Associated Papers
Association of TRPV5 gene polymorphism with calcium urolithiasis: a case-control study from West Bengal, India.
Mitra P et al.
World Journal of Urology, 2020
Modeling the structural and dynamical changes of the epithelial calcium channel TRPV5 caused by the A563T variation based on the structure of TRPV6.
Wang L et al.
Journal of Biomolecular Structure & Dynamics, 2019
The L530R variation associated with recurrent kidney stones impairs the structure and function of TRPV5.
Wang L et al.
Biochemical and Biophysical Research Communications, 2017
Molecular Modeling of the Structural and Dynamical Changes in Calcium Channel TRPV5 Induced by the African-Specific A563T Variation.
Wang L et al.
Biochemistry, 2016
A Single Nucleotide Polymorphism (rs4236480) in TRPV5 Calcium Channel Gene Is Associated with Stone Multiplicity in Calcium Nephrolithiasis Patients.
Khaleel A et al.
Mediators of Inflammation, 2015
TRPV5: a Ca(2+) channel for the fine-tuning of Ca(2+) reabsorption.
Na T et al.
Handbook of Experimental Pharmacology, 2014
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.
Loh NY et al.
Plos One, 2013
Why is hypercalciuria absent at diagnosis in some children with ATP6V1B1 mutation?
Tsai HY et al.
Pediatric Nephrology (berlin, Germany), 2011
The A563T variation of the renal epithelial calcium channel TRPV5 among African Americans enhances calcium influx.
Na T et al.
American Journal of Physiology. Renal Physiology, 2009
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