Maxime Denis

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Angela Brooks‐Wilson, Michel Marcil, Susanne M. Clee et al. · Nature Genetics · 1999 · 1.7K citations

Mendelian Disorder, Disease Mechanism, Genetic Disorder +13

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

Michel Marcil, Angela Brooks‐Wilson, Susanne M. Clee et al. · The Lancet · 1999 · 357 citations

Abc 1, Mendelian Disorder, Familial Hdl Deficiency +12

Gene Inactivation of Proprotein Convertase Subtilisin/Kexin Type 9 Reduces Atherosclerosis in Mice

Maxime Denis, Jadwiga Marcinkiewicz, Ahmed Zaid et al. · Circulation · 2012 · 227 citations · Full text

ATP-binding Cassette Transporter A1 Expression Disrupts Raft Membrane Microdomains through Its ATPase-related Functions

Yves Landry, Maxime Denis, Shilpi Nandi et al. · Journal of Biological Chemistry · 2006 · 205 citations · Full text

Abca1 Expression Results, Proteinlipid Interaction, Molecular Biology +19

Molecular interactions between apoE and ABCA1

Larbi Krimbou, Maxime Denis, Bassam Haidar et al. · Journal of Lipid Research · 2004 · 132 citations · Full text