Ryanodine receptors: structure, expression, molecular details, and function in calcium release

JT Lanner, DK Georgiou, AD Joshi… - Cold Spring Harbor …, 2010 - cshperspectives.cshlp.org
Ryanodine receptors (RyRs) are located in the sarcoplasmic/endoplasmic reticulum
membrane and are responsible for the release of Ca2+ from intracellular stores during …

Ryanodine receptors and ventricular arrhythmias: emerging trends in mutations, mechanisms and therapies

CH George, H Jundi, NL Thomas, DL Fry… - Journal of molecular and …, 2007 - Elsevier
It has been six years since the first reported link between mutations in the cardiac ryanodine
receptor Ca2+ release channel (RyR2) and catecholaminergic polymorphic ventricular …

Presenilins regulate calcium homeostasis and presynaptic function via ryanodine receptors in hippocampal neurons

B Wu, H Yamaguchi, FA Lai… - Proceedings of the …, 2013 - National Acad Sciences
Presenilin (PS) plays a central role in the pathogenesis of Alzheimer's disease, and loss of
PS causes progressive memory impairment and age-related neurodegeneration in the …

Early Remodeling of Perinuclear Ca2+ Stores and Nucleoplasmic Ca2+ Signaling During the Development of Hypertrophy and Heart Failure

S Ljubojevic, S Radulovic, G Leitinger, S Sedej… - Circulation, 2014 - Am Heart Assoc
Background—A hallmark of heart failure is impaired cytoplasmic Ca2+ handling of
cardiomyocytes. It remains unknown whether specific alterations in nuclear Ca2+ handling …

[HTML][HTML] Ryanodine receptor-mediated arrhythmias and sudden cardiac death

LM Blayney, FA Lai - Pharmacology & therapeutics, 2009 - Elsevier
The cardiac ryanodine receptor-Ca2+ release channel (RyR2) is an essential sarcoplasmic
reticulum (SR) transmembrane protein that plays a central role in excitation–contraction …

Mechanisms of Disease: ryanodine receptor defects in heart failure and fatal arrhythmia

M Yano, T Yamamoto, Y Ikeda… - Nature Clinical Practice …, 2006 - nature.com
Abnormal regulation of intracellular Ca2+ by sarcoplasmic reticulum plays a part in the
mechanism underlying contractile and relaxation dysfunction in heart failure (HF). The …

Patient-specific human induced pluripotent stem cell model assessed with electrical pacing validates S107 as a potential therapeutic agent for catecholaminergic …

K Sasaki, T Makiyama, Y Yoshida, Y Wuriyanghai… - PLoS …, 2016 - journals.plos.org
Introduction Human induced pluripotent stem cells (hiPSCs) offer a unique opportunity for
disease modeling. However, it is not invariably successful to recapitulate the disease …

Synthesis of the Ca2+-mobilizing messengers NAADP and cADPR by intracellular CD38 enzyme in the mouse heart: Role in β-adrenoceptor signaling

WK Lin, EL Bolton, WA Cortopassi, Y Wang… - Journal of Biological …, 2017 - ASBMB
Nicotinic acid adenine dinucleotide phosphate (NAADP) and cyclic ADP-ribose (cADPR) are
Ca 2+-mobilizing messengers important for modulating cardiac excitation–contraction …

FK506 binding proteins: cellular regulators of intracellular Ca2+ signalling

D MacMillan - European journal of pharmacology, 2013 - Elsevier
In many cell types the intracellular Ca2+ store performs a central role in the regulation of the
cytosolic Ca2+ concentration ([Ca2+] c), the elevation of which triggers diverse and …

Ryanodine receptors

EM Capes, R Loaiza, HH Valdivia - Skeletal muscle, 2011 - Springer
Excitation-contraction coupling involves the faithful conversion of electrical stimuli to
mechanical shortening in striated muscle cells, enabled by the ubiquitous second …