Query author contributions in Reactome

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Details on Person Willer, Tobias

Class:Id	Person:5617132
_displayName	Willer, Tobias
_timestamp	2014-07-31 10:03:39
created	[InstanceEdit:5617130] Jassal, Bijay, 2014-07-31
firstname	Tobias
initial	T
surname	Willer
(author)	[LiteratureReference:5617139] Xylosyl- and glucuronyltransferase functions of LARGE in ?-dystroglycan modification are conserved in LARGE2 [LiteratureReference:8855877] Endogenous glucuronyltransferase activity of LARGE or LARGE2 required for functional modification of α-dystroglycan in cells and tissues [LiteratureReference:8879116] SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function [LiteratureReference:8931643] Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan [LiteratureReference:8931899] The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation [LiteratureReference:9933085] Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion [LiteratureReference:9940658] An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene [LiteratureReference:9940680] ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome [LiteratureReference:9940755] The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition
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No pathways have been reviewed or authored by Willer, Tobias (5617132)