| P50 | author | Kanneboyina Nagaraju | Q27662260 |
| | Jyoti K. Jaiswal | Q50648507 |
| | Marshall W Hogarth | Q51089640 |
| | Adam Horn | Q57881682 |
| P2093 | author name string | Kristy J Brown | |
| | Yetrib Hathout | |
| | Sree Rayavarapu | |
| | Shin'ichi Takeda | |
| | Aurelia Defour | |
| | Jack H Van der Meulen | |
| | Maria C Vila | |
| P2860 | cites work | Rescue of dystrophic skeletal muscle by PGC-1α involves a fast to slow fiber type shift in the mdx mouse | Q27310125 |
| | Metabolic dysfunction and altered mitochondrial dynamics in the utrophin-dystrophin deficient mouse model of duchenne muscular dystrophy | Q28546070 |
| | Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development | Q28594513 |
| | Use of quantitative membrane proteomics identifies a novel role of mitochondria in healing injured muscles. | Q30524775 |
| | Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion. | Q30582564 |
| | Alteration in calcium handling at the subcellular level in mdx myotubes. | Q31456406 |
| | Dysferlin and the plasma membrane repair in muscular dystrophy | Q33201061 |
| | Efficacy of MitoTracker Green and CMXrosamine to measure changes in mitochondrial membrane potentials in living cells and tissues | Q33207057 |
| | Chronic administration of membrane sealant prevents severe cardiac injury and ventricular dilatation in dystrophic dogs | Q33755416 |
| | Enhanced Ca²⁺ influx from STIM1-Orai1 induces muscle pathology in mouse models of muscular dystrophy. | Q33784460 |
| | Imaging cell membrane injury and subcellular processes involved in repair | Q33872310 |
| | Membrane sealant Poloxamer P188 protects against isoproterenol induced cardiomyopathy in dystrophin deficient mice | Q33901556 |
| | Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures | Q33975979 |
| | Non-invasive optical imaging of muscle pathology in mdx mice using cathepsin caged near-infrared imaging | Q34928429 |
| | VBP15, a novel anti-inflammatory and membrane-stabilizer, improves muscular dystrophy without side effects | Q34981147 |
| | Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse | Q35009267 |
| | Mechanism of Ca²⁺-triggered ESCRT assembly and regulation of cell membrane repair | Q35099073 |
| | Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice | Q35779807 |
| | How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouse | Q35821127 |
| | Regulation of cytosolic calcium in skeletal muscle cells of the mdx mouse under conditions of stress | Q35873884 |
| | Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma | Q36025454 |
| | A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. | Q36232550 |
| | Mechanical function of dystrophin in muscle cells | Q36235185 |
| | Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy. | Q52527217 |
| | Contraction-induced injury to single permeabilized muscle fibers from mdx, transgenic mdx, and control mice. | Q52541082 |
| | High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disorders. | Q53964474 |
| | Dystrophin levels and clinical severity in Becker muscular dystrophy patients. | Q54508616 |
| | Time course of changes in plasma membrane permeability in the dystrophin-deficient mdx mouse | Q58487605 |
| | Dysferlin, annexin A1, and mitsugumin 53 are upregulated in muscular dystrophy and localize to longitudinal tubules of the T-system with stretch. | Q64981707 |
| | Changes in muscle plasma membranes in young mice with X chromosome-linked muscular dystrophy: a freeze-fracture study | Q68049296 |
| | Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer | Q82892069 |
| | Use of stable isotope labeling by amino acids in cell culture as a spike-in standard in quantitative proteomics | Q83366737 |
| | Peroxisome proliferator-activated receptor γ coactivator1- gene α transfer restores mitochondrial biomass and improves mitochondrial calcium handling in post-necrotic mdx mouse skeletal muscle | Q84829768 |
| | Increased dysferlin expression in Duchenne muscular dystrophy | Q95403251 |
| | Dystrophin protects the sarcolemma from stresses developed during muscle contraction | Q36259954 |
| | Elusive sources of variability of dystrophin rescue by exon skipping | Q36340978 |
| | Metabolic remodeling agents show beneficial effects in the dystrophin-deficient mdx mouse model | Q36351079 |
| | Stem and progenitor cells in skeletal muscle development, maintenance, and therapy | Q36771273 |
| | Poloxamer 188 reduces the contraction-induced force decline in lumbrical muscles from mdx mice | Q36805372 |
| | Identification of disease specific pathways using in vivo SILAC proteomics in dystrophin deficient mdx mouse. | Q36832437 |
| | Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies | Q37276061 |
| | Visualization of ATP levels inside single living cells with fluorescence resonance energy transfer-based genetically encoded indicators | Q37327467 |
| | Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism | Q37419160 |
| | Exogenous cytochrome C restores myocardial cytochrome oxidase activity into the late phase of sepsis | Q37673307 |
| | Muscular dystrophy in dysferlin-deficient mouse models | Q38087717 |
| | Dystrophin abnormalities in Duchenne/Becker muscular dystrophy | Q38768990 |
| | Chronic AMPK activation evokes the slow, oxidative myogenic program and triggers beneficial adaptations in mdx mouse skeletal muscle | Q39527529 |
| | Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles | Q39571496 |
| | Dominant-negative inhibition of Ca2+ influx via TRPV2 ameliorates muscular dystrophy in animal models | Q39909880 |
| | Increased activity of calcium leak channels caused by proteolysis near sarcolemmal ruptures | Q41752594 |
| | Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers | Q41882302 |
| | Post-natal induction of PGC-1α protects against severe muscle dystrophy independently of utrophin. | Q41911490 |
| | Reciprocal amplification of ROS and Ca(2+) signals in stressed mdx dystrophic skeletal muscle fibers. | Q42452644 |
| | Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin | Q44177784 |
| | Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse. | Q45140549 |
| | Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice | Q46266620 |
| | Calcium entry through stretch-inactivated ion channels in mdx myotubes | Q46603395 |
| | Dystrophic heart failure blocked by membrane sealant poloxamer | Q46604988 |
| | Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse | Q47878704 |
| P275 | copyright license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International | Q42553662 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 2 | |
| P921 | main subject | mitochondrion | Q39572 |
| P304 | page(s) | 330-342 | |
| P577 | publication date | 2016-11-11 | |
| P1433 | published in | Cell Death & Differentiation | Q2943974 |
| P1476 | title | Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy | |
| P478 | volume | 24 | |