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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.
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… 
2013
2013
Ocular involvement in a child with medullary nephrocalcinosis: Answers
1. Because of the diagnostic triad composed of hypomagnesemia, hypercalciuria, and nephrocalcinosis, familial hypomagnesemia with… 
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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