Evidence map›Paper›PMID 31641069›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Aged hind-limb clasping experimental autoimmune encephalomyelitis models aspects of the neurodegenerative process seen in multiple sclerosis.

Lindsay S Cahill, Monan Angela Zhang, Valeria Ramaglia, Heather Whetstone, Melika Pahlevan Sabbagh, Tae Joon Yi, Laura Woo, Thomas S Przybycien, Marina Moshkova, Fei Linda Zhao and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Modeling cerebral palsy in animals.Developmental medicine and child neurology · 2026
    Review
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  6. Conditional Astrocyte Rac1KO Attenuates Hyperreflexia after Spinal Cord Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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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

16 authors at 5 institutions in 2 countries.

Lindsay S CahillMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON M5T 3H7, Canada.
Monan Angela ZhangDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Valeria RamagliaDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Heather WhetstonePeter Gilgan Centre for Research and Learning, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Melika Pahlevan SabbaghDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Tae Joon YiDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Laura WooMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON M5T 3H7, Canada.
Thomas S PrzybycienDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Marina MoshkovaToronto General Research Institute, University Health Network, Toronto, ON M5G 2C4, Canada.
Fei Linda ZhaoDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Olga L RojasDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Josephine GomesDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Stefanie KuertenInstitute of Anatomy and Cell Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054 Erlangen, Germany.ORCID 0000-0001-6119-605X
Jennifer L GommermanDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada.
John G SledMouse Imaging Centre, The Hospital for Sick Children, Toronto, ON M5T 3H7, Canada.
Shannon E DunnDepartment of Immunology, University of Toronto, Toronto, ON M5S 1A8, Canada; Shannon.Dunn@unityhealth.to.
University of Toronto · CAHospital for Sick Children · CAFriedrich-Alexander-Universität Erlangen-Nürnberg · DESt. Michael's Hospital · CAUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Experimental autoimmune encephalomyelitis (EAE) is the most common model of multiple sclerosis (MS). This model has been instrumental in understanding the events that lead to the initiation of central nervous system (CNS) autoimmunity. Though EAE has been an effective screening tool for identifying novel therapies for relapsing-remitting MS, it has proven to be less successful in identifying therapies for progressive forms of this disease. Though axon injury occurs in EAE, it is rapid and acute, making it difficult to intervene for the purpose of evaluating neuroprotective therapies. Here, we describe a variant of spontaneous EAE in the 2D2 T cell receptor transgenic mouse (2D2

Indexed as

HindlimbAgingAnimalsEncephalomyelitis, Autoimmune, ExperimentalGray MatterMiceMice, Inbred C57BLMice, TransgenicMultiple SclerosisPPAR alphaWhite MatterPPAR alphaPpara protein, mousemultiple sclerosis modelneurodegenerationprogressive

Identifiers

PMID31641069
PMCPMC6842635
OpenAlexW2981904633

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.