A Novel in Vivo Lecithin-Cholesterol Acyltransferase (LCAT)-Deficient Mouse Expressing Predominantly LpX Is Associated with Spontaneous Glomerulopathy

Complete lecithin cholesterol acyltransferase (LCAT) deficiency is a rare genetic cause of extreme reduction in high density lipoproteins and there is a high prevalence of chronic renal dysfunction that may progress to renal failure. Previous in vitro studies suggest the vesicular lipoprotein X (LpX...

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Detalhes bibliográficos
Main Authors: Zhu, Xianghong, Herzenberg, Andrew M., Eskandarian, Mohammad, Maguire, Graham F., Scholey, James W., Connelly, Philip W., Ng, Dominic S.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2004
Assuntos:
Regular Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3118835/
https://ncbi.nlm.nih.gov/pubmed/15466392
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