(Q24307957)

22 June 2017

title

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism (English)

1 reference

22 June 2017

0 references

Neuroligin 4 X-linked

1 reference

GOA release 2020-03-11

vocalization behavior

1 reference

GOA release 2020-03-11

Neuroligin 4-like

1 reference

GOA release 2020-03-11

1 reference

14

0 references

Jens Frahm

11

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Susann Boretius

5

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Nils Brose

15

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Frédérique Varoqueaux

6

1 reference

ORCID Public Data File 2021

Julia Fischer

12

0 references

Thomas Bourgeron

13

0 references

Sylvie Granon

object named as

Sylvie Granon

4

0 references

Kurt Hammerschmidt

3

object named as

Kurt Hammerschmidt

1 reference

22 June 2017

10

Dorina Winter

1 reference

22 June 2017

Stephane Jamain

1

1 reference

22 June 2017

Konstantin Radyushkin

2

1 reference

22 June 2017

Nelina Ramanantsoa

7

1 reference

22 June 2017

Jorge Gallego

8

1 reference

22 June 2017

Anja Ronnenberg

9

1 reference

22 June 2017

language of work or name

English

0 references

publication date

28 January 2008

1 reference

Proceedings of the National Academy of Sciences of the United States of America

22 June 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

22 June 2017

volume

105

1 reference

22 June 2017

issue

5

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22 June 2017

page(s)

1710-1715

1 reference

on focus list of Wikimedia project

22 June 2017

ScienceSource

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cites work

A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Strong association of de novo copy number mutations with autism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Ultrasonic songs of male mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Somatostatin receptor interacting protein defines a novel family of multidomain proteins present in human and rodent brain

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

The genetics of autistic disorders and its clinical relevance: a review of the literature

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Neurobiological Correlates of Autism: A Review of Recent Research

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Neuroligins determine synapse maturation and function

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Pten regulates neuronal arborization and social interaction in mice

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Epidemiology of autistic disorder and other pervasive developmental disorders

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

The calcium-independent receptor for alpha-latrotoxin from human and rodent brains interacts with members of the ProSAP/SSTRIP/Shank family of multidomain proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Regulation of neuronal morphology and function by the tumor suppressors Tsc1 and Tsc2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Control of excitatory and inhibitory synapse formation by neuroligins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

A mouse model for the learning and memory deficits associated with neurofibromatosis type I

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Reversal of neurological defects in a mouse model of Rett syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Regulation of dendritic spine morphology and synaptic function by Shank and Homer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Fragile X syndrome and autism at the intersection of genetic and neural networks

10 May 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Social behavior deficits in the Fmr1 mutant mouse

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

PTEN mutation in a family with Cowden syndrome and autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Fragile X mice develop sensory hyperreactivity to auditory stimuli

27 September 2017

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Tsc2 null murine neuroepithelial cells are a model for human tuber giant cells, and show activation of an mTOR pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

The Drosophila easily shocked gene: a mutation in a phospholipid synthetic pathway causes seizure, neuronal failure, and paralysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Heterozygosity for the tuberous sclerosis complex (TSC) gene products results in increased astrocyte numbers and decreased p27-Kip1 expression in TSC2+/- cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Astrocyte-specific TSC1 conditional knockout mice exhibit abnormal neuronal organization and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Analysis of four neuroligin genes as candidates for autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0711555105

Abnormal fear conditioning and amygdala processing in an animal model of autism

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2234209

Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18227507

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0711555105

1 reference

release_zikqxe6vybgm5ijon3wkahnowa

22 June 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/zikqxe6vybgm5ijon3wkahnowa

mapped directly with Wikidata item

24 November 2022

based on heuristic

OpenCitations bibliographic resource ID

1033817

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1033817

1 reference