Evidence map›Paper›PMID 32188695›Full record

ArticleThe Journal of biological chemistry2020

Deletion of fatty acid transport protein 2 (FATP2) in the mouse liver changes the metabolic landscape by increasing the expression of PPARα-regulated genes.

Vincent M Perez, Jeffrey Gabell, Mark Behrens, Nishikant Wase, Concetta C DiRusso, Paul N Black

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

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  5. Insulin Resistance and Inflammation.International journal of molecular sciences · 2026
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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

6 authors at 1 institution in 1 country.

Vincent M PerezDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588.
Jeffrey GabellDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588.
Mark BehrensDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588.
Nishikant WaseDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588.
Concetta C DiRussoDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588; Nebraska Center for Integrated Biomolecular Communication, University of Nebraska, Lincoln, Nebraska 68588.
Paul N BlackDepartment of Biochemistry, University of Nebraska, Lincoln, Nebraska 68588. Electronic address: pblack2@unl.edu.
University of Nebraska–Lincoln · US

Funding

Targeted mass spectrometry approaches to understand CART processing and recepter interactionsP20GM113126 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI GUO, JIANTAO · 2016 to 2025
$20.8M
NIGMS NIH HHS P20 GM113126
6 · The paper itself

Abstract

Fatty acid transport protein 2 (FATP2) is highly expressed in the liver, small intestine, and kidney, where it functions in both the transport of exogenous long-chain fatty acids and the activation of very-long-chain fatty acids. Here, using a murine model, we investigated the phenotypic impacts of deleting FATP2, followed by a transcriptomic analysis using unbiased RNA-Seq to identify concomitant changes in the liver transcriptome. WT and FATP2-null (

Indexed as

Gene DeletionAnimalsCoenzyme A LigasesFemaleGene Expression RegulationLipid MetabolismLiverMaleMetabolomeMiceMice, Inbred C57BLPPAR alphaTranscriptomeCoenzyme A LigasesFATP2 protein, mousePPAR alphafatty acid transport protein 2 (FATP2)gene regulationlipid metabolismlivermetabolic landscapemetabolomicsperoxisome proliferator–activated receptor α (PPARα)RNA-Seqtranscriptomics

Identifiers

PMID32188695
PMCPMC7186177
OpenAlexW3010751007

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.