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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Details on Person von Figura, K

Class:Id	Person:71282
_displayName	von Figura, K
_timestamp	0000-00-00 00:00:00
firstname	K
initial	K
surname	von Figura
(author)	[LiteratureReference:71277] Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man. [LiteratureReference:449268] Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik [LiteratureReference:449330] A new type of congenital disorders of glycosylation (CDG-Ii) provides new insights into the early steps of dolichol-linked oligosaccharide biosynthesis [LiteratureReference:1015828] Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId [LiteratureReference:1663155] A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme [LiteratureReference:2314581] Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes [LiteratureReference:3781879] Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy [LiteratureReference:4720455] Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase [LiteratureReference:9841171] Mr 46,000 mannose 6-phosphate specific receptor: its role in targeting of lysosomal enzymes [LiteratureReference:9841185] In vitro mutagenesis of potential N-glycosylation sites of arylsulfatase A. Effects on glycosylation, phosphorylation, and intracellular sorting
[Change default viewing format]

No pathways have been reviewed or authored by von Figura, K (71282)