| 1 |
34761296 | Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features. | 2022 Apr |
1 |
| 2 |
30621608 | Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations. | 2019 Jan 8 |
2 |
| 3 |
31357502 | In-Depth Bioinformatic Study of the CLDN16 Gene and Protein: Prediction of Subcellular Localization to Mitochondria. | 2019 Jul 26 |
1 |
| 4 |
27530400 | Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. | 2017 Jan |
1 |
| 5 |
27878608 | Claudins in barrier and transport function-the kidney. | 2017 Jan |
1 |
| 6 |
27191348 | Claudins and mineral metabolism. | 2016 Jul |
1 |
| 7 |
25557732 | The claudin-16 channel gene is transcriptionally inhibited by 1,25-dihydroxyvitamin D. | 2015 Jan |
2 |
| 8 |
26613020 | Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis: clinical and molecular characteristics. | 2015 Dec |
2 |
| 9 |
22846351 | [Magnesium homeostasis and its disturbances]. | 2012 Aug |
1 |
| 10 |
21848011 | A novel mutation of the claudin 16 gene in familial hypomagnesemia with hypercalciuria and nephrocalcinosis mimicking rickets. | 2011 |
3 |
| 11 |
19165416 | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family. | 2009 Aug |
1 |
| 12 |
19721377 | [Molecular physiological study of electrolyte transporters in renal tubular epithelial cells]. | 2009 Sep |
1 |
| 13 |
18253757 | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: report of three Turkish siblings. | 2008 Jun |
1 |
| 14 |
18442037 | Claudin-16 reduces the aggressive behavior of human breast cancer cells. | 2008 Sep 1 |
2 |
| 15 |
18562569 | Molecular determinants of magnesium homeostasis: insights from human disease. | 2008 Aug |
2 |
| 16 |
24459527 | Magnesium metabolism. | 2008 Dec |
2 |
| 17 |
17347984 | Hypomagnesemia and nephrocalcinosis in a patient with two heterozygous mutations in the CLDN16 gene. | 2007 Jan-Feb |
1 |
| 18 |
17551748 | Identification and subcellular localization of paracellin-1 (claudin-16) in human salivary glands. | 2007 Jul |
3 |
| 19 |
17918133 | Disorders of renal magnesium handling explain renal magnesium transport. | 2007 Sep-Oct |
2 |
| 20 |
16705067 | Unusual clinical presentation and possible rescue of a novel claudin-16 mutation. | 2006 Aug |
1 |
| 21 |
15845589 | A critical role of TRPM channel-kinase for human magnesium transport. | 2005 Jul 15 |
6 |
| 22 |
16047219 | Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations. | 2005 Oct |
1 |
| 23 |
14730510 | Inherited hypercalciuric syndromes: Dent's disease (CLC-5) and familial hypomagnesemia with hypercalciuria (paracellin-1). | 2004 Jan |
1 |
| 24 |
15001450 | Insights into the molecular nature of magnesium homeostasis. | 2004 Apr |
3 |
| 25 |
15574250 | [Familial hypomagnesemia with hypercalciuria and nephrocalcinosis. Association with ocular abnormalities]. | 2004 Dec |
2 |
| 26 |
14628289 | A novel claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting. | 2003 Dec |
1 |
| 27 |
11836293 | Genetic heterogeneity in familial renal magnesium wasting. | 2002 Feb |
2 |
| 28 |
12185465 | Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene. | 2002 Aug |
2 |
| 29 |
11380823 | Paracellin-1 is critical for magnesium and calcium reabsorption in the human thick ascending limb of Henle. | 2001 Jun |
5 |
| 30 |
11729235 | Primary gene structure and expression studies of rodent paracellin-1. | 2001 Dec |
1 |
| 31 |
10915631 | Molecular physiology and pathophysiology of tight junctions I. Tight junction structure and function: lessons from mutant animals and proteins. | 2000 Aug |
1 |