Maternal ABCA1 genotype is associated with severity of Smith–Lemli–Opitz syndrome and with viability of patients homozygous for null mutations

ATP-binding cassette transporter A1 gene polymorphisms and serum lipid levels in young Greek nurses

(2011) Vana Kolovou et al.   Lipids in Health and Disease

Expression and localization pattern of ABCA1 in diverse human placental primary cells and tissues

(2011) L. Nikitina et al.   PLACENTA

Placental ABCA1 and ABCG1 transporters efflux cholesterol and protect trophoblasts from oxysterol induced toxicity

(2010) Irving L.M.H. Aye et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS

The Molecular Mechanisms of HDL and Associated Vesicular Trafficking Mechanisms to Mediate Cellular Lipid Homeostasis

(2009) Gerd Schmitz et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Human Endothelial Cells of the Placental Barrier Efficiently Deliver Cholesterol to the Fetal Circulation via ABCA1 and ABCG1

(2009) Jasminka Stefulj et al.   CIRCULATION RESEARCH

High-density lipoprotein metabolism and the human embryo

(2009) V. Y. Fujimoto et al.   HUMAN REPRODUCTION UPDATE

Characterization of placental cholesterol transport: ABCA1 is a potential target for in utero therapy of Smith-Lemli-Opitz syndrome

(2008) M. L. Lindegaard et al.   HUMAN MOLECULAR GENETICS

Genetic Variation in ABCA1 Predicts Ischemic Heart Disease in the General Population

(2007) Ruth Frikke-Schmidt et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY