Membrane repair: mechanisms and pathophysiology
ST Cooper, PL McNeil - Physiological reviews, 2015 - journals.physiology.org
Eukaryotic cells have been confronted throughout their evolution with potentially lethal
plasma membrane injuries, including those caused by osmotic stress, by infection from …
plasma membrane injuries, including those caused by osmotic stress, by infection from …
[PDF][PDF] Mechanisms of muscle injury, repair, and regeneration
JG Tidball - Comprehensive physiology, 2011 - drive.google.com
Skeletal muscle continuously adapts to changes in its mechanical environment through
modifications in gene expression and protein stability that affect its physiological function …
modifications in gene expression and protein stability that affect its physiological function …
[HTML][HTML] The role of calpains in skeletal muscle remodeling with exercise and inactivity-induced atrophy
Calpains are cysteine proteases expressed in skeletal muscle fibers and other cells.
Although calpain was first reported to act as a kinase activating factor in skeletal muscle, the …
Although calpain was first reported to act as a kinase activating factor in skeletal muscle, the …
X-ROS signaling in the heart and skeletal muscle: stretch-dependent local ROS regulates [Ca2+] i
BL Prosser, RJ Khairallah, AP Ziman, CW Ward… - Journal of molecular and …, 2013 - Elsevier
X-ROS signaling is a novel redox signaling pathway that links mechanical stress to changes
in [Ca2+] i. This pathway is activated rapidly and locally within a muscle cell under …
in [Ca2+] i. This pathway is activated rapidly and locally within a muscle cell under …
Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane
JP Kerr, AP Ziman, AL Mueller… - Proceedings of the …, 2013 - National Acad Sciences
Dysferlinopathies, most commonly limb girdle muscular dystrophy 2B and Miyoshi
myopathy, are degenerative myopathies caused by mutations in the DYSF gene encoding …
myopathy, are degenerative myopathies caused by mutations in the DYSF gene encoding …
Molecular, physiological, and motor performance defects in DMSXL mice carrying> 1,000 CTG repeats from the human DM1 locus
A Huguet, F Medja, A Nicole, A Vignaud… - PLoS …, 2012 - journals.plos.org
Myotonic dystrophy type 1 (DM1) is caused by an unstable CTG repeat expansion in the 3′
UTR of the DM protein kinase (DMPK) gene. DMPK transcripts carrying CUG expansions …
UTR of the DM protein kinase (DMPK) gene. DMPK transcripts carrying CUG expansions …
The dystrophin‐glycoprotein complex in the prevention of muscle damage
JD Gumerson, DE Michele - BioMed Research International, 2011 - Wiley Online Library
Muscular dystrophies are genetically diverse but share common phenotypic features of
muscle weakness, degeneration, and progressive decline in muscle function. Previous work …
muscle weakness, degeneration, and progressive decline in muscle function. Previous work …
Muscle membrane repair and inflammatory attack in dysferlinopathy
R Han - Skeletal muscle, 2011 - Springer
Repair of plasma membrane tears is an important normal physiological process that enables
the cells to survive a variety of physiological and pathological membrane lesions. Dysferlin …
the cells to survive a variety of physiological and pathological membrane lesions. Dysferlin …
Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice
R Han, EM Frett, JR Levy, EP Rader… - The Journal of …, 2010 - Am Soc Clin Investig
Mutations in the dysferlin gene underlie a group of autosomal recessive muscle-wasting
disorders denoted as dysferlinopathies. Dysferlin has been shown to play roles in muscle …
disorders denoted as dysferlinopathies. Dysferlin has been shown to play roles in muscle …
Dysferlin at transverse tubules regulates Ca2+ homeostasis in skeletal muscle
The class of muscular dystrophies linked to the genetic ablation or mutation of dysferlin,
including Limb Girdle Muscular Dystrophy 2B (LGMD2B) and Miyoshi Myopathy (MM), are …
including Limb Girdle Muscular Dystrophy 2B (LGMD2B) and Miyoshi Myopathy (MM), are …