(Q38914392)

English

Exploring the potential role of disease-causing mutation in a gene desert: duplication of noncoding elements 5' of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

retracted paper

2 references

Dataset for "Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine"

Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine

Exploring the potential role of disease-causing mutation in a gene desert: duplication of noncoding elements 5' of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

0 references

0 references

X-linked intellectual disability

0 references

Laurence Faivre

9

object named as

Laurence Faivre

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Christel Thauvin-Robinet

8

object named as

Christel Thauvin-Robinet

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Alice Masurel-Paulet

2

object named as

Alice Masurel-Paulet

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Patrick Callier

5

object named as

Patrick Callier

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Francine Mugneret

6

object named as

Francine Mugneret

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

author name string

Céline Bonnet

1

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Asma Ali Khan

3

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Mylène Béri-Dexheimer

4

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Christophe Philippe

7

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Philippe Jonveaux

10

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

publication date

28 November 2011

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

33

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

355-358

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Partial tandem duplication of GRIA3 in a male with mental retardation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

Long-range control of gene expression: emerging mechanisms and disruption in disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

Regulatory potential scores from genome-wide three-way alignments of human, mouse, and rat

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

ECRbase: database of evolutionary conserved regions, promoters, and transcription factor binding sites in vertebrate genomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

21 January 2018

Aberrant GRIA3 transcripts with multi-exon duplications in a family with X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21649

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.21649

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

ResearchGate publication ID

0 references

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=Q38914392&oldid=2149118498"