Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q30488800)
Watch
English
Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
title
Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
main subject
phenotype
1 reference
based on heuristic
inferred from title
author
Maria Luisa Scattoni
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Nathaniel Heintz
series ordinal
6
object named as
Nathaniel Heintz
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
author name string
Kathryn K Chadman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Shiaoching Gong
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Sarah E Boltuck
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Shruti U Gandhy
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
Jacqueline N Crawley
series ordinal
7
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
publication date
1 June 2008
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
published in
Autism Research
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
volume
1
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
page(s)
147-158
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
cites work
Familial deletion within NLGN4 associated with autism and Tourette syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Disruption of neurexin 1 associated with autism spectrum disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Reduced ultrasonic vocalizations in vasopressin 1b knockout mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Contribution of SHANK3 mutations to autism spectrum disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Social deficits in BTBR T+tf/J mice are unchanged by cross-fostering with C57BL/6J mothers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Neuroligin-3 is a neuronal adhesion protein at GABAergic and glutamatergic synapses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Autism-like behavioral phenotypes in BTBR T+tf/J mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Neurexin-neuroligin signaling in synapse development
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Galanin receptor subtype 2 (GalR2) null mutant mice display an anxiogenic-like phenotype specific to the elevated plus-maze
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
The postsynaptic architecture of excitatory synapses: a more quantitative view
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Neuroligins determine synapse maturation and function
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Mouse behavioral tasks relevant to autism: phenotypes of 10 inbred strains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Molecular and phenotypic characterization of ring chromosome 22
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Control of excitatory and inhibitory synapse formation by neuroligins
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
Preliminary report of a simple animal behavior model for the anxiolytic effects of benzodiazepines
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
20 June 2018
A crystal-clear interaction: relating neuroligin/neurexin complex structure to function at the synapse.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
Neuroscience. Autism's cause may reside in abnormalities at the synapse.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
Postsynaptic neuroligin enhances presynaptic inputs at neuronal nicotinic synapses
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
Social approach behaviors in oxytocin knockout mice: comparison of two independent lines tested in different laboratory environments.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
Analysis of four neuroligin genes as candidates for autism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
The acoustic startle response in DBA/2 and C57BL/6 mice: relationship to auditory neuronal response properties and hearing impairment.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701211
retrieved
26 November 2018
Identifiers
DOI
10.1002/AUR.22
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PMCID
2701211
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
PubMed ID
19360662
1 reference
stated in
Europe PubMed Central
PMCID
2701211
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19360662%20AND%20SRC:MED&resulttype=core&format=json
retrieved
25 January 2020
ResearchGate publication ID
24272127
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit