scholarly article | Q13442814 |
P50 | author | Tony Lai | Q73106357 |
Nia Lowri Thomas | Q79276359 | ||
P2093 | author name string | Spyros Zissimopoulos | |
Wan W Jamaluddin | |||
P2860 | cites work | Invited Review: redox modulation of skeletal muscle contraction: what we know and what we don't | Q34131741 |
Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2. | Q34312242 | ||
Mice with the R176Q cardiac ryanodine receptor mutation exhibit catecholamine-induced ventricular tachycardia and cardiomyopathy. | Q35033228 | ||
Ryanodine receptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies | Q36642953 | ||
Redox sensitivity of the ryanodine receptor interaction with FK506-binding protein. | Q52575969 | ||
The role of oxidative stress in the genesis of heart disease. | Q55032862 | ||
Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model | Q79851890 | ||
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2) | Q24290749 | ||
Removal of FKBP12.6 does not alter the conductance and activation of the cardiac ryanodine receptor or the susceptibility to stress-induced ventricular arrhythmias | Q24296752 | ||
Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak | Q24296910 | ||
Ryanodine receptor mutations associated with stress-induced ventricular tachycardia mediate increased calcium release in stimulated cardiomyocytes | Q24315860 | ||
FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death | Q28183817 | ||
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia | Q28201561 | ||
FKBP12 binding modulates ryanodine receptor channel gating | Q28208762 | ||
Enhanced store overload-induced Ca2+ release and channel sensitivity to luminal Ca2+ activation are common defects of RyR2 mutations linked to ventricular tachycardia and sudden death | Q28278262 | ||
Catecholaminergic polymorphic ventricular tachycardia | Q28287523 | ||
Interaction of FKBP12.6 with the cardiac ryanodine receptor C-terminal domain | Q28297732 | ||
Stabilization of cardiac ryanodine receptor prevents intracellular calcium leak and arrhythmias | Q28586317 | ||
Functional heterogeneity of ryanodine receptor mutations associated with sudden cardiac death. | Q31111627 | ||
Bidirectional ventricular tachycardia and fibrillation elicited in a knock-in mouse model carrier of a mutation in the cardiac ryanodine receptor. | Q33152686 | ||
Role of oxidative stress in cardiovascular diseases | Q33953686 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Ryanodine receptor 2 | Q3415811 |
heart disease | Q190805 | ||
response to redox state | Q21101822 | ||
FKBP prolyl isomerase 1B | Q21106584 | ||
P1104 | number of pages | 6 | |
P304 | page(s) | 273-278 | |
P577 | publication date | 2009-04-01 | |
P1433 | published in | Biochemical Journal | Q864221 |
P1476 | title | FKBP12.6 binding of ryanodine receptors carrying mutations associated with arrhythmogenic cardiac disease | |
P478 | volume | 419 |
Q47709918 | Association of FK506 binding proteins with RyR channels - effect of CLIC2 binding on sub-conductance opening and FKBP binding. |
Q28821966 | Genetic and Biochemical Approaches for In Vivo and In Vitro Assessment of Protein Oligomerization: The Ryanodine Receptor Case Study |
Q89799576 | Identification of an amino-terminus determinant critical for ryanodine receptor/Ca2+ release channel function |
Q41397431 | Is ryanodine receptor phosphorylation key to the fight or flight response and heart failure? |
Q33911293 | Mapping the ryanodine receptor FK506-binding protein subunit using fluorescence resonance energy transfer |
Q37671414 | N-terminus oligomerization is conserved in intracellular calcium release channels |
Q37687548 | Ryanodine receptor mutations in arrhythmia: The continuing mystery of channel dysfunction. |
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