Evidence map›Paper›PMID 34073530›Full record

ReviewCells2021

EFA6 in Axon Regeneration, as a Microtubule Regulator and as a Guanine Nucleotide Exchange Factor.

Gilberto Gonzalez, Lizhen Chen

RetractedOpen access · goldAbstract readReviewRetracted Publication
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Gilberto GonzalezBarshop Institute for Longevity and Aging Studies, Department of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0002-3660-9673
Lizhen ChenBarshop Institute for Longevity and Aging Studies, Department of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA.ORCID 0000-0001-5313-7340
The University of Texas Health Science Center at San Antonio · US

Funding

NIH HHS 1R01AG070214-01
6 · The paper itself

Abstract

Axon regeneration after injury is a conserved biological process that involves a large number of molecular pathways, including rapid calcium influx at injury sites, retrograde injury signaling, epigenetic transition, transcriptional reprogramming, polarized transport, and cytoskeleton reorganization. Despite the numerous efforts devoted to understanding the underlying cellular and molecular mechanisms of axon regeneration, the search continues for effective target molecules for improving axon regeneration. Although there have been significant historical efforts towards characterizing pro-regenerative factors involved in axon regeneration, the pursuit of intrinsic inhibitors is relatively recent. EFA6 (exchange factor for ARF6) has been demonstrated to inhibit axon regeneration in different organisms. EFA6 inhibition could be a promising therapeutic strategy to promote axon regeneration and functional recovery after axon injury. This review summarizes the inhibitory role on axon regeneration through regulating microtubule dynamics and through affecting ARF6 (ADP-ribosylation factor 6) GTPase-mediated integrin transport.

Indexed as

ADP-Ribosylation Factor 6ADP-Ribosylation FactorsAxonsCell MembraneGuanine Nucleotide Exchange FactorsHumansMicrotubulesNerve RegenerationADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF6 protein, humanGuanine Nucleotide Exchange FactorsARF6axon injuryaxon regenerationEFA6integrinmicrotubule dynamics

Identifiers

PMID34073530
PMCPMC8226579
OpenAlexW3165159928

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.