MeSH term | MeSH ID | Detail |
---|---|---|
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 |
---|---|---|
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:16669652 | ||||
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Lee H et al. | An integrated approach to the prediction of domain-domain interactions. | 2006 | BMC Bioinformatics | pmid:16725050 |
pmid:16729985 | ||||
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pmid:16770810 | ||||
pmid:16814740 | ||||
pmid:16835851 | ||||
pmid:16855207 | ||||
pmid:16861247 | ||||
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Brown RM et al. | Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. | 2006 | Dev Med Child Neurol | pmid:16904023 |
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pmid:16945443 | ||||
pmid:17017892 | ||||
pmid:17033778 | ||||
Lee EH et al. | A Korean female patient with thiamine-responsive pyruvate dehydrogenase complex deficiency due to a novel point mutation (Y161C)in the PDHA1 gene. | 2006 | J. Korean Med. Sci. | pmid:17043409 |
pmid:17052205 | ||||
Kunieda T et al. | Carbohydrate metabolism genes and pathways in insects: insights from the honey bee genome. | 2006 | Insect Mol. Biol. | pmid:17069632 |