(Q30540894)

English

Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.

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scholarly article

1 reference

Europe PubMed Central

17 November 2017

Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36. (English)

1 reference

Europe PubMed Central

17 November 2017

1 reference

based on heuristic

inferred from title

quantitative trait locus

1 reference

based on heuristic

inferred from title

Martin Hrabě de Angelis

4

object named as

Martin Hrabé de Angelis

0 references

Gregory I Frolenkov

object named as

Gregory Frolenkov

6

0 references

Tomoko Makishima

object named as

Tomoko Makishima

3

0 references

author name string

Yoshihiro Noguchi

1

1 reference

Europe PubMed Central

17 November 2017

Kiyoto Kurima

2

1 reference

Europe PubMed Central

17 November 2017

Helmut Fuchs

5

1 reference

Europe PubMed Central

17 November 2017

Ken Kitamura

7

1 reference

Europe PubMed Central

17 November 2017

Andrew J Griffith

8

1 reference

Europe PubMed Central

17 November 2017

language of work or name

0 references

publication date

28 April 2006

1 reference

Europe PubMed Central

17 November 2017

1 reference

Europe PubMed Central

17 November 2017

173

1 reference

Europe PubMed Central

17 November 2017

4

1 reference

Europe PubMed Central

17 November 2017

2111-2119

1 reference

Europe PubMed Central

17 November 2017

Bioinformatics toolbox for narrowing rodent quantitative trait loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Genetic insights into the morphogenesis of inner ear hair cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Human Nonsyndromic Sensorineural Deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Genetic modifiers of vision and hearing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Map Manager QTX, cross-platform software for genetic mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Modifier genes of hereditary hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Localization of the bronx waltzer (bv) deafness gene to mouse chromosome 5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Auditory neuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Distortion product otoacoustic emissions in hearing-impaired mutant mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Postnatal development in the acoustic system of the house mouse in the light of developing masked thresholds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

20 June 2018

Listening to genetic background noise.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14-21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

The guide to plotting a cochleogram.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

A chemical-genetic strategy implicates myosin-1c in adaptation by hair cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Inner ear pathology in the deafness mutant mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1569729

26 November 2018

Cochlear origin of 2f1-f2 distortion products assessed by using 2 types of mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16648588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1534/GENETICS.106.057372

1 reference

Europe PubMed Central

17 November 2017

1 reference

Europe PubMed Central

17 November 2017

1 reference

Europe PubMed Central

17 November 2017

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0 references

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