The inositol trisphosphate/calcium signaling pathway in health and disease
MJ Berridge - Physiological reviews, 2016 - journals.physiology.org
Many cellular functions are regulated by calcium (Ca2+) signals that are generated by
different signaling pathways. One of these is the inositol 1, 4, 5-trisphosphate/calcium …
different signaling pathways. One of these is the inositol 1, 4, 5-trisphosphate/calcium …
Abnormal calcium handling in Duchenne muscular dystrophy: mechanisms and potential therapies
Duchenne muscular dystrophy (DMD) is an X-linked muscle-wasting disease caused by the
loss of dystrophin. DMD is associated with muscle degeneration, necrosis, inflammation …
loss of dystrophin. DMD is associated with muscle degeneration, necrosis, inflammation …
Ion channels of the sarcolemma and intracellular organelles in Duchenne muscular dystrophy: a role in the dysregulation of ion homeostasis and a possible target for …
Duchenne muscular dystrophy (DMD) is caused by the absence of the dystrophin protein
and a properly functioning dystrophin-associated protein complex (DAPC) in muscle cells …
and a properly functioning dystrophin-associated protein complex (DAPC) in muscle cells …
Prednisolone rescues Duchenne muscular dystrophy phenotypes in human pluripotent stem cell–derived skeletal muscle in vitro
Duchenne muscular dystrophy (DMD) is a devastating genetic disease leading to
degeneration of skeletal muscles and premature death. How dystrophin absence leads to …
degeneration of skeletal muscles and premature death. How dystrophin absence leads to …
PAX7, a key for myogenesis modulation in muscular dystrophies through multiple signaling pathways: a systematic review
Muscular dystrophy is a heterogenous group of hereditary muscle disorders caused by
mutations in the genes responsible for muscle development, and is generally defined by a …
mutations in the genes responsible for muscle development, and is generally defined by a …
Bioenergetic and metabolic impairments in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene and
dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality in DMD patients …
dilated cardiomyopathy (DCM) is a major cause of morbidity and mortality in DMD patients …
A Review of the Role of Endo/Sarcoplasmic Reticulum-Mitochondria Ca2+ Transport in Diseases and Skeletal Muscle Function
The physical contact site between a mitochondrion and endoplasmic reticulum (ER), named
the mitochondria-associated membrane (MAM), has emerged as a fundamental platform for …
the mitochondria-associated membrane (MAM), has emerged as a fundamental platform for …
[HTML][HTML] IP3 receptor blockade restores autophagy and mitochondrial function in skeletal muscle fibers of dystrophic mice
Duchenne muscular dystrophy (DMD) is characterized by a severe and progressive
destruction of muscle fibers associated with altered Ca 2+ homeostasis. We have previously …
destruction of muscle fibers associated with altered Ca 2+ homeostasis. We have previously …
Genome-wide analysis reveals extensive changes in LncRNAs during skeletal muscle development in Hu sheep
As an important type of noncoding RNA molecules, long non-coding RNAs (lncRNAs) act as
versatile players in various biological processes. However, little is known about lncRNA …
versatile players in various biological processes. However, little is known about lncRNA …
Skeletal ryanodine receptors are involved in impaired myogenic differentiation in Duchenne muscular dystrophy patients
P Meyer, C Notarnicola, AC Meli, S Matecki… - International Journal of …, 2021 - mdpi.com
Duchenne muscular dystrophy (DMD) is characterized by progressive muscle wasting
following repeated muscle damage and inadequate regeneration. Impaired myogenesis and …
following repeated muscle damage and inadequate regeneration. Impaired myogenesis and …