Evidence map›Paper›PMID 29053141›Full record

ArticleCell death and differentiation2018

Loss of BIM increases mitochondrial oxygen consumption and lipid oxidation, reduces adiposity and improves insulin sensitivity in mice.

Jibran A Wali, Sandra Galic, Christina Yr Tan, Esteban N Gurzov, Ann E Frazier, Timothy Connor, Jingjing Ge, Evan G Pappas, David Stroud, L Chitra Varanasi and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Frontiers in endocrinology · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Metabolic characteristics of CD8Nature communications · 2020
    Article
  16. 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

18 authors at 6 institutions in 1 country.

Jibran A WaliSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Sandra GalicSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Christina Yr TanSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Esteban N GurzovSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.ORCID 0000-0003-4642-0273
Ann E FrazierMurdoch Childrens Research Institute and The University of Melbourne Department of Paediatrics, Royal Childrens Hospital, Parkville, VIC 3052, Australia.
Timothy ConnorMetabolic Reprogramming Laboratory, Metabolic Research Unit, School of Medicine, Deakin University, Geelong, VIC 3216, Australia.
Jingjing GeSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Evan G PappasSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
David StroudDepartment of Biochemistry and Molecular Biology, Monash University, VIC 3800, Australia.
L Chitra VaranasiSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Claudia SelckSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Michael T RyanDepartment of Biochemistry and Molecular Biology, Monash University, VIC 3800, Australia.ORCID 0000-0003-2586-8829
David R ThorburnMurdoch Childrens Research Institute and The University of Melbourne Department of Paediatrics, Royal Childrens Hospital, Parkville, VIC 3052, Australia.ORCID 0000-0002-7725-9470
Bruce E KempSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Balasubramanian KrishnamurthySt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Thomas Wh KaySt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
Sean L McGeeMetabolic Reprogramming Laboratory, Metabolic Research Unit, School of Medicine, Deakin University, Geelong, VIC 3216, Australia.
Helen E ThomasSt. Vincent's Institute, Fitzroy, VIC 3065, Australia.
St Vincents Institute of Medical Research · AUThe University of Melbourne · AUDeakin University · AUMonash University · AURoyal Children's Hospital · AUSt Vincent's Hospital Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BCL-2 proteins are known to engage each other to determine the fate of a cell after a death stimulus. However, their evolutionary conservation and the many other reported binding partners suggest an additional function not directly linked to apoptosis regulation. To identify such a function, we studied mice lacking the BH3-only protein BIM. BIM

Indexed as

AdiposityLipid MetabolismAnimalsBcl-2-Like Protein 11Electron Transport Complex IVEnergy MetabolismGlucoseHepatocytesInsulin ResistanceLiverMembrane Potential, MitochondrialMiceMitochondriaOxidation-ReductionOxygen ConsumptionWeight LossBcl2l11 protein, mouseBcl-2-Like Protein 11Electron Transport Complex IVGlucose

Identifiers

PMID29053141
PMCPMC5729528
OpenAlexW2767101040

What OpenQuestion holds

Textmetadata
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.