| scholarly article | Q13442814 |
| P50 | author | Angus Lindsay | Q50991524 |
| Dawn A Lowe | Q59688933 | ||
| P2093 | author name string | James M Ervasti | |
| David D Thomas | |||
| James S Hodges | |||
| Cory W Baumann | |||
| Razvan L Cornea | |||
| William M Southern | |||
| Samantha L Yuen | |||
| Robyn T Rebbeck | |||
| P2860 | cites work | Dystrophin expression following the transplantation of normal muscle precursor cells protects mdx muscle from contraction-induced damage | Q84585433 |
| High-Throughput Screens to Discover Small-Molecule Modulators of Ryanodine Receptor Calcium Release Channels | Q88589870 | ||
| Neopterin/7,8-dihydroneopterin is elevated in Duchenne muscular dystrophy patients and protects mdx skeletal muscle function | Q88785440 | ||
| Truncated dystrophin ameliorates the dystrophic phenotype of mdx mice by reducing sarcolipin-mediated SERCA inhibition | Q91593994 | ||
| Plasmalemma Function Is Rapidly Restored in Mdx Muscle after Eccentric Contractions | Q92637741 | ||
| Variable cytoplasmic actin expression impacts the sensitivity of different dystrophin-deficient mdx skeletal muscles to eccentric contraction | Q92818986 | ||
| Hypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscle | Q24308714 | ||
| The dystrophin complex forms a mechanically strong link between the sarcolemma and costameric actin | Q28145442 | ||
| Dystrophin: the protein product of the Duchenne muscular dystrophy locus | Q29618077 | ||
| Microtubules underlie dysfunction in duchenne muscular dystrophy. | Q30557507 | ||
| Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber | Q30951467 | ||
| High-throughput FRET assay yields allosteric SERCA activators | Q34393960 | ||
| Expression of full-length utrophin prevents muscular dystrophy in mdx mice | Q34482808 | ||
| Determinants of the repeated-bout effect after lengthening contractions | Q35204675 | ||
| SERCA1 overexpression minimizes skeletal muscle damage in dystrophic mouse models | Q35572589 | ||
| A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy | Q36151226 | ||
| Dystrophin protects the sarcolemma from stresses developed during muscle contraction | Q36259954 | ||
| Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. | Q36273863 | ||
| Muscle-specific expression of insulin-like growth factor I counters muscle decline in mdx mice | Q36324105 | ||
| Small Molecular Allosteric Activator of the Sarco/Endoplasmic Reticulum Ca2+-ATPase (SERCA) Attenuates Diabetes and Metabolic Disorders | Q36650350 | ||
| Adeno-associated virus-mediated microdystrophin expression protects young mdx muscle from contraction-induced injury. | Q36968852 | ||
| Overexpression of Galgt2 in skeletal muscle prevents injury resulting from eccentric contractions in both mdx and wild-type mice | Q37139061 | ||
| Microtubule binding distinguishes dystrophin from utrophin | Q37711984 | ||
| Discovery of enzyme modulators via high-throughput time-resolved FRET in living cells. | Q39033560 | ||
| Eliminating Nox2 reactive oxygen species production protects dystrophic skeletal muscle from pathological calcium influx assessed in vivo by manganese-enhanced magnetic resonance imaging | Q39459441 | ||
| Overexpression of SERCA1a in the mdx diaphragm reduces susceptibility to contraction-induced damage | Q41118342 | ||
| Characteristics of lengthening contractions associated with injury to skeletal muscle fibers | Q41471206 | ||
| Leaky ryanodine receptors in β-sarcoglycan deficient mice: a potential common defect in muscular dystrophy. | Q42149020 | ||
| Prosurvival Factors Improve Functional Engraftment of Myogenically Converted Dermal Cells into Dystrophic Skeletal Muscle. | Q42391300 | ||
| Essential role of TRPV2 ion channel in the sensitivity of dystrophic muscle to eccentric contractions | Q43258728 | ||
| Susceptibility to sarcomere injury induced by single stretches of maximally activated muscles of mdx mice. | Q44722909 | ||
| Acute failure of action potential conduction in mdx muscle reveals new mechanism of contraction-induced force loss. | Q44985983 | ||
| Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse. | Q45140549 | ||
| A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy | Q45857200 | ||
| Insulin-like growth factor-I analogue protects muscles of dystrophic mdx mice from contraction-mediated damage | Q46528995 | ||
| N-Acetylcysteine ameliorates skeletal muscle pathophysiology in mdx mice | Q46765634 | ||
| Ryanodine channel complex stabilizer compound S48168/ARM210 as a disease modifier in dystrophin-deficient mdx mice: proof-of-concept study and independent validation of efficacy | Q47665947 | ||
| Streptomycin reduces stretch-induced membrane permeability in muscles from mdx mice | Q50475477 | ||
| Variable rescue of microtubule and physiological phenotypes in mdx muscle expressing different miniaturized dystrophins. | Q54241942 | ||
| Restoration of SERCA ATPase prevents oxidative stress-related muscle atrophy and weakness | Q57191111 | ||
| Targeting protein-protein interactions for therapeutic discovery via FRET-based high-throughput screening in living cells | Q58722435 | ||
| Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle | Q59799234 | ||
| Injury to muscle fibres after single stretches of passive and maximally stimulated muscles in mice | Q70917677 | ||
| Increased susceptibility of EDL muscles from mdx mice to damage induced by contractions with stretch | Q72102757 | ||
| Eccentric contraction-induced injury in normal and hindlimb-suspended mouse soleus and EDL muscles | Q72464292 | ||
| Mechanical factors in the initiation of eccentric contraction-induced injury in rat soleus muscle | Q72578539 | ||
| Rapid recovery following contraction-induced injury to in situ skeletal muscles in mdx mice | Q74425819 | ||
| The effects of stretch parameters on eccentric exercise-induced damage to toad skeletal muscle | Q74534142 | ||
| The relation between force and speed in muscular contraction | Q80330090 | ||
| Branched fibers in dystrophic mdx muscle are associated with a loss of force following lengthening contractions | Q80475156 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 3 | |
| P577 | publication date | 2020-02-01 | |
| P1433 | published in | Skeletal Muscle | Q27723741 |
| P1476 | title | Mechanical factors tune the sensitivity of mdx muscle to eccentric strength loss and its protection by antioxidant and calcium modulators | |
| P478 | volume | 10 |
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