Evidence map›Paper›PMID 29483192›Full record

ArticleThe Journal of biological chemistry2018

Alternative splicing variant of the scaffold protein APPL1 suppresses hepatic adiponectin signaling and function.

Amanda K Galan-Davila, Jiyoon Ryu, Kun Dong, Yang Xiao, Zhe Dai, Deling Zhang, Zhi Li, Amanda M Dick, Kevin D Liu, Amrita Kamat and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  9. APPL1 negatively regulates bone mass, possibly by controlling the fate of bone marrow mesenchymal progenitor cells.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2020
    Article
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

14 authors at 4 institutions in 1 country.

Amanda K Galan-DavilaFrom the Departments of Cell Systems and Anatomy.
Jiyoon RyuFrom the Departments of Cell Systems and Anatomy.
Kun DongFrom the Departments of Cell Systems and Anatomy.
Yang XiaoFrom the Departments of Cell Systems and Anatomy.
Zhe DaiFrom the Departments of Cell Systems and Anatomy.
Deling ZhangFrom the Departments of Cell Systems and Anatomy.
Zhi LiFrom the Departments of Cell Systems and Anatomy.
Amanda M DickFrom the Departments of Cell Systems and Anatomy.
Kevin D LiuFrom the Departments of Cell Systems and Anatomy.
Amrita KamatMedicine and.
Min Luthe Department of Medicine, University of California, San Diego, La Jolla, California 92093.
Qunfeng Dongthe Center for Biomedical Informatics, Department of Public Health Sciences, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois 60153, and.
Feng LiuThe Barshop Center for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio, Texas 78229-3900.
Lily Q DongFrom the Departments of Cell Systems and Anatomy, DongQ@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USLoyola University Chicago · USUniversity of California, San Diego · USUniversity of the Incarnate Word · US

Funding

Regulation and Function of Adiponectin OligomerizationR01DK076902 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LIU, FENG · 2008 to 2017
$2.9M
The role of TCTP in regulating adiponectin signalingR01DK102965 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DONG, LILY Q · 2015 to 2019
$1.7M
Lipid Metabolism and Steatosis in LiverI01BX001744 · VA · SOUTH TEXAS VETERANS HEALTH CARE SYSTEM · PI KAMAT, AMRITA · 2013 to 2016
–
BLRD VA I01 BX001744NIDDK NIH HHS R01 DK076902NIDDK NIH HHS R01 DK102965
6 · The paper itself

Abstract

Adiponectin is an adipocyte-derived hormone with antidiabetic activities that include increasing the sensitivity of cells to insulin. Adaptor protein containing pleckstrin homology domain, phosphotyrosine-binding domain, and leucine zipper motif (APPL1) stimulates adiponectin signaling and promotes adiponectin's insulin-sensitizing effects by binding to two adiponectin receptors, AdipoR1 and AdipoR2, and the insulin receptor. In this study, we report an alternative splicing variant of APPL1 (APPL1sv) that is highly expressed in mouse liver, pancreas, and spleen tissues. The expression levels of APPL1sv in liver tissues were enhanced in a mouse model of obesity and diabetic dyslipidemia (

Indexed as

Alternative SplicingInsulin ResistanceSignal TransductionAdaptor Proteins, Signal TransducingAdiponectinAnimalsCells, CulturedDiabetes Mellitus, Type 2DyslipidemiasHumansLiverMaleMice, Inbred C57BLObesityUp-RegulationAdaptor Proteins, Signal TransducingAdiponectinAppl1 protein, mouseadiponectinalternative splicingAMP-activated kinase (AMPK)APPL1APPL1svdiabetesinsulin resistancelivermetabolic disordermetabolism

Identifiers

PMID29483192
PMCPMC5912452
OpenAlexW2789795395

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.