Shank3 mutant mice display autistic-like behaviours and striatal dysfunction (Q24597501)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21423165%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

title

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction (English)

1 reference

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positive regulation of AMPA receptor activity

26 January 2020

main subject

autism

0 references

1 reference

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:2000969

SH3 and multiple ankyrin repeat domains 3

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

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26 January 2020

Catia Feliciano

2

1 reference

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26 January 2020

Jonathan T Ting

3

1 reference

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26 January 2020

Wenting Wang

4

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26 January 2020

author name string

Michael F Wells

5

1 reference

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26 January 2020

Talaignair N Venkatraman

6

1 reference

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26 January 2020

Christopher D Lascola

7

1 reference

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26 January 2020

Zhanyan Fu

8

1 reference

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26 January 2020

Guoping Feng

9

1 reference

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26 January 2020

language of work or name

English

0 references

publication date

20 March 2011

1 reference

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26 January 2020

1 reference

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26 January 2020

volume

472

1 reference

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26 January 2020

page(s)

437-442

1 reference

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26 January 2020

issue

7344

1 reference

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describes a project that uses

26 January 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3090611/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

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Contribution of SHANK3 mutations to autism spectrum disorder

24 March 2017

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

24 March 2017

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Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice.

24 March 2017

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

24 March 2017

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Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome

24 March 2017

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Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms

24 March 2017

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

24 March 2017

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GKAP, a novel synaptic protein that interacts with the guanylate kinase-like domain of the PSD-95/SAP90 family of channel clustering molecules

24 March 2017

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Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive-like behaviors in mice

24 March 2017

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Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1.

24 March 2017

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24 March 2017

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Pten regulates neuronal arborization and social interaction in mice

24 March 2017

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Differential mRNA expression and protein localization of the SAP90/PSD-95-associated proteins (SAPAPs) in the nervous system of the mouse

24 March 2017

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Binding of neuroligins to PSD-95

24 March 2017

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24 March 2017

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24 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

7 April 2017

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7 April 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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30 May 2018

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Novel de novo SHANK3 mutation in autistic patients

28 November 2018

1 reference

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The role of protein synthesis in striatal long-term depression.

28 November 2018

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

28 November 2018

1 reference

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The NMDA-to-AMPA ratio at synapses onto layer 2/3 pyramidal neurons is conserved across prefrontal and visual cortices

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3090611

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.

28 November 2018

1 reference

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An MRI study of the basal ganglia in autism.

28 November 2018

1 reference

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28 November 2018

Identifiers

DOI

10.1038/NATURE09965

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21423165%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

26 January 2020

1023637164

0 references

OpenCitations bibliographic resource ID

1132182

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1132182

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21423165%20AND%20SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21423165%20AND%20SRC:MED&resulttype=core&format=json