Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, et al. (June 2003). "Mutations in PCSK9 cause autosomal dominant hypercholesterolemia". Nature Genetics. 34 (2): 154–156. doi:10.1038/ng1161. PMID12730697. S2CID19462210.
Abifadel M, Elbitar S, El Khoury P, Ghaleb Y, Chémaly M, Moussalli ML, et al. (September 2014). "Living the PCSK9 adventure: from the identification of a new gene in familial hypercholesterolemia towards a potential new class of anticholesterol drugs". Current Atherosclerosis Reports. 16 (9): 439. doi:10.1007/s11883-014-0439-8. PMID25052769. S2CID207325099 – via SpringerLink.
Cunningham D, Danley DE, Geoghegan KF, Griffor MC, Hawkins JL, Subashi TA, et al. (May 2007). "Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia". Nature Structural & Molecular Biology. 14 (5): 413–419. doi:10.1038/nsmb1235. PMID17435765. S2CID37890299.
Peng W, Qiang F, Peng W, Qian Z, Ke Z, Yi L, et al. (November 2016). "Therapeutic efficacy of PCSK9 monoclonal antibodies in statin-nonresponsive patients with hypercholesterolemia and dyslipidemia: A systematic review and meta-analysis". International Journal of Cardiology. 222: 119–129. doi:10.1016/j.ijcard.2016.07.239. PMID27494723.
Berger JM, Vaillant N, Le May C, Calderon C, Brégeon J, Prieur X, et al. (March 2015). "PCSK9-deficiency does not alter blood pressure and sodium balance in mouse models of hypertension". Atherosclerosis. 239 (1): 252–259. doi:10.1016/j.atherosclerosis.2015.01.012. PMID25621930.
Norata GD, Pirillo A, Ammirati E, Catapano AL (January 2012). "Emerging role of high density lipoproteins as a player in the immune system". Atherosclerosis. 220 (1): 11–21. doi:10.1016/j.atherosclerosis.2011.06.045. PMID21783193.
Chen YQ, Troutt JS, Konrad RJ (May 2014). "PCSK9 is present in human cerebrospinal fluid and is maintained at remarkably constant concentrations throughout the course of the day". Lipids. 49 (5): 445–455. doi:10.1007/s11745-014-3895-6. PMID24659111. S2CID4052058.
Lopez D (2008). "Inhibition of PCSK9 as a novel strategy for the treatment of hypercholesterolemia". Drug News & Perspectives. 21 (6): 323–330. doi:10.1358/dnp.2008.21.6.1246795. PMID18836590.
Stein EA, Raal FJ (December 2014). "New therapies for reducing low-density lipoprotein cholesterol". Endocrinology and Metabolism Clinics of North America. 43 (4): 1007–1033. doi:10.1016/j.ecl.2014.08.008. PMID25432394.
Navarese EP, Kolodziejczak M, Schulze V, Gurbel PA, Tantry U, Lin Y, et al. (July 2015). "Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies in Adults With Hypercholesterolemia: A Systematic Review and Meta-analysis". Annals of Internal Medicine. 163 (1): 40–51. doi:10.7326/M14-2957. PMID25915661. S2CID207538324.
Durairaj A, Sabates A, Nieves J, Moraes B, Baum S (August 2017). "Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data". Current Treatment Options in Cardiovascular Medicine. 19 (8): 58. doi:10.1007/s11936-017-0556-0. PMID28639183. S2CID25301414.
Khan S (2022). "PCSK9 inhibitors and ezetimibe with or without statin therapy for cardiovascular risk reduction: a systematic review and network meta-analysis". BMJ. 377. Clinical Research Ed.: e069116. doi:10.1136/bmj-2021-069116. PMID35508321.
Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, et al. (June 2003). "Mutations in PCSK9 cause autosomal dominant hypercholesterolemia". Nature Genetics. 34 (2): 154–156. doi:10.1038/ng1161. PMID12730697. S2CID19462210.
Abifadel M, Elbitar S, El Khoury P, Ghaleb Y, Chémaly M, Moussalli ML, et al. (September 2014). "Living the PCSK9 adventure: from the identification of a new gene in familial hypercholesterolemia towards a potential new class of anticholesterol drugs". Current Atherosclerosis Reports. 16 (9): 439. doi:10.1007/s11883-014-0439-8. PMID25052769. S2CID207325099 – via SpringerLink.
Cunningham D, Danley DE, Geoghegan KF, Griffor MC, Hawkins JL, Subashi TA, et al. (May 2007). "Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia". Nature Structural & Molecular Biology. 14 (5): 413–419. doi:10.1038/nsmb1235. PMID17435765. S2CID37890299.
