Biochemistry of muscle membranes in Duchenne muscular dystrophy.
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Biochemical characterization of plasma membrane isolated from human skeletal muscleThe golden retriever model of Duchenne muscular dystrophy.Plasma membrane cytoskeleton of muscle: a fine structural analysis.Exploration of lipid metabolism in relation with plasma membrane properties of Duchenne muscular dystrophy cells: influence of L-carnitineIncreased concentration of spectrin is observed in avian dystrophic muscle.Differential degradation of [35S]methionine polypeptides in Duchenne muscular dystrophy skin fibroblasts in vitro.Pathogenesis of Duchenne muscular dystrophy: the calcium hypothesis revisited.Teaching monograph: pathology of skeletal muscle diseases.The role of cytoskeletal and cytocontractile elements in pathologic processes.Studies of water permeability and proteins of erythrocyte membranes in patients with Duchenne muscular dystrophy.Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscle.Isolation and characterization of human muscle cellsSuccessful treatment of murine muscular dystrophy with the proteinase inhibitor leupeptinLocalization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle.The subcellular distribution of dystrophin in mouse skeletal, cardiac, and smooth muscle.Sodium channel and sodium pump in normal and pathological muscles from patients with myotonic muscular dystrophy and lower motor neuron impairment.Monensin-induced inhibition of cell spreading in normal and dystrophic human fibroblasts.Defective Ca2+ metabolism in Duchenne muscular dystrophy: effects on cellular and viral growth.Increased rate of cell-substratum detachment of fibroblasts from patients with Duchenne muscular dystrophy.Dystrophin-related muscular dystrophies.Dantrolene enhances antisense-mediated exon skipping in human and mouse models of Duchenne muscular dystrophy.Overexpression of follistatin in human myoblasts increases their proliferation and differentiation, and improves the graft success in SCID mice.Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin.Duchenne/Becker muscular dystrophy: A report on clinical, biochemical, and genetic study in Gujarat population, IndiaRelease of sarcoplasmic enzymes from frog skeletal muscle.Isolation and characterization of different C-terminal fragments of dystrophin expressed in Escherichia coli.Cell fractionation studies indicate that dystrophin is a protein of surface membranes of skeletal muscle.Increased muscle calcium. A possible cause of mitochondrial dysfunction and cellular necrosis in denervated rat skeletal muscle.Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophy.Changes in plasma enzyme activity after intramuscular injection of bupivacaine into the human biceps brachii.Release of creatine kinase from frog muscle by osmotic changes.Stra13 regulates oxidative stress mediated skeletal muscle degeneration.
P2860
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P2860
Biochemistry of muscle membranes in Duchenne muscular dystrophy.
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
1980年论文
@zh
1980年论文
@zh-cn
name
Biochemistry of muscle membranes in Duchenne muscular dystrophy.
@en
type
label
Biochemistry of muscle membranes in Duchenne muscular dystrophy.
@en
prefLabel
Biochemistry of muscle membranes in Duchenne muscular dystrophy.
@en
P2860
P356
P1433
P1476
Biochemistry of muscle membranes in Duchenne muscular dystrophy.
@en
P2093
Rowland LP
P2860
P356
10.1002/MUS.880030103
P577
1980-01-01T00:00:00Z