Pin1 and secondary hyperparathyroidism of chronic kidney disease: gene polymorphisms and protein levels.

CONCLUSION: The -667T genetic variants in the Pin1 promoter contribute to an increased risk of CKD SHPT and may be biomarkers of susceptibility to CKD SHPT. PMID: 27876426 [PubMed - as supplied by publisher]
Source: Renal Failure - Category: Urology & Nephrology Tags: Ren Fail Source Type: research