Evidence map›Paper›PMID 30864232›Full record

ArticleHepatology (Baltimore, Md.)2019

Bile Acid Homeostasis in a Cholesterol 7α-Hydroxylase and Sterol 27-Hydroxylase Double Knockout Mouse Model.

Daniel Rizzolo, Kyle Buckley, Bo Kong, Le Zhan, Jianliang Shen, Mary Stofan, Anita Brinker, Michael Goedken, Brian Buckley, Grace L Guo

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. 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
3.2field-weighted citation impact, top 7% 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, 76 citations in OpenAlex.

  1. Role of Bile Acid Receptors in Non-Infectious Diarrhea: A Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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  8. Article
  9. Bile acids and their receptors in hepatic immunity.Liver research (Beijing, China) · 2025
    Review
  10. Experimental and therapeutic medicine · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Liver-gut axis signaling regulates circadian energy metabolism in shift workers.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  15. Article
  16. Characterization of individual bile acids in vivo utilizing a novel low bile acid mouse model.Toxicological sciences : an official journal of the Society of Toxicology · 2024
    Article
  17. Article
  18. Article
  19. In vivo mouse models to study bile acid synthesis and signaling.Hepatobiliary & pancreatic diseases international : HBPD INT · 2023
    Review
  20. Review
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

10 authors at 5 institutions in 1 country.

Daniel RizzoloDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Kyle BuckleyDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Bo KongDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Le ZhanRutgers Cancer Institute of New Jersey, New Brunswick, NJ.
Jianliang ShenDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Mary StofanDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Anita BrinkerDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Michael GoedkenOffice of Research and Economic Development, Research Pathology Services, Rutgers University, Piscataway, NJ.
Brian BuckleyDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Grace L GuoDepartment of Pharmacology and Toxicology, School of Pharmacy, Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, NJ.
Rutgers, The State University of New Jersey · USEnvironmental and Occupational Health Sciences Institute · USRutgers Cancer Institute of New JerseyVA New Jersey Health Care System · USVA Office of Research and Development · US

Funding

Translational Research Support CoreP30ES005022 · NIEHS · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Debra L Laskin · 1988 to 2026
$47.4M
TRAINING IN EVIRONMENTAL TOXICOLOGYT32ES007148 · NIEHS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI Lauren M Aleksunes · 1987 to 2026
$11.4M
Gut bile acids, Fxr, & Fgf15 in total parenteral nutrition-associated cholestasisR01GM104037 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI GUO, GRACE L · 2013 to 2016
$1.1M
Differential roles of FXR and FGF15 in liver fibrosis developmentR21ES029258 · NIEHS · RUTGERS, THE STATE UNIV OF N.J. · PI GUO, GRACE L · 2018 to 2019
$426k
Role of Intestinal Bile Acid Signaling in Liver DiseasesI01BX002741 · VA · VA NEW JERSEY HEALTH CARE SYSTEM · PI GRACE L GUO · 2018 to 2026
–
BLRD VA I01 BX002741National Institutes of Health and Department of Veterans Affairs BX002741National Institutes of Health and Department of Veterans Affairs T32ES007148NIEHS NIH HHS P30 ES005022NIEHS NIH HHS R21 ES029258NIEHS NIH HHS T32 ES007148NIGMS NIH HHS R01 GM104037
6 · The paper itself

Abstract

Bile acids (BAs) are diverse molecules that are synthesized from cholesterol in the liver. The synthesis of BAs has traditionally been shown to occur through two pathways. Cholesterol 7α-hydroxylase (CYP7A1) performs the initial and rate-limiting step in the classical pathway, and sterol 27-hydroxylase (CYP27A1) initiates the hydroxylation of cholesterol in the alternative pathway. While the role of individual BA species as physiological detergents is relatively ubiquitous, their endocrine functions as signaling molecules and roles in disease pathogenesis have been emerging to be BA species-specific. In order to better understand the pharmacologic and toxicologic roles of individual BA species in an in vivo model, we created cholesterol 7α-hydroxylase (Cyp7a1) and sterol 27-hydroxylase (Cyp27a1) double knockout (DKO) mice by cross-breeding single knockout mice (Cyp7a1

Indexed as

Models, AnimalAnimalsBile Acids and SaltsCholestanetriol 26-MonooxygenaseCholesterol 7-alpha-HydroxylaseHomeostasisMaleMice, KnockoutBile Acids and SaltsCholestanetriol 26-MonooxygenaseCholesterol 7-alpha-HydroxylaseCyp27a1 protein, mouseCyp7a1 protein, mouse

Identifiers

PMID30864232
PMCPMC7893641
OpenAlexW2922325860

What OpenQuestion holds

Textmetadata
LicenceTDM
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.