Evidence map›Paper›PMID 33545428›Full record

ArticleCellular and molecular gastroenterology and hepatology2021

SMN Depleted Mice Offer a Robust and Rapid Onset Model of Nonalcoholic Fatty Liver Disease.

Marc-Olivier Deguise, Chantal Pileggi, Yves De Repentigny, Ariane Beauvais, Alexandra Tierney, Lucia Chehade, Jean Michaud, Maica Llavero-Hurtado, Douglas Lamont, Abdelmadjid Atrih and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  6. Peripheral defects precede neuromuscular pathology in theJournal of neuromuscular diseases · 2024
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  12. Mitochondrial Dysfunction in Spinal Muscular Atrophy.International journal of molecular sciences · 2022
    Review
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  14. Article
  15. Review
  16. Metabolic Dysfunction in Spinal Muscular Atrophy.International journal of molecular sciences · 2021
    Review
  17. 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

16 authors at 5 institutions in 3 countries.

Marc-Olivier DeguiseRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; Centre for Neuromuscular Disease, University of Ottawa, Ottawa, Ontario, Canada.
Chantal PileggiDepartment of Biochemistry, Microbiology and Immunology, Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada.
Yves De RepentignyRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Ariane BeauvaisRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Alexandra TierneyRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Lucia ChehadeRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; Centre for Neuromuscular Disease, University of Ottawa, Ottawa, Ontario, Canada.
Jean MichaudDepartment of Pathology and Laboratory Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Maica Llavero-HurtadoEuan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh, United Kingdom; The Roslin Institute, Royal (Dick) School of Veterinary Studies, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Douglas LamontFingerPrints Proteomics Facility, University of Dundee, Dundee, United Kingdom.
Abdelmadjid AtrihFingerPrints Proteomics Facility, University of Dundee, Dundee, United Kingdom.
Thomas M WishartEuan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh, United Kingdom; The Roslin Institute, Royal (Dick) School of Veterinary Studies, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Thomas H GillingwaterEuan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh, United Kingdom; College of Medicine & Veterinary Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Bernard L SchneiderBrain Mind Institute, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland; Bertarelli Foundation Gene Therapy Platform, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne (EPFL), Geneva, Switzerland.
Mary-Ellen HarperDepartment of Biochemistry, Microbiology and Immunology, Ottawa Institute of Systems Biology, University of Ottawa, Ottawa, Ontario, Canada.
Simon H ParsonEuan MacDonald Centre for Motor Neurone Disease Research, University of Edinburgh, Edinburgh, United Kingdom; Institute of Medical Sciences, University of Aberdeen, Aberdeen, United Kingdom.
Rashmi KotharyRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada; Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada; Centre for Neuromuscular Disease, University of Ottawa, Ottawa, Ontario, Canada; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada. Electronic address: rkothary@ohri.ca.
University of Ottawa · CAMott MacDonald (United Kingdom) · GBOttawa Hospital · CAUniversity of Dundee · GBÉcole Polytechnique Fédérale de Lausanne · CH

Funding

Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
UMass Mouse Metabolic Phenotyping Center - Metabolism CoreU2CDK093000 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI KIM, JASON K · 2016 to 2021
$4.6M
Biotechnology and Biological Sciences Research CouncilCIHR 575466CIHR ERL-138414CIHR FDN 143278CIHR PJT-156379NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U2C DK093000
6 · The paper itself

Abstract

BACKGROUND &

aimsNonalcoholic fatty liver disease (NAFLD) is considered a health epidemic with potential devastating effects on the patients and the healthcare systems. Current preclinical models of NAFLD are invariably imperfect and generally take a long time to develop. A mouse model of survival motor neuron (SMN) depletion (Smn

methodsBiochemical, histologic, electron microscopy, proteomic, and high-resolution respirometry were used.

resultsThe Smn

conclusionsThe Smn

Indexed as

Disease Models, AnimalAnimalsFatty LiverMiceMice, Inbred C57BLMice, KnockoutNon-alcoholic Fatty Liver DiseaseSurvival of Motor Neuron 1 ProteinSmn1 protein, mouseSurvival of Motor Neuron 1 ProteinMetabolismNAFLDNASHSMN

Identifiers

PMID33545428
PMCPMC8257458
OpenAlexW3125737167

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.