Ryanodine receptors: how many, where and why?
V Sorrentino, P Volpe - Trends in pharmacological sciences, 1993 - cell.com
Vincenzo Sorrentino and Pompeo Volpe review some recent deve~ o~ menis~ the
ryanodine receptor channels have now been found to be expressed in the central nervous …
ryanodine receptor channels have now been found to be expressed in the central nervous …
Repairing mitochondrial dysfunction in disease
V Sorrentino, KJ Menzies… - Annual review of …, 2018 - annualreviews.org
Mitochondria are essential organelles for many aspects of cellular homeostasis, including
energy harvesting through oxidative phosphorylation. Alterations of mitochondrial function …
energy harvesting through oxidative phosphorylation. Alterations of mitochondrial function …
Mutations in the Cardiac Ryanodine Receptor Gene (hRyR2) Underlie Catecholaminergic Polymorphic Ventricular Tachycardia
Background—Catecholaminergic polymorphic ventricular tachycardia is a genetic
arrhythmogenic disorder characterized by stress-induced, bidirectional ventricular …
arrhythmogenic disorder characterized by stress-induced, bidirectional ventricular …
Cytosolic proteostasis networks of the mitochondrial stress response
Mitochondrial stress requires timely intervention to prevent mitochondrial and cellular
dysfunction. Re-establishing the correct protein homeostasis is crucial for coping with …
dysfunction. Re-establishing the correct protein homeostasis is crucial for coping with …
The ryanodine receptor/calcium channel genes are widely and differentially expressed in murine brain and peripheral tissues.
G Giannini, A Conti, S Mammarella… - The Journal of cell …, 1995 - rupress.org
Ryanodine receptors (RyRs) are intracellular calcium release channels that participate in
controlling cytosolic calcium levels. At variance with the probably ubiquitous inositol 1, 4, 5 …
controlling cytosolic calcium levels. At variance with the probably ubiquitous inositol 1, 4, 5 …
Enhancing mitochondrial proteostasis reduces amyloid-β proteotoxicity
Alzheimer's disease is a common and devastating disease characterized by aggregation of
the amyloid-β peptide. However, we know relatively little about the underlying molecular …
the amyloid-β peptide. However, we know relatively little about the underlying molecular …
NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation
D Ryu, H Zhang, ER Ropelle, V Sorrentino… - Science translational …, 2016 - science.org
Neuromuscular diseases are often caused by inherited mutations that lead to progressive
skeletal muscle weakness and degeneration. In diverse populations of normal healthy mice …
skeletal muscle weakness and degeneration. In diverse populations of normal healthy mice …
Regulation and expression of a growth arrest-specific gene (gas5) during growth, differentiation, and development
EM Coccia, C Cicala, A Charlesworth… - … and cellular biology, 1992 - Am Soc Microbiol
The growth arrest-specific gas5 gene was isolated from mouse genomic DNA and
structurally characterized. The transcriptional unit is divided into 12 exons that span around …
structurally characterized. The transcriptional unit is divided into 12 exons that span around …
[HTML][HTML] MECP2 mutation in male patients with non-specific X-linked mental retardation
In contrast to the preponderance of affected males in families with X-linked mental
retardation, Rett syndrome (RTT) is a neurological disorder occurring almost exclusively in …
retardation, Rett syndrome (RTT) is a neurological disorder occurring almost exclusively in …
Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles
P Bagnato, V Barone, E Giacomello, D Rossi… - The Journal of cell …, 2003 - rupress.org
Assembly of specialized membrane domains, both of the plasma membrane and of the ER,
is necessary for the physiological activity of striated muscle cells. The mechanisms that …
is necessary for the physiological activity of striated muscle cells. The mechanisms that …