Evidence map›Paper›PMID 28351971›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by

James N Sleigh, John M Dawes, Steven J West, Na Wei, Emily L Spaulding, Adriana Gómez-Martín, Qian Zhang, Robert W Burgess, M Zameel Cader, Kevin Talbot and 3 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 75 citations in OpenAlex.

  1. The neuropathy-causingbioRxiv : the preprint server for biology · 2026
    Article
  2. Junctions in Jeopardy: the neuromuscular junction is a selective pathological target in Charcot-Marie-Tooth disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  3. Disruption of BDNF signalling in neuropathologies.Biochemical Society transactions · 2026
    Review
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Mimicking the Human Articular Joint withInternational journal of stem cells · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Neuronal signaling · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Genes · 2021
    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

13 authors at 4 institutions in 2 countries.

James N SleighSobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom; j.sleigh@ucl.ac.uk giampietro.schiavo@ucl.ac.uk.ORCID 0000-0002-3782-9045
John M DawesNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom.
Steven J WestNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom.
Na WeiDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037.
Emily L SpauldingThe Jackson Laboratory, Bar Harbor, ME 04609.
Adriana Gómez-MartínSobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom.
Qian ZhangDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037.
Robert W BurgessThe Jackson Laboratory, Bar Harbor, ME 04609.
M Zameel CaderNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom.
Kevin TalbotNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom.ORCID 0000-0001-5490-1697
Xiang-Lei YangDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA 92037.
David L BennettNuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DU, United Kingdom.
Giampietro SchiavoSobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, University College London, London WC1N 3BG, United Kingdom; j.sleigh@ucl.ac.uk giampietro.schiavo@ucl.ac.uk.ORCID 0000-0002-4319-8745
John Radcliffe Hospital · GBScripps Research Institute · USUniversity College London · GBJackson Laboratory · US

Funding

Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR01NS054154 · NINDS · JACKSON LABORATORY · PI BURGESS, ROBERT W. · 2006 to 2019
$6.0M
The Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR37NS054154 · NINDS · JACKSON LABORATORY · PI Robert W. Burgess · 2020 to 2026
$5.9M
Extra-translational roles of aminoacyl tRNA synthetases in connection to diseaseR01GM088278 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI YANG, XIANG-LEI · 2010 to 2019
$3.7M
Genetics of the Neuromuscular Junction: Mechanisms and Disease ModelsR56NS054154 · NINDS · JACKSON LABORATORY · PI BURGESS, ROBERT W. · 2015 to 2015
$613k
Transcriptional and Translational Profiling of Motor Neurons in Two Mouse Models of Charcot-Marie-Tooth Disease Type 2DF31NS100328 · NINDS · JACKSON LABORATORY · PI SPAULDING, EMILY LOUISA · 2017 to 2019
$87k
Medical Research Council G0601887NIGMS NIH HHS R01 GM088278NINDS NIH HHS F31 NS100328NINDS NIH HHS R01 NS054154NINDS NIH HHS R37 NS054154NINDS NIH HHS R56 NS054154Wellcome TrustWellcome Trust 103191/A/13/ZWellcome Trust 107116/Z/15/Z
6 · The paper itself

Abstract

Charcot-Marie-Tooth disease type 2D (CMT2D) is a peripheral nerve disorder caused by dominant, toxic, gain-of-function mutations in the widely expressed, housekeeping gene,

Indexed as

MutationAnimalsCells, CulturedCharcot-Marie-Tooth DiseaseFemaleGlycine-tRNA LigaseHumansMaleMiceMice, KnockoutReceptor, trkASensory Receptor CellsGlycine-tRNA LigaseReceptor, trkAaminoacyl-tRNA synthetaseCharcot–Marie–Tooth diseasedistal spinal muscular atrophy type Vneurodevelopmentneuromuscular disease

Identifiers

PMID28351971
PMCPMC5402433
OpenAlexW2603775236

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.