Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities. - Wikidata - wikimedia - TriplyDB

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

http://www.wikidata.org/entity/Q30479480

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Fuchs endothelial corneal dystrophy: current perspectives SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial Dystrophy SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria.Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transporters Immunocytochemical distribution of WARP (von Willebrand A domain-related protein) in the inner ear.Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line.Glutaminolysis is Essential for Energy Production and Ion Transport in Human Corneal Endothelium.Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.The SLC4 family of bicarbonate (HCO₃⁻) transporters.Fuchs endothelial corneal dystrophy Human SLC4A11-C functions as a DIDS-stimulatable H⁺(OH⁻) permeation pathway: partial correction of R109H mutant transport.Molecular bases of corneal endothelial dystrophies.Human SLC4A11 Is a Novel NH3/H+ Co-transporter.The genetics of Fuchs' corneal dystrophy SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulator.Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia.Mis-trafficking of bicarbonate transporters: implications to human diseases.Na(+) dependent acid-base transporters in the choroid plexus; insights from slc4 and slc9 gene deletion studies.Immunocytochemical localization of the translocase of the outer mitochondrial membrane (Tom20) in the human cochlea.Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies.Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants.Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy.Vps35-deficiency impairs SLC4A11 trafficking and promotes corneal dystrophy.Dietary supplementation of boron differentially alters expression of borate transporter (NaBCl) mRNA by jejunum and kidney of growing pigs.Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH- conductance pathway that is stimulated by rises in intracellular and extracellular pH.

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P2860

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

http://www.wikidata.org/entity/Q30479480

description

2009 nî lūn-bûn

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2009 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2009 թվականի հուլիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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JBC.M109.008102

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Journal of Biological Chemistry

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Slc4a11 gene disruption in mice: cellular targets of sensorineuronal abnormalities.

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P2093

Alexander Pushkin

http://www.w3.org/2001/XMLSchema#string

Charles Kim

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Debra Newman

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Gary C Galbraith

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Ira Kurtz

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Liyo Kao

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Mark I Rosenblatt

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Natalia Abuladze

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Sherri M Jones

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Stacey Yeh

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P2860

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

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

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

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

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

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

Arabidopsis boron transporter for xylem loading.

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

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

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

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26882-26896

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10.1074/JBC.M109.008102

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39

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