(Q54336549)

English

1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay.

scientific article published on 25 November 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

1p34.3 deletion involving GRIK3: Further clinical implication of GRIK family glutamate receptors in the pathogenesis of developmental delay. (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Takao Takahashi

5

object named as

Takao Takahashi

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

author name string

Toshiki Takenouchi

1

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Noriko Hashida

2

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Chiharu Torii

3

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Rika Kosaki

4

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Kenjiro Kosaki

6

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

language of work or name

0 references

publication date

25 November 2013

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

number of pages

5

1 reference

based on heuristic

inferred from page(s)

American Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

164A

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

2

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

456-460

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Association between the ionotropic glutamate receptor kainate 3 (GRIK3) ser310ala polymorphism and schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Cloning of a putative glutamate receptor: a low affinity kainate-binding subunit

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Kainate receptors are involved in synaptic plasticity

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Evolution in health and medicine Sackler colloquium: Comparative genomics of autism and schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Cloning of a cDNA for a glutamate receptor subunit activated by kainate but not AMPA

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

High-affinity kainate receptor subunits are necessary for ionotropic but not metabotropic signaling

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

A de novo 8.8-Mb deletion of 21q21.1-q21.3 in an autistic male with a complex rearrangement involving chromosomes 6, 10, and 21.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Association study of GRIK1 gene polymorphisms in schizophrenia: case-control and family-based studies.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Linkage and association of the glutamate receptor 6 gene with autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Are GRIK3 (T928G) gene variants in schizophrenia patients different from those in their first-degree relatives?

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

CNVs: harbingers of a rare variant revolution in psychiatric genetics

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Overview of glutamatergic neurotransmission in the nervous system.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Atypical functional properties of GluK3-containing kainate receptors.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Cytogenetic and genetic evidence supports a role for the kainate-type glutamate receptor gene, GRIK4, in schizophrenia and bipolar disorder.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

GluR7 is an essential subunit of presynaptic kainate autoreceptors at hippocampal mossy fiber synapses

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Association between polymorphisms in GRIK2 gene and obsessive-compulsive disorder: a family-based study.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Association of the human kainate receptor GluR7 gene (GRIK3) with recurrent major depressive disorder

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Rat GluR7 and a carboxy-terminal splice variant, GluR7b, are functional kainate receptor subunits with a low sensitivity to glutamate

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Presynaptic kainate receptor mediation of frequency facilitation at hippocampal mossy fiber synapses

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Pharmacology of ionotropic glutamate receptors: A structural perspective

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

A novel microdeletion in 1(p34.2p34.3), involving the SLC2A1 (GLUT1) gene, and severe delayed development

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Genome-wide association study on bipolar disorder in the Bulgarian population

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.36240

21 January 2018

Identifiers

10.1002/AJMG.A.36240

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 May 2018

http://europepmc.org/abstract/MED/24449200

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q54336549&oldid=1776819613"