[HTML][HTML] Sgk1 sensitive pendrin expression in murine platelets
L Pelzl, H Fakhri, AT Umbach, M Gawaz… - Cellular physiology and …, 2013 - karger.com
Background: The anion exchanger pendrin (SLC26A4) is required for proper development
of the inner ear, and contributes to iodide organification in thyroid glands as well as anion …
of the inner ear, and contributes to iodide organification in thyroid glands as well as anion …
DOCA sensitive pendrin expression in kidney, heart, lung and thyroid tissues
Abstract Background/Aims: Pendrin (SLC26A4), a transporter accomplishing anion
exchange, is expressed in inner ear, thyroid gland, kidneys, lung, liver and heart. Loss or …
exchange, is expressed in inner ear, thyroid gland, kidneys, lung, liver and heart. Loss or …
New insights into the role of pendrin (SLC26A4) in inner ear fluid homeostasis
LA Everett - Epithelial Anion Transport in Health and Disease …, 2006 - Wiley Online Library
For over 100 years after the first description of the disorder, the molecular pathology
underlying the deafness and thyroid pathology in Pendred syndrome (PS) remained …
underlying the deafness and thyroid pathology in Pendred syndrome (PS) remained …
The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currents
S Dossena, A Maccagni, V Vezzoli… - European journal of …, 2005 - academic.oup.com
Abstract Objective The SLC26A4 protein (pendrin) seems to be involved in the exchange of
chloride with other anions, therefore being responsible for iodide organification in the thyroid …
chloride with other anions, therefore being responsible for iodide organification in the thyroid …
Molecular and functional characterization of human pendrin and its allelic variants
Abstract Pendrin (SLC26A4, PDS) is an electroneutral anion exchanger transporting I-, Cl-,
HCO3-, OH-, SCN-and formate. In the thyroid, pendrin is expressed at the apical membrane …
HCO3-, OH-, SCN-and formate. In the thyroid, pendrin is expressed at the apical membrane …
Mouse models reveal the role of pendrin in the inner ear
P Wangemann, AJ Griffith - The Role of Pendrin in Health and Disease …, 2017 - Springer
Abstract In 1896, Vaughan Pendred, MD, wrote a case report about two siblings that
presented with hearing loss and goiter. This initial report was followed over the next 100 …
presented with hearing loss and goiter. This initial report was followed over the next 100 …
Functional characterization of pendrin in a polarized cell system: evidence for pendrin-mediated apical iodide efflux
MP Gillam, AR Sidhaye, EJ Lee, J Rutishauser… - Journal of Biological …, 2004 - ASBMB
Pendred's syndrome is an autosomal recessive disorder characterized by sensorineural
deafness, goiter, and impaired iodide organification. It is caused by mutations in the …
deafness, goiter, and impaired iodide organification. It is caused by mutations in the …
Pendred syndrome
JL Wémeau, P Kopp - Best Practice & Research Clinical Endocrinology & …, 2017 - Elsevier
Pendred syndrome is an autosomal recessive disorder that is classically defined by the
combination of sensorineural deafness/hearing impairment, goiter, and an abnormal …
combination of sensorineural deafness/hearing impairment, goiter, and an abnormal …
Pendrin function in airway epithelia
C Nofziger, S Dossena, S Suzuki, K Izuhara… - Cellular Physiology and …, 2011 - karger.com
The expression and function of the anion exchanger pendrin (SLC26A4) was thought to be
limited mainly to the inner ear, kidney and thyroid. Recent data indicates that pendrin is also …
limited mainly to the inner ear, kidney and thyroid. Recent data indicates that pendrin is also …
Impact of bicarbonate, ammonium chloride, and acetazolamide on hepatic and renal SLC26A4 expression
I Alesutan, A Daryadel, N Mohebbi, L Pelzl… - Cellular physiology and …, 2011 - karger.com
SLC26A4 encodes pendrin, a transporter exchanging anions such as chloride, bicarbonate,
and iodide. Loss of function mutations of SLC26A4 cause Pendred syndrome characterized …
and iodide. Loss of function mutations of SLC26A4 cause Pendred syndrome characterized …