Tauroursodeoxycholic acid

Tauroursodeoxycholic acid is a lipid of Sterol Lipids (ST) class. Tauroursodeoxycholic acid is associated with abnormalities such as Hyperglycemia, Obesity, Wiskott-Aldrich Syndrome, neurogenic hypertension and Cholestatic liver disease. The involved functions are known as Cell Death, Apoptosis, Homeostasis, Process and mRNA Expression. Tauroursodeoxycholic acid often locates in Body tissue, Endoplasmic Reticulum, Hepatic, Blood and Protoplasm. The associated genes with Tauroursodeoxycholic acid are Homologous Gene and Mutant Proteins. The related lipids are cholanic acid, taurolithocholic acid 3-sulfate, Sterols, 7-dehydrocholesterol and tauromuricholic acid. The related experimental models are Disease model.

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Introduction

To understand associated biological information of Tauroursodeoxycholic acid, 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 Tauroursodeoxycholic acid?

Tauroursodeoxycholic acid is suspected in Endothelial dysfunction, Hyperglycemia, Obesity, neurogenic hypertension, Cholestatic liver disease, Heart failure 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 Tauroursodeoxycholic acid

MeSH term MeSH ID Detail
Hypertension D006973 115 associated lipids
Insulin Resistance D007333 99 associated lipids
Total 2

PubChem Associated disorders and diseases

What pathways are associated with Tauroursodeoxycholic acid

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 Tauroursodeoxycholic acid?

Related references are published most in these journals:

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What functions are associated with Tauroursodeoxycholic acid?


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What lipids are associated with Tauroursodeoxycholic acid?

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What genes are associated with Tauroursodeoxycholic acid?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Tauroursodeoxycholic acid?

Disease model

Disease model are used in the study 'Bile Acids Reduce Prion Conversion, Reduce Neuronal Loss, and Prolong Male Survival in Models of Prion Disease.' (Cortez LM et al., 2015).

Related references are published most in these journals:

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NCBI Entrez Crosslinks

All references with Tauroursodeoxycholic acid

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Authors Title Published Journal PubMed Link
Ramalho RM et al. Tauroursodeoxycholic acid suppresses amyloid β-induced synaptic toxicity in vitro and in APP/PS1 mice. 2013 Neurobiol. Aging pmid:22621777
Balasubramanyam M et al. Molecular intricacies and the role of ER stress in diabetes. 2012 Exp Diabetes Res pmid:22701473
Lenin R et al. Amelioration of glucolipotoxicity-induced endoplasmic reticulum stress by a "chemical chaperone" in human THP-1 monocytes. 2012 Exp Diabetes Res pmid:22550476
Xu J et al. Endoplasmic reticulum stress and diabetic cardiomyopathy. 2012 Exp Diabetes Res pmid:22144992
Matsubara T et al. TGF-β-SMAD3 signaling mediates hepatic bile acid and phospholipid metabolism following lithocholic acid-induced liver injury. 2012 J. Lipid Res. pmid:23034213
Drack AV et al. TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice. 2012 Invest. Ophthalmol. Vis. Sci. pmid:22110077
Amin A et al. Chronic inhibition of endoplasmic reticulum stress and inflammation prevents ischaemia-induced vascular pathology in type II diabetic mice. 2012 J. Pathol. pmid:22081301
Fonseca MB et al. c-Jun regulates the stability of anti-apoptotic ΔNp63 in amyloid-β-induced apoptosis. 2012 J. Alzheimers Dis. pmid:22045494
Studer E et al. Conjugated bile acids activate the sphingosine-1-phosphate receptor 2 in primary rodent hepatocytes. 2012 Hepatology pmid:21932398
Brites D The evolving landscape of neurotoxicity by unconjugated bilirubin: role of glial cells and inflammation. 2012 Front Pharmacol pmid:22661946
Farrell GC et al. NASH is an Inflammatory Disorder: Pathogenic, Prognostic and Therapeutic Implications. 2012 Gut Liver pmid:22570745
Hassan IH et al. Influenza A viral replication is blocked by inhibition of the inositol-requiring enzyme 1 (IRE1) stress pathway. 2012 J. Biol. Chem. pmid:22194594
Rieusset J et al. Reduction of endoplasmic reticulum stress using chemical chaperones or Grp78 overexpression does not protect muscle cells from palmitate-induced insulin resistance. 2012 Biochem. Biophys. Res. Commun. pmid:22177958
Cash JG et al. Apolipoprotein E4 impairs macrophage efferocytosis and potentiates apoptosis by accelerating endoplasmic reticulum stress. 2012 J. Biol. Chem. pmid:22730380
Zhang JY et al. Inhibition of endoplasmic reticulum stress improves mouse embryo development. 2012 PLoS ONE pmid:22808162
Galán M et al. A novel role for epidermal growth factor receptor tyrosine kinase and its downstream endoplasmic reticulum stress in cardiac damage and microvascular dysfunction in type 1 diabetes mellitus. 2012 Hypertension pmid:22665120
Young CN et al. ER stress in the brain subfornical organ mediates angiotensin-dependent hypertension. 2012 J. Clin. Invest. pmid:23064361
Henkel AS et al. Reducing endoplasmic reticulum stress does not improve steatohepatitis in mice fed a methionine- and choline-deficient diet. 2012 Am. J. Physiol. Gastrointest. Liver Physiol. pmid:22556147
Daood MJ et al. Lipid peroxidation is not the primary mechanism of bilirubin-induced neurologic dysfunction in jaundiced Gunn rat pups. 2012 Pediatr. Res. pmid:22902434
Cheng F et al. Refined Qingkailing Protects MCAO Mice from Endoplasmic Reticulum Stress-Induced Apoptosis with a Broad Time Window. 2012 Evid Based Complement Alternat Med pmid:22536287