Pages that link to "Q37338902"

The following pages link to Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling (Q37338902):

Displaying 44 items.

• Critical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and Disease (Q26770423) (← links)
• Alternating bipolar field stimulation identifies muscle fibers with defective excitability but maintained local Ca(2+) signals and contraction. (Q27321327) (← links)
• Altered nuclear dynamics in MDX myofibers (Q30275220) (← links)
• Incidence and severity of myofiber branching with regeneration and aging (Q33646492) (← links)
• Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle (Q33647871) (← links)
• Human skeletal muscle xenograft as a new preclinical model for muscle disorders (Q33649287) (← links)
• Eccentric exercise in aging and diseased skeletal muscle: good or bad? (Q33708184) (← links)
• A new function for odorant receptors: MOR23 is necessary for normal tissue repair in skeletal muscle (Q34445314) (← links)
• Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy. (Q34473309) (← links)
• Engraftment potential of dermal fibroblasts following in vivo myogenic conversion in immunocompetent dystrophic skeletal muscle (Q34794545) (← links)
• The role of proteases in excitation-contraction coupling failure in muscular dystrophy (Q34800803) (← links)
• Temporal changes in magnetic resonance imaging in the mdx mouse (Q34803416) (← links)
• Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury (Q34807765) (← links)
• Assessment of calcium sparks in intact skeletal muscle fibers (Q35123222) (← links)
• Use of BODIPY (493/503) to visualize intramuscular lipid droplets in skeletal muscle (Q35232331) (← links)
• SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models (Q35572589) (← links)
• Pre- and postsynaptic changes in the neuromuscular junction in dystrophic mice (Q36038762) (← links)
• Abnormalities in brain structure and biochemistry associated with mdx mice measured by in vivo MRI and high resolution localized (1)H MRS. (Q36075156) (← links)
• Structural and functional evaluation of branched myofibers lacking intermediate filaments (Q36114637) (← links)
• Early metabolic changes measured by 1H MRS in healthy and dystrophic muscle after injury (Q36320857) (← links)
• Nanospan, an alternatively spliced isoform of sarcospan, localizes to the sarcoplasmic reticulum in skeletal muscle and is absent in limb girdle muscular dystrophy 2F. (Q36394350) (← links)
• Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. (Q36422465) (← links)
• Decrease of myofiber branching via muscle-specific expression of the olfactory receptor mOR23 in dystrophic muscle leads to protection against mechanical stress (Q36485571) (← links)
• Using a novel coculture model to dissect the role of intramuscular lipid load on skeletal muscle insulin responsiveness under reduced estrogen conditions (Q36923620) (← links)
• Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane (Q37409431) (← links)
• Proteomic profiling of x-linked muscular dystrophy (Q37676955) (← links)
• Proteomics of skeletal muscle differentiation, neuromuscular disorders and fiber aging. (Q37727204) (← links)
• The dystrophin-glycoprotein complex in the prevention of muscle damage (Q37946876) (← links)
• Chaperoning heat shock proteins: proteomic analysis and relevance for normal and dystrophin-deficient muscle. (Q38217473) (← links)
• Myofibrillar misalignment correlated to triad disappearance of mdx mouse gastrocnemius muscle probed by SHG microscopy (Q38363484) (← links)
• Drug Discovery of Therapies for Duchenne Muscular Dystrophy (Q38480698) (← links)
• Establishment of a human skeletal muscle-derived cell line: biochemical, cellular and electrophysiological characterization. (Q39117156) (← links)
• Myofiber branching rather than myofiber hyperplasia contributes to muscle hypertrophy in mdx mice (Q40372230) (← links)
• Disruption of action potential and calcium signaling properties in malformed myofibers from dystrophin-deficient mice (Q40488151) (← links)
• Detection of calcium sparks in intact and permeabilized skeletal muscle fibers (Q40841956) (← links)
• PGC-1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress (Q41487839) (← links)
• Effects of in vivo injury on the neuromuscular junction in healthy and dystrophic muscles (Q45220017) (← links)
• Imaging Analysis of the Neuromuscular Junction in Dystrophic Muscle (Q46327049) (← links)
• Brain and heart magnetic resonance imaging/spectroscopy in duchenne muscular dystrophy (Q47619099) (← links)
• Combined XIL-6R and urocortin-2 treatment restores MDX diaphragm muscle force (Q47949346) (← links)
• Nanoscale remodeling of ryanodine receptor cluster size underlies cerebral microvascular dysfunction in Duchenne muscular dystrophy (Q57292416) (← links)
• Optical prediction of single muscle fiber force production using a combined biomechatronics and second harmonic generation imaging approach (Q58118806) (← links)
• Mitochondrial oxidative stress impairs contractile function but paradoxically increases muscle mass via fibre branching (Q64229243) (← links)
• Abnormalities in Brain and Muscle Microstructure and Neurochemistry of the DMD Rat Measured by in vivo Diffusion Tensor Imaging and High Resolution Localized 1H MRS (Q98224403) (← links)