(Q27334217)

26 June 2017

title

Heterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia (English)

1 reference

26 June 2017

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1

James Dachtler

1 reference

26 June 2017

Jose L Ivorra

2

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26 June 2017

Tessa E Rowland

3

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26 June 2017

Colin Lever

4

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26 June 2017

R John Rodgers

5

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26 June 2017

Steven J Clapcote

6

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26 June 2017

language of work or name

English

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publication date

1 December 2015

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full work available at URL

26 June 2017

http://eprints.whiterose.ac.uk/91227/

content deliverer

White Rose Research Online

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published in

Behavioral Neuroscience

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26 June 2017

volume

129

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26 June 2017

issue

6

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26 June 2017

page(s)

765-776

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Creative Commons Attribution 3.0 Unported

26 June 2017

copyright license

start time

23 November 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4655861/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior

21 March 2017

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CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila

21 March 2017

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Mouse neurexin-1alpha deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments

21 March 2017

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Neurexin 1 (NRXN1) deletions in schizophrenia

21 March 2017

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21 March 2017

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21 March 2017

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Deletion of α-neurexin II results in autism-related behaviors in mice

21 March 2017

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21 March 2017

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Genetic heterogeneity between the three components of the autism spectrum: a twin study

21 March 2017

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Structures, alternative splicing, and neurexin binding of multiple neuroligins

21 March 2017

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Gating and habituation of the startle reflex in schizophrenic patients

21 March 2017

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Neurexin I alpha is a major alpha-latrotoxin receptor that cooperates in alpha-latrotoxin action

21 March 2017

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Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors

21 March 2017

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Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

21 March 2017

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Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behavior in mice

21 March 2017

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Maternal care, gene expression, and the transmission of individual differences in stress reactivity across generations

7 April 2017

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Synaptic assembly of the brain in the absence of neurotransmitter secretion

7 April 2017

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Altered social behaviours in neurexin 1α knockout mice resemble core symptoms in neurodevelopmental disorders.

7 April 2017

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Comprehensive behavioral analysis of ENU-induced Disc1-Q31L and -L100P mutant mice

28 September 2017

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Sex-dependent novelty response in neurexin-1α mutant mice

28 September 2017

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Automated three-chambered social approach task for mice

28 September 2017

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The role of neurexins in schizophrenia and autistic spectrum disorder.

28 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation

28 September 2017

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Behavioral phenotyping strategies for mutant mice

28 September 2017

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Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans

28 September 2017

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Behavioural studies of spatial working memory dysfunction in schizophrenia: a quantitative literature review.

28 September 2017

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Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

28 September 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Epidemiological surveys of autism and other pervasive developmental disorders: an update

28 September 2017

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Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics

28 September 2017

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Intelligence in schizophrenia: meta-analysis of the research

28 September 2017

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28 September 2017

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The use of a plus-maze to measure anxiety in the mouse

2 June 2018

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Anxiolytic and anxiogenic drug effects on exploratory activity in an elevated plus-maze: a novel test of anxiety in the rat.

2 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Etiological yield of SNP microarrays in idiopathic intellectual disability

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Munc18-1 haploinsufficiency results in enhanced anxiety-like behavior as determined by heart rate responses in mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

IQ change over time in schizophrenia and healthy individuals: a meta-analysis.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

A de novo 0.57 Mb microdeletion in chromosome 11q13.1 in a patient with speech problems, autistic traits, dysmorphic features and multiple endocrine neoplasia type 1.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Differential involvement of the dorsal hippocampus in passive avoidance in C57bl/6J and DBA/2J mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Behavioral phenotypes of Disc1 missense mutations in mice

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Assessing nest building in mice.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Sensorimotor gating deficits in adults with autism

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4655861

Investigation of NRXN1 deletions: clinical and molecular characterization

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26595880

12 December 2020

inferred from PubMed ID database lookup

Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26595880

12 December 2020

inferred from PubMed ID database lookup

Genetic influences on maternal care

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26595880

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1037/BNE0000108

1 reference

Dimensions Publication ID

26 June 2017

0 references

0 references

1006074792

0 references

OpenCitations bibliographic resource ID

5081226

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5081226

1 reference