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Journal Abstract Search
229 related items for PubMed ID: 26089600
1. A Single Nucleotide Polymorphism (rs4236480) in TRPV5 Calcium Channel Gene Is Associated with Stone Multiplicity in Calcium Nephrolithiasis Patients. Khaleel A, Wu MS, Wong HS, Hsu YW, Chou YH, Chen HY. Mediators Inflamm; 2015; 2015():375427. PubMed ID: 26089600 [Abstract] [Full Text] [Related]
2. TRPV5 in renal tubular calcium handling and its potential relevance for nephrolithiasis. van der Wijst J, van Goor MK, Schreuder MF, Hoenderop JG. Kidney Int; 2019 Dec; 96(6):1283-1291. PubMed ID: 31471161 [Abstract] [Full Text] [Related]
3. Association of TRPV5, CASR, and CALCR genetic variants with kidney stone disease susceptibility in Egyptians through main effects and gene-gene interactions. Ali FT, El-Azeem EMA, Hekal HFA, El-Gizawy MM, Sayed MS, Mandoh AY, Soliman AF. Urolithiasis; 2022 Dec; 50(6):701-710. PubMed ID: 36088585 [Abstract] [Full Text] [Related]
5. A polymorphism of the ORAI1 gene is associated with the risk and recurrence of calcium nephrolithiasis. Chou YH, Juo SH, Chiu YC, Liu ME, Chen WC, Chang CC, Chang WP, Chang JG, Chang WC. J Urol; 2011 May; 185(5):1742-6. PubMed ID: 21420116 [Abstract] [Full Text] [Related]
6. A genetic polymorphism (rs17251221) in the calcium-sensing receptor gene (CASR) is associated with stone multiplicity in calcium nephrolithiasis. Chou YH, Woon PY, Chen WC, Hsu YW, Chang JM, Hwang DY, Chiu YC, Kuo HC, Chang WP, Hou MF, Liu ME, Chang JG, Chang WC. PLoS One; 2011 May; 6(9):e25227. PubMed ID: 21966463 [Abstract] [Full Text] [Related]
7. Mucin-1 Increases Renal TRPV5 Activity In Vitro, and Urinary Level Associates with Calcium Nephrolithiasis in Patients. Nie M, Bal MS, Yang Z, Liu J, Rivera C, Wenzel A, Beck BB, Sakhaee K, Marciano DK, Wolf MT. J Am Soc Nephrol; 2016 Nov; 27(11):3447-3458. PubMed ID: 27036738 [Abstract] [Full Text] [Related]
8. The melatonin receptor 1A (MTNR1A) gene is associated with recurrent and idiopathic calcium nephrolithiasis. Esposito T, Rendina D, Aloia A, Formicola D, Magliocca S, De Filippo G, Muscariello R, Mossetti G, Gianfrancesco F, Strazzullo P. Nephrol Dial Transplant; 2012 Jan; 27(1):210-8. PubMed ID: 21652546 [Abstract] [Full Text] [Related]
9. Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5. Loh NY, Bentley L, Dimke H, Verkaart S, Tammaro P, Gorvin CM, Stechman MJ, Ahmad BN, Hannan FM, Piret SE, Evans H, Bellantuono I, Hough TA, Fraser WD, Hoenderop JG, Ashcroft FM, Brown SD, Bindels RJ, Cox RD, Thakker RV. PLoS One; 2013 Jan; 8(1):e55412. PubMed ID: 23383183 [Abstract] [Full Text] [Related]
10. Role of the calcium-sensing receptor in reducing the risk for calcium stones. Renkema KY, Bindels RJ, Hoenderop JG. Clin J Am Soc Nephrol; 2011 Aug; 6(8):2076-82. PubMed ID: 21784822 [Abstract] [Full Text] [Related]
11. TRPV5: a Ca(2+) channel for the fine-tuning of Ca(2+) reabsorption. Na T, Peng JB. Handb Exp Pharmacol; 2014 Aug; 222():321-57. PubMed ID: 24756712 [Abstract] [Full Text] [Related]
12. Association of TRPV5 gene polymorphism with calcium urolithiasis: a case-control study from West Bengal, India. Mitra P, Pal DK, Das M. World J Urol; 2020 May; 38(5):1311-1322. PubMed ID: 31428848 [Abstract] [Full Text] [Related]
13. 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, Holmes RP, Peng JB. J Biomol Struct Dyn; 2019 Aug; 37(13):3506-3512. PubMed ID: 30175942 [Abstract] [Full Text] [Related]
14. Study of the association between ITPKC genetic polymorphisms and calcium nephrolithiasis. Kan WC, Chou YH, Chiu SJ, Hsu YW, Lu HF, Hsu W, Chang WC. Biomed Res Int; 2014 Aug; 2014():397826. PubMed ID: 24800221 [Abstract] [Full Text] [Related]
15. Calcium-sensing receptor gene polymorphisms in patients with calcium nephrolithiasis. Vezzoli G, Terranegra A, Soldati L. Curr Opin Nephrol Hypertens; 2012 Jul; 21(4):355-61. PubMed ID: 22660550 [Abstract] [Full Text] [Related]
16. Calcium-sensing receptor: evidence and hypothesis for its role in nephrolithiasis. Vezzoli G, Macrina L, Magni G, Arcidiacono T. Urolithiasis; 2019 Feb; 47(1):23-33. PubMed ID: 30446806 [Abstract] [Full Text] [Related]
17. Association of sirtuin 1 gene polymorphisms with nephrolithiasis in Eastern chinese population. Hou J, Ding J, Li L, Peng Y, Gao X, Guo Z. Ren Fail; 2019 Nov; 41(1):34-41. PubMed ID: 30714469 [Abstract] [Full Text] [Related]
19. Genetics of hypercalciuric stone forming diseases. Devuyst O, Pirson Y. Kidney Int; 2007 Nov; 72(9):1065-72. PubMed ID: 17687260 [Abstract] [Full Text] [Related]
20. Association between single nucleotide polymorphism (rs4252424) in TRPV5 calcium channel gene and lead poisoning in Chinese workers. Liu J, Zhang L, Feng L, Xu M, Gao Y, Zhou P, Yu Z, Zhu B, An Y, Zhang H. Mol Genet Genomic Med; 2019 Mar; 7(3):e562. PubMed ID: 30666830 [Abstract] [Full Text] [Related] Page: [Next] [New Search]