Evidence map›Paper›PMID 30135087›Full record

ArticleThe Biochemical journal2018

Isoform-specific AMPK association with TBC1D1 is reduced by a mutation associated with severe obesity.

Elaine C Thomas, Sharon C Hook, Alexander Gray, Alexandra Chadt, David Carling, Hadi Al-Hasani, Kate J Heesom, D Grahame Hardie, Jeremy M Tavaré

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Elaine C ThomasSchool of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol, U.K. elaine.thomas@bristol.ac.uk.ORCID 0000-0002-9435-3653
Sharon C HookSchool of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol, U.K.
Alexander GrayDivision of Cell Signalling & Immunology, School of Life Sciences, University of Dundee, Dundee, U.K.
Alexandra ChadtGerman Diabetes Center, Leibniz Center for Diabetes Research, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
David CarlingCellular Stress Group, Medical Research Council London Institute of Medical Sciences, Hammersmith Hospital, Imperial College, London, U.K.
Hadi Al-HasaniGerman Diabetes Center, Leibniz Center for Diabetes Research, Heinrich-Heine-University, Medical Faculty, Düsseldorf, Germany.
Kate J HeesomSchool of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol, U.K.
D Grahame HardieDivision of Cell Signalling & Immunology, School of Life Sciences, University of Dundee, Dundee, U.K.
Jeremy M TavaréSchool of Biochemistry, Biomedical Sciences Building, University of Bristol, Bristol, U.K.
University of Bristol · GBDeutsches Diabetes-Zentrum e.V. · DEUniversity of Dundee · GBHammersmith Hospital · GB

Funding

British Heart Foundation PG/10/008/28186Wellcome Trust 204766/Z/16/Z
6 · The paper itself

Abstract

AMP-activated protein kinase (AMPK) is a key regulator of cellular and systemic energy homeostasis which achieves this through the phosphorylation of a myriad of downstream targets. One target is TBC1D1 a Rab-GTPase-activating protein that regulates glucose uptake in muscle cells by integrating insulin signalling with that promoted by muscle contraction. Ser

Indexed as

Mutation, MissenseAmino Acid SubstitutionAminoimidazole CarboxamideAMP-Activated Protein KinasesAnimalsFemaleGTPase-Activating ProteinsIsoenzymesMaleMiceMice, TransgenicObesityPhosphorylationRibonucleotidesSex CharacteristicsAICA ribonucleotideAminoimidazole CarboxamideAMP-Activated Protein KinasesGTPase-Activating ProteinsIsoenzymesRibonucleotidesTbc1d1 protein, mouseAMPKglucose transportobesityprotein–protein interactionsRab-GAPsignalling

Identifiers

PMID30135087
PMCPMC6156765
OpenAlexW2888538512

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.