Caveolin-deficient mice: insights into caveolar function human disease

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Caveolin-deficient mice: insights into caveolar function human disease is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

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P356DOI10.1172/JCI200114611
P932PMC publication ID201001
P698PubMed publication ID11733547

P2093author name stringM P Lisanti
B Razani
P2860cites workIdentification, sequence, and expression of caveolin-2 defines a caveolin gene familyQ24315913
Cell-type and tissue-specific expression of caveolin-2. Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivoQ24324547
Caveolae-deficient Endothelial Cells Show Defects in the Uptake and Transport of Albuminin VivoQ57371858
Non-coated membrane invaginations are involved in binding and internalization of cholera and tetanus toxinsQ59078570
In vivo delivery of the caveolin-1 scaffolding domain inhibits nitric oxide synthesis and reduces inflammationQ60695434
Targeted down-regulation of caveolin-3 is sufficient to inhibit myotube formation in differentiating C2C12 myoblasts. Transient activation of p38 mitogen-activated protein kinase is required for induction of caveolin-3 expression and subsequent myotQ73066721
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophyQ28139430
Caveolin-3 deficiency causes muscle degeneration in miceQ28140304
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemiaQ28140434
Caveolin-2 localizes to the golgi complex but redistributes to plasma membrane, caveolae, and rafts when co-expressed with caveolin-1Q28143130
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle diseaseQ28204157
Caveolin-1, a putative tumour suppressor geneQ28212075
Caveolae, caveolin and caveolin-rich membrane domains: a signalling hypothesisQ28239626
Caveolin-3 in muscular dystrophyQ28267179
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophyQ28267252
Molecular cloning of caveolin-3, a novel member of the caveolin gene family expressed predominantly in muscleQ28273695
Endothelial nitric oxide synthase is regulated by tyrosine phosphorylation and interacts with caveolin-1Q28296135
Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activityQ28510735
Caveolin-3 associates with developing T-tubules during muscle differentiationQ28511690
Expression of caveolin-3 in skeletal, cardiac, and smooth muscle cells. Caveolin-3 is a component of the sarcolemma and co-fractionates with dystrophin and dystrophin-associated glycoproteinsQ28585091
Caveolin-3 null mice show a loss of caveolae, changes in the microdomain distribution of the dystrophin-glycoprotein complex, and t-tubule abnormalitiesQ28592366
Reciprocal regulation of endothelial nitric-oxide synthase by Ca2+-calmodulin and caveolinQ28609899
Loss of caveolae, vascular dysfunction, and pulmonary defects in caveolin-1 gene-disrupted miceQ29615180
Caveolin, a protein component of caveolae membrane coatsQ29619795
Caveolins, liquid-ordered domains, and signal transductionQ33752828
Caveolae and caveolin-3 in muscular dystrophyQ33845396
Targeted downregulation of caveolin-1 is sufficient to drive cell transformation and hyperactivate the p42/44 MAP kinase cascadeQ33890028
Cholesterol and caveolae: structural and functional relationshipsQ34101258
Clathrin-mediated endocytosis: membrane factors pull the triggerQ34341954
Emerging themes in lipid rafts and caveolae.Q34348709
The fine structure of the gall bladder epithelium of the mouse.Q34537858
Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiencyQ35788659
Characterization of caveolin-rich membrane domains isolated from an endothelial-rich source: implications for human diseaseQ36234407
Filipin-sensitive caveolae-mediated transport in endothelium: reduced transcytosis, scavenger endocytosis, and capillary permeability of select macromoleculesQ36234903
Expression of caveolin-1 is required for the transport of caveolin-2 to the plasma membrane. Retention of caveolin-2 at the level of the golgi complexQ40932810
Acylation targets emdothelial nitric-oxide synthase to plasmalemmal caveolaeQ41215934
Recombinant expression of caveolin-1 in oncogenically transformed cells abrogates anchorage-independent growthQ42440094
Limb-girdle muscular dystrophy (LGMD-1C) mutants of caveolin-3 undergo ubiquitination and proteasomal degradation. Treatment with proteasomal inhibitors blocks the dominant negative effect of LGMD-1C mutanta and rescues wild-type caveolin-3.Q42797699
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 complexQ42811534
Invasion activating caveolin-1 mutation in human scirrhous breast cancers.Q42830165
Caveolin-1 null mice are viable but show evidence of hyperproliferative and vascular abnormalitiesQ43678714
Involvement of caveolin-1 in meiotic cell-cycle progression in Caenorhabditis elegansQ47069442
Involvement of cellular caveolae in bacterial entry into mast cells.Q52540262
Caveolin proteins in signaling, oncogenic transformation and muscular dystrophy.Q53409448
P433issue11
P407language of work or nameEnglishQ1860
P304page(s)1553-1561
P577publication date2001-12-01
P1433published inJournal of Clinical InvestigationQ3186904
P1476titleCaveolin-deficient mice: insights into caveolar function human disease
P478volume108

Reverse relations

cites work (P2860)
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