“Sequence variations in PCSK9, low LDL, and protection against coronary heart disease”. The New England Journal of Medicine354 (12): 1264–72. (March 2006). doi:10.1056/NEJMoa054013. PMID16554528.
“Inhibition of PCSK9 as a novel strategy for the treatment of hypercholesterolemia”. Drug News Perspect.21 (6): 323–30. (2008). doi:10.1358/dnp.2008.21.6.1246795. PMID18836590.
“Annexin A2 is a C-terminal PCSK9-binding protein that regulates endogenous low density lipoprotein receptor levels”. J. Biol. Chem.283 (46): 31791–801. (November 2008). doi:10.1074/jbc.M805971200. PMID18799458.
“New therapies for reducing low-density lipoprotein cholesterol”. Endocrinology and Metabolism Clinics of North America43 (4): 1007–33. (December 2014). doi:10.1016/j.ecl.2014.08.008. PMID25432394.
“Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies in Adults With Hypercholesterolemia: A Systematic Review and Meta-analysis”. Annals of Internal Medicine163 (1): 40–51. (July 2015). doi:10.7326/M14-2957. PMID25915661.
“Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data”. Current Treatment Options in Cardiovascular Medicine19 (8): 58. (August 2017). doi:10.1007/s11936-017-0556-0. PMID28639183.
“PCSK9 binds to multiple receptors and can be functionally inhibited by an EGF-A peptide”. Biochem. Biophys. Res. Commun.375 (1): 69–73. (October 2008). doi:10.1016/j.bbrc.2008.07.106. PMID18675252.
“The effects of berberine on blood lipids: a systemic review and meta-analysis of randomized controlled trials”. Planta Medica79 (6): 437–46. (April 2013). doi:10.1055/s-0032-1328321. PMID23512497.
“Sequence variations in PCSK9, low LDL, and protection against coronary heart disease”. The New England Journal of Medicine354 (12): 1264–72. (March 2006). doi:10.1056/NEJMoa054013. PMID16554528.
“Inhibition of PCSK9 as a novel strategy for the treatment of hypercholesterolemia”. Drug News Perspect.21 (6): 323–30. (2008). doi:10.1358/dnp.2008.21.6.1246795. PMID18836590.
“Annexin A2 is a C-terminal PCSK9-binding protein that regulates endogenous low density lipoprotein receptor levels”. J. Biol. Chem.283 (46): 31791–801. (November 2008). doi:10.1074/jbc.M805971200. PMID18799458.
“New therapies for reducing low-density lipoprotein cholesterol”. Endocrinology and Metabolism Clinics of North America43 (4): 1007–33. (December 2014). doi:10.1016/j.ecl.2014.08.008. PMID25432394.
“Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies in Adults With Hypercholesterolemia: A Systematic Review and Meta-analysis”. Annals of Internal Medicine163 (1): 40–51. (July 2015). doi:10.7326/M14-2957. PMID25915661.
“Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data”. Current Treatment Options in Cardiovascular Medicine19 (8): 58. (August 2017). doi:10.1007/s11936-017-0556-0. PMID28639183.
“PCSK9 binds to multiple receptors and can be functionally inhibited by an EGF-A peptide”. Biochem. Biophys. Res. Commun.375 (1): 69–73. (October 2008). doi:10.1016/j.bbrc.2008.07.106. PMID18675252.
“The effects of berberine on blood lipids: a systemic review and meta-analysis of randomized controlled trials”. Planta Medica79 (6): 437–46. (April 2013). doi:10.1055/s-0032-1328321. PMID23512497.