Inching toward a Greater Understanding of Genetic Hypercalciuria: The Role of Claudins.
作者信息
Shah Ronak Jagdeep, Lieske John C
机构信息
Division of Nephrology and Hypertension, Mayo Clinic College of Medicine, Rochester, Minnesota.
出版信息
Clin J Am Soc Nephrol. 2018 Oct 8;13(10):1460-1462. doi: 10.2215/CJN.10030818. Epub 2018 Sep 19.
Abstract
摘要
相似文献
1
Inching toward a Greater Understanding of Genetic Hypercalciuria: The Role of Claudins.逐步深入了解遗传性高钙尿症：紧密连接蛋白的作用
Clin J Am Soc Nephrol. 2018 Oct 8;13(10):1460-1462. doi: 10.2215/CJN.10030818. Epub 2018 Sep 19.
2
Claudins and nephrolithiasis.紧密连接蛋白与肾结石病。
Curr Opin Nephrol Hypertens. 2018 Jul;27(4):268-276. doi: 10.1097/MNH.0000000000000426.
3
Role of claudins in idiopathic hypercalciuria and renal lithiasis.紧密连接蛋白在特发性高钙尿症和肾结石中的作用。
Int Urol Nephrol. 2022 Sep;54(9):2197-2204. doi: 10.1007/s11255-022-03119-2. Epub 2022 Jan 27.
4
An unusual patient with hypercalciuria, recurrent nephrolithiasis, hypomagnesemia and G227R mutation of Paracellin-1. An unusual patient with hypercalciuria and hypomagnesemia unresponsive to thiazide diuretics.一名患有高钙尿症、复发性肾结石、低镁血症且存在Paracellin-1基因G227R突变的特殊患者。一名患有高钙尿症和低镁血症且对噻嗪类利尿剂无反应的特殊患者。
Horm Res. 2006;66(4):175-81. doi: 10.1159/000094253. Epub 2006 Jun 27.
5
The role of claudin in hypercalciuric nephrolithiasis.Claudin 在高钙尿性肾结石中的作用。
Curr Urol Rep. 2013 Feb;14(1):5-12. doi: 10.1007/s11934-012-0289-2.
6
Molecular mechanisms altering tubular calcium reabsorption.改变管状钙重吸收的分子机制。
Pediatr Nephrol. 2022 Apr;37(4):707-718. doi: 10.1007/s00467-021-05049-0. Epub 2021 Apr 1.
7
Claudins and mineral metabolism.紧密连接蛋白与矿物质代谢。
Curr Opin Nephrol Hypertens. 2016 Jul;25(4):308-13. doi: 10.1097/MNH.0000000000000239.
8
A variant in a cis-regulatory element enhances claudin-14 expression and is associated with pediatric-onset hypercalciuria and kidney stones.顺式调控元件中的一个变体增强了claudin-14的表达，并与儿童期高钙尿症和肾结石有关。
Hum Mutat. 2017 Jun;38(6):649-657. doi: 10.1002/humu.23202. Epub 2017 Mar 21.
9
Genetic causes of hypercalciuric nephrolithiasis.高钙尿性肾结石的遗传病因。
Pediatr Nephrol. 2009 Dec;24(12):2321-32. doi: 10.1007/s00467-008-0807-0. Epub 2008 Apr 30.
10
A novel CLDN16 mutation in a large family with familial hypomagnesaemia with hypercalciuria and nephrocalcinosis.一个患有家族性低镁血症伴高钙尿症和肾钙质沉着症的大家庭中的一种新型CLDN16突变。
BMC Res Notes. 2013 Dec 10;6:527. doi: 10.1186/1756-0500-6-527.
引用本文的文献
1
Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease.综合基因分析揭示单基因尿路结石病的复杂性。
Kidney Int Rep. 2021 Sep 8;6(11):2862-2884. doi: 10.1016/j.ekir.2021.08.033. eCollection 2021 Nov.
2
Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.钙、镁和尿酸24小时尿排泄量的全基因组关联研究
Mayo Clin Proc Innov Qual Outcomes. 2019 Nov 22;3(4):448-460. doi: 10.1016/j.mayocpiqo.2019.08.007. eCollection 2019 Dec.
Zotero 插件