SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria.
about
SLC4A11 and the Pathophysiology of Congenital Hereditary Endothelial DystrophyThe divergence, actions, roles, and relatives of sodium-coupled bicarbonate transportersDepletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line.Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.The SLC4 family of bicarbonate (HCO₃⁻) transporters.Hearing disability in patients with Fuchs' endothelial corneal dystrophy: unrecognized co-pathology?Molecular bases of corneal endothelial dystrophies.Human SLC4A11 Is a Novel NH3/H+ Co-transporter.The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11.Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell culture.Ion transport function of SLC4A11 in corneal endothelium.SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulator.Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.Mis-trafficking of bicarbonate transporters: implications to human diseases.Molecular physiology of the medullary collecting duct.Na(+) dependent acid-base transporters in the choroid plexus; insights from slc4 and slc9 gene deletion studies.Corneal dystrophies and genetics in the International Committee for Classification of Corneal Dystrophies era: a review.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.Deficiency in the α1 subunit of Na+/K+-ATPase enhances the anti-proliferative effect of high osmolality in nucleus pulposus intervertebral disc cells.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.H(OH), H(OH), H(OH): a holiday perspective. Focus on "Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH- conductance pathway that is stimulated by rises in intracellular and extracellular pH".Water Transport Mediated by Other Membrane Proteins.
P2860
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P2860
SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria.
description
2010 nî lūn-bûn
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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
SLC4A11 prevents osmotic imbal ...... trophy, deafness, and polyuria
@nl
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@ast
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@en
type
label
SLC4A11 prevents osmotic imbal ...... trophy, deafness, and polyuria
@nl
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@ast
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@en
prefLabel
SLC4A11 prevents osmotic imbal ...... trophy, deafness, and polyuria
@nl
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@ast
SLC4A11 prevents osmotic imbal ...... rophy, deafness, and polyuria.
@en
P2093
P2860
P356
P1476
SLC4A11 prevents osmotic imbal ...... trophy, deafness, and polyuria
@en
P2093
Andrea Olbrich
Hannes Maier
Henning Fröhlich
Nicole Gröger
Sawa Kostin
Thomas Boettger
P2860
P304
14467-14474
P356
10.1074/JBC.M109.094680
P407
P50
P577
2010-02-25T00:00:00Z