Abnormal Lipoproteins Trigger Oxidative Stress-Mediated Apoptosis of Renal Cells in LCAT Deficiency

Familial lecithin:cholesterol acyltransferase (LCAT) deficiency (FLD) is a rare genetic disease caused by the loss of function mutations in the LCAT gene. LCAT deficiency is characterized by an abnormal lipoprotein profile with severe reduction in plasma levels of high-density lipoprotein (HDL) chol...

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Detalles Bibliográficos
Autores principales: Gomaraschi, Monica, Turri, Marta, Strazzella, Arianna, Lhomme, Marie, Pavanello, Chiara, Le Goff, Wilfried, Kontush, Anatol, Calabresi, Laura, Ossoli, Alice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451761/
https://www.ncbi.nlm.nih.gov/pubmed/37627492
http://dx.doi.org/10.3390/antiox12081498

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10451761/
https://www.ncbi.nlm.nih.gov/pubmed/37627492
http://dx.doi.org/10.3390/antiox12081498

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