Reactome | Campbell, KP

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Campbell, KP Show undefined attributes

created	[InstanceEdit:2328179] Jupe, S, 2012-06-25
dbId	2328163
displayName	Campbell, KP
firstname	Kevin P
initial	KP
modified	[InstanceEdit:8953528] D'Eustachio, Peter, 2016-12-23
publications	[LiteratureReference:2328132] Membrane organization of the dystrophin-glycoprotein complex [LiteratureReference:2328093] Muscular dystrophies and the dystrophin-glycoprotein complex [LiteratureReference:2328126] Molecular basis of muscular dystrophies [LiteratureReference:2328097] A role for dystroglycan in basement membrane assembly [LiteratureReference:9939298] Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane [LiteratureReference:2328092] A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin [LiteratureReference:2328124] A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering [LiteratureReference:2426614] Dystroglycan is a binding protein of laminin and merosin in peripheral nerve [LiteratureReference:3597683] Dystroglycan loss disrupts polarity and beta-casein induction in mammary epithelial cells by perturbing laminin anchoring [LiteratureReference:8849759] Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE [LiteratureReference:5617139] Xylosyl- and glucuronyltransferase functions of LARGE in ?-dystroglycan modification are conserved in LARGE2 [LiteratureReference:9940861] HNK-1 sulfotransferase modulates ?-dystroglycan glycosylation by 3-O-sulfation of glucuronic acid on matriglycan [LiteratureReference:9619577] Characterization of dystroglycan-laminin interaction in peripheral nerve [LiteratureReference:9913174] O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding [LiteratureReference:8931899] The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated ?-dystroglycan functional glycosylation [LiteratureReference:8879116] SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function [LiteratureReference:9940755] The functional O-mannose glycan on ?-dystroglycan contains a phospho-ribitol primed for matriglycan addition [LiteratureReference:9940680] ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome [LiteratureReference:8931643] Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of ?-dystroglycan
schemaClass	Person
surname	Campbell

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