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A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies
(American Chemical Society, 2011-03)
Mutations in the SLC4A11 protein, reported as a sodium-coupled borate transporter of the human plasma membrane, are responsible for three corneal dystrophies (CD): congenital hereditary endothelial dystrophy type 2, Harboyan ...
Iron homeostasis in the lung
(Sociedad de Biología de Chile, 2006)
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies
(American Physiological Society, 2016-08)
SLC4A11, a member of the SLC4 family of bicarbonate transporters, is a widely expressed integral membrane protein, abundant in kidney and cornea. Mutations of SLC4A11 cause some cases of the blinding corneal dystrophies, ...
Decreased Expression of the Human Urea Transporter SLC14A1 in Bone is Induced by Cytokines and Stimulates Adipogenesis of Mesenchymal Progenitor Cells
(Johann Ambrosius Barth Verlag Medizinverlage Heidelberg Gmbh, 2020-09)
The human urea transporter SLC14A1 (HUT11/UT-B) has been suggested as a marker for the adipogenic differentiation of bone cells with a relevance for bone diseases. We investigated the function of SLC14A1 in different cells ...
SLC2A4 gene: a promising target for pharmacogenomics of insulin resistance
(Ashley PublicationsLondres, 2013-06)