Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Connexin26 and -30 in the Cochlea and their clinical relevance].

Laryngo- rhino- otologie - 1 Dec 2001

Lautermann J, Gabriel H D, Kupsch P, Winterhager E, Jahnke K

Abstract excerpt

INTRODUCTION: Gap junction channels consist of different connexin proteins and play an important role in the physiology of hearing. Connexin26 and connexin30 have been demonstrated in the inner ear by immunohistochemistry and Northern Blot analysis. Mutations in the genes for connexin26 and connexin30 have been described to be responsible for non-syndromic hearing loss. METHODS: We investigated the prevalence of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Connexin 26
Share to Connexin 30
Share to Connexins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to Ear, Inner

Share to Gap Junctions

Share to Pregnancy Trimester, Second

Share to Rats, Wistar

Source

Identifiers

PMID: 11793268
DOI: 10.1055/s-2001-19576

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Connexin26 and -30 in the Cochlea and their clinical relevance].PMID 11793268Read ↗

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population.Semantic proximity Read ↗

Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene.Semantic proximity Read ↗

Connexins in hearing loss: a comprehensive overview.Semantic proximity Read ↗

[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].Semantic proximity Read ↗

Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling.Semantic proximity Read ↗

[Phenotype of patients showing hearing impairment based on the 35delG mutation in the connexin 26 gene].Semantic proximity Read ↗

Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey.Semantic proximity Read ↗

Hearing is normal without connexin30.Semantic proximity Read ↗

Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment.Semantic proximity Read ↗

A novel compound heterozygous mutation (35delG, 363delC) in the Connexin 26 gene causes non-syndromic autosomal recessive hearing loss.Semantic proximity Read ↗

[From gene to disease: deafness and connexin 26].Semantic proximity Read ↗

Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.