Plasma PCSK9 concentrations correlate with LDL and total cholesterol in diabetic patients and are decreased by fenofibrate treatment.
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A. Keech | P. Barter | K. Rye | F. Charlton | D. Sullivan | G. Lambert | J. Cohn | J. Pilot | N. Ancellin | Sanjay R. Patel | D. Comas
[1] Proprotein convertase subtilisin kexin type 9 (PCSK9) , 2010 .
[2] P. Barter,et al. Identification and characterization of two non-secreted PCSK9 mutants associated with familial hypercholesterolemia in cohorts from New Zealand and South Africa. , 2008, Atherosclerosis.
[3] W. Alborn,et al. Atorvastatin increases human serum levels of proprotein convertase subtilisin/kexin type 9 Published, JLR Papers in Press, November 21, 2007. , 2008, Journal of Lipid Research.
[4] P. Barter,et al. Is there a role for fibrates in the management of dyslipidemia in the metabolic syndrome? , 2007, Arteriosclerosis, thrombosis, and vascular biology.
[5] F. Gonzalez,et al. The PPAR alpha-humanized mouse: a model to investigate species differences in liver toxicity mediated by PPAR alpha. , 2008, Toxicological sciences : an official journal of the Society of Toxicology.
[6] F. Gonzalez,et al. The PPARα-Humanized Mouse: A Model to Investigate Species Differences in Liver Toxicity Mediated by PPARα , 2008 .
[7] J. Repa,et al. Fenofibrate reduces intestinal cholesterol absorption via PPARalpha-dependent modulation of NPC1L1 expression in mouse. , 2007, Journal of lipid research.
[8] Y. Qian,et al. Serum proprotein convertase subtilisin kexin type 9 is correlated directly with serum LDL cholesterol. , 2007, Clinical chemistry.
[9] N. Seidah,et al. Plasma PCSK9 levels correlate with cholesterol in men but not in women. , 2007, Biochemical and biophysical