(Q42634137)

4 November 2017

Zebrafish short fin mutations in connexin43 lead to aberrant gap junctional intercellular communication (English)

1 reference

Gap junction protein alpha 1b

4 November 2017

0 references

1 reference

GOA release 2020-03-11

1 reference

4

1 reference

4 November 2017

Angela D Hoptak-Solga

1

1 reference

4 November 2017

Kathryn A Klein

2

1 reference

4 November 2017

Adam M DeRosa

3

1 reference

4 November 2017

M Kathryn Iovine

5

1 reference

4 November 2017

language of work or name

English

0 references

publication date

21 June 2007

1 reference

4 November 2017

6

1 reference

based on heuristic

inferred from page(s)

published in

FEBS Letters

1 reference

4 November 2017

581

1 reference

4 November 2017

17

1 reference

4 November 2017

3297-3302

1 reference

Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Spot pattern of leopard Danio is caused by mutation in the zebrafish connexin41.8 gene

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Life cycle of connexins in health and disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Oculodentodigital dysplasia connexin43 mutations result in non-functional connexin hemichannels and gap junctions in C6 glioma cells

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Connexin-based gap junction hemichannels: gating mechanisms

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Gap junction- and hemichannel-independent actions of connexins

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Modifications in the biophysical properties of connexin43 channels by a peptide of the cytoplasmic loop region

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Gap junctions and the connexin protein family

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Genetic diseases and gene knockouts reveal diverse connexin functions.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Connexin40, a component of gap junctions in vascular endothelium, is restricted in its ability to interact with other connexins

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Equilibrium properties of a voltage-dependent junctional conductance.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Gap junctions formed by connexins 26 and 32 alone and in combination are differently affected by applied voltage

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Mutations in connexin43 (GJA1) perturb bone growth in zebrafish fins

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Oculodentodigital dysplasia-causing connexin43 mutants are non-functional and exhibit dominant effects on wild-type connexin43.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Specific amino-acid residues in the N-terminus and TM3 implicated in channel function and oligomerization compatibility of connexin43.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2044562

Functional Characterization of Connexin43 Mutations Found in Patients With Oculodentodigital Dysplasia

16 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2007.06.030

Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17599838

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17599838

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.FEBSLET.2007.06.030

1 reference

4 November 2017

1 reference

4 November 2017

PubMed publication ID

17599838

1 reference