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Query author contributions in Reactome

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Details on Person Stephan, Ralf, 2023-07-28

Class:IdInstanceEdit:9840815
_displayNameStephan, Ralf, 2023-07-28
_timestamp2023-07-28 09:13:39
author[Person:804962] Stephan, Ralf
dateTime2023-07-28 09:13:17
(created)[Person:9840816] Harzer, K
[LiteratureReference:9840817] Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage disease
[Complex:9840818] PSAP(195-273):LacCer:PE [lysosomal lumen] [Homo sapiens]
[Person:9840819] Smíd, F
[Person:9840820] Bradová, V
[Complex:9840821] PSAP(195-273):GM3:PE [lysosomal lumen] [Homo sapiens]
[Person:9840822] Roggendorf, W
[Person:9840823] Ulrich-Bott, B
[Person:9840824] Fürst, W
[LiteratureReference:9840825] Metabolism of GM1 ganglioside in cultured skin fibroblasts: anomalies in gangliosidoses, sialidoses, and sphingolipid activator protein (SAP, saposin) 1 and prosaposin deficient disorders
List all 15 refering instances
(modified)[PathwayDiagram:554229] Diagram of Sphingolipid metabolism
[Summation:1605714] Ganglioside GM3, mobilized by Saposin B (PSAP(195-273)), is ...
[Reaction:1605724] NEU1,4 hydrolyze PSAP(195-273):GM3:PE [Homo sapiens]
[Summation:9840330] After its transport to lysosomes, prosaposin (PSAP) gets cle...
[BlackBoxEvent:9840334] PSAP is cleaved [Homo sapiens]
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No pathways have been reviewed or authored by Stephan, Ralf, 2023-07-28 (9840815)
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