Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction.
about
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populationsGenetics of hypertension and cardiovascular disease and their interconnected pathways: lessons from large studies.Endoplasmic reticulum Ca(2+) handling in excitable cells in health and diseaseMutation-linked defective interdomain interactions within ryanodine receptor cause aberrant Ca²⁺release leading to catecholaminergic polymorphic ventricular tachycardia.Regulation of ryanodine receptor RyR2 by protein-protein interactions: prediction of a PKA binding site on the N-terminal domain of RyR2 and its relation to disease causing mutationsDantrolene rescues arrhythmogenic RYR2 defect in a patient-specific stem cell model of catecholaminergic polymorphic ventricular tachycardia.A mechanistic description of gating of the human cardiac ryanodine receptor in a regulated minimal environment.A human pluripotent stem cell model of catecholaminergic polymorphic ventricular tachycardia recapitulates patient-specific drug responses.The structural biology of ryanodine receptors.The structure and functioning of the couplon in the mammalian cardiomyocyte.Calcium Signaling and Cardiac Arrhythmias.Pharyngeal spasticity due to dantrolene
P2860
Q29417027-B366B04A-1C22-4B54-B08E-23E4B1CC83E2Q34713661-EDA929E5-5189-4CDD-8387-E5B0360E597AQ35122788-BC92194D-3966-48AE-A2CB-0DC8B54F6931Q35156823-0EC609A2-3E05-48F7-A1E8-BBDF3FE3E577Q35611218-26CA2A56-A817-4366-A08F-66F497755CA9Q36037969-ADCE7464-6CF2-4E45-BD1C-39D29823CF89Q36130339-2B2CC045-64F1-4872-838F-B8280CC6C490Q37305886-8B4575C7-7B9C-4DA8-A1CA-0BC47D25E5E4Q37904888-116179C8-0EA9-4920-A91C-0C4FBAB98160Q37953250-0AFC648F-EDB8-4744-A5AA-A670BA518398Q39360546-27F85F2C-E0A5-4488-BC88-89E0C591CC43Q58049720-15D046DA-59F5-44E6-929D-414F0BAB3831
P2860
Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 02 February 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@en
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@nl
type
label
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@en
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@nl
prefLabel
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@en
Ryanodine receptor mutations i ...... ystery of channel dysfunction.
@nl
P2860
P50
P1433
P1476
Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction
@en
P2093
Chloé Maxwell
P2860
P304
P356
10.1016/J.FEBSLET.2010.01.057
P407
P577
2010-02-02T00:00:00Z