Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex.
about
The caveolin proteinsCaveolin-1 and caveolin-3 form heterooligomeric complexes in atrial cardiac myocytes that are required for doxorubicin-induced apoptosisDifferential effects of myopathy-associated caveolin-3 mutants on growth factor signalingCaveolinopathies: from the biology of caveolin-3 to human diseasesCaV1.2 signaling complexes in the heartLipid modulation of skeletal muscle mass and functionMutations in the caveolin-3 gene: When are they pathogenic?Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlinCaveolin regulates endocytosis of the muscle repair protein, dysferlinModulation of myoblast fusion by caveolin-3 in dystrophic skeletal muscle cells: implications for Duchenne muscular dystrophy and limb-girdle muscular dystrophy-1CSpatial and temporal regulation of GLUT4 translocation by flotillin-1 and caveolin-3 in skeletal muscle cellsThe interaction of caveolin 3 protein with the potassium inward rectifier channel Kir2.1: physiology and pathology related to long qt syndrome 9 (LQT9)Caveolin-3 null mice show a loss of caveolae, changes in the microdomain distribution of the dystrophin-glycoprotein complex, and t-tubule abnormalitiesCholesterol and fatty acids regulate dynamic caveolin trafficking through the Golgi complex and between the cell surface and lipid bodies.Confinement of β(1)- and β(2)-adrenergic receptors in the plasma membrane of cardiomyocyte-like H9c2 cells is mediated by selective interactions with PDZ domain and A-kinase anchoring proteins but not caveolae.Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophiesCaveolins, liquid-ordered domains, and signal transduction.Satellite cells and the muscle stem cell nicheExpression of caveolin-1 induces premature cellular senescence in primary cultures of murine fibroblasts.Identification and functional analysis of a new putative caveolin-3 variant found in a patient with sudden unexplained deathCaveolin-1 expression negatively regulates cell cycle progression by inducing G(0)/G(1) arrest via a p53/p21(WAF1/Cip1)-dependent mechanism.N-terminal protein acylation confers localization to cholesterol, sphingolipid-enriched membranes but not to lipid rafts/caveolae.Caveolin 3 is associated with the calcium release complex and is modified via in vivo triadin modification.Membrane traffic and muscle: lessons from human diseaseCaveolin-deficient mice: insights into caveolar function human diseaseCaveolin-3 regulates compartmentation of cardiomyocyte beta2-adrenergic receptor-mediated cAMP signaling.Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscleImpairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency.Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteinsPhosphofructokinase muscle-specific isoform requires caveolin-3 expression for plasma membrane recruitment and caveolar targeting: implications for the pathogenesis of caveolin-related muscle diseases.Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesDiagnostic immunohistochemistry in neuromuscular disorders.The MARVEL domain protein, Singles Bar, is required for progression past the pre-fusion complex stage of myoblast fusion.Spatial control of the βAR system in heart failure: the transverse tubule and beyond.Overexpression of caveolin-1 is sufficient to phenocopy the behavior of a disease-associated mutantA pH-Mediated Topological Switch within the N-Terminal Domain of Human Caveolin-3.Caveolin-3 regulates myostatin signaling. Mini-review.Clinical and translational implications of the caveolin gene family: lessons from mouse models and human genetic disorders.From embryonic development to human diseases: The functional role of caveolae/caveolin.Caveolins and cavins in the trafficking, maturation, and degradation of caveolae: implications for cell physiology.
P2860
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P2860
Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Phenotypic behavior of caveoli ...... ants within the golgi complex.
@en
Phenotypic behavior of caveoli ...... limb girdle muscular dystrophy
@nl
type
label
Phenotypic behavior of caveoli ...... ants within the golgi complex.
@en
Phenotypic behavior of caveoli ...... limb girdle muscular dystrophy
@nl
prefLabel
Phenotypic behavior of caveoli ...... ants within the golgi complex.
@en
Phenotypic behavior of caveoli ...... limb girdle muscular dystrophy
@nl
P2093
P2860
P356
P1476
Phenotypic behavior of caveoli ...... ants within the golgi complex.
@en
P2093
P2860
P304
25632-25641
P356
10.1074/JBC.274.36.25632
P407
P577
1999-09-01T00:00:00Z