(Q50439331)

English

Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss.

scientific article published on 4 February 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss. (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

1 reference

based on heuristic

inferred from title

author name string

Hui-Mei Hong

1

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

Jiann-Jou Yang

2

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

Jia-Ching Shieh

3

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

Mei-Ling Lin

4

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

Shuan-Yow Li

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

publication date

4 February 2010

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

127

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

5

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

545-551

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

https://scigraph.springernature.com/pub.10.1007/s00439-010-0791-x

0 references

Plasma membrane channels formed by connexins: their regulation and functions.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-010-0791-X

21 January 2018

Structural and functional diversity of connexin genes in the mouse and human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin43 pseudogene is expressed in tumor cells and inhibits growth

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac malformation in neonatal mice lacking connexin43.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolic Coupling, Ionic Coupling and Cell Contacts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human connexin43 gene locus, GJA1 sublocalized to band 6q21→q23.2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin gene mutations in human genetic diseases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of human cardiac gap junction channel mutants

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid determination of gap junction formation using HeLa cells microinjected with cDNAs encoding wild-type and chimeric connexins

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics, genomics and gene discovery in the auditory system

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20130915

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-010-0791-X

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 March 2018

http://europepmc.org/abstract/MED/20130915

ResearchGate publication ID

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