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

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Özgün Gökçe

5

object named as

Ozgun Gokce

1 reference

25 June 2017

Marc V Fuccillo

2

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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

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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

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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

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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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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

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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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7 April 2017

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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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7 April 2017

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7 April 2017

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The role of the basal ganglia in habit formation

7 April 2017

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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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28 September 2017

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28 September 2017

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28 September 2017

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28 September 2017

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Aberrant striatal functional connectivity in children with autism

28 September 2017

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

28 September 2017

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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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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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28 September 2017

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28 November 2018

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28 November 2018

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28 November 2018

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28 November 2018

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Striatal volume on magnetic resonance imaging and repetitive behaviors in autism

28 November 2018

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28 November 2018

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PTEN mutation in a family with Cowden syndrome and autism

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

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

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

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Disruption of neurexin 1 associated with autism spectrum disorder

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

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

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

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Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors

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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.

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Novel PTEN mutations in neurodevelopmental disorders and macrocephaly

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

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

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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