(Q30479480)

20 August 2017

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities (English)

1 reference

20 August 2017

1

1 reference

20 August 2017

7

Debra Newman

1 reference

20 August 2017

Mark I Rosenblatt

2

1 reference

20 August 2017

Charles Kim

3

1 reference

20 August 2017

Gary C Galbraith

4

1 reference

20 August 2017

Sherri M Jones

5

1 reference

20 August 2017

Liyo Kao

6

1 reference

20 August 2017

Weixin Liu

8

1 reference

20 August 2017

Stacey Yeh

9

1 reference

20 August 2017

Alexander Pushkin

10

1 reference

20 August 2017

Natalia Abuladze

11

1 reference

20 August 2017

Ira Kurtz

12

1 reference

20 August 2017

language of work or name

English

0 references

publication date

8 July 2009

1 reference

Journal of Biological Chemistry

20 August 2017

1 reference

20 August 2017

284

1 reference

20 August 2017

39

1 reference

20 August 2017

26882-26896

1 reference

Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

A mouse model with postnatal endolymphatic hydrops and hearing loss

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Mutational spectrum of the SLC4A11 gene in autosomal recessive congenital hereditary endothelial dystrophy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Functional significance of channels and transporters expressed in the inner ear and kidney

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Genetic analysis of two Indian families affected with congenital hereditary endothelial dystrophy: two novel mutations in SLC4A11

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

20 June 2018

Gene trap mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Aquaporins and Meniere's disease.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Impaired growth and neurological abnormalities in branched-chain alpha-keto acid dehydrogenase kinase-deficient mice.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

SLC4 base (HCO3 -, CO3 2-) transporters: classification, function, structure, genetic diseases, and knockout models

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Hypothesis: could Meniere's disease be a channelopathy?

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Arabidopsis boron transporter for xylem loading.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Dynamics of noise-induced cellular injury and repair in the mouse cochlea

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Corneal dystrophy and perceptive deafness (Harboyan syndrome): CDPD1 maps to 20p13

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

High-level and high-throughput recombinant protein production by transient transfection of suspension-growing human 293-EBNA1 cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Spiral ligament pathology: a major aspect of age-related cochlear degeneration in C57BL/6 mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Between sound and perception: reviewing the search for a neural code

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

A further observation of corneal dystrophy and perceptive deafness in two siblings.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Interpretation of the vertex short-latency acoustic response: A study of single neurons in the brain stem

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Auditory brainstem volume-conducted responses: origins in the laboratory mouse

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Vital staining of the corneal endothelium with Rose Bengal and Alizarin Red S

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785376

Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy

20 June 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Time course of auditory impairment in mice lacking the electroneutral sodium bicarbonate cotransporter NBC3 (slc4a7).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Murine auditory brainstem evoked response: putative two-channel differentiation of peripheral and central neural pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Auditory evoked responses in the rat: transverse mastoid needle electrodes register before cochlear nucleus and do not reflect later inferior colliculus activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Borate transport and cell growth and proliferation. Not only in plants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M109.008102

Ultrastructural co-localization of cochlin and type II collagen in the rat semicircular canal

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19586905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Endothelial repair in the rat cornea

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19586905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Histopathology of the peripheral vestibular system after cochlear implantation in the human

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19586905

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1074/JBC.M109.008102

1 reference

20 August 2017

1 reference

20 August 2017

1 reference