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Pin1 and secondary hyperparathyroidism of chronic kidney disease: gene polymorphisms and protein levels
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 S...
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| Publicat a: | Ren Fail |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Taylor & Francis
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6014329/ https://ncbi.nlm.nih.gov/pubmed/27876426 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/0886022X.2016.1256310 |
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