Evidence map›Paper›PMID 26468186›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Transcriptomic Approaches to Neural Repair.

Jennifer N Dulin, Ana Antunes-Martins, Vijayendran Chandran, Michael Costigan, Jessica K Lerch, Dianna E Willis, Mark H Tuszynski

Abstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  4. Spinal cord injury regulates circular RNA expression in axons.Frontiers in molecular neuroscience · 2023
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  5. Review
  6. Article
  7. Review
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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

7 authors.

Jennifer N DulinDepartment of Neurosciences, University of California, San Diego, La Jolla, California 92093, jdulin@ucsd.edu.ORCID http://orcid.org/0000-0001-5767-4290
Ana Antunes-MartinsWolfson Centre for Age-Related Disease, King's College London, London SE1 1UL, United Kingdom.
Vijayendran ChandranProgram in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095.
Michael CostiganF.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, Massachusetts 02115, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, Department of Anesthesia, Boston Children's Hospital, Boston, Massachusetts 02115.
Jessica K LerchDepartment of Neuroscience, Center for Brain and Spinal Cord Repair, The Ohio State University, Columbus, Ohio 43210.
Dianna E WillisBurke-Cornell Medical Research Institute, White Plains, New York 10605, Feil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, New York 10065, and.ORCID http://orcid.org/0000-0003-1442-3533
Mark H TuszynskiDepartment of Neurosciences, University of California, San Diego, La Jolla, California 92093, Veterans Affairs Medical Center, San Diego, California 92161.

Funding

The mechanisms of action of T-lymphocytes in neuropathic painR01NS074430 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI COSTIGAN, MICHAEL · 2012 to 2016
$2.0M
Axonal Transport and Local Translation in Neuropathic PainR00NR010797 · NINR · WINIFRED MASTERSON BURKE MED RES INST · PI WILLIS, DIANNA E. · 2010 to 2012
$733k
Axonal Transport and Local Translation in Neuropathic PainK99NR010797 · NINR · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI WILLIS, DIANNA E. · 2007 to 2008
$174k
NINDS NIH HHS R01 NS074430NINR NIH HHS K99 NR010797NINR NIH HHS NR-010797NINR NIH HHS R00 NR010797
6 · The paper itself

Abstract

Understanding why adult CNS neurons fail to regenerate their axons following injury remains a central challenge of neuroscience research. A more complete appreciation of the biological mechanisms shaping the injured nervous system is a crucial prerequisite for the development of robust therapies to promote neural repair. Historically, the identification of regeneration associated signaling pathways has been impeded by the limitations of available genetic and molecular tools. As we progress into an era in which the high-throughput interrogation of gene expression is commonplace and our knowledge base of interactome data is rapidly expanding, we can now begin to assemble a more comprehensive view of the complex biology governing axon regeneration. Here, we highlight current and ongoing work featuring transcriptomic approaches toward the discovery of novel molecular mechanisms that can be manipulated to promote neural repair. SIGNIFICANCE STATEMENT: Transcriptional profiling is a powerful technique with broad applications in the field of neuroscience. Recent advances such as single-cell transcriptomics, CNS cell type-specific and developmental stage-specific expression libraries are rapidly enhancing the power of transcriptomics for neuroscience applications. However, extracting biologically meaningful information from large transcriptomic datasets remains a formidable challenge. This mini-symposium will highlight current work using transcriptomic approaches to identify regulatory networks in the injured nervous system. We will discuss analytical strategies for transcriptomics data, the significance of noncoding RNA networks, and the utility of multiomic data integration. Though the studies featured here specifically focus on neural repair, the approaches highlighted in this mini-symposium will be of broad interest and utility to neuroscientists working in diverse areas of the field.

Indexed as

AnimalsCentral Nervous System DiseasesGene Expression ProfilingHumansNerve RegenerationTranscriptome

Identifiers

PMID26468186
PMCPMC4604224

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.