Evidence map›Paper›PMID 27263037›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2017

mTOR inhibitor reverses autistic-like social deficit behaviours in adult rats with both Tsc2 haploinsufficiency and developmental status epilepticus.

Miriam Schneider, Petrus J de Vries, Kai Schönig, Veit Rößner, Robert Waltereit

Abstract read
PubMed Publisher
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Brain Symptoms of Tuberous Sclerosis Complex: Pathogenesis and Treatment.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Overlapping Molecular Pathways Leading to Autism Spectrum Disorders, Fragile X Syndrome, and Targeted Treatments.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Review
  14. Article
  15. Review
  16. Review
  17. [Research advances in the role of mTOR signaling pathway in autism spectrum disorder].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019
    Article
  18. Article
  19. Cell Clearing Systems Bridging Neuro-Immunity and Synaptic Plasticity.International journal of molecular sciences · 2019
    Review
  20. Epilepsy in Children with Autistic Spectrum Disorder.Children (Basel, Switzerland) · 2019
    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 at 3 institutions in 2 countries.

Miriam SchneiderResearch Group Developmental Neuropsychopharmacology, Institute of Psychopharmacology, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Petrus J de VriesDivision of Child and Adolescent Psychiatry, University of Cape Town, Cape Town, South Africa.
Kai SchönigDepartment of Molecular Biology, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany.
Veit RößnerDepartment of Child and Adolescent Psychiatry, University Hospital Carl Gustav Carus, Faculty of Medicine, Technical University of Dresden, Dresden, Germany.
Robert WaltereitDepartment of Child and Adolescent Psychiatry, University Hospital Carl Gustav Carus, Faculty of Medicine, Technical University of Dresden, Dresden, Germany. robert.waltereit@uniklinikum-dresden.de.ORCID http://orcid.org/0000-0002-5338-2765
Heidelberg University · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Cape Town · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epilepsy is a major risk factor for autism spectrum disorder (ASD) and complicates clinical manifestations and management of ASD significantly. Tuberous sclerosis complex (TSC), caused by TSC1 or TSC2 mutations, is one of the medical conditions most commonly associated with ASD and has become an important model to examine molecular pathways associated with ASD. Previous research showed reversal of autism-like social deficits in Tsc1

Indexed as

AnimalsAnimals, NewbornAutism Spectrum DisorderBody WeightDisease Models, AnimalEverolimusHaploinsufficiencyInterpersonal RelationsLocomotionRatsRats, TransgenicRecognition, PsychologySocial Behavior DisordersStatus EpilepticusTOR Serine-Threonine KinasesTuberous Sclerosis Complex 2 ProteinEverolimusTOR Serine-Threonine KinasesTsc2 protein, mouseTsc2 protein, ratTuberous Sclerosis Complex 2 ProteinTumor Suppressor ProteinsAnimal modelAutism spectrum disorderEverolimusExperimental therapySocial cognitionTuberous sclerosis complex

Identifiers

PMID27263037
OpenAlexW2460508745

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.