Detalhe da pesquisa
1.
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
2.
Impaired chromaffin cell excitability and exocytosis in autistic Timothy syndrome TS2-neo mouse rescued by L-type calcium channel blockers.
J Physiol
; 597(6): 1705-1733, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30629744
3.
The human channel gating-modifying A749G CACNA1D (Cav1.3) variant induces a neurodevelopmental syndrome-like phenotype in mice.
JCI Insight
; 8(20)2023 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37698939
4.
ß2-subunit alternative splicing stabilizes Cav2.3 Ca2+ channel activity during continuous midbrain dopamine neuron-like activity.
Elife
; 112022 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35792082
5.
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
6.
Biophysical classification of a CACNA1D de novo mutation as a high-risk mutation for a severe neurodevelopmental disorder.
Mol Autism
; 11(1): 4, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31921405