(Q28213840)

2

0 references

Wei-Li Di

3

0 references

Irene M Leigh

4

0 references

Edel A O'Toole

5

0 references

David P Kelsell

Biochemical and Biophysical Research Communications

6

0 references

language of work or name

English

0 references

publication date

15 November 2002

0 references

published in

0 references

volume

298

0 references

issue

5

0 references

page(s)

651-6

0 references

cites work

Connexins: a connection with the skin

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Connexin mutations in skin disease and hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Multiple epidermal connexins are expressed in different keratinocyte subpopulations including connexin 31

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Expression of connexin 30 in the developing mouse cochlea.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

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%2902517-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Mutations in GJB6 cause hidrotic ectodermal dysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

A novel connexin 30 mutation in Clouston syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Clouston syndrome: an ectodermal dysplasia without significant dental findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Oral findings of Clouston's syndrome (hidrotic ectodermal dysplasia)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2

A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2902517-2