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Human hereditary hearing impairment: mouse models can help to solve the puzzle

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Europe PubMed Central

PubMed publication ID

26 July 2017

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Europe PubMed Central

Human hereditary hearing impairment: mouse models can help to solve the puzzle (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

based on heuristic

inferred from title

object named as

Guy Van Camp

3

0 references

author name string

Karen Vrijens

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Lut Van Laer

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

11 September 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

124

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

325-348

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

A fast motile response in guinea-pig outer hair cells: the cellular basis of the cochlear amplifier

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

Genetic associations in age-related hearing thresholds

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

Identification of the protein product of the Coch gene (hereditary deafness gene) as the major component of bovine inner ear protein

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

Ca2+ signaling in the inner ear.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

Mitochondrial DNA Deletions Associated With Aging and Presbyacusis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-008-0556-Y

21 January 2018

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-links between stereocilia in the guinea pig cochlea.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unconventional Myosins in Cell Movement, Membrane Traffic, and Signal Transduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gap junction systems in the mammalian cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphological differences among radial afferent fibers in the cat cochlea: an electron-microscopic study of serial sections

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA damage by oxygen-derived species Its mechanism and measurement in mammalian systems

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Classical cadherin adhesion molecules: coordinating cell adhesion, signaling and the cytoskeleton

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gender differences in a longitudinal study of age-associated hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and environmental influences on self-reported reduced hearing in the old and oldest old.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unconventional myosins in inner-ear sensory epithelia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Developmental expression patterns of connexin26 and -30 in the rat cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro and in vivo suppression of GJB2 expression by RNA interference.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of the hair bundle and mechanotransduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anatomy of cochlear innervation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrokinetic shape changes of cochlear outer hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mechanism for active hearing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new age in the genetics of deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel frameshift mutations in the procollagen 2 gene (COL2A1) associated with Stickler syndrome (hereditary arthro-ophthalmopathy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evoked mechanical responses of isolated cochlear outer hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elongation of hair cell stereocilia is defective in the mouse mutant whirler

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vlgr1 knockout mice show audiogenic seizure susceptibility.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Knockout mouse models in pain research

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping quantitative trait loci for hearing loss in Black Swiss mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathology and molecular genetics of hearing loss in the human

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic and gene knock-out techniques and burn research.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of electromotility in the cochlear outer hair cell

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Claudin-based barrier in simple and stratified cellular sheets

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and characterisation of human Junctional Adhesion Molecule (JAM)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype-phenotype correlations for SLC26A4-related deafness.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of Cochlear Blood Supply with Mitochondrial DNA Common Deletion in Presbyacusis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Description and primary results from an audiometric study of male twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GATA3 haplo-insufficiency causes human HDR syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two quantitative trait loci affecting progressive hearing loss in 101/H mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid renewal of auditory hair bundles

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multifunctional strands in tight junctions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of outer hair cell motility in cochlear tuning

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gap junctions and cochlear homeostasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Espins are multifunctional actin cytoskeletal regulatory proteins in the microvilli of chemosensory and mechanosensory cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ahl3, a third locus on mouse chromosome 17 affecting age-related hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A deafness mutation isolates a second role for the tectorial membrane in hearing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cochlear dysfunction in the jerker mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noise-induced transient microlesions in the cell membranes of auditory hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in members of the connexin gene family as a cause of nonsyndromic deafness in Taiwan.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Auditory function associated with Col11a1 haploinsufficiency in chondrodysplasia (cho) mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of myosin VI in the differentiation of cochlear hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fine structure of freeze-fractured intercellular junctions in the guinea pig inner ear

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

K+ cycling and the endocochlear potential

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connexin 26 as a cause of hereditary hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NMR structure of the LCCL domain and implications for DFNA9 deafness disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a gene encoding a novel member of the nuclear receptor superfamily from the critical region of Usher syndrome type IIa at 1q41

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in PDS causes non-syndromic recessive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical dissection of stereovilli from fish inner ear reveals differences from intestinal microvilli

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development and properties of stereociliary link types in hair cells of the mouse cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stickler syndrome. A mutation in the nonhelical 3' end of type II procollagen gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural findings in the inner ear of Jackson shaker mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cadherin 23 is a component of the tip link in hair-cell stereocilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 3D structure of the tectorial membrane determined by second-harmonic imaging microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions in the network of Usher syndrome type 1 proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Initial sequencing and comparative analysis of the mouse genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma Membrane Ca2+-ATPase Extrudes Ca2+from Hair Cell Stereocilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The need for universal neonatal hearing screening--some aspects of epidemiology and identification

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-links between stereocilia in the guinea pig organ of Corti, and their possible relation to sensory transduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Origin of Jerker, a New Gene Mutation of the House Mouse, and Linkage Studies Made with It

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression pattern and functional characterization of connexin29 in transgenic mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Composition and supramolecular organization of the tectorial membrane.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular mechanisms of age-related hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DFNA9 is a progressive audiovestibular dysfunction with a microfibrillar deposit in the inner ear.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The circling mouse (C57BL/6J-cir) has a 40-kilobase genomic deletion that includes the transmembrane inner ear (tmie) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of MYO6 are associated with recessive deafness, DFNB37

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acoustic startle and prepulse inhibition in 40 inbred strains of mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cochlear mitochondrial DNA3867bp deletion in aged mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Modification of human hearing loss by plasma-membrane calcium pump PMCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cross-links between stereocilia in the human organ of Corti

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strain background effects and genetic modifiers of hearing in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ahl2, a second locus affecting age-related hearing loss in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eya4-deficient mice are a model for heritable otitis media

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of the 275 kD hair cell antigen and cell surface specialisations on auditory and vestibular hair bundles in the chicken inner ear

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hearing: the effects of chemicals

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18784944

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-008-0556-Y

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Sitelinks

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