Evidence map›Paper›PMID 23536326›Full record

ReviewDevelopmental neurobiology2014

Therapeutic approaches for shankopathies.

Xiaoming Wang, Alexandra L Bey, Leeyup Chung, Andrew D Krystal, Yong-Hui Jiang

Abstract readReview
In one paragraph

Review in Developmental neurobiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Autism patient-derived SHANK2BMolecular psychiatry · 2024
    Article
  2. Review
  3. Review
  4. Article
  5. Autism-associatedeLife · 2021
    Article
  6. Article
  7. Article
  8. Frontiers in cellular neuroscience · 2019
    Article
  9. Article
  10. Cell-Type-SpecificThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. 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

5 authors.

Xiaoming WangDepartment of Pediatrics, Duke University School of Medicine Durham, North Carolina, 27710.
Alexandra L Bey
Leeyup Chung
Andrew D Krystal
Yong-Hui Jiang

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Center for Molecular &Cellular Studies of Ped DiseaseK12HD043494 · NICHD · DUKE UNIVERSITY · PI REED, ANN M. · 2003 to 2017
$5.2M
Analysis of Shank3 Complete and Temporal and Spatial Specific Knockout MiceR01MH098114 · NIMH · DUKE UNIVERSITY · PI JIANG, YONG-HUI · 2012 to 2016
$2.2M
Autism Speaks AS4936Autism Speaks AS6123NICHD NIH HHS 5K12-HD0043494-08NICHD NIH HHS K12 HD043494NIGMS NIH HHS T32 GM007171NIMH NIH HHS MH098114NIMH NIH HHS R01 MH098114
6 · The paper itself

Abstract

Despite recent advances in understanding the molecular mechanisms of autism spectrum disorders (ASD), the current treatments for these disorders are mostly focused on behavioral and educational approaches. The considerable clinical and molecular heterogeneity of ASD present a significant challenge to the development of an effective treatment targeting underlying molecular defects. Deficiency of SHANK family genes causing ASD represent an exciting opportunity for developing molecular therapies because of strong genetic evidence for SHANK as causative genes in ASD and the availability of a panel of Shank mutant mouse models. In this article, we review the literature suggesting the potential for developing therapies based on molecular characteristics and discuss several exciting themes that are emerging from studying Shank mutant mice at the molecular level and in terms of synaptic function.

Indexed as

AnimalsChild Development Disorders, PervasiveHumansMutationNerve Tissue ProteinsSynaptic TransmissionTranscranial Magnetic StimulationNerve Tissue ProteinsSHANK1 protein, humanSHANK2 protein, humanSHANK3 protein, humanautism spectrum disordersbrain stimulationmouse modelSHANK family proteinsynapses

Identifiers

PMID23536326
PMCPMC3883807

What OpenQuestion holds

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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.