Dihydrolipoamide

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.

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Introduction

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.

What diseases are associated with Dihydrolipoamide?

Dihydrolipoamide is suspected in and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Dihydrolipoamide

MeSH term MeSH ID Detail
Parkinsonian Disorders D020734 20 associated lipids
Total 1

PubChem Associated disorders and diseases

What pathways are associated with Dihydrolipoamide

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Dihydrolipoamide?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with Dihydrolipoamide?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Dihydrolipoamide?

There are no associated biomedical information in the current reference collection.

What genes are associated with Dihydrolipoamide?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Dihydrolipoamide?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Dihydrolipoamide

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Authors Title Published Journal PubMed Link
Jeffery CJ Proteins with neomorphic moonlighting functions in disease. 2011 IUBMB Life pmid:21698752
Golas A et al. Sperm mitochondria diaphorase activity--a gene mapping study of recombinant inbred strains of mice. 2010 Int. J. Dev. Biol. pmid:20209439
Ninomiya M et al. PBC: Animal Models of Cholangiopathies and Possible Endogenous Viral Infections. 2012 Int J Hepatol pmid:22007316
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
Trofimova L et al. Behavioral impact of the regulation of the brain 2-oxoglutarate dehydrogenase complex by synthetic phosphonate analog of 2-oxoglutarate: implications into the role of the complex in neurodegenerative diseases. 2010 Int J Alzheimers Dis pmid:21049004
Chadwick W et al. Complex and multidimensional lipid raft alterations in a murine model of Alzheimer's disease. 2010 Int J Alzheimers Dis pmid:21151659
Kunieda T et al. Carbohydrate metabolism genes and pathways in insects: insights from the honey bee genome. 2006 Insect Mol. Biol. pmid:17069632
Odièvre MH et al. A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency. 2005 Hum. Mutat. pmid:15712224
Mersey BD et al. Human microRNA (miR29b) expression controls the amount of branched chain alpha-ketoacid dehydrogenase complex in a cell. 2005 Hum. Mol. Genet. pmid:16203741
Schlüter A et al. Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy. 2012 Hum. Mol. Genet. pmid:22095690
Narisawa A et al. Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans. 2012 Hum. Mol. Genet. pmid:22171071
Vasiliou V et al. Update of the NAD(P)H:quinone oxidoreductase (NQO) gene family. 2006 Hum. Genomics pmid:16595077
Ottosson F et al. Genetic variation in three species of Hordeum, and the selection of accessions for the Barley Core Collection. 2002 Hereditas pmid:12564627
Sasaki M and Nakanuma Y Biliary epithelial apoptosis, autophagy, and senescence in primary biliary cirrhosis. 2010 Hepat Res Treat pmid:21152179
Bull TJ et al. A rhodanine agent active against non-replicating intracellular Mycobacterium avium subspecies paratuberculosis. 2009 Gut Pathog pmid:20030828
Griffin JL and Des Rosiers C Applications of metabolomics and proteomics to the mdx mouse model of Duchenne muscular dystrophy: lessons from downstream of the transcriptome. 2009 Genome Med pmid:19341503
Wang N et al. Cloning, expression and characterization of alcohol dehydrogenases in the silkworm Bombyx mori. 2011 Genet. Mol. Biol. pmid:21734824
Kim SY and Kim J Roles of dihydrolipoamide dehydrogenase Lpd1 in Candida albicans filamentation. 2010 Fungal Genet. Biol. pmid:20601046
Finnegan PM and Chen W Arsenic toxicity: the effects on plant metabolism. 2012 Front Physiol pmid:22685440
Sharma A et al. Interactomic and pharmacological insights on human sirt-1. 2012 Front Pharmacol pmid:22470339