Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers.
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Molecular organization of sarcoglycan complex in mouse myotubes in cultureBrain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophyDeficiency in Cardiac Dystrophin Affects the Abundance of the $\alpha$ -/ $\beta$ -Dystroglycan ComplexThe biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscleProteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathyFlow (shear stress)-induced endothelium-dependent dilation is altered in mice lacking the gene encoding for dystrophinThere is more than one way to model an elephant. Experiment-driven modeling of the actin cytoskeletonProteomic profiling of antisense-induced exon skipping reveals reversal of pathobiochemical abnormalities in dystrophic mdx diaphragm.Proteomic profiling of mdx-4cv serum reveals highly elevated levels of the inflammation-induced plasma marker haptoglobin in muscular dystrophy.New pathobiochemical insights into dystrophinopathy from the proteomics of senescent mdx mouse muscleProteomic Profiling of the Dystrophin-Deficient MDX Heart Reveals Drastically Altered Levels of Key Metabolic and Contractile Proteins.Contractile function, sarcolemma integrity, and the loss of dystrophin after skeletal muscle eccentric contraction-induced injuryIn situ molecular association of dystrophin with actin revealed by sensitized emission immuno-resonance energy transfer.Extensive but coordinated reorganization of the membrane skeleton in myofibers of dystrophic (mdx) mice.Label-free mass spectrometric analysis reveals complex changes in the brain proteome from the mdx-4cv mouse model of Duchenne muscular dystrophy.Profiling of age-related changes in the tibialis anterior muscle proteome of the mdx mouse model of dystrophinopathyMass spectrometric identification of dystrophin, the protein product of the Duchenne muscular dystrophy gene, in distinct muscle surface membranes.Drastic reduction of sarcalumenin in Dp427 (dystrophin of 427 kDa)-deficient fibres indicates that abnormal calcium handling plays a key role in muscular dystrophy.Interaction of dystrophin fragments with model membranesAbsence of dystrophin in mice reduces NO-dependent vascular function and vascular density: total recovery after a treatment with the aminoglycoside gentamicin.Loss of dystrophin staining in cardiomyocytes: a novel method for detection early myocardial infarction.Isoproterenol induces primary loss of dystrophin in rat hearts: correlation with myocardial injury.Comparative gel-based proteomic analysis of chemically crosslinked complexes in dystrophic skeletal muscle.
P2860
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P2860
Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Towards an understanding of th ...... cytoskeleton in muscle fibers.
@en
type
label
Towards an understanding of th ...... cytoskeleton in muscle fibers.
@en
prefLabel
Towards an understanding of th ...... cytoskeleton in muscle fibers.
@en
P1476
Towards an understanding of th ...... cytoskeleton in muscle fibers
@en
P2093
Ohlendieck K
P577
1996-01-01T00:00:00Z