Evidence map›Paper›PMID 24713578›Full record

ReviewCurrent opinion in neurobiology2014

BMP signaling in axon regeneration.

Jian Zhong, Hongyan Zou

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in neurobiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

36 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  3. Article
  4. Review
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  6. Article
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  8. Review
  9. Review
  10. Article
  11. Review
  12. BMP/TGF-β signaling as a modulator of neurodegeneration in ALS.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Article
  13. Article
  14. Review
  15. Recurrent rewiring of the adult hippocampal mossy fiber system by a single transcriptional regulator, Id2.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Review
  17. Article
  18. The stem cell markerProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  19. Review
  20. Emerging molecular therapeutic targets for spinal cord injury.Expert opinion on therapeutic targets · 2019
    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

2 authors at 2 institutions in 1 country.

Jian ZhongBurke Medical Research Institute, 785 Mamaroneck Ave., White Plains, NY 10605, United States; Brain and Mind Research Institute, Weill Medical College of Cornell University, New York, NY 10065, United States.
Hongyan ZouFishberg Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States; Department of Neurosurgery, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, United States. Electronic address: hongyan.zou@mssm.edu.
Burke Medical Research Institute · USIcahn School of Medicine at Mount Sinai · US

Funding

B-RAF drives regenerative axon growth in the optic nerve in vivoR01EY022409 · NEI · WINIFRED MASTERSON BURKE MED RES INST · PI ZHONG, JIAN · 2012 to 2016
$2.4M
Promoting axon regeneration by activation of the Smad1 signaling pathwayR01NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2011 to 2015
$1.7M
Promoting Axon regeneration in Spinal Cord Injury by Epigenetic ModulationR56NS073596 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZOU, HONGYAN JENNY · 2017 to 2017
$431k
NEI NIH HHS R01 EY022409NEI NIH HHS R01EY022409NEI NIH HHS R01EY022409-01S1NINDS NIH HHS NS073596NINDS NIH HHS R01 NS073596NINDS NIH HHS R56 NS073596
6 · The paper itself

Abstract

Neuronal competence to re-extend axons and a permissive environment that allows growth cone navigation are two major determinants for successful axon regeneration. Here, we review the roles of bone morphogenetic protein (BMP) signaling in mediating both neuronal and glial injury responses after CNS injury. BMPs can activate a pro-regenerative transcription program in neurons through Smad-mediated canonical pathway, or act locally on cytoskeleton assembly at distal axons via non-canonical pathways. Emerging evidence implicates retrograde BMP signalosomes in connecting the cytoskeletal and nuclear responses. In addition, BMP/Smad signaling modulates neurotrophin-mediated axonal outgrowth, and interacts with the epigenetic machinery to initiate epigenetic reprogramming for axon regeneration. Besides their influences on neurons, BMPs also regulate astrogliosis, inflammatory processes, and neural progenitor cell differentiation at the injury site, all of which can either positively or negatively modify the injury microenvironment. Lastly, an increasing number of BMP signaling partners, sensitizers, and downstream effectors collectively fine-tune the signaling intensity and spatiotemporal dynamics of BMP activity in an integrated signaling network during axon regeneration.

Indexed as

Central Nervous System DiseasesAnimalsAxonsBone Morphogenetic ProteinsHumansNeural Stem CellsRegenerationSignal TransductionBone Morphogenetic Proteins

Identifiers

PMID24713578
PMCPMC4122622
OpenAlexW2060022091

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.