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CLDN16 gene

Known as: PCLN1, CLAUDIN 16, HOMG3 
National Institutes of Health

Related topics

Related topics

2 relations
Primary hypomagnesemia (disorder)claudin 16 protein

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
BackgroundFamilial hypomagnesaemia with hypercalciuria and nephrocalcinosis type 1 is an autosomal recessive disease… 
2016
2016
A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
2014
2014
Tight Junctional Localization of Claudin-16 Is Regulated by Syntaxin 8 in Renal Tubular Epithelial Cells*
Background: Disease-associated claudin-16 mutants cause mislocalization and decrease reabsorption of Mg2+ in the kidney. Results… 
Review
2009
Review
2009
Magnesium disorders: clinical experience and review of the literature.
Magnesium (Mg) is the most abudant living cation in prokaryotic and mammalian cells, with a total cellular concentration of 15-25… 
Highly Cited
2006
Highly Cited
2006
Phosphorylation of paracellin-1 at Ser217 by protein kinase A is essential for localization in tight junctions
Although paracellin-1 (PCLN-1) is known to have a crucial role in the control of Mg2+ reabsorption in the kidney, the molecular… 
Review
2004
Review
2004
Mg2+ transport in the kidney
Magnesium is abundant in biological systems and an important divalent cation in the human body. Mg2+ helps mediate cellular… 
2003
2003
Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss.
BACKGROUND Based on genetic studies in families with hereditary renal Mg(2+) reabsorption disorders, several genes were shown to… 
2003
2003
Exclusion of mutations in FXYD 2 , CLDN 16 and SLC 12 A 3 in two families with primary renal Mg 2 q loss
Background. Based on genetic studies in families with hereditary renal Mg reabsorption disorders, several genes were shown to be… 
2001
2001
Literature abstracts
2000
2000
Functional evidence that paracellin-1 is critical for calcium and magnesium reabsorption in the human thick ascending limb of henle
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