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Lipoprotein X Causes Renal Disease in LCAT Deficiency
Human familial lecithin:cholesterol acyltransferase (LCAT) deficiency (FLD) is characterized by low HDL, accumulation of an abnormal cholesterol-rich multilamellar particle called lipoprotein-X (LpX) in plasma, and renal disease. The aim of our study was to determine if LpX is nephrotoxic and to gai...
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| Pubblicato in: | PLoS One |
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| Autori principali: | , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4769176/ https://ncbi.nlm.nih.gov/pubmed/26919698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0150083 |
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