(Q28244149)

English

Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease

scientific article (publication date: 2011)

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scholarly article

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Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease (English)

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object named as

Muhammad Naeem

1

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author name string

Sofia Hussain

2

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Naureen Akhtar

3

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language of work or name

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publication date

2011

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American Journal of Nephrology

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34

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3

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241-8

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The human paracellin-1 gene (hPCLN-1): renal epithelial cell-specific expression and regulation

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Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

1 reference

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Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

1 reference

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The roles of claudin superfamily proteins in paracellular transport

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Kidney claudin-19: localization in distal tubules and collecting ducts and dysregulation in polycystic renal disease

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Rho signaling and tight junction functions

1 reference

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Biology of claudins.

1 reference

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The role of tight junctions in paracellular ion transport in the renal tubule: lessons learned from a rare inherited tubular disorder

1 reference

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Renal, ocular, and neuromuscular involvements in patients with CLDN19 mutations

1 reference

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Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

1 reference

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Paracellin-1 and the modulation of ion selectivity of tight junctions

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Comparative effects of potassium chloride and bicarbonate on thiazide-induced reduction in urinary calcium excretion

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10.1159/000330854

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