A Molecular Insight of the Role of PIN-1 Promoter Polymorphism (− 667C > T; rs2233679) in Chronic Kidney Disease Patients with Secondary Hyperparathyroidism

Author:

Patel Digishaben D.,Parchwani DeepakORCID,Vachhani Uday,Parchwani Tanishk,Raghavani Pratik,Rajput Ajay,Dholariya Sagar,Singh Ragini

Publisher

Springer Science and Business Media LLC

Subject

Clinical Biochemistry

Reference29 articles.

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2. KDOQI Clinical Practice Guidelines and Clinical Practice Recommendations for Anemia in Chronic Kidney Disease KDOQI; National Kidney Foundation. Am J Kidney Dis 2006;47:S11–145.

3. Zhao Y, Zhang LL, Ding FX, Cao P, Qi YY, Wang J. Pin1 and secondary hyperparathyroidism of chronic kidney disease: gene polymorphisms and protein levels. Ren Fail. 2017;39(1):159–65.

4. Kidney Disease: Improving Global Outcomes (KDIGO) CKD-MBD Work Group. KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of chronic kidney disease-mineral and bone disorder (CKD-MBD). Kidney Int Suppl. 2009;76(S113):S1-130.

5. Nechama M, Uchida T, Mor Yosef-Levi I, Silver J, Naveh-Many T. The peptidyl-prolyl isomerase Pin1 determines parathyroid hormone mRNA levels and stability in rat models of secondary hyperparathyroidism. J Clin Invest. 2009;119(10):3102–14.

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