The membrane hypothesis of duchenne muscular dystrophy: Quest for functional evidence

No abstract is available for this paper.

• Publication year

  1992

• Venue

  Journal of Inherited Metabolic Disease

• Publication date

  1992-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF01799615PMID 1528017
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Binding sites involved in the interaction of actin with the N‐terminal region of dystrophin

  1992cited by this paper
• Contractile properties and susceptibility to exercise-induced damage of normal and mdx mouse tibialis anterior muscle.

  1992cited by this paper
• Dystrophin is required for normal thin filament-membrane associations at myotendinous junctions.

  1991cited by this paper
• Mechanical properties of normal andmdx mouse sarcolemma: Bearing on function of dystrophin

  1991cited by this paper
• Canine X‐linked muscular dystrophy studied with in vivo phosphorus magnetic resonance spectroscopy

  1991cited by this paper
• Decreased osmotic stability of dystrophin-less muscle cells from the mdx mouse

  1991cited by this paper
• The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle

  1991cited by this paper
• Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

  1991cited by this paper
• Effects of contractile activity on muscle damage in the dystrophin-deficient mdx mouse.

  1991cited by this paper
• Membrane organization of the dystrophin-glycoprotein complex.

  1991cited by this paper
• Mammalian subtilisins: the long-sought dibasic processing endoproteases.

  1991cited by this paper
• Dystrophin is tightly associated with the sarcolemma of mammalian skeletal muscle fibers.

  1991cited by this paper
• Calcium entry through stretch-inactivated ion channels in mdx myotubes

  1990cited by this paper
• Lateral mobility of membrane glycoprotein in chick myotubes and in skeletal muscle fibres isolated from normal and MDX mice

  1990cited by this paper
• Elastic deformation and failure of lipid bilayer membranes containing cholesterol.

  1990cited by this paper
• Changes in surface morphology and basal lamina of cultured muscle cells from Duchenne muscular dystrophy patients.

  1990cited by this paper
• Detailed analysis of the repeat domain of dystrophin reveals four potential hinge segments that may confer flexibility.

  1990cited by this paper
• Immunocytochemical study of dystrophin at the myotendinous junction

  1990cited by this paper
• Dystrophin-deficient mdx muscle fibers are preferentially vulnerable to necrosis induced by experimental lengthening contractions.

  1990cited by this paper
• Ultrastructural localization of dystropin in human muscle by using gold immunolabelling

  1990cited by this paper
• The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.

  1989cited by this paper
• Animal models of Duchenne and Becker muscular dystrophy.

  1989cited by this paper
• Association of dystrophin and an integral membrane glycoprotein

  1989cited by this paper
• The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein.

  1988cited by this paper
• The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

  1988cited by this paper
• Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.

  1988cited by this paper
• Increased protein degradation results from elevated free calcium levels found in muscle from mdx mice

  1988cited by this paper
• Reductions of erythrocyte membrane viscoelastic coefficients reflect spectrin deficiencies in hereditary spherocytosis.

  1988cited by this paper
• Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

  1988cited by this paper
• Free cytoplasmic Ca++ at rest and after cholinergic stimulus is increased in cultured muscle cells from Duchenne muscular dystrophy patients

  1988cited by this paper
• Single‐channel activity in sarcolemmal vesicles from human and other mammalian muscles

  1988cited by this paper
• Dystrophin: the protein product of the Duchenne muscular dystrophy locus.

  1987cited by this paper
• Protein sequence of DMD gene is related to actin-binding domain of alpha-actinin.

  1987cited by this paper
• Effects of intracellular Ca2+ and proteolytic digestion of the membrane skeleton on the mechanical properties of the red blood cell membrane.

  1987cited by this paper
• Immunocytochemical localisation of complement components C8 and C9 in human diseased muscle. The role of complement in muscle fibre damage.

  1987cited by this paper
• Protein sequence of DMD gene is related to actin-binding domain of α-actinin

  1987cited by this paper
• An examination of some factors influencing creatine kinase in the blood of patients with muscular dystrophy

  1987cited by this paper
• Measurements of calcium and other elements in muscle biopsy samples from patients with Duchenne muscular dystrophy.

  1985cited by this paper
• X chromosome-linked muscular dystrophy (mdx) in the mouse.

  1984cited by this paper
• Stretch‐activated single ion channel currents in tissue‐cultured embryonic chick skeletal muscle.

  1984cited by this paper
• Membrane skeletal dynamics: role in modulation of red cell deformability, mobility of transmembrane proteins, and shape.

  1983cited by this paper
• Ultrastructural changes after concentric and eccentric contractions of human muscle.

  1983cited by this paper
• Geometric parameters of pipettes and membrane patches

  1983cited by this paper
• Element analysis of skeletal muscle in duchenne muscular dystrophy using x‐ray fluorescence spectrometry

  1980cited by this paper
• Duchenne muscular dystrophy: plasma membrane loss initiates muscle cell necrosis unless it is repaired.

  1979cited by this paper
• Intracellular calcium accumulation in Duchenne dystrophy and other myopathies

  1978cited by this paper
• Pathogenesis of muscular dystrophies.

  1976cited by this paper
• Elastic area compressibility modulus of red cell membrane.

  1976cited by this paper
• The relative contributions of the folds and caveolae to the surface membrane of frog skeletal muscle fibres at different sarcomere lengths.

  1975cited by this paper
• New membrane concept applied to the analysis of fluid shear- and micropipette-deformed red blood cells.

