(Q57923060)

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Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Radoslaw Dobrowolski

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

author name string

Annette Sommershof

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Klaus Willecke

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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9 August 2007

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Europe PubMed Central

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3 January 2020

number of pages

9

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Journal of Membrane Biology

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

219

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Europe PubMed Central

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3 January 2020

1-3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

9-17

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

https://scigraph.springernature.com/pub.10.1007/s00232-007-9055-7

0 references

Connexin 43 hemi channels mediate Ca2+-regulated transmembrane NAD+ fluxes in intact cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conductance of connexin hemichannels segregates with the first transmembrane segment

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gap junction cellular internet: connexin hemichannels enter the signalling limelight

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Cα Model for the Transmembrane α Helices of Gap Junction Intercellular Channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transient, recurrent, white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexin 32 mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Change in permeant size selectivity by phosphorylation of connexin 43 gap-junctional hemichannels by PKC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The optimal use of IRES (internal ribosome entry site) in expression vectors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional expression in Xenopus oocytes of gap-junctional hemichannels formed by a cysteine-less connexin 43.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of gap junctional communication-deficient mutants of a rat liver epithelial cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gap junction turnover, intracellular trafficking, and phosphorylation of connexin43 in brefeldin A-treated rat mammary tumor cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The pattern of disulfide linkages in the extracellular loop regions of connexin 32 suggests a model for the docking interface of gap junctions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biophysics of gap junctions

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of Connexin43 phosphorylated at S325, S328 and S330 in normoxic and ischemic heart

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of gap junction formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

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/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple pathways in the trafficking and assembly of connexin 26, 32 and 43 into gap junction intercellular communication channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe neuropathy with leaky connexin32 hemichannels.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of Cx26, Cx32 AND Cx43 gap junction proteins in normal and neoplastic human tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An update on connexin genes and their nomenclature in mouse and man.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphorylated carboxy terminal serine residues stabilize the mouse gap junction protein connexin45 against degradation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin hemichannels and gap junction channels are differentially influenced by lipopolysaccharide and basic fibroblast growth factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin-based gap junction hemichannels: gating mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intercellular calcium signaling in astrocytes via ATP release through connexin hemichannels

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

pH-dependent intramolecular binding and structure involving Cx43 cytoplasmic domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional connexin “hemichannels”: A critical appraisal

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mechanism for connexin 26 mutation linked deafness: cell death caused by leaky gap junction hemichannels

1 reference

https://pubmed.ncbi.nlm.nih.gov/17687502

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00232-007-9055-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17687502%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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