(Q50486953)

14 March 2018

title

Hearing loss: frequency and functional studies of the most common connexin26 alleles. (English)

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14 March 2018

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Paola D'Andrea

1

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14 March 2018

Valentina Veronesi

2

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14 March 2018

Massimiliano Bicego

3

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14 March 2018

Salvatore Melchionda

4

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14 March 2018

Leopoldo Zelante

5

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14 March 2018

Enzo Di Iorio

6

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14 March 2018

Roberto Bruzzone

7

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14 March 2018

Paolo Gasparini

8

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14 March 2018

language of work or name

English

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publication date

1 August 2002

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14 March 2018

Biochemical and Biophysical Research Communications

published in

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14 March 2018

volume

296

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14 March 2018

issue

3

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14 March 2018

page(s)

685-691

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14 March 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connections with connexins: the molecular basis of direct intercellular signaling

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Molecular genetics of hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connexin-26 mutations in sporadic and inherited sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connexin mutations and hearing loss.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Meta-analysis of GJB2 mutation 35delG frequencies in Europe

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

High carrier frequency of the 35delG deafness mutation in European populations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Three novel connexin26 gene mutations in autosomal recessive non-syndromic deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Prevalent connexin 26 gene (GJB2) mutations in Japanese

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Properties of connexin26 gap junctional proteins derived from mutations associated with non-syndromal heriditary deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Connexin mutations in deafness.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900891-4

Altered trafficking of mutant connexin32

7 January 2021

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10.1016/S0006-291X(02)00891-4

7 January 2021

Identifiers

DOI

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14 March 2018

1 reference

14 March 2018