Evidence map›Paper›PMID 20696251›Full record

ArticleMolecular and cellular neurosciences2011

Transcriptional profiling of intrinsic PNS factors in the postnatal mouse.

Robin P Smith, Jessica K Lerch-Haner, Jose R Pardinas, William J Buchser, John L Bixby, Vance P Lemmon

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Circuit formation in the adult brain.The European journal of neuroscience · 2022
    Review
  4. Article
  5. Article
  6. The Life of a Trailing Spouse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  7. Article
  8. Review
  9. HSP90 is a chaperone for DLK and is required for axon injury signaling.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  10. Review
  11. Article
  12. Article
  13. Intrinsic mechanisms of neuronal axon regeneration.Nature reviews. Neuroscience · 2018
    Review
  14. Axonal regeneration in zebrafish spinal cord.Regeneration (Oxford, England) · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Differential Expression ofFrontiers in molecular neuroscience · 2017
    Article
  20. 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

6 authors at 1 institution in 1 country.

Robin P SmithThe Miami Project to Cure Paralysis, Department of Neurological Surgery, Miller School of Medicine, University of Miami, 1400 NW 12th Ave, Miami, FL 33136, USA.
Jessica K Lerch-Haner
Jose R Pardinas
William J Buchser
John L Bixby
Vance P Lemmon
University of Miami · US

Funding

Novel Gene Targets for CNS Axonal RegenerationR01HD057632 · NICHD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BIXBY, JOHN L, LEMMON, VANCE P · 2007 to 2018
$4.7M
Novel Compounds That Overcome Glial Inhibition of Axonal RegenerationR01NS059866 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BIXBY, JOHN L · 2009 to 2013
$1.7M
NICHD NIH HHS HD057632NICHD NIH HHS R01 HD057632NINDS NIH HHS NS059866NINDS NIH HHS R01 NS059866
6 · The paper itself

Abstract

Neurons in the peripheral nervous system (PNS) display a higher capacity to regenerate after injury than those in the central nervous system, suggesting cell specific transcriptional modules underlying axon growth and inhibition. We report a systems biology based search for PNS specific transcription factors (TFs). Messenger RNAs enriched in dorsal root ganglion (DRG) neurons compared to cerebellar granule neurons (CGNs) were identified using subtractive hybridization and DNA microarray approaches. Network and transcription factor binding site enrichment analyses were used to further identify TFs that may be differentially active. Combining these techniques, we identified 32 TFs likely to be enriched and/or active in the PNS. Twenty-five of these TFs were then tested for an ability to promote CNS neurite outgrowth in an overexpression screen. Real-time PCR and immunohistochemical studies confirmed that one representative TF, STAT3, is intrinsic to PNS neurons, and that constitutively active STAT3 is sufficient to promote CGN neurite outgrowth.

Indexed as

Transcription, GeneticAnimalsCerebellumGanglia, SpinalGene Expression ProfilingMiceMice, Inbred C57BLMicroarray AnalysisNeuronsNucleic Acid HybridizationPeripheral Nervous SystemRNA, MessengerSignal TransductionSTAT3 Transcription FactorTranscription FactorsRNA, MessengerSTAT3 Transcription FactorTranscription Factors

Identifiers

PMID20696251
PMCPMC3003944
OpenAlexW2031543128

What OpenQuestion holds

Textmetadata
LicenceTDM
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.