-
Pendrin is an
anion exchange protein that in
humans is
encoded by the SLC26A4 gene (solute
carrier family 26,
member 4).
Pendrin was
initially identified...
-
Kirsten M.; Nielsen, Søren (2002-10-01). "Immunocytochemical
localization of
pendrin in
intercalated cell
subtypes in rat and
mouse kidney".
American Journal...
- It has been
linked to
mutations in the PDS gene,
which codes for the
pendrin protein (solute
carrier family 26,
member 4, SLC26A4). The gene is located...
- side,
iodide is
shuttled across the
apical membrane into the
colloid via
pendrin,
after which thyroid peroxidase oxidizes iodide to
atomic iodine (I) or...
- α-ketoglutarate's
binding to, and
thereby inhibits its
activation of OXGR1. The
pendrin protein promotes the
electroneutral exchange of
tissue chloride (Cl−) for...
- then
travels from
within the cell into the lumen,
through the
action of
pendrin, an iodide-chloride antiporter. In the
follicular lumen, the
iodide is...
- tubule,
epithelial sodium channels, and chloride-bicarbonate
exchanger pendrin. This will
promote sodium reabsorption and
fluid retention,
causing diuretic...
-
iodide is
secreted into the
colloid by the chloride/iodide
transporter pendrin.
Thyroid diverticulum List of
human cell
types derived from the germ layers...
-
Resting and IL-4-Stimulated
Human Bronchial Epithelial Cells: Role of
Pendrin and
Anion Channels".
Journal of Immunology. 178 (8): 5144–5153. doi:10...
-
attributable entirely to
chloride depletion,
which leads to a
failure of
pendrin, a chloride/bicarbonate
exchanger in the
collecting duct.
Diagnosis of...
