Evidence map›Paper›PMID 23540496›Full record

ReviewClinics in liver disease2013

Nuclear receptors as drug targets in cholestatic liver diseases.

Emina Halilbasic, Anna Baghdasaryan, Michael Trauner

Open access · hybridAbstract readReview
In one paragraph

Review in Clinics in liver disease, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 98 citations in OpenAlex.

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  9. The Farnesoid X Receptor as a Master Regulator of Hepatotoxicity.International journal of molecular sciences · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Emina HalilbasicDivision of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Anna Baghdasaryan
Michael Trauner
Medical University of Vienna · AT

Funding

Austrian Science Fund FWF F 3008Austrian Science Fund FWF F 3517
6 · The paper itself

Abstract

Cholestatic liver diseases encompass a wide spectrum of disorders with different causes, resulting in impaired bile flow and accumulation of bile acids and other potentially hepatotoxic cholephils. The understanding of the molecular mechanisms of bile formation and cholestasis has recently improved significantly through new insights into nuclear receptor (patho)biology. Nuclear receptors are ligand-activated transcription factors, which act as central players in the regulation of genes responsible for elimination and detoxification of biliary constituents accumulating in cholestasis. They also control other pathophysiologic processes such as inflammation, fibrogenesis, and carcinogenesis involved in the pathogenesis and disease progression of cholestasis liver diseases.

Indexed as

AnimalsBile Acids and SaltsCholagogues and CholereticsCholestasisConstitutive Androstane ReceptorHomeostasisHumansLigandsPeroxisome Proliferator-Activated ReceptorsPregnane X ReceptorReceptor, Farnesoid X-ActivatedReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, GlucocorticoidReceptors, SteroidSignal TransductionBile Acids and SaltsCholagogues and CholereticsConstitutive Androstane ReceptorLigandsPeroxisome Proliferator-Activated ReceptorsPregnane X ReceptorReceptor, Farnesoid X-ActivatedReceptors, CalcitriolReceptors, Cytoplasmic and NuclearReceptors, GlucocorticoidReceptors, SteroidUrsodeoxycholic Acid

Identifiers

PMID23540496
PMCPMC3633080
OpenAlexW1976811057

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.