(Q28268807)

SH3 and multiple ankyrin repeat domains 2

9 April 2017

main subject

autism

0 references

1 reference

GOA release 2020-03-11

author

Eckart D. Gundelfinger

26

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Ehab Shiban

Ehab Shiban

9

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Stephanie Wegener

Stephanie Wegener

3

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Nicolas Torquet

Nicolas Torquet

18

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Christina Spilker

Christina Spilker

10

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Andreas M. Grabrucker

Andreas M Grabrucker

Andreas M. Grabrucker

21

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Philippe Faure

Philippe Faure

17

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Roberto Toro

Roberto Toro

20

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Dirk Montag

Dirk Montag

15

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Thomas Bourgeron

Thomas Bourgeron

25

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Claire S Leblond

16

Claire S. Leblond

1 reference

9 April 2017

16

Claire S Leblond

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author name string

Michael J Schmeisser

1

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Elodie Ey

2

1 reference

9 April 2017

Juergen Bockmann

4

1 reference

9 April 2017

A Vanessa Stempel

5

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Angelika Kuebler

6

1 reference

9 April 2017

Anna-Lena Janssen

7

1 reference

9 April 2017

Patrick T Udvardi

8

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Detlef Balschun

11

1 reference

9 April 2017

Boris V Skryabin

12

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Susanne tom Dieck

13

1 reference

9 April 2017

Karl-Heinz Smalla

14

1 reference

9 April 2017

Anne-Marie Le Sourd

19

1 reference

9 April 2017

Sarah A Shoichet

22

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Dietmar Schmitz

23

1 reference

9 April 2017

Michael R Kreutz

24

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Tobias M Boeckers

27

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Michael J. Schmeisser

1

1 reference

9 April 2017

A. Vanessa Stempel

5

1 reference

9 April 2017

Patrick T. Udvardi

8

1 reference

9 April 2017

Boris V. Skryabin

12

1 reference

9 April 2017

Sarah A. Shoichet

22

1 reference

9 April 2017

Michael R. Kreutz

24

1 reference

9 April 2017

Tobias M. Boeckers

27

1 reference

9 April 2017

language of work or name

English

0 references

publication date

29 April 2012

1 reference

9 April 2017

1 reference

Advances in autism genetics: on the threshold of a new neurobiology

9 April 2017

volume

486

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issue

7402

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page(s)

256-60

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

An autism-associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor-mediated synaptic transmission in hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Novel de novo SHANK3 mutation in autistic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

An architectural framework that may lie at the core of the postsynaptic density

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Concerted action of zinc and ProSAP/Shank in synaptogenesis and synapse maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Key role for gene dosage and synaptic homeostasis in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Enhanced polyubiquitination of Shank3 and NMDA receptor in a mouse model of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Inherited and de novo SHANK2 variants associated with autism spectrum disorder impair neuronal morphogenesis and physiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Motor and cognitive stereotypies in the BTBR T+tf/J mouse model of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Sociability and motor functions in Shank1 mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Behavioral profiles of mouse models for autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Synaptic cross-talk between N-methyl-D-aspartate receptors and LAPSER1-beta-catenin at excitatory synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Somatostatin receptor interacting protein defines a novel family of multidomain proteins present in human and rodent brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Presynaptic kainate receptors impart an associative property to hippocampal mossy fiber long-term potentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Automated apparatus for quantitation of social approach behaviors in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Misguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Unusual repertoire of vocalizations in adult BTBR T+tf/J mice during three types of social encounters

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22699619

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Animal Models of Autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE11015

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NATURE11015

2 references

9 April 2017

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1020582984

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

22699619

1 reference

Consolidated OpenCitations Corpus – April 2017