(Q28511260)

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Connexin29 is highly expressed in cochlear Schwann cells, and it is required for the normal development and function of the auditory nerve of mice

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PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Connexin29 is highly expressed in cochlear Schwann cells, and it is required for the normal development and function of the auditory nerve of mice (English)

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Gap junction protein, gamma 3

1 reference

GOA release 2020-03-11

0 references

author name string

Wenxue Tang

1

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Yanping Zhang

2

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Qing Chang

3

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Shoab Ahmad

4

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Ian Dahlke

5

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Hong Yi

6

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Ping Chen

7

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Xi Lin

9

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

David L Paul

8

1 reference

Europe PubMed Central

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16 January 2020

language of work or name

0 references

publication date

1 February 2006

1 reference

Europe PubMed Central

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16 January 2020

Journal of Neuroscience

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

26

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

7

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1991-1999

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

Altered formation of hemichannels and gap junction channels caused by C-terminal connexin-32 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

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/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexins and gap junctions of astrocytes and oligodendrocytes in the CNS

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelination defects and neuronal hyperexcitability in the neocortex of connexin 32-deficient mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The varieties of auditory neuropathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse gap junction gene connexin29 is highly expressed in sciatic nerve and regulated during brain development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Speech perception and cortical event related potentials in children with auditory neuropathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin29 expression, immunocytochemistry and freeze-fracture replica immunogold labelling (FRIL) in sciatic nerve

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 47 (Cx47)-deficient mice with enhanced green fluorescent protein reporter gene reveal predominant oligodendrocytic expression of Cx47 and display vacuolized myelin in the CNS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexins are critical for normal myelination in the CNS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease mechanisms in inherited neuropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Group I metabotropic glutamate receptors in spiral ganglion neurons contribute to excitatory neurotransmissions in the cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A reporter allele for investigating connexin 26 gene expression in the mouse brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four classes of intercellular channels between glial cells in the CNS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acid-sensing ion channel 2 contributes a major component to acid-evoked excitatory responses in spiral ganglion neurons and plays a role in noise susceptibility of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perceptual consequences of disrupted auditory nerve activity.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of three gap junction proteins in developing and mature brain tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Qualitative and quantitative observations of spiral ganglion development in the rat.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelin-associated glycoprotein is not detectable in perikaryal myelin of spiral ganglion neurons of adult mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin mutations in X-linked Charcot-Marie-Tooth disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32 is a myelin-related protein in the PNS and CNS

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Auditory neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties and regulation of gap junctional hemichannels in the plasma membranes of cultured cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin32-null mice develop demyelinating peripheral neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional gap junctions in the schwann cell myelin sheath

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Auditory neuropathy in childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16481432

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.5055-05.2006

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

2 references

PubMed publication ID

25 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16481432%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

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