(Q30454214)

12 August 2017

Identifying the genes of hearing, deafness, and dysequilibrium (English)

1 reference

12 August 2017

1 reference

Corwin JT

1

1 reference

PMCID

33905

12 August 2017

language of work or name

English

0 references

publication date

1 October 1998

1 reference

Proceedings of the National Academy of Sciences of the United States of America

12 August 2017

1 reference

12 August 2017

95

1 reference

12 August 2017

21

1 reference

12 August 2017

12080-12082

1 reference

Molecular markers for cell types of the inner ear and candidate genes for hearing disorders

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Cell death, cell proliferation, and estimates of hair cell life spans in the vestibular organs of chicks

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Fish n' chicks: model recipes for hair-cell regeneration?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

The role of neurotrophic factors in regulating the development of inner ear innervation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Inherited hearing defects in mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Defective myosin VIIA gene responsible for Usher syndrome type 1B

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Molecular cloning of chick beta-tectorin, an extracellular matrix molecule of the inner ear

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

cDNA cloning, tissue distribution, and chromosomal localization of Ocp2, a gene encoding a putative transcription-associated factor predominantly expressed in the auditory organs

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Hair cell distributions in the normal human cochlea.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

The Prevalence of Hearing Impairment and Reported Hearing Disability among Adults in Great Britain

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Genetic epidemiology of hearing impairment

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Brain-derived neurotrophic factor and neurotrophin 3 mRNAs in the peripheral target fields of developing inner ear ganglia.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

28 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.21.12080

Connexin 26 gene linked to a dominant deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.21.12080

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.21.12080

Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.21.12080

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.21.12080

Mutations affecting development of the zebrafish inner ear and lateral line.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

Differential expression of bone morphogenetic proteins in the developing vestibular and auditory sensory organs.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=33905

26 November 2018

Identifiers

DOI

10.1073/PNAS.95.21.12080

1 reference

release_ez5jy35l4rfw3cc437jzbbcg4u

12 August 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ez5jy35l4rfw3cc437jzbbcg4u

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

33905

1 reference

12 August 2017

1 reference

PMCID

33905