Pages that link to "Q43695009"

The following pages link to Adult dystrophic (mdx) endplates exhibit reduced quantal size and enhanced quantal variation (Q43695009):

Displaying 18 items.

• Truncated dystrophins can influence neuromuscular synapse structure. (Q33676836) (← links)
• The nicotinic acetylcholine receptor and the Na,K-ATPase alpha2 isoform interact to regulate membrane electrogenesis in skeletal muscle (Q34121222) (← links)
• Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubes (Q36033118) (← links)
• Pre- and postsynaptic changes in the neuromuscular junction in dystrophic mice (Q36038762) (← links)
• Sarcolemmal ion channels in dystrophin-deficient skeletal muscle fibres (Q36549694) (← links)
• The value of mammalian models for duchenne muscular dystrophy in developing therapeutic strategies (Q37383091) (← links)
• The roles of the dystrophin-associated glycoprotein complex at the synapse (Q37629726) (← links)
• Reduced resting potentials in dystrophic (mdx) muscle fibers are secondary to NF-κB-dependent negative modulation of ouabain sensitive Na+–K+ pump activity (Q42106765) (← links)
• Resting Ca2+ influx does not contribute to anoxia-induced cell death in adult rat cardiac myocytes (Q42453827) (← links)
• Acute failure of action potential conduction in mdx muscle reveals new mechanism of contraction-induced force loss. (Q44985983) (← links)
• Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles (Q45220017) (← links)
• Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models. (Q51535716) (← links)
• Cycles of myofiber degeneration and regeneration lead to remodeling of the neuromuscular junction in two mammalian models of Duchenne muscular dystrophy (Q58091143) (← links)
• Extrajunctional resting Ca2+ influx is not increased in a severely dystrophic expiratory muscle (triangularis sterni) of the mdx mouse (Q59489917) (← links)
• Recovery of electrogenesis in skeletal muscles after cell therapy of myodystrophy in MDX mice (Q83194157) (← links)
• Fiber Type Composition of the Sternomastoid and Diaphragm Muscles of Dystrophin‐Deficient mdx Mice (Q84786967) (← links)
• Inspiratory pressure-generating capacity is preserved during ventilatory and non-ventilatory behaviours in young dystrophic mdx mice despite profound diaphragm muscle weakness (Q90661005) (← links)
• Muscle specific kinase protects dystrophic mdx mouse muscles from eccentric contraction-induced loss of force-producing capacity (Q92149794) (← links)