Producing Adenomas: Histopathology-Genotype Correlation and Identification of a Novel CACNA1D Mutation.
Hypertension
; 70(1): 129-136, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28584016
13.
Splice variants of the CaV1.3 L-type calcium channel regulate dendritic spine morphology.
Sci Rep
; 6: 34528, 2016 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27708393
14.
Pharmacology of L-type Calcium Channels: Novel Drugs for Old Targets?
Curr Mol Pharmacol
; 8(2): 110-22, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25966690
15.
CACNA1D de novo mutations in autism spectrum disorders activate Cav1.3 L-type calcium channels.
Biol Psychiatry
; 77(9): 816-22, 2015 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25620733
16.
L-type Ca2+ channels in heart and brain.
Wiley Interdiscip Rev Membr Transp Signal
; 3(2): 15-38, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24683526