Search Results - Foster, William
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Succinyl-CoA:3-oxoacid coenzyme a transferase (SCOT) deficiency: a rare and potentially fatal metabolic disease by Grünert, Sarah (Author) , Foster, William (Author) , Schumann, Anke (Author) , Lund, Allan (Author) , Pontes, Christina (Author) , Roloff, Sylvia (Author) , Weinhold, Natalie (Author) , Yue, Wyatt W. (Author) , AlAsmari, Ali (Author) , Obaid, Osama A. (Author) , Faqeih, Eissa Ali (Author) , Stübbe, Lisa (Author) , Yamamoto, Raina (Author) , Gemperle-Britschgi, Corinne (Author) , Walter, Melanie (Author) , Spiekerkoetter, Ute (Author) , Mackinnon, Sabrina (Author) , Sass, Jörn Oliver (Author) ,
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Crystal structure and interaction studies of human DHTKD1 provide insight into a mitochondrial megacomplex in lysine catabolism by Bezerra, Gustavo A. (Author) , Foster, William R. (Author) , Bailey, Henry J. (Author) , Hicks, Kevin G. (Author) , Sauer, Sven (Author) , Dimitrov, Bianca (Author) , McCorvie, Thomas J. (Author) , Okun, Jürgen G. (Author) , Rutter, Jared (Author) , Kölker, Stefan (Author) , Yue, Wyatt W. (Author) ,
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Related Subjects
2-oxoacid dehydrogenase
2-oxoadipate
2-oxoglutarate dehydrogenase
Inborn error of metabolism
Ketoacidosis
Ketolysis
Ketone body utilization
Metabolic acidosis
acid
alpha-ketoacid dehydrogenase
complex
cryo-EM
cubic-core
enzyme mechanisms
generation
human DHTKD1
ketoglutarate dehydrogenase
lysine catabolism
multi-protein complexes
subunit
superoxide/hydrogen peroxide
thiamine diphosphate