(Q45183609)

10 December 2017

Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness (English)

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10 December 2017

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Martina Beltramello

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10 December 2017

Valeria Piazza

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10 December 2017

Feliksas F Bukauskas

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3

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10 December 2017

Tullio Pozzan

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4

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10 December 2017

Fabio Mammano

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5

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10 December 2017

12 December 2004

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10 December 2017

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10 December 2017

7

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10 December 2017

1

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10 December 2017

63-69

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https://scigraph.springernature.com/pub.10.1038/ncb1205

10 December 2017

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cites work

Connexin disorders of the ear, skin, and lens.

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7 January 2021

Neuronal KCNQ potassium channels: physiology and role in disease.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T.

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7 January 2021

Connexin 26 studies in patients with sensorineural hearing loss.

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7 January 2021

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

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7 January 2021

Functional analysis of connexin-26 mutants associated with hereditary recessive deafness

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7 January 2021

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

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7 January 2021

Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells

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7 January 2021

Chemical gating of gap junction channels; roles of calcium, pH and calmodulin

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7 January 2021

Gap junction channel gating

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7 January 2021

Microscopic properties of elementary Ca2+ release sites in non-excitable cells.

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7 January 2021

Hepatocyte gap junctions are permeable to the second messenger, inositol 1,4,5-trisphosphate, and to calcium ions

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7 January 2021

Transfer of second messengers through gap junction connexin 43 channels reconstituted in liposomes.

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7 January 2021

Strongly decreased gap junctional permeability to inositol 1,4, 5-trisphosphate in connexin32 deficient hepatocytes

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7 January 2021

Purinoceptors: are there families of P2X and P2Y purinoceptors?

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7 January 2021

New roles for astrocytes: Gap junction hemichannels have something to communicate

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7 January 2021

Beyond the gap: functions of unpaired connexon channels

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7 January 2021

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

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7 January 2021

A mechanism for sensing noise damage in the inner ear.

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7 January 2021

Changes in permeability caused by connexin 32 mutations underlie X-linked Charcot-Marie-Tooth disease

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7 January 2021

Frequency dependence of electrical coupling in Deiters' cells of the guinea pig cochlea.

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7 January 2021

Purinergic control of intercellular communication between Hensen's cells of the guinea-pig cochlea

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7 January 2021

Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4.

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7 January 2021

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

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7 January 2021

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

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7 January 2021

Identifiers

DOI

10.1038/NCB1205

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Dimensions Publication ID

10 December 2017

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