sulfate transporter

Known as: pendrin 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2017
010203019992017

Papers overview

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Highly Cited
2004
Highly Cited
2004
Slc26a4 (Pds, pendrin) is an anion transporter expressed in the apical region of type B and non-A, non-B intercalated cells of… (More)
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2004
2004
Pendred's syndrome is an autosomal recessive disorder characterized by sensorineural deafness, goiter, and impaired iodide… (More)
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Highly Cited
2003
Highly Cited
2003
Pendrin is an anion exchanger expressed in type B intercalated cells of the cortical collecting duct (CCD). Whether pendrin… (More)
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Highly Cited
2003
Highly Cited
2003
Pendrin is an anion exchanger expressed along the apical plasma membrane and apical cytoplasmic vesicles of type B and of non-A… (More)
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2003
2003
The anion exchanger pendrin is present in the apical plasma membrane of type B and non-A-non-B intercalated cells of the cortical… (More)
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Highly Cited
2003
Highly Cited
2003
Ammonia is both produced and transported by renal epithelial cells, and it regulates renal ion transport. Recent studies have… (More)
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Highly Cited
2002
Highly Cited
2002
Aberrant HCO(3)(-) transport is a hallmark of cystic fibrosis (CF) and is associated with aberrant Cl(-)-dependent HCO(3… (More)
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Highly Cited
2001
Highly Cited
2001
Pendrin is an anion transporter encoded by the PDS/Pds gene. In humans, mutations in PDS cause the genetic disorder Pendred… (More)
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Highly Cited
2001
Highly Cited
2001
The identities of the apical Cl-/base exchangers in kidney proximal tubule and cortical collecting duct (CCD) cells remain… (More)
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Highly Cited
1999
Highly Cited
1999
Pendred syndrome is the most common form of syndromic deafness and characterized by congenital sensorineural hearing loss and… (More)
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