MeSH term | MeSH ID | Detail |
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Parkinsonian Disorders | D020734 | 20 associated lipids |
Dihydrolipoamide is a lipid of Fatty Acyls (FA) class. Dihydrolipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Citric Acid Cycle, Electron Transport, NADH oxidation, Oxidation and Oxidants. Dihydrolipoamide often locates in Mitochondria, Mitochondrial matrix and Chloroplasts. The associated genes with Dihydrolipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, Genes, Mitochondrial and alanylproline.
To understand associated biological information of Dihydrolipoamide, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.
Dihydrolipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
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We collected disease MeSH terms mapped to the references associated with Dihydrolipoamide
MeSH term | MeSH ID | Detail |
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Parkinsonian Disorders | D020734 | 20 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
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Function | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Gene | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Authors | Title | Published | Journal | PubMed Link |
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pmid:22100759 | ||||
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Vazquez A et al. | Serine biosynthesis with one carbon catabolism and the glycine cleavage system represents a novel pathway for ATP generation. | 2011 | PLoS ONE | pmid:22073143 |
Ninomiya M et al. | PBC: Animal Models of Cholangiopathies and Possible Endogenous Viral Infections. | 2012 | Int J Hepatol | pmid:22007316 |
Stobbe MD et al. | Critical assessment of human metabolic pathway databases: a stepping stone for future integration. | 2011 | BMC Syst Biol | pmid:21999653 |
Sasaki M and Nakanuma Y | Novel approach to bile duct damage in primary biliary cirrhosis: participation of cellular senescence and autophagy. | 2012 | Int J Hepatol | pmid:21994884 |
Sandoval JM et al. | Glucose-6-phosphate dehydrogenase protects Escherichia coli from tellurite-mediated oxidative stress. | 2011 | PLoS ONE | pmid:21984934 |
Skapski A et al. | Genome-scale analysis of Mycoplasma agalactiae loci involved in interaction with host cells. | 2011 | PLoS ONE | pmid:21966487 |
Vaubel RA et al. | Mutations in the dimer interface of dihydrolipoamide dehydrogenase promote site-specific oxidative damages in yeast and human cells. | 2011 | J. Biol. Chem. | pmid:21930696 |