Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Berger, EG

Class:IdPerson:449301
_displayNameBerger, EG
_timestamp2009-12-02 11:34:34
created[InstanceEdit:449318] Jassal, B, 2009-12-02
initialEG
surnameBerger
(author)[LiteratureReference:449224] Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik
[LiteratureReference:449292] Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL
[LiteratureReference:449643] A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic
[LiteratureReference:977005] Molecular cloning of a human UDP-galactose:GlcNAcbeta1,3GalNAc beta1, 3 galactosyltransferase gene encoding an O-linked core3-elongation enzyme
[LiteratureReference:977014] Localization of three human polypeptide GalNAc-transferases in HeLa cells suggests initiation of O-linked glycosylation throughout the Golgi apparatus
[LiteratureReference:1015824] Transition of galactosyltransferase 1 from trans-Golgi cisterna to the trans-Golgi network is signal mediated
[LiteratureReference:1015828] Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
[LiteratureReference:1889993] A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases
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No pathways have been reviewed or authored by Berger, EG (449301)