Peng W, Qiang F, Peng W, Qian Z, Ke Z, Yi L, et al. (November 2016). "Therapeutic efficacy of PCSK9 monoclonal antibodies in statin-nonresponsive patients with hypercholesterolemia and dyslipidemia: A systematic review and meta-analysis". International Journal of Cardiology. 222: 119–129. doi:10.1016/j.ijcard.2016.07.239. PMID27494723.
Berger JM, Vaillant N, Le May C, Calderon C, Brégeon J, Prieur X, et al. (March 2015). "PCSK9-deficiency does not alter blood pressure and sodium balance in mouse models of hypertension". Atherosclerosis. 239 (1): 252–259. doi:10.1016/j.atherosclerosis.2015.01.012. PMID25621930.
Norata GD, Pirillo A, Ammirati E, Catapano AL (January 2012). "Emerging role of high density lipoproteins as a player in the immune system". Atherosclerosis. 220 (1): 11–21. doi:10.1016/j.atherosclerosis.2011.06.045. PMID21783193.
Chen YQ, Troutt JS, Konrad RJ (May 2014). "PCSK9 is present in human cerebrospinal fluid and is maintained at remarkably constant concentrations throughout the course of the day". Lipids. 49 (5): 445–455. doi:10.1007/s11745-014-3895-6. PMID24659111. S2CID4052058.
Lopez D (2008). "Inhibition of PCSK9 as a novel strategy for the treatment of hypercholesterolemia". Drug News & Perspectives. 21 (6): 323–330. doi:10.1358/dnp.2008.21.6.1246795. PMID18836590.
Stein EA, Raal FJ (December 2014). "New therapies for reducing low-density lipoprotein cholesterol". Endocrinology and Metabolism Clinics of North America. 43 (4): 1007–1033. doi:10.1016/j.ecl.2014.08.008. PMID25432394.
Navarese EP, Kolodziejczak M, Schulze V, Gurbel PA, Tantry U, Lin Y, et al. (July 2015). "Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies in Adults With Hypercholesterolemia: A Systematic Review and Meta-analysis". Annals of Internal Medicine. 163 (1): 40–51. doi:10.7326/M14-2957. PMID25915661. S2CID207538324.
Durairaj A, Sabates A, Nieves J, Moraes B, Baum S (August 2017). "Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data". Current Treatment Options in Cardiovascular Medicine. 19 (8): 58. doi:10.1007/s11936-017-0556-0. PMID28639183. S2CID25301414.
Khan S (2022). "PCSK9 inhibitors and ezetimibe with or without statin therapy for cardiovascular risk reduction: a systematic review and network meta-analysis". BMJ. 377. Clinical Research Ed.: e069116. doi:10.1136/bmj-2021-069116. PMID35508321.
Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, et al. (June 2003). "Mutations in PCSK9 cause autosomal dominant hypercholesterolemia". Nature Genetics. 34 (2): 154–156. doi:10.1038/ng1161. PMID12730697. S2CID19462210.
Abifadel M, Elbitar S, El Khoury P, Ghaleb Y, Chémaly M, Moussalli ML, et al. (September 2014). "Living the PCSK9 adventure: from the identification of a new gene in familial hypercholesterolemia towards a potential new class of anticholesterol drugs". Current Atherosclerosis Reports. 16 (9): 439. doi:10.1007/s11883-014-0439-8. PMID25052769. S2CID207325099 – via SpringerLink.
Cunningham D, Danley DE, Geoghegan KF, Griffor MC, Hawkins JL, Subashi TA, et al. (May 2007). "Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia". Nature Structural & Molecular Biology. 14 (5): 413–419. doi:10.1038/nsmb1235. PMID17435765. S2CID37890299.
Chen YQ, Troutt JS, Konrad RJ (May 2014). "PCSK9 is present in human cerebrospinal fluid and is maintained at remarkably constant concentrations throughout the course of the day". Lipids. 49 (5): 445–455. doi:10.1007/s11745-014-3895-6. PMID24659111. S2CID4052058.
Navarese EP, Kolodziejczak M, Schulze V, Gurbel PA, Tantry U, Lin Y, et al. (July 2015). "Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Antibodies in Adults With Hypercholesterolemia: A Systematic Review and Meta-analysis". Annals of Internal Medicine. 163 (1): 40–51. doi:10.7326/M14-2957. PMID25915661. S2CID207538324.
Durairaj A, Sabates A, Nieves J, Moraes B, Baum S (August 2017). "Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) and Its Inhibitors: a Review of Physiology, Biology, and Clinical Data". Current Treatment Options in Cardiovascular Medicine. 19 (8): 58. doi:10.1007/s11936-017-0556-0. PMID28639183. S2CID25301414.