[HTML][HTML] Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone disease

JN Curry, M Saurette, M Askari, L Pei… - The Journal of …, 2020 - Am Soc Clin Investig
The major risk factor for kidney stone disease is idiopathic hypercalciuria. Recent evidence
implicates a role for defective calcium reabsorption in the renal proximal tubule. We …

Claudins in barrier and transport function—the kidney

Y Gong, J Hou - Pflügers Archiv-European Journal of Physiology, 2017 - Springer
Claudins are discovered to be key players in renal epithelial physiology. They are involved
in developmental, physiological, and pathophysiological differentiation. In the glomerular …

[HTML][HTML] Claudin-12 knockout mice demonstrate reduced proximal tubule calcium permeability

A Plain, W Pan, D O'Neill, M Ure, MR Beggs… - International journal of …, 2020 - mdpi.com
The renal proximal tubule (PT) is responsible for the reabsorption of approximately 65% of
filtered calcium, primarily via a paracellular pathway. However, which protein (s) contribute …

Claudin-2 and claudin-12 form independent, complementary pores required to maintain calcium homeostasis

MR Beggs, K Young, W Pan… - Proceedings of the …, 2021 - National Acad Sciences
Calcium (Ca2+) homeostasis is maintained through coordination between intestinal
absorption, renal reabsorption, and bone remodeling. Intestinal and renal (re) absorption …

Claudins and the kidney.

AS Yu - Journal of the American Society of Nephrology: JASN, 2014 - europepmc.org
Claudins are tight-junction membrane proteins that function as both pores and barriers in the
paracellular pathway in epithelial cells. In the kidney, claudins determine the permeability …

[HTML][HTML] Deletion of claudin-10 rescues claudin-16–deficient mice from hypomagnesemia and hypercalciuria

T Breiderhoff, N Himmerkus, H Drewell, A Plain… - Kidney international, 2018 - Elsevier
The tight junction proteins claudin-10 and-16 are crucial for the paracellular reabsorption of
cations along the thick ascending limb of Henle's loop in the kidney. In patients, mutations in …

[HTML][HTML] Claudins in renal physiology and pathology

C Prot-Bertoye, P Houillier - Genes, 2020 - mdpi.com
Claudins are integral proteins expressed at the tight junctions of epithelial and endothelial
cells. In the mammalian kidney, every tubular segment express a specific set of claudins that …

[PDF][PDF] A novel claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting

D Müller, PJ Kausalya, F Claverie-Martin, IC Meij… - The American Journal of …, 2003 - cell.com
Mutations in the gene coding for the renal tight junction protein claudin 16 cause familial
hypomagnesemia with hypercalciuria and nephrocalcinosis, an autosomal recessive …

Claudins and the kidney

J Hou, M Rajagopal, ASL Yu - Annual review of physiology, 2013 - annualreviews.org
Claudins are tight junction membrane proteins that regulate paracellular permeability of
renal epithelia to small ions, solutes, and water. Claudins interact within the cell membrane …

Renal salt wasting and chronic dehydration in claudin-7-deficient mice

R Tatum, Y Zhang, K Salleng, Z Lu… - American Journal …, 2010 - journals.physiology.org
Claudin-7, a member of the claudin family, is highly expressed in distal nephrons of kidneys
and has been reported to be involved in the regulation of paracellular Cl− permeability in …