Query author contributions in Reactome

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Details on Person Rothfels, Karen, 2024-08-13

Class:Id	InstanceEdit:9917785
_displayName	Rothfels, Karen, 2024-08-13
_timestamp	2024-08-13 12:58:05
author	[Person:1226097] Rothfels, Karen
dateTime	2024-08-13 12:58:01
(modified)	[Pathway:9865113] Loss-of-function mutations in DBT cause MSUD2 [Homo sapiens] [Pathway:9865114] Maple Syrup Urine Disease [Homo sapiens] [FailedReaction:9865115] DBT loss-of-function mutants don't synthesize BCAA-CoA [Homo sapiens] [Pathway:9865118] Diseases of branched-chain amino acid catabolism [Homo sapiens] [FailedReaction:9865121] BCKDHA or BCKDHB loss-of-function mutants don't synthesize BCAA-CoA [Homo sapiens] [Pathway:9865125] Loss-of-function mutations in BCKDHA or BCKDHB cause MSUD [Homo sapiens] [Pathway:9907570] Loss-of-function mutations in DLD cause MSUD3/DLDD [Homo sapiens] [FailedReaction:9907572] Loss-of-function DLD mutants don't dehydrogenate dihydrolipoyl DBT [Homo sapiens] [Pathway:9909438] 3-Methylcrotonyl-CoA carboxylase deficiency [Homo sapiens] [FailedReaction:9909466] MCCC mutants don't synthesize beta-methylglutaconyl-CoA [Homo sapiens] List all 24 refering instances
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No pathways have been reviewed or authored by Rothfels, Karen, 2024-08-13 (9917785)