(Q36168861)

English

Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder

scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

0 references

autism spectrum disorder

0 references

author name string

Kumiko Yanagi

1

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Tadashi Kaname

2

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Keiko Wakui

3

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Ohiko Hashimoto

4

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Yoshimitsu Fukushima

5

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Kenji Naritomi

6

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

publication date

16 July 2012

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Autism Research & Treatment

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

2012

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

724072

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Utility of lymphoblastoid cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Neuroligins and neurexins link synaptic function to cognitive disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Familial deletion within NLGN4 associated with autism and Tourette syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

A "silent" polymorphism in the MDR1 gene changes substrate specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Disorder-associated mutations lead to functional inactivation of neuroligins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Product differentiation by analysis of DNA melting curves during the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3420546

1 October 2017

Analysis of four neuroligin genes as candidates for autism.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F724072

21 January 2018

Association between the neurofibromatosis-1 (NF1) locus and autism in the Japanese population.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F724072

21 January 2018

Detection of factor VIII gene mutations by high-resolution melting analysis

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F724072

21 January 2018

Why does the mutation G17736A/Val107Val (silent) in the F9 gene cause mild haemophilia B in five Swedish families?

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F724072

21 January 2018

The sounds of silence: synonymous mutations affect function

1 reference

https://pubmed.ncbi.nlm.nih.gov/22934180

12 December 2020

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inferred from PubMed ID database lookup

Identifiers

10.1155/2012/724072

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

ResearchGate publication ID

0 references

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