Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse.
about
Genetic evidence in the mouse solidifies the calcium hypothesis of myofiber death in muscular dystrophyThe golden retriever model of Duchenne muscular dystrophy.Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophiesMolecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapiesA proteasome inhibitor fails to attenuate dystrophic pathology in mdx mice.Orai1 mediates exacerbated Ca(2+) entry in dystrophic skeletal muscleThe role of proteases in excitation-contraction coupling failure in muscular dystrophy.Regulation of the calpain and ubiquitin-proteasome systems in a canine model of muscular dystrophy.SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models.Chronic administration of a leupeptin-derived calpain inhibitor fails to ameliorate severe muscle pathology in a canine model of duchenne muscular dystrophycAMP signaling in skeletal muscle adaptation: hypertrophy, metabolism, and regenerationLinking cytoarchitecture to metabolism: sarcolemma-associated plectin affects glucose uptake by destabilizing microtubule networks in mdx myofibers.Leupeptin-based inhibitors do not improve the mdx phenotype.Calpain-mediated proteolysis of tropomodulin isoforms leads to thin filament elongation in dystrophic skeletal muscle.The effects of Capn1 gene inactivation on skeletal muscle growth, development, and atrophy, and the compensatory role of other proteolytic systemsCell-matrix interactions in muscle disease.The dystrophin-glycoprotein complex in the prevention of muscle damage.The physiological response of protease inhibition in dystrophic muscle.Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion.Overexpression of SERCA1a in the mdx diaphragm reduces susceptibility to contraction-induced damage.Immunoproteasome in animal models of Duchenne muscular dystrophy.Effects of feeding hexane-extracts of a shochu distillery by-product on skeletal muscle protein degradation in broiler chicken.Mouse models of two missense mutations in actin binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy.Platelet m-calpain: a facile marker and STR polymorphism analysis for the identification of true carriers of Duchenne muscular dystrophy.The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy.Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.Exercise prevents impaired autophagy and proteostasis in a model of neurogenic myopathy
P2860
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P2860
Effect of calpain and proteasome inhibition on Ca2+-dependent proteolysis and muscle histopathology in the mdx mouse.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@en
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@nl
type
label
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@en
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@nl
prefLabel
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@en
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@nl
P2093
P356
P1433
P1476
Effect of calpain and proteaso ...... stopathology in the mdx mouse.
@en
P2093
Alexandre Briguet
Cyrille Lescop
Gesa Santos
Günther Metz
Hervé Siendt
Holger Herzner
Isabelle Courdier-Fruh
Josef P Magyar
Judith Dubach-Powell
Marco Henneboehle
P304
P356
10.1096/FJ.07-099036
P407
P577
2008-08-26T00:00:00Z