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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Format: | Article |
Language: | English |
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Elsevier
2022-10-01
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Series: | Journal of Pharmacological Sciences |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S1347861322000548 |