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
pmid:22100759
Schlüter A et al. Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy. 2012 Hum. Mol. Genet. pmid:22095690
Schmidt MC et al. Efficient α, β-motif finder for identification of phenotype-related functional modules. 2011 BMC Bioinformatics pmid:22078292
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