(Q24649430)

English

Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18674745%20AND%20SRC:MED&resulttype=core&format=json

11 January 2020

Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice (English)

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11 January 2020

nonsyndromic deafness

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based on heuristic

inferred from title

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based on heuristic

inferred from title

3

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11 January 2020

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11 January 2020

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11 January 2020

Richard J Smith

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11 January 2020

author name string

Jérôme Ruel

1

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11 January 2020

Sarah Emery

2

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11 January 2020

Tiphaine Bersot

4

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11 January 2020

Bénédicte Amilhon

5

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11 January 2020

Jana M Van Rybroek

6

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11 January 2020

Guy Rebillard

7

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11 January 2020

Marc Lenoir

8

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11 January 2020

Benjamin Delprat

10

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11 January 2020

Theru A Sivakumaran

11

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11 January 2020

Salah El Mestikawy

13

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11 January 2020

Marci M Lesperance

16

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11 January 2020

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1 August 2008

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11 January 2020

American Journal of Human Genetics

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11 January 2020

83

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11 January 2020

2

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11 January 2020

278-292

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11 January 2020

describes a project that uses

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2495073/fullTextXML

based on heuristic

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Docking and homology modeling explain inhibition of the human vesicular glutamate transporters

1 reference

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7 April 2017

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

1 reference

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7 April 2017

DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2495073

7 April 2017

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

1 reference

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7 April 2017

The structure of haplotype blocks in the human genome

1 reference

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7 April 2017

Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3.

1 reference

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7 April 2017

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

1 reference

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7 April 2017

Organic anion transport is the primary function of the SLC17/type I phosphate transporter family

1 reference

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7 April 2017

The identification of vesicular glutamate transporter 3 suggests novel modes of signaling by glutamate

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7 April 2017

Molecular cloning and functional identification of mouse vesicular glutamate transporter 3 and its expression in subsets of novel excitatory neurons

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7 April 2017

A third vesicular glutamate transporter expressed by cholinergic and serotoninergic neurons

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7 April 2017

RIBEYE, a component of synaptic ribbons: a protein's journey through evolution provides insight into synaptic ribbon function

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Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat

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7 April 2017

Expression of the vesicular glutamate transporters during development indicates the widespread corelease of multiple neurotransmitters

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7 April 2017

An essential role for vesicular glutamate transporter 1 (VGLUT1) in postnatal development and control of quantal size

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Structure and function of the hair cell ribbon synapse

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28 September 2017

CaV1.3 channels are essential for development and presynaptic activity of cochlear inner hair cells.

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28 September 2017

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28 September 2017

RIBEYE, a Component of Synaptic Ribbons

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2495073

28 September 2017

Kinetics of exocytosis and endocytosis at the cochlear inner hair cell afferent synapse of the mouse

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28 September 2017

Prevalence of hearing loss in older adults in Beaver Dam, Wisconsin. The Epidemiology of Hearing Loss Study

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28 September 2017

Synaptic distribution of the AMPA-GluR2 subunit and its colocalization with calcium-binding proteins in rat cerebral cortex: an immunohistochemical study using a GluR2-specific monoclonal antibody

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28 September 2017

Chemical synaptic transmission in the cochlea

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28 September 2017

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28 September 2017

Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells.

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30 May 2018

Persistence of Ca(v)1.3 Ca2+ channels in mature outer hair cells supports outer hair cell afferent signaling.

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Neurotrophin 3 potentiates glutamatergic responses of IHC afferents in the cochlea in vivo

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30 May 2018

Glutamate receptor activity is required for normal development of tectal cell dendrites in vivo.

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30 May 2018

Cigarette smoking and hearing loss: the epidemiology of hearing loss study.

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30 May 2018

Immunochemical characterization of the non-NMDA glutamate receptor using subunit-specific antibodies. Evidence for a hetero-oligomeric structure in rat brain

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30 May 2018

The vesicular glutamate transporter VGLUT3 synergizes striatal acetylcholine tone

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28 November 2018

Temperature enhances exocytosis efficiency at the mouse inner hair cell ribbon synapse.

1 reference

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28 November 2018

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28 November 2018

Synaptic organization in cochlear inner hair cells deficient for the CaV1.3 (alpha1D) subunit of L-type Ca2+ channels.

1 reference

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28 November 2018

Hair cell synaptic ribbons are essential for synchronous auditory signalling.

1 reference

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28 November 2018

Inhibitory synapses in the developing auditory system are glutamatergic.

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28 November 2018

Developmental pattern of three vesicular glutamate transporters in the rat superior olivary complex

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28 November 2018

Transient Ca2+-permeable AMPA receptors in postnatal rat primary auditory neurons.

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28 November 2018

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

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28 November 2018

Localization of VGLUT3, the vesicular glutamate transporter type 3, in the rat brain

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28 November 2018

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

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28 November 2018

Catecholamine-independent transient expression of tyrosine hydroxylase in primary auditory neurons is coincident with the onset of hearing in the rat cochlea

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28 November 2018

Phenotypic characterization of hereditary hearing impairment linked to DFNA25.

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28 November 2018

Cysteine-string protein in inner hair cells of the organ of Corti: synaptic expression and upregulation at the onset of hearing.

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28 November 2018

Genetic associations in age-related hearing thresholds.

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28 November 2018

Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)

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28 November 2018

Genotypic differences in behavioral, physiological and anatomical expressions of age-related hearing loss in the laboratory mouse.

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28 November 2018

Summary health statistics for u.s. Adults: national health interview survey, 2003.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18674745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of AMPA, kainate, and NMDA receptor subunits in cochlear and vestibular ganglia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18674745

12 December 2020

based on heuristic

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Organization of AMPA receptor subunits at a glutamate synapse: a quantitative immunogold analysis of hair cell synapses in the rat organ of Corti

1 reference

https://pubmed.ncbi.nlm.nih.gov/18674745

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2008.07.008

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Europe PubMed Central

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11 January 2020

1 reference

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11 January 2020

1 reference

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11 January 2020

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