(Q26269833)

25 June 2017

title

Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors (English)

1 reference

25 June 2017

0 references

1 reference

9

Thomas C Südhof

0 references

Özgün Gökçe

5

object named as

Ozgun Gokce

1 reference

25 June 2017

Marc V Fuccillo

2

0 references

Stephan Maxeiner

object named as

Stephan Maxeiner

3

0 references

Robert Malenka

8

object named as

Robert C Malenka

1 reference

25 June 2017

6

Byung Kook Lim

1 reference

25 June 2017

Patrick E Rothwell

1

1 reference

25 June 2017

Scott J Hayton

4

1 reference

25 June 2017

Stephen C Fowler

7

1 reference

25 June 2017

language of work or name

English

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publication date

1 July 2014

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25 June 2017

number of pages

15

0 references

published in

Cell

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25 June 2017

volume

158

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25 June 2017

issue

1

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25 June 2017

page(s)

198-212

1 reference

Presynaptic neurexin-3 alternative splicing trans-synaptically controls postsynaptic AMPA receptor trafficking

25 June 2017

cites work

1 reference

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Autism-associated neuroligin-3 mutations commonly disrupt tonic endocannabinoid signaling

7 April 2017

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Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function

7 April 2017

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Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

7 April 2017

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7 April 2017

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

7 April 2017

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Neuroligins and neurexins link synaptic function to cognitive disease

7 April 2017

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

7 April 2017

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

7 April 2017

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The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

7 April 2017

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

7 April 2017

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Cocaine seeking habits depend upon dopamine-dependent serial connectivity linking the ventral with the dorsal striatum

7 April 2017

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Disrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatum

7 April 2017

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

7 April 2017

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Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

7 April 2017

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Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits

7 April 2017

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Animal models of neuropsychiatric disorders

7 April 2017

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A translational profiling approach for the molecular characterization of CNS cell types

7 April 2017

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The role of the basal ganglia in habit formation

7 April 2017

1 reference

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Excitatory/inhibitory synaptic imbalance leads to hippocampal hyperexcitability in mouse models of tuberous sclerosis

7 April 2017

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Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities

28 September 2017

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Mutations causing syndromic autism define an axis of synaptic pathophysiology

28 September 2017

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Nucleus accumbens μ-opioid receptors mediate social reward

28 September 2017

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Mechanisms of inhibition within the telencephalon: "where the wild things are".

28 September 2017

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Modulation of striatal projection systems by dopamine

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4120877

Aberrant striatal functional connectivity in children with autism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4120877

Postsynaptic TRPV1 triggers cell type-specific long-term depression in the nucleus accumbens

28 September 2017

1 reference

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Human and rodent homologies in action control: corticostriatal determinants of goal-directed and habitual action

28 September 2017

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Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice

28 September 2017

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Dynamic reorganization of striatal circuits during the acquisition and consolidation of a skill.

28 September 2017

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Striatal plasticity and basal ganglia circuit function

28 September 2017

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Habits, rituals, and the evaluative brain

28 September 2017

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28 September 2017

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Central mechanisms of motor skill learning

28 September 2017

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A force-plate actometer for quantitating rodent behaviors: illustrative data on locomotion, rotation, spatial patterning, stereotypies, and tremor

28 September 2017

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Striatonigrostriatal pathways in primates form an ascending spiral from the shell to the dorsolateral striatum

28 September 2017

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The nucleus accumbens: gateway for limbic structures to reach the motor system?

28 September 2017

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Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism.

28 September 2017

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Genetically increased cell-intrinsic excitability enhances neuronal integration into adult brain circuits

28 November 2018

1 reference

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Changes in the developmental trajectories of striatum in autism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4120877

D2R striatopallidal neurons inhibit both locomotor and drug reward processes

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4120877

Neuroligin-3-deficient mice: model of a monogenic heritable form of autism with an olfactory deficit.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4120877

Striatal volume on magnetic resonance imaging and repetitive behaviors in autism.

28 November 2018

1 reference

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Differential corticostriatal plasticity during fast and slow motor skill learning in mice.

28 November 2018

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PTEN mutation in a family with Cowden syndrome and autism

28 November 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment

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7 January 2021

Bannayan–Riley–Ruvalcaba syndrome with reactive nodular lymphoid hyperplasia and autism and a PTEN mutation

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7 January 2021

Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

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7 January 2021

Brief report: duplication of chromosome 15q11-13 in two individuals with autistic disorder

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7 January 2021

Leftward shift in the acquisition of cocaine self-administration in isolation-reared rats: relationship to extracellular levels of dopamine, serotonin and glutamate in the nucleus accumbens and amygdala-striatal FOS expression.

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7 January 2021

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Disruption of neurexin 1 associated with autism spectrum disorder

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Structural variation of chromosomes in autism spectrum disorder

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Using whole-exome sequencing to identify inherited causes of autism

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7 January 2021

Automated tests for measuring the effects of antidepressants in mice.

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7 January 2021

A neural basis for social cooperation.

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7 January 2021

Talking about a Revolution

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7 January 2021

Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety

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7 January 2021

High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP

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7 January 2021

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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7 January 2021

Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin

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7 January 2021

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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7 January 2021

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

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7 January 2021

Erroneous analyses of interactions in neuroscience: a problem of significance.

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7 January 2021

Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors

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7 January 2021

Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

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7 January 2021

Calmodulin suppresses synaptotagmin-2 transcription in cortical neurons

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7 January 2021

Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders

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7 January 2021

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

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7 January 2021

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Novel PTEN mutations in neurodevelopmental disorders and macrocephaly.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Developmental changes of GABA synaptic transient in cerebellar granule cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Strong association of de novo copy number mutations with autism

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

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7 January 2021

In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

A patient with vertebral, cognitive and behavioural abnormalities and a de novo deletion of NRXN1alpha

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https://api.crossref.org/works/10.1016%2FJ.CELL.2014.04.045

7 January 2021

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

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7 January 2021

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

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7 January 2021

A developmental switch in the response of DRG neurons to ETS transcription factor signaling

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7 January 2021

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

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7 January 2021

A comparison of striatal-dependent behaviors in wild-type and hemizygous Drd1a and Drd2 BAC transgenic mice

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7 January 2021

Strain-specific regulation of striatal phenotype in Drd2-eGFP BAC transgenic mice

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7 January 2021

Striatonigrostriatal Pathways in Primates Form an Ascending Spiral from the Shell to the Dorsolateral Striatum

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7 January 2021

Targeting Cre recombinase to specific neuron populations with bacterial artificial chromosome constructs

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7 January 2021

Drd1a-tdTomato BAC transgenic mice for simultaneous visualization of medium spiny neurons in the direct and indirect pathways of the basal ganglia.

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7 January 2021

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Identifiers

DOI

1 reference

OpenCitations bibliographic resource ID

25 June 2017

1462188

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1462188

1 reference