Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle - Wikidata - awgldk - TriplyDB

Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle

Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle

http://www.wikidata.org/entity/Q36290588

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Contribution of the different modules in the utrophin carboxy-terminal region to the formation and regulation of the DAP complex DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes Biglycan binds to alpha- and gamma-sarcoglycan and regulates their expression during development A technicolour approach to the connectome Different dystrophin-like complexes are expressed in neurons and glia In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4 Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling Proteomic analysis reveals new cardiac-specific dystrophin-associated proteins Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain Identification of new dystroglycan complexes in skeletal muscle Characterization of human alpha-dystrobrevin isoforms in HL-60 human promyelocytic leukemia cells undergoing granulocytic differentiation.Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.Beta-synemin expression in cardiotoxin-injected rat skeletal muscle.Blastocyst injection of wild type embryonic stem cells induces global corrections in mdx mice.Utrophin binds laterally along actin filaments and can couple costameric actin with sarcolemma when overexpressed in dystrophin-deficient muscle.Plasma membrane cytoskeleton of muscle: a fine structural analysis.Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice Alpha-dystrobrevin-1 recruits alpha-catulin to the alpha1D-adrenergic receptor/dystrophin-associated protein complex signalosome.Disruption of basal lamina components in neuromotor synapses of children with spastic quadriplegic cerebral palsy Dystrobrevin controls neurotransmitter release and muscle Ca(2+) transients by localizing BK channels in Caenorhabditis elegans The effect of respiratory muscle training with CO2 breathing on cellular adaptation of mdx mouse diaphragm.Interaction of α-catulin with dystrobrevin contributes to integrity of dystrophin complex in muscle Comparative proteomic profiling of dystroglycan-associated proteins in wild type, mdx, and Galgt2 transgenic mouse skeletal muscle.A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells.Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain Role of extracellular matrix proteins and their receptors in the development of the vertebrate neuromuscular junction Tyrosine-phosphorylated and nonphosphorylated isoforms of alpha-dystrobrevin: roles in skeletal muscle and its neuromuscular and myotendinous junctions.Combinatorial therapeutic activation with heparin and AICAR stimulates additive effects on utrophin A expression in dystrophic muscles.Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.Ring chromosome 18 in combination with 18q12.1 (DTNA) interstitial microdeletion in a patient with multiple congenital defects.Α-Dystrobrevin-1 recruits Grb2 and α-catulin to organize neurotransmitter receptors at the neuromuscular junction.C-terminal-truncated microdystrophin recruits dystrobrevin and syntrophin to the dystrophin-associated glycoprotein complex and reduces muscular dystrophy in symptomatic utrophin/dystrophin double-knockout mice Sub-physiological sarcoglycan expression contributes to compensatory muscle protection in mdx mice Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy.The roles of the dystrophin-associated glycoprotein complex at the synapse Aquaporin expression in normal and pathological skeletal muscles: a brief review with focus on AQP4 The role of α-dystrobrevin in striated muscle.Progress in therapy for Duchenne muscular dystrophy.Differential Vicia villosa agglutinin reactivity identifies three distinct dystroglycan complexes in skeletal muscle.

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P2860

Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle

http://www.wikidata.org/entity/Q36290588

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1998 nî lūn-bûn

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1998年の論文

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1998年学术文章

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1998年学术文章

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1998年学术文章

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1998年学术文章

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1998年学术文章

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1998年學術文章

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1998年學術文章

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1998年學術文章

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name

Differential membrane localiza ...... in isoforms in skeletal muscle

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Differential membrane localiza ...... in isoforms in skeletal muscle

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type

label

Differential membrane localiza ...... in isoforms in skeletal muscle

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Differential membrane localiza ...... in isoforms in skeletal muscle

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Differential membrane localiza ...... in isoforms in skeletal muscle

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Differential membrane localiza ...... in isoforms in skeletal muscle

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H M Sadoulet-Puccio

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J R Sanes

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L M Kunkel

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M F Peters

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M R Grady

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N R Kramarcy

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R Sealock

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S C Froehner

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P2860

Syntrophin binds to an alternatively spliced exon of dystrophin

Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane

Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene

The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives

Dystrobrevin and dystrophin: an interaction through coiled-coil motifs

beta-dystrobrevin, a member of the dystrophin-related protein family

Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels

A novel genetic system to detect protein-protein interactions

Characterization of DRP2, a novel human dystrophin homologue

Primary structure of dystrophin-related protein

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9732287

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2149339

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