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Article

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

Renal failure - 1 Nov 2017

Zhao Yu, Zhang Li-Li, Ding Fa-Xian, Cao Ping, Qi Yuan-Yuan, Wang Jing

Abstract excerpt

BACKGROUND: Peptidyl-prolyl cis/trans isomerase NIMA-interacting 1 (Pin1) is a key regulator of PTH mRNA stability. Secondary hyperparathyroidism (SHPT), which is characterized by elevated serum PTH levels, is a common complication of CKD. We investigated the possible associations between CKD with SHPT (CKD SHPT) and single-nucleotide polymorphisms of the Pin1 gene and compared the levels of the Pin1 protein in...

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Source

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Identifiers

PMID: 27876426
DOI: 10.1080/0886022X.2016.1256310
PMCID: PMC6014329

Genes

PTH

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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