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1 current amplitude or open probability of the cardiac ryanodine receptor.
2 body MA3-916, also raised against the canine cardiac ryanodine receptor.
3 es and regulation by CaM of the skeletal and cardiac ryanodine receptors.
4 alcium release activity of both skeletal and cardiac ryanodine receptors.
6 rm a protein complex that is associated with cardiac ryanodine receptor 2 (RyR2) SR Ca(2+) release ch
7 ired beta-agonist-induced denitrosylation of cardiac ryanodine receptor 2 (RyR2), resulting in calciu
9 2+-binding protein that associates with both cardiac ryanodine receptors and L-type Ca2+ channels and
10 Ca(2+)-ATPase [SERCA2a], phospholamban, and cardiac ryanodine receptor), and contractile function (m
11 nteract with and disrupt the function of the cardiac ryanodine receptor Ca(2+) release channel (RyR2)
12 ith PKA-mediated hyperphosphorylation of the cardiac ryanodine receptor/Ca(2+)-release channel, which
13 arcoplasmic reticulum (SR) Ca2+ leak via the cardiac ryanodine receptor/calcium release channel (RyR2
14 ple targets in cardiac muscle, including the cardiac ryanodine receptor/calcium release channel (RyR2
16 constructed models of the pore region of the cardiac ryanodine receptor channel (RyR2) monomer and te
17 study, we addressed whether Zn(2+) modulates cardiac ryanodine receptor gating and Ca(2+) dynamics in
19 ia syndrome associated with mutations in the cardiac ryanodine receptor gene (Ryr2) in the majority o
20 prevalence of mutations in the RYR2-encoded cardiac ryanodine receptor in cases with exertional sync
21 These results appear to indicate that the cardiac ryanodine receptor is capable of being activated
22 hmias in a mouse model of CPVT by inhibiting cardiac ryanodine receptor-mediated Ca(2+) release and t
23 including voltage-gated Na and Ca channels, cardiac ryanodine receptors, Na/Ca-exchanger, and SR Ca-
24 hypothesis for elevated Ca(2+) leak through cardiac ryanodine receptors (ryanodine receptor 2 [RyR2]
26 ion to determine whether Ca(2+) can regulate cardiac ryanodine receptor (RyR) channel gating from wit
30 with mutations in the genes encoding for the cardiac ryanodine receptor (RyR2) and cardiac calsequest
32 ic disorder associated with mutations in the cardiac ryanodine receptor (RyR2) and cardiac calsequest
33 determine the CaM binding properties of the cardiac ryanodine receptor (RyR2) and to identify potent
34 d its metabolite, doxorubicinol, bind to the cardiac ryanodine receptor (RyR2) and to the sarco/endop
38 a widely used pharmacological agonist of the cardiac ryanodine receptor (RyR2) Ca(2+) release channel
39 To study the function and regulation of the cardiac ryanodine receptor (RyR2) Ca(2+) release channel
40 CPVT) require spontaneous Ca(2+) release via cardiac ryanodine receptor (RyR2) channels affected by g
41 e crossing region (the proposed gate) of the cardiac ryanodine receptor (RyR2) completely abolishes l
45 NH2-terminal region (residues 1-543) of the cardiac ryanodine receptor (RyR2) harbors a large number
47 m the sarcoplasmic reticulum mediated by the cardiac ryanodine receptor (RyR2) is a fundamental event
49 t the single-channel level, oxidation of the cardiac ryanodine receptor (RyR2) is known to activate a
51 Ca from sarcoplasmic reticulum (SR) via the cardiac ryanodine receptor (RyR2) may contribute to cont
52 s a hetero-oligomer with FKBP12, whereas the cardiac ryanodine receptor (RyR2) more selectively assoc
55 tachycardia (CPVT) is caused by mutations in cardiac ryanodine receptor (RyR2) or calsequestrin (Casq
56 n kinase A (PKA) hyperphosphorylation of the cardiac ryanodine receptor (RyR2) resulting in dissociat
57 riments we characterized another site on the cardiac ryanodine receptor (RyR2) with which ryanoids in
58 rdiac death due to missense mutations in the cardiac ryanodine receptor (RyR2), an intracellular Ca2+
59 lation of the calcium (Ca2+) release channel/cardiac ryanodine receptor (RyR2), required for cardiac
64 sphodiesterase 4D3 (PDE4D3) was found in the cardiac ryanodine receptor (RyR2)/calcium-release-channe
65 ssible for flecainide to directly affect the cardiac ryanodine receptor (RyR2); however, an extracell
66 lasmic reticulum (SR) Ca(2+) release through cardiac ryanodine receptors (RyR2) aggravate cardiac rem
68 kinase A (PKA)-dependent phosphorylation of cardiac ryanodine receptors (RyR2) is linked to the deve
69 eins FKBP12.6 and FKBP12 are associated with cardiac ryanodine receptors (RyR2), and cAMP-dependent p
70 ses sudden cardiac death due to mutations in cardiac ryanodine receptors (RyR2), calsequestrin, or ca
71 r tachyarrhythmias (VTs) in a mouse model of cardiac ryanodine-receptor (RyR2)-linked catecholaminerg
74 nels is a critical step in the activation of cardiac ryanodine receptors (RyRs) and release of Ca2+ v
76 cytes and single channel recordings from rat cardiac ryanodine receptors (RyRs) incorporated into pla
77 ein kinase A-mediated phosphorylation of the cardiac ryanodine receptor (the Ca(2+) release channel o
78 rdia (CPVT) is a familial disorder caused by cardiac ryanodine receptor type 2 (RyR2) or calsequestri
82 tabolic labeling experiments showed that the cardiac ryanodine receptor was phosphorylated at additio
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