(Q28590867)

22 June 2017

title

Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss (English)

1 reference

22 June 2017

main subject

transmembrane protein

0 references

Hepsin

1 reference

GOA release 2020-03-11

1 reference

Robert K Shepherd

8

0 references

Hamish S. Scott

object named as

Hamish S Scott

9

0 references

author name string

Michel Guipponi

1

1 reference

22 June 2017

Justin Tan

2

1 reference

22 June 2017

Lauren Donley

4

1 reference

22 June 2017

Pauline Crewther

5

1 reference

22 June 2017

Maria Clarke

6

1 reference

22 June 2017

Qingyu Wu

7

1 reference

22 June 2017

Ping Z F Cannon

3

1 reference

22 June 2017

language of work or name

English

0 references

publication date

9 July 2007

1 reference

The American Journal of Pathology

22 June 2017

published in

1 reference

22 June 2017

volume

171

1 reference

22 June 2017

issue

2

1 reference

22 June 2017

page(s)

608-616

1 reference

describes a project that uses

22 June 2017

ImageQuant

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1934525/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Control of peripheral nerve myelination by the beta-secretase BACE1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein

17 March 2017

1 reference

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Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss

17 March 2017

1 reference

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Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Mutations of MYO6 are associated with recessive deafness, DFNB37

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Expression of Ca2+-activated BK channel mRNA and its splice variants in the rat cochlea

17 March 2017

1 reference

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

17 March 2017

1 reference

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Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients

17 March 2017

1 reference

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

17 March 2017

1 reference

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Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

17 March 2017

1 reference

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

17 March 2017

1 reference

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Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant mouse

17 March 2017

1 reference

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Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing

17 March 2017

1 reference

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The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

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

17 March 2017

1 reference

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Thyroid hormone receptor beta is essential for development of auditory function

17 March 2017

1 reference

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Polypeptide composition of the mammalian tectorial membrane

17 March 2017

1 reference

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Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing

17 March 2017

1 reference

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Chronic depolarization enhances the trophic effects of brain-derived neurotrophic factor in rescuing auditory neurons following a sensorineural hearing loss.

29 September 2017

1 reference

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Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

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29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Molecular mechanisms of age-related hearing loss

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

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

29 September 2017

1 reference

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Generation and characterization of mice deficient in hepsin, a hepatic transmembrane serine protease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Genetic epidemiology of hearing impairment

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Effects of hypothyroidism on the structural development of the organ of Corti in the rat.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Periods of sensitivity to thyroid hormone during the development of the organ of Corti.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Contribution of BK Ca2+-activated K+ channels to auditory neurotransmission in the Guinea pig cochlea.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Retardation of cochlear maturation and impaired hair cell function caused by deletion of all known thyroid hormone receptors.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Thyroid hormone affects Schwann cell and oligodendrocyte gene expression at the glial transition zone of the VIIIth nerve prior to cochlea function.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Hearing loss and cochlear abnormalities in the congenital hypothyroid (hyt/hyt) mouse.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1934525

Type II transmembrane serine proteases

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17620368

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.2353/AJPATH.2007.070068

1 reference

22 June 2017

0 references

1 reference