  1973cited by this paper
• Lipids and fatty acids of sarcolemma, sarcoplasmic reticulum, and mitochondria from rat skeletal muscle.

  1971cited by this paper
• A Textbook of General Physiology

  1960cited by this paper
• Red cell structure and its breakdown

  1955cited by this paper
• Potassium accumulation in muscle and associated changes.

  1941cited by this paper
• Potassium accumulation in muscle and associated changes 1

  1941cited by this paper
• Textbook of general physiology

  1937cited by this paper

• CTLA4-Ig reduces muscle fiber damage in a model of Duchenne muscular dystrophy by attenuating pro-inflammatory gene expression in myeloid lineage cells.

  2025cites this paper
• Long-term Observation in Patients with Duchenne Muscular Dystrophy with Early Introduction of a Standing Program Using Knee–ankle–foot Orthoses

  2023cites this paper
• Is the fundamental pathology in Duchenne's muscular dystrophy caused by a failure of glycogenolysis–glycolysis in costameres?

  2023cites this paper
• Disrupted Calcium Homeostasis in Duchenne Muscular Dystrophy: A Common Mechanism behind Diverse Consequences

  2021cites this paper
• Dystrophin-negative slow-twitch soleus muscles are not susceptible to eccentric contraction induced injury over the lifespan of the mdx mouse.

  2021cites this paper
• Cytotoxic Swelling of Sick Excitable Cells - Impaired Ion Homeostasis and Membrane Tension Homeostasis in Muscle and Neuron.

  2018cites this paper
• Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.

  2016cites this paper
• Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan.

  2016cites this paper
• resistant to injury from acute mechanical stress Fast-twitch skeletal muscles of dystrophic mouse pups are

  2016cites this paper
• Muscle and bone health in adult males with muscular dystrophy

  2015cites this paper
• Chapter 30 – Dystrophinopathies

  2015cites this paper
• Diagnóstico da cardiomiopatia na distrofia muscular progressiva por ressonância magnética cardiovascular - correlação com tratamento, prognóstico e preditores genéticos

  2013cites this paper
• Stretch-induced membrane damage in muscle: comparison of wild-type and mdx mice.

  2010cites this paper
• Inhibitory Control Over Ca2+ Sparks via Mechanosensitive Channels Is Disrupted in Dystrophin Deficient Muscle but Restored by Mini-Dystrophin Expression

  2008cites this paper
• BIBLIOGRAPHY OF DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY: SELECTED BOOKS AND ARTICLES RECEIVED IN 1992

  2007cites this paper
• Mechanical Properties of Maturing Dystrophic Skeletal Muscle

  2007cites this paper
• MUSCLE DAMAGE IN MDX (DYSTROPHIC) MICE: ROLE OF CALCIUM AND REACTIVE OXYGEN SPECIES

  2006cites this paper
• Corticosteroid Treatment and Functional Improvement in Duchenne Muscular Dystrophy: Long-Term Effect

  2005cites this paper
• Immune Response Markers are Prevalent in the mRNA Expression Profile of Maturing Dystrophic Murine Skeletal Muscle

  2005cites this paper
• EDL and soleus muscles of the C57BL6J/dy2j laminin‐α2‐deficient dystrophic mouse are not vulnerable to eccentric contractions

  2004cites this paper
• Mini‐dystrophin restores L‐type calcium currents in skeletal muscle of transgenic mdx mice

  2004cites this paper
• Gadolinium reduces short‐term stretch‐induced muscle damage in isolated mdx mouse muscle fibres

  2003cites this paper
• Function and genetics of dystrophin and dystrophin-related proteins in muscle.

  2002cites this paper
• Response to resistive strengthening exercise training in humans with neuromuscular disease.

  2002cites this paper
• Fast-twitch skeletal muscles of dystrophic mouse pups are resistant to injury from acute mechanical stress.

  2002cites this paper
• Eccentric contraction injury in dystrophic canine muscle.

  2002cites this paper
• Cell Surface Area Regulation and Membrane Tension

  2001cites this paper
• Sarcoglycans in muscular dystrophy

  2000cites this paper
• Management of neuromuscular scoliosis.

  1999cites this paper
• Muscle degeneration without mechanical injury in sarcoglycan deficiency.

  1999cites this paper
• Mechanisms of resistance to pathogenesis in muscular dystrophies

  1999cites this paper
• Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers.

  1996cites this paper
• Duchenne muscular dystrophy.

  1995cites this paper
• Profiles of neuromuscular diseases. Duchenne muscular dystrophy.

  1995cites this paper
• Effect of voluntary wheel-running exercise on muscles of the mdx mouse.

  1995cites this paper
• Extent of shock-induced membrane leakage in human and mouse myotubes depends on dystrophin.

  1995cites this paper
• The use of fluorescent dextrans as a marker of sarcolemmal injury.

  1994cites this paper
• New cell biological applications of the laser microbeam technique: the microdissection and skinning of muscle fibers and the perforation and fusion of sarcolemma vesicles.

  1994cites this paper
• Dystrophin deficiency, altered cell signalling and fibre hypertrophy.

  1994cites this paper
• Organization of single motor units in feline sartorius.

  1994cites this paper
• In‐series fiber architecture in long human muscles

  1993cites this paper
• The structural and functional diversity of dystrophin

  1993cites this paper
• Molecular mechanisms of muscle damage.

  1993cites this paper