RNA Interference Prevents Autosomal-Dominant Hearing Loss. (Q37004981)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27236922%20AND%20SRC:MED&resulttype=core&format=json

3 April 2020

title

RNA Interference Prevents Autosomal-Dominant Hearing Loss (English)

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3 April 2020

Seiji B Shibata

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3 April 2020

Paul T Ranum

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3 April 2020

Hideaki Moteki

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3 April 2020

Bifeng Pan

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Alexander T Goodwin

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3 April 2020

Shawn S Goodman

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3 April 2020

Paul J Abbas

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Jeffrey R Holt

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3 April 2020

language of work or name

English

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publication date

26 May 2016

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American Journal of Human Genetics

3 April 2020

published in

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volume

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issue

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page(s)

1101-1113

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describes a project that uses

3 April 2020

ImageJ

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11 June 2022

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based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss.

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TMC1 and TMC2 Localize at the Site of Mechanotransduction in Mammalian Inner Ear Hair Cell Stereocilia

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A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

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A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family

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Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice

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TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear

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Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2

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Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness

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Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes

29 September 2017

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A novel mutation adjacent to the Bth mouse mutation in the TMC1 gene makes this mouse an excellent model of human deafness at the DFNA36 locus.

29 September 2017

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29 September 2017

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29 September 2017

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A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.

29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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4 September 2018

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4 September 2018

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4 September 2018

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4 September 2018

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10.1016/J.AJHG.2016.03.028

4 September 2018

Identifiers

DOI

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3 April 2020

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3 April 2020

PubMed publication ID

27236922

1 reference

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