A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.
about
Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interactionSkeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.Form and function: the laminin family of heterotrimersCaveolin-3 directly interacts with the C-terminal tail of beta -dystroglycan. Identification of a central WW-like domain within caveolin family membersO Mannosylation of alpha-dystroglycan is essential for lymphocytic choriomeningitis virus receptor functionDystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGEB4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycanProcessing and secretion of the N-terminal domain of alpha-dystroglycan in cell culture mediaSpecific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19.Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferaseAbsence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12A role of fukutin, a gene responsible for Fukuyama type congenital muscular dystrophy, in cancer cells: a possible role to suppress cell proliferationMutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanA comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severitySarcospan-deficient mice maintain normal muscle functionDefective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophyIncreasing complexity of the dystrophin-associated protein complexPikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpressionDevelopmental and pathogenic mechanisms of basement membrane assemblyMouse fukutin deletion impairs dystroglycan processing and recapitulates muscular dystrophyVisual impairment in the absence of dystroglycanStructure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparinFilamin 2 (FLN2): A muscle-specific sarcoglycan interacting proteinPost-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localizationSildenafil and cardiomyocyte-specific cGMP signaling prevent cardiomyopathic changes associated with dystrophin deficiencyZZ domain of dystrophin and utrophin: topology and mapping of a beta-dystroglycan interaction siteThe small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscleMolecular organization of sarcoglycan complex in mouse myotubes in cultureDetection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencingA stoichiometric complex of neurexins and dystroglycan in brainThe biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscleDystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophiesThe potential of sarcospan in adhesion complex replacement therapeutics for the treatment of muscular dystrophyAutonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin-angiotensin systemProteomic profiling of the dystrophin-deficient mdx phenocopy of dystrophinopathy-associated cardiomyopathyOn the Teneurin track: a new synaptic organization molecule emergesMulti-parametric MRI at 14T for muscular dystrophy mice treated with AAV vector-mediated gene therapyβ2-Syntrophin is a Cdk5 substrate that restrains the motility of insulin secretory granulesThe Crystal Structures of Dystrophin and Utrophin Spectrin Repeats: Implications for Domain BoundariesExpression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex
P2860
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P2860
A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
A role for the dystrophin-glyc ...... ker between laminin and actin.
@ast
A role for the dystrophin-glyc ...... ker between laminin and actin.
@en
type
label
A role for the dystrophin-glyc ...... ker between laminin and actin.
@ast
A role for the dystrophin-glyc ...... ker between laminin and actin.
@en
prefLabel
A role for the dystrophin-glyc ...... ker between laminin and actin.
@ast
A role for the dystrophin-glyc ...... ker between laminin and actin.
@en
P2860
P356
P1476
A role for the dystrophin-glyc ...... nker between laminin and actin
@en
P2093
J M Ervasti
P2860
P304
P356
10.1083/JCB.122.4.809
P407
P577
1993-08-01T00:00:00Z