(Q24297920)

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0097104

neuroligin family protein binding

1 reference

Gene Ontology release 2020-05-02

1 reference

Neurexin-1

1 reference

Neuroligin 2

1 reference

Neurexin II

1 reference

Neurexin-1

1 reference

author

Guy A. Rouleau

21

0 references

Tabrez J. Siddiqui

Tabrez J Siddiqui

2

0 references

Marie-Odile Krebs

Marie-Odile Krebs

13

0 references

Éric Fombonne

Eric Fombonne

16

0 references

Laurent Mottron

15

Laurent Mottron

0 references

Dan Spiegelman

8

Dan Spiegelman

0 references

Julie Gauthier

1

Julie Gauthier

0 references

Jacques L. Michaud

17

Jacques L Michaud

0 references

Ann Marie Craig

20

Ann Marie Craig

0 references

Pierre Drapeau

18

Pierre Drapeau

0 references

Anne Noreau

9

Anne Noreau

0 references

Nathalie Champagne

6

Nathalie Champagne

0 references

Mathieu Lapointe

7

Mathieu Lapointe

0 references

Ronald G. Lafrenière

10

Ronald G Lafrenière

0 references

Ferid Fathalli

11

Ferid Fathalli

0 references

Salvatore Carbonetto

19

Salvatore Carbonetto

0 references

author name string

Peng Huashan

3

0 references

Daisaku Yokomaku

4

0 references

Fadi F Hamdan

5

0 references

Ridha Joober

12

0 references

Lynn E DeLisi

on focus list of Wikimedia project

14

0 references

language of work or name

English

0 references

publication date

October 2011

0 references

published in

Human Genetics

0 references

volume

130

0 references

issue

4

0 references

page(s)

563-73

0 references

ScienceSource

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

LRRTMs and neuroligins bind neurexins with a differential code to cooperate in glutamate synapse development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Disruption of the neurexin 1 gene is associated with schizophrenia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neuroligins and neurexins link synaptic function to cognitive disease

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Structural variation of chromosomes in autism spectrum disorder

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Disruption of neurexin 1 associated with autism spectrum disorder

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Contribution of SHANK3 mutations to autism spectrum disorder

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neurexin-neuroligin signaling in synapse development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

High frequency of neurexin 1beta signal peptide structural variants in patients with autism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neurexins: synaptic cell surface proteins related to the alpha-latrotoxin receptor and laminin

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

A stoichiometric complex of neurexins and dystroglycan in brain

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Trans-synaptic interaction of GluRdelta2 and Neurexin through Cbln1 mediates synapse formation in the cerebellum

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neurexins: three genes and 1001 products

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Alpha-neurexins couple Ca2+ channels to synaptic vesicle exocytosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

A splice code for trans-synaptic cell adhesion mediated by binding of neuroligin 1 to alpha- and beta-neurexins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neuroligin 1: a splice site-specific ligand for beta-neurexins

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Neurexin 1alpha structural variants associated with autism

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Induction of GABAergic postsynaptic differentiation by alpha-neurexins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

How to build a central synapse: clues from cell culture

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Autism as a disorder of neural information processing: directions for research and targets for therapy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

The neuropathology of schizophrenia. A critical review of the data and their interpretation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Assessing the validity of an animal model of deficient sensorimotor gating in schizophrenic patients

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Sensorimotor gating and schizophrenia. Human and animal model studies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Deletion of alpha-neurexins does not cause a major impairment of axonal pathfinding or synapse formation.

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-011-0975-Z

CASK and protein 4.1 support F-actin nucleation on neurexins

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204930

Mixed-culture assays for analyzing neuronal synapse formation

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21424692

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00439-011-0975-Z

0 references

Dimensions Publication ID

1009556400

0 references

Fatcat ID

release_6ja36i4dtvf7tdxb5uufvtlx6y

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6ja36i4dtvf7tdxb5uufvtlx6y