Evidence map›Paper›PMID 19360662›Full record

ArticleAutism research : official journal of the International Society for Autism Research2008

Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice.

Kathryn K Chadman, Shiaoching Gong, Maria L Scattoni, Sarah E Boltuck, Shruti U Gandhy, Nathaniel Heintz, Jacqueline N Crawley

Open access · bronzeAbstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 155 papers.

0numbers the graph read from it
0cells of the map it votes in
155citing papers in PubMed
8.6field-weighted citation impact, top 2% 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

155 citing papers in PubMed, 297 citations in OpenAlex.

  1. Article
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  15. Rodent Models for ASD Biomarker Development.Advances in neurobiology · 2024
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

95 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 3 countries.

Kathryn K ChadmanLaboratory of Behavioral Neuroscience, Intramural Research Program, National Institute of Mental Health, Bethesda, Maryland 20892-3730, USA. kathryn.chadman@gmail.com
Shiaoching Gong
Maria L Scattoni
Sarah E Boltuck
Shruti U Gandhy
Nathaniel Heintz
Jacqueline N Crawley
National Institute of Mental Health · USHoward Hughes Medical Institute · USNational Institute of Mental Health · CZRockefeller University · US

Funding

Animal Models Of Neuropsychiatric DisordersZIAMH002179 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI CRAWLEY, JACQUELINE N · 2009 to 2012
$6.4M
HAMSTER SEPARATION MODEL OF DEPRESSIONZ01MH002179 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI CRAWLEY, JACQUELINE N · 1985 to 2008
$3.4M
Howard Hughes Medical InstituteIntramural NIH HHS Z01 MH002179PHS HHS ISS-NIH 0F14
6 · The paper itself

Abstract

Neuroligin-3 is a member of the class of cell adhesion proteins that mediate synapse development and have been implicated in autism. Mice with the human R451C mutation (NL3), identical to the point mutation found in two brothers with autism spectrum disorders, were generated and phenotyped in multiple behavioral assays with face validity to the diagnostic symptoms of autism. No differences between NL3 and their wildtype (WT) littermate controls were detected on measures of juvenile reciprocal social interaction, adult social approach, cognitive abilities, and resistance to change in a spatial habit, findings which were replicated in several cohorts of males and females. Physical and procedural abilities were similar across genotypes on measures of general health, sensory abilities, sensorimotor gating, motor functions, and anxiety-related traits. Minor developmental differences were detected between NL3 and WT, including slightly different rates of somatic growth, slower righting reflexes at postnatal days 2-6, faster homing reflexes in females, and less vocalizations on postnatal day 8 in males. Significant differences in NL3 adults included somewhat longer latencies to fall from the rotarod, less vertical activity in the open field, and less acoustic startle to high decibel tones. The humanized R451C mutation in mice did not result in apparent autism-like phenotypes, but produced detectable functional consequences that may be interpreted in terms of physical development and/or reduced sensitivity to stimuli.

Indexed as

PhenotypeAnimalsAutistic DisorderCell Adhesion Molecules, NeuronalDisease Models, AnimalFemaleGene Knock-In TechniquesMaleMembrane ProteinsMiceMice, KnockoutNerve Tissue ProteinsPoint MutationSocial BehaviorCell Adhesion Molecules, NeuronalMembrane ProteinsNerve Tissue Proteinsneuroligin 3

Identifiers

PMID19360662
PMCPMC2701211
OpenAlexW1967112350

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.