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Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium

Claudins are tight junction integral membrane proteins that are key regulators of the paracellular pathway. Defects in claudin-16 (CLDN16) and CLDN19 function result in the inherited human renal disorder familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC). Previous studies showe...

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Main Authors: Hou, Jianghui, Renigunta, Aparna, Gomes, Antonio S., Hou, Mingli, Paul, David L., Waldegger, Siegfried, Goodenough, Daniel A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: National Academy of Sciences 2009
Ábhair:
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC2741254/
https://ncbi.nlm.nih.gov/pubmed/19706394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0907724106
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