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

Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.

PloS one - 7 Jul 2010

Noben-Trauth Konrad, Latoche Joseph R, Neely Harold R, Bennett Beth

Abstract excerpt

Progressive sensorineural hearing loss is the most common form of acquired hearing impairment in the human population. It is also highly prevalent in inbred strains of mice, providing an experimental avenue to systematically map genetic risk factors and to dissect the molecular pathways that orch...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 10
Share to Cochlea
Share to Ear, Inner

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Evoked Potentials, Auditory

Share to Hearing Loss, Sensorineural

Share to Quantitative Trait Loci

Share to Regression Analysis

Source

Open in PubMed Open full text

Identifiers

PMID: 20628639
DOI: 10.1371/journal.pone.0011459
PMCID: PMC2898796

Genes

ABR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20628639-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.PMID 20628639Read ↗

Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.Semantic proximity Read ↗

Inheritance patterns of progressive hearing loss in laboratory strains of mice.Semantic proximity Read ↗

Hearing loss and tinnitus: association studies for complex-hearing disorders in mouse and man.Semantic proximity Read ↗

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.Semantic proximity Read ↗

Large-scale phenotyping of noise-induced hearing loss in 100 strains of mice.Semantic proximity Read ↗

Genome-wide association study for age-related hearing loss in CFW miceSemantic proximity Read ↗

Mapping quantitative trait loci for hearing loss in Black Swiss mice.Semantic proximity Read ↗

Inherited hearing defects in mice.Semantic proximity Read ↗

Distinct cochlear cell types associated with genetic susceptibility to sensory and metabolic hearing loss in older adults from the CLSASemantic proximity Read ↗

Analysis of the QTL for sleep homeostasis in mice: Homer1a is a likely candidate.Semantic proximity Read ↗

Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.Semantic proximity Read ↗

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.Semantic proximity Read ↗

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