Evidence map›Paper›PMID 28507260›Full record

ArticleNeurology2017

Reprogramming cells from Gulf War veterans into neurons to study Gulf War illness.

Liang Qiang, Anand N Rao, Gustavo Mostoslavsky, Marianne F James, Nicole Comfort, Kimberly Sullivan, Peter W Baas

Abstract read
In one paragraph

Article in Neurology, 2017. 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
0.6field-weighted citation impact, top 35% 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, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. A cellular approach to understanding and treating Gulf War Illness.Cellular and molecular life sciences : CMLS · 2021
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. 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

7 authors at 1 institution in 1 country.

Liang QiangFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Anand N RaoFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Gustavo MostoslavskyFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Marianne F JamesFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Nicole ComfortFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Kimberly SullivanFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA.
Peter W BaasFrom the Department of Neurobiology and Anatomy (L.Q., A.N.R., P.W.B.), Drexel University, Philadelphia, PA; and Center for Regenerative Medicine (G.M., M.F.J.) and School of Public Health (N.C., K.S.), Boston University, Boston, MA. pbaas@drexelmed.edu.
Drexel University · US

Funding

Establishment and Preservation of Microtubule Polarity in the AxonF31NS093748 · NINDS · DREXEL UNIVERSITY · PI RAO, ANAND NANDAKUMAR · 2015 to 2016
$72k
NINDS NIH HHS F31 NS093748
6 · The paper itself

Abstract

Gulf War illness (GWI), which afflicts at least 25% of veterans who served in the 1990-1991 war in the Persian Gulf, is thought to be caused by deployment exposures to various neurotoxicants, including pesticides, anti-nerve gas pills, and low-level nerve agents including sarin/cyclosarin. GWI is a multisymptom disorder characterized by fatigue, joint pain, cognitive problems, and gastrointestinal complaints. The most prominent symptoms of GWI (memory problems, poor attention/concentration, chronic headaches, mood alterations, and impaired sleep) suggest that the disease primarily affects the CNS. Development of urgently needed treatments depends on experimental models appropriate for testing mechanistic hypotheses and for screening therapeutic compounds. Rodent models have been useful thus far, but are limited by their inability to assess the contribution of genetic or epigenetic background to the disease, and because disease-vulnerable proteins and pathways may be different in humans relative to rodents. As of yet, no postmortem tissue from the veterans has become available for research. We are moving forward with a paradigm shift in the study of GWI, which utilizes contemporary stem cell technology to convert somatic cells from Gulf War veterans into pluripotent cell lines that can be differentiated into various cell types, including neurons, glia, muscle, or other relevant cell types. Such cell lines are immortal and will be a resource for GWI researchers to pursue mechanistic hypotheses and therapeutics.

Indexed as

Cellular ReprogrammingGulf WarNeuronsVeteransAnimalsCerebral CortexHumansInduced Pluripotent Stem CellsMiceNeurilemmaPersian Gulf SyndromeResearch Design

Identifiers

PMID28507260
PMCPMC5444312
OpenAlexW2615053672

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.