Background: Kidney stone disease is one of the most common disorders of urinary tract, manifesting with high clinical and genetic heterogeneity in population. Sestrin 2 is involved in many essential processes, especially oxidative and genotoxic stress. Regarding the importance of oxidative stress pathway deregulation in systemic diseases such as kidney disorders, this study was conducted to investigate the association between rs7526084 3′ downstream polymorphism of the sestrin 2 gene and risk of kidney stone in south Iranian patients. Materials and Methods: In this case-control study, 150 patients with kidney stone disease and 180 age- and gender-matched healthy individuals were participated from March to December 2015. Genotyping of the ...
Background: Inflammation may be one cause of nephrolithiasis and the interleukin-18 (IL-18) encoding...
<div><p>Kidney stone disease (KSD) is a major clinical problem imposing a large burden for both heal...
Abstract Cystinuria (OMIM 220100) is an inborn congenital disorder characterised by a defective cyst...
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein-...
There is strong evidence for a familial basis to renal stone disease. However, apart from a number o...
Kidney stone disease (nephrolithiasis) is a common problem that can be associated with alterations i...
To access publisher's full text version of this article click on the hyperlink belowKidney stone dis...
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein ...
Kidney stone disease is a complex disorder with a strong genetic component. We conducted a genome-wi...
OBJECTIVE: Primary hyperparathyroidism (PHPT) is often complicated by kidney stones. Hypercalciuria ...
Copyright © 2013 Paul A. Dawson et al.This is an open access article distributed under the Creative ...
Renal stone formation is a common multifactorial disorder, of unknown etiology, with an established ...
Purpose To study whether −160 C > A (rs16260) and −347 G > GA (rs5030625) single nucleotide polymorp...
Contains fulltext : 81561.pdf (publisher's version ) (Closed access)Kidney stone d...
Kidney stones are a global health problem, incurring massive health costs annually. Why stones recur...
Background: Inflammation may be one cause of nephrolithiasis and the interleukin-18 (IL-18) encoding...
<div><p>Kidney stone disease (KSD) is a major clinical problem imposing a large burden for both heal...
Abstract Cystinuria (OMIM 220100) is an inborn congenital disorder characterised by a defective cyst...
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein-...
There is strong evidence for a familial basis to renal stone disease. However, apart from a number o...
Kidney stone disease (nephrolithiasis) is a common problem that can be associated with alterations i...
To access publisher's full text version of this article click on the hyperlink belowKidney stone dis...
We previously reported the association between prothrombin (F2), encoding a stone inhibitor protein ...
Kidney stone disease is a complex disorder with a strong genetic component. We conducted a genome-wi...
OBJECTIVE: Primary hyperparathyroidism (PHPT) is often complicated by kidney stones. Hypercalciuria ...
Copyright © 2013 Paul A. Dawson et al.This is an open access article distributed under the Creative ...
Renal stone formation is a common multifactorial disorder, of unknown etiology, with an established ...
Purpose To study whether −160 C > A (rs16260) and −347 G > GA (rs5030625) single nucleotide polymorp...
Contains fulltext : 81561.pdf (publisher's version ) (Closed access)Kidney stone d...
Kidney stones are a global health problem, incurring massive health costs annually. Why stones recur...
Background: Inflammation may be one cause of nephrolithiasis and the interleukin-18 (IL-18) encoding...
<div><p>Kidney stone disease (KSD) is a major clinical problem imposing a large burden for both heal...
Abstract Cystinuria (OMIM 220100) is an inborn congenital disorder characterised by a defective cyst...