Pages that link to "Q68025103"
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The following pages link to The mdx mouse skeletal muscle myopathy: II. Contractile properties (Q68025103):
Displaying 50 items.
- Non-invasive MRI and spectroscopy of mdx mice reveal temporal changes in dystrophic muscle imaging and in energy deficits (Q28544896) (← links)
- Mechanisms of resistance to pathogenesis in muscular dystrophies (Q33680413) (← links)
- The chondrogenic response to exercise in the proximal femur of normal and mdx mice (Q33683997) (← links)
- Understanding dystrophinopathies: an inventory of the structural and functional consequences of the absence of dystrophin in muscles of the mdx mouse (Q33836366) (← links)
- Effects of prednisolone on skeletal muscle contractility in mdx mice (Q33887318) (← links)
- Role of dystrophin in airway smooth muscle phenotype, contraction and lung function (Q33939933) (← links)
- Skeletal muscle homeostasis in duchenne muscular dystrophy: modulating autophagy as a promising therapeutic strategy (Q33944130) (← links)
- The different impact of a high fat diet on dystrophic mdx and control C57Bl/10 mice (Q34077151) (← links)
- Are human and mouse satellite cells really the same? (Q34216980) (← links)
- Mammalian models of Duchenne Muscular Dystrophy: pathological characteristics and therapeutic applications (Q34497055) (← links)
- Early right ventricular fibrosis and reduction in biventricular cardiac reserve in the dystrophin-deficient mdx heart. (Q35086442) (← links)
- Expression of the dystrophin isoform Dp116 preserves functional muscle mass and extends lifespan without preventing dystrophy in severely dystrophic mice (Q35565691) (← links)
- Disease course in mdx:utrophin+/- mice: comparison of three mouse models of Duchenne muscular dystrophy (Q35588699) (← links)
- Duchenne's muscular dystrophy: animal models used to investigate pathogenesis and develop therapeutic strategies (Q35591025) (← links)
- Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia. (Q35616824) (← links)
- Identification in GRMD dog muscle of critical miRNAs involved in pathophysiology and effects associated with MuStem cell transplantation. (Q36015171) (← links)
- Alpha1-syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration. (Q36324019) (← links)
- Loss of cIAP1 attenuates soleus muscle pathology and improves diaphragm function in mdx mice (Q36580725) (← links)
- Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophy (Q36841572) (← links)
- Animal models of muscular dystrophy – what can they teach us? (Q36856649) (← links)
- Animal models of muscular dystrophy (Q36915922) (← links)
- Biology of the striated muscle dystrophin-glycoprotein complex (Q37085050) (← links)
- Sparing of the dystrophin-deficient cranial sartorius muscle is associated with classical and novel hypertrophy pathways in GRMD dogs (Q37271889) (← links)
- Calpain-mediated proteolysis of tropomodulin isoforms leads to thin filament elongation in dystrophic skeletal muscle (Q37635343) (← links)
- Cellular mechanisms and local progenitor activation to regulate skeletal muscle mass. (Q37701307) (← links)
- The paradox of muscle hypertrophy in muscular dystrophy. (Q37975319) (← links)
- Mechanisms of muscle injury, repair, and regeneration (Q38111732) (← links)
- Myo-mechanical analysis of isolated skeletal muscle (Q38274894) (← links)
- What has the mdx mouse model of Duchenne muscular dystrophy contributed to our understanding of this disease? (Q38351283) (← links)
- Plantarflexion contracture in the mdx mouse. (Q39771895) (← links)
- Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice (Q40372230) (← links)
- Myoblast transfer and gene therapy in muscular dystrophies (Q40437473) (← links)
- Expression of dystrophin driven by the 1.35-kb MCK promoter ameliorates muscular dystrophy in fast, but not in slow muscles of transgenic mdx mice (Q40576976) (← links)
- Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice (Q40667755) (← links)
- Increased levels of interleukin-6 exacerbate the dystrophic phenotype in mdx mice. (Q41045084) (← links)
- Influence of Botulinumtoxin A on the Expression of Adult MyHC Isoforms in the Masticatory Muscles in Dystrophin-Deficient Mice (Mdx-Mice). (Q41096343) (← links)
- Laminin-111: a potential therapeutic agent for Duchenne muscular dystrophy (Q41197789) (← links)
- Normal myogenic cells from newborn mice restore normal histology to degenerating muscles of the mdx mouse (Q41902045) (← links)
- Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice (Q42067795) (← links)
- Distinct effects of contraction-induced injury in vivo on four different murine models of dysferlinopathy. (Q42129224) (← links)
- Dystrophin deficiency is associated with myotendinous junction defects in prenecrotic and fully regenerated skeletal muscle. (Q42755001) (← links)
- Distinctive patterns of basic fibroblast growth factor (bFGF) distribution in degenerating and regenerating areas of dystrophic (mdx) striated muscles (Q43876648) (← links)
- Consequence of parvalbumin deficiency in the mdx mouse: histological, biochemical and mechanical phenotype of a new double mutant. (Q44473148) (← links)
- Regenerative capacity of mdx mouse muscles after repeated applications of myo-necrotic bupivacaine (Q51616543) (← links)
- Administration of chinese herbal medicines facilitates the locomotor activity in dystrophin-deficient mice. (Q53475327) (← links)
- Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse. (Q54127324) (← links)
- Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin-deficient mice and Duchenne muscular dystrophy. (Q55622381) (← links)
- Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice (Q57050163) (← links)
- The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy (Q59051261) (← links)
- ZEB1 protects skeletal muscle from damage and is required for its regeneration (Q64056143) (← links)