Plasma PCSK9 levels and lipoprotein distribution are preserved in carriers of genetic HDL disorders.
Ruscica, Massimiliano; Simonelli, Sara; Botta, Margherita; Ossoli, Alice; Lupo, Maria Giovanna; Magni, Paolo; Corsini, Alberto; Arca, Marcello; Pisciotta, Livia; Veglia, Fabrizio; Franceschini, Guido; Ferri, Nicola; Calabresi, Laura.
Biochim Biophys Acta Mol Cell Biol Lipids
; 1863(9): 991-997, 2018 09.
Artigo em Inglês | MEDLINE | ID: mdl-29852278
Charged Residues in the C-Terminal Domain of Apolipoprotein A-I Modulate Oligomerization.
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HDL from apoA1 transgenic mice expressing the 4WF isoform is resistant to oxidative loss of function.
Apolipoprotein A-I and adenosine triphosphate-binding cassette transporter A1 expression alleviates lipid accumulation in hepatocytes.