(Q42716740)

5 November 2017

The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants (English)

1 reference

5 November 2017

1 reference

Dale W Laird

5

0 references

author name string

Jared M Churko

1

1 reference

5 November 2017

Stephanie Langlois

2

1 reference

5 November 2017

Xinyue Pan

3

1 reference

5 November 2017

Qing Shao

4

1 reference

5 November 2017

language of work or name

English

0 references

publication date

1 August 2010

1 reference

5 November 2017

1 reference

5 November 2017

429

1 reference

5 November 2017

3

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5 November 2017

473-483

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Creative Commons Attribution-NonCommercial 2.5 Generic

5 November 2017

start time

25 July 2019

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2907710/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Oculo-dento-digital dysplasia: lack of genotype-phenotype correlation for GJA1 mutations and usefulness of neuro-imaging.

1 reference

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Connexin 43 and plakophilin-2 as a protein complex that regulates blood-testis barrier dynamics

27 May 2018

1 reference

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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

27 May 2018

1 reference

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ERp29 restricts Connexin43 oligomerization in the endoplasmic reticulum

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Conformational maturation and post-ER multisubunit assembly of gap junction proteins

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Cellular responses to disruption of the permeability barrier in a three-dimensional organotypic epidermal model

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Possible involvement of gap junctions in the barrier function of tight junctions of brain and lung endothelial cells

27 May 2018

1 reference

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

27 May 2018

1 reference

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From deafness genes to hearing mechanisms: harmony and counterpoint

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Protein kinase C spatially and temporally regulates gap junctional communication during human wound repair via phosphorylation of connexin43 on serine368.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43.

27 May 2018

1 reference

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Functional domain mapping and selective trans-dominant effects exhibited by Cx26 disease-causing mutations

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

The molecular basis of hereditary palmoplantar keratodermas.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Comparative analysis and application of fluorescent protein-tagged 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=2907710

Conduction slowing and sudden arrhythmic death in mice with cardiac-restricted inactivation of connexin43

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease.

27 May 2018

1 reference

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In vivo modulation of connexins 43 and 26 of human epidermis by topical retinoic acid treatment

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Connexins, connexons, and intercellular communication

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Wounding alters epidermal connexin expression and gap junction-mediated intercellular communication

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Expression of gap junction proteins Cx26, Cx31.1, Cx37, and Cx43 in developing and mature rat epidermis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

The Growth and Differentiation of Cultured Newborn Rat Keratinocytes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Connexin43: a protein from rat heart homologous to a gap junction protein from liver

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Hereditary palmoplantar keratodermas.

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Cx43 has distinct mobility within plasma-membrane domains, indicative of progressive formation of gap-junction plaques.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

A novel missense mutation in GJB2 disturbs gap junction protein transport and causes focal palmoplantar keratoderma with deafness.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Connexin levels regulate keratinocyte differentiation in the epidermis

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Altered connexin expression and wound healing in the epidermis of connexin-deficient mice

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Functional characteristics of skate connexin35, a member of the gamma subfamily of connexins expressed in the vertebrate retina.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Novel Connexin 43 (GJA1) mutation causes oculo-dento-digital dysplasia with curly hair

16 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1042%2FBJ20100155

Skin changes in oculo-dento-digital dysplasia are correlated with C-terminal truncations of connexin 43

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2907710

Functional Characterization of aGJA1Frameshift Mutation Causing Oculodentodigital Dysplasia and Palmoplantar Keratoderma

1 December 2018

1 reference

12 December 2020

Changing patterns of gap junctional intercellular communication and connexin distribution in mouse epidermis and hair follicles during embryonic development

1 reference

12 December 2020

A HEREDITARY SYNDROME: "DYSPLASIA OCULODENTODIGITALIS

1 reference

12 December 2020

New evidence for the correlation of the p.G130V mutation in the GJB2 gene and syndromic hearing loss with palmoplantar keratoderma

1 reference

12 December 2020

Connexin disorders of the skin

1 reference

12 December 2020

Gap-junctional protein connexin 43 is expressed in dermis and epidermis of human skin: differential modulation by retinoids

1 reference

12 December 2020

Morphological and molecular alterations at the junctional complex in irradiated human colon adenocarcinoma cells, Caco-2

1 reference

12 December 2020

A 2-bp deletion in the GJA1 gene is associated with oculo-dento-digital dysplasia with palmoplantar keratoderma

1 reference

12 December 2020

Optical and biochemical dissection of connexin and disease-linked connexin mutants in 3D organotypic epidermis

1 reference

12 December 2020

Hyperkeratosis of palms and soles : clinical study

1 reference

12 December 2020

Striate palmoplantar keratoderma (Brunauer-Fohs-Siemens syndrome)

1 reference

12 December 2020

Identifiers

DOI

10.1042/BJ20100155

1 reference

5 November 2017

1 reference

5 November 2017

PubMed publication ID

20515445

1 reference