HDL, cholesterol efflux, and ABCA1: Free from good and evil dualism

Homozygotes for loss-of-function mutations in ABCA1 cause Tangier disease. The phenotype of their markedly reduced or loss of blood high-density lipoprotein (HDL) cholesterol, as well as examination of ATP-binding cassette transporter A1 (ABCA1)-deficient mice, proved that ABCA1 is a key player in H...

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Autor principal: Masatsune Ogura (Autor)
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Publicado: Elsevier, 2022-10-01T00:00:00Z.
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