Detalles de la búsqueda
1.
Generation of a lymphoblastoid-derived induced pluripotent stem cell line (CBRCULi015-A) from a patient with congenital myotonic dystrophy.
Stem Cell Res
; 77: 103430, 2024 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-38704930
2.
Cloning, functional expression, and pharmacological characterization of inwardly rectifying potassium channels (Kir) from Apis mellifera.
Sci Rep
; 14(1): 7834, 2024 04 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38570597
3.
Biophysical properties of NaV1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells.
Sci Rep
; 13(1): 20685, 2023 11 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-38001331
4.
Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels.
Front Physiol
; 14: 1258318, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37791351
5.
iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities.
Sci Rep
; 11(1): 2500, 2021 01 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-33510259
6.
Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State.
CJC Open
; 3(3): 256-266, 2021 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-33778442
7.
A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs.
Sci Rep
; 8(1): 16681, 2018 11 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30420713
8.
The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT.
Gene
; 536(2): 348-56, 2014 Feb 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-24334129
9.
A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype.
PLoS One
; 7(5): e38331, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22675453
10.
Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.
Can J Physiol Pharmacol
; 81(2): 129-34, 2003 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-12710526
Resultados
1 -
10
de 10
1
Próxima >
>>