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

Expression of connexin 31 in the developing mouse cochlea.

Neuroreport - 3 Aug 2000

Xia A P, Ikeda K, Katori Y, Oshima T, Kikuchi T, Takasaka T

Abstract excerpt

Connexin 31 (Cx31) mutations cause an autosomal dominant form of high-frequency hearing loss. The immunohistochemical localization of Cx31 in mouse cochlea was studied at different ages between 0 and 60 days after birth (DAB). Cx31-like immunoreactivity was detected in fibrocytes of spiral ligament and spiral limbus at 12 DAB, gradually enhanced with the increase of age and reached the adult pattern on 60 DAB....

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Animals, Newborn
Share to Cochlea

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Connexin 26

Share to Connexins

Share to Gene Expression Regulation, Developmental

Share to Mice, Inbred CBA

Share to Organ of Corti

Source

Identifiers

PMID: 10943702
DOI: 10.1097/00001756-200008030-00022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Expression of connexin 31 in the developing mouse cochlea.PMID 10943702Read ↗

Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss.Semantic proximity Read ↗

Unique expression of connexins in the human cochlea.Semantic proximity Read ↗

The connexin 30.3 of zebrafish homologue of human connexin 26 may play similar role in the inner ear.Semantic proximity Read ↗

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential.Semantic proximity Read ↗

Inner Ear Connexin Channels: Roles in Development and Maintenance of Cochlear Function.Semantic proximity Read ↗

Dynamic Spatiotemporal Expression Changes in Connexins of the Developing Primate's Cochlea.Semantic proximity Read ↗

Connexin 26 in human fetal development of the inner ear.Semantic proximity Read ↗

The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice.Semantic proximity Read ↗

Engraftment of Human Pluripotent Stem Cell-derived Progenitors in the Inner Ear of Prenatal MiceSemantic proximity Read ↗

Hearing is normal without connexin30.Semantic proximity Read ↗

Degradation and modification of cochlear gap junction proteins in the early development of age-related hearing loss.Semantic proximity Read ↗

Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses.Semantic proximity Read ↗

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