CLDN16 gene

Known as: PCLN1, CLAUDIN 16, HOMG3 
 

Topic mentions per year

Topic mentions per year

2003-2018
02420032018

Papers overview

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2011
2011
RATIONALE Hyperaldosteronism, important in hypertension, is associated with electrolyte alterations, including hypomagnesemia… (More)
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Highly Cited
2009
Highly Cited
2009
Claudins are tight junction integral membrane proteins that are key regulators of the paracellular pathway. Defects in claudin-16… (More)
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2009
2009
Tight junction (TJ) properties are determined by membrane protein complexes of neighboring cells that form both a barrier and a… (More)
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2008
2008
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive tubular disorder caused by… (More)
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Highly Cited
2008
Highly Cited
2008
Tight junctions (TJs) play a key role in mediating paracellular ion reabsorption in the kidney. Familial hypomagnesemia with… (More)
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2008
2008
BACKGROUND Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC) is an autosomal recessive disorder of renal… (More)
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2006
2006
Although paracellin-1 (PCLN-1) is known to have a crucial role in the control of Mg2+ reabsorption in the kidney, the molecular… (More)
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2006
2006
BACKGROUND Hydrochlorothiazide (HCT) is applied in the therapy of familial hypomagnesaemia with hypercalciuria and… (More)
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2005
2005
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), an autosomal recessive renal tubular disorder, is… (More)
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2003
2003
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC, MIN 248250) is a rare autosomal recessive tubular… (More)
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