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Journal Abstract Search
2609 related items for PubMed ID: 23973703
1. Targeting the proprotein convertase subtilisin/kexin type 9 for the treatment of dyslipidemia and atherosclerosis. Urban D, Pöss J, Böhm M, Laufs U. J Am Coll Cardiol; 2013 Oct 15; 62(16):1401-8. PubMed ID: 23973703 [Abstract] [Full Text] [Related]
2. Proprotein convertase subtilisin/kexin type 9 inhibition: a new therapeutic mechanism for reducing cardiovascular disease risk. Bergeron N, Phan BA, Ding Y, Fong A, Krauss RM. Circulation; 2015 Oct 27; 132(17):1648-66. PubMed ID: 26503748 [Abstract] [Full Text] [Related]
3. PCSK9 inhibition in LDL cholesterol reduction: genetics and therapeutic implications of very low plasma lipoprotein levels. Marais AD, Kim JB, Wasserman SM, Lambert G. Pharmacol Ther; 2015 Jan 27; 145():58-66. PubMed ID: 25046268 [Abstract] [Full Text] [Related]
4. On the function and homeostasis of PCSK9: reciprocal interaction with LDLR and additional lipid effects. Tavori H, Rashid S, Fazio S. Atherosclerosis; 2015 Feb 27; 238(2):264-70. PubMed ID: 25544176 [Abstract] [Full Text] [Related]
5. Molecular and cellular function of the proprotein convertase subtilisin/kexin type 9 (PCSK9). Schulz R, Schlüter KD, Laufs U. Basic Res Cardiol; 2015 Mar 27; 110(2):4. PubMed ID: 25600226 [Abstract] [Full Text] [Related]
6. Evaluation of proprotein convertase subtilisin/kexin type 9: focus on potential clinical and therapeutic implications for low-density lipoprotein cholesterol lowering. Lose JM, Dorsch MP, Bleske BE. Pharmacotherapy; 2013 Apr 27; 33(4):447-60. PubMed ID: 23553812 [Abstract] [Full Text] [Related]
7. New CETP inhibitor K-312 reduces PCSK9 expression: a potential effect on LDL cholesterol metabolism. Miyosawa K, Watanabe Y, Murakami K, Murakami T, Shibata H, Iwashita M, Yamazaki H, Yamazaki K, Ohgiya T, Shibuya K, Mizuno K, Tanabe S, Singh SA, Aikawa M. Am J Physiol Endocrinol Metab; 2015 Jul 15; 309(2):E177-90. PubMed ID: 26015437 [Abstract] [Full Text] [Related]
8. An antibody against the C-terminal domain of PCSK9 lowers LDL cholesterol levels in vivo. Schiele F, Park J, Redemann N, Luippold G, Nar H. J Mol Biol; 2014 Feb 20; 426(4):843-52. PubMed ID: 24252255 [Abstract] [Full Text] [Related]
9. New LDL-cholesterol lowering therapies: pharmacology, clinical trials, and relevance to acute coronary syndromes. Sahebkar A, Watts GF. Clin Ther; 2013 Aug 20; 35(8):1082-98. PubMed ID: 23932550 [Abstract] [Full Text] [Related]
10. New developments in atherosclerosis: clinical potential of PCSK9 inhibition. Giunzioni I, Tavori H. Vasc Health Risk Manag; 2015 Aug 20; 11():493-501. PubMed ID: 26345307 [Abstract] [Full Text] [Related]
13. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors: Present perspectives and future horizons. Yadav K, Sharma M, Ferdinand KC. Nutr Metab Cardiovasc Dis; 2016 Oct 20; 26(10):853-62. PubMed ID: 27352986 [Abstract] [Full Text] [Related]
14. The next generation of novel low-density lipoprotein cholesterol-lowering agents: proprotein convertase subtilisin/kexin 9 inhibitors. Shen L, Peng H, Xu D, Zhao S. Pharmacol Res; 2013 Jul 20; 73():27-34. PubMed ID: 23578522 [Abstract] [Full Text] [Related]
15. Proprotein convertase subtilisin kexin type 9 (PCSK9) secreted by cultured smooth muscle cells reduces macrophages LDLR levels. Ferri N, Tibolla G, Pirillo A, Cipollone F, Mezzetti A, Pacia S, Corsini A, Catapano AL. Atherosclerosis; 2012 Feb 20; 220(2):381-6. PubMed ID: 22176652 [Abstract] [Full Text] [Related]
16. LDL-R promoting activity of peptides derived from human PCSK9 catalytic domain (153-421): design, synthesis and biochemical evaluation. Alghamdi RH, O'Reilly P, Lu C, Gomes J, Lagace TA, Basak A. Eur J Med Chem; 2015 Mar 06; 92():890-907. PubMed ID: 25679794 [Abstract] [Full Text] [Related]
19. β-Estradiol results in a proprotein convertase subtilisin/kexin type 9-dependent increase in low-density lipoprotein receptor levels in human hepatic HuH7 cells. Starr AE, Lemieux V, Noad J, Moore JI, Dewpura T, Raymond A, Chrétien M, Figeys D, Mayne J. FEBS J; 2015 Jul 06; 282(14):2682-96. PubMed ID: 25913303 [Abstract] [Full Text] [Related]