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SLC26A4 gene

Known as: SLC26A4, PENDRIN, PDS 
National Institutes of Health

Related topics

Related topics

1 relation
Pendred's syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Genetic Screening of GJB2 and SLC26A4 in Korean Cochlear Implantees: Experience of Soree Ear Clinic
Objectives Genetic hearing loss is highly heterogeneous and more than 100 genes are predicted to cause this disorder in humans… 
Review
2012
Review
2012
Indian Social Safety Net Programs as Platforms for Introducing Wheat Flour Fortification: A Case Study of Gujarat, India
Background Micronutrient deficiencies exact an enormous health burden on India. The release of the National Family Health Survey… 
2011
2011
Impact of Bicarbonate, Ammonium Chloride, and Acetazolamide on Hepatic and Renal SLC26A4 Expression
SLC26A4 encodes pendrin, a transporter exchanging anions such as chloride, bicarbonate, and iodide. Loss of function mutations of… 
2010
2010
A coherent organization of differentiation proteins is required to maintain an appropriate thyroid function in the Pendred thyroid.
CONTEXT Pendred syndrome is caused by mutations in the gene coding for pendrin, an apical Cl-/I- exchanger. OBJECTIVE To… 
Review
2010
Review
2010
Pendrin and sodium channels: relevance to hypertension.
Renal intercalated cells mediate the secretion or the absorption of OH-/H+ equivalents and Cl- in the distal convoluted tubule… 
2008
2008
Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene.
Pendrin, a Cl(-)/anion exchanger encoded by the gene PDS, is highly expressed in the kidney, thyroid, and inner ear epithelia and… 
2006
2006
Distribution of pendrin in the organ of Corti of mice observed by electron immunomicroscopy
The distribution of pendrin, which is encoded by the Pendred syndrome gene, has been investigated immunohistochemically in the… 
2005
2005
Expression of pendrin in benign and malignant human thyroid tissues
The Pendred syndrome gene (PDS) encodes a transmembrane protein, pendrin, which is expressed in follicular thyroid cells and… 
2004
2004
The immunohistochemical analysis of pendrin in the mouse inner ear
2000
2000
A novel mutation in the pendrin gene associated with Pendred's syndrome
Pendred's syndrome is an autosomal recessive disorder characterized by goitre, sensorineural deafness and iodide organification… 
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