(Q28206633)

gap junction protein beta 6

GOA release 2020-03-11

1 reference

gap junction-mediated intercellular transport

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1

Martina Beltramello

0 references

Fabio Mammano

object named as

Fabio Mammano

5

1 reference

ORCID Public Data File 2021

author name string

Massimiliano Bicego

2

0 references

Valeria Piazza

3

0 references

Catalin D Ciubotaru

4

0 references

Paola D'Andrea

Biochemical and Biophysical Research Communications

6

0 references

language of work or name

English

0 references

publication date

13 June 2003

0 references

published in

0 references

volume

305

0 references

issue

4

0 references

page(s)

1024-33

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Connexin46 mutations in autosomal dominant congenital cataract

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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%2803%2900868-4

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Mutations in GJB6 cause hidrotic ectodermal dysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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%2803%2900868-4

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%2803%2900868-4

Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Functional studies of human skin disease- and deafness-associated connexin 30 mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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%2803%2900868-4

Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Clustering of connexin 43-enhanced green fluorescent protein gap junction channels and functional coupling in living cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Connexin-GFPs shed light on regulation of cell-cell communication by gap junctions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Single-channel currents of an intercellular junction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Trafficking, assembly, and function of a connexin43-green fluorescent protein chimera in live mammalian cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

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%2803%2900868-4

Voltage clamp limitations of dual whole-cell gap junction current and voltage recordings. I. Conductance measurements

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Electrophysiological properties of gap junction channels in hepatocytes isolated from connexin32-deficient and wild-type mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Biophysical properties of mouse connexin30 gap junction channels studied in transfected human HeLa cells.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4

Connexin mutations in deafness.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2803%2900868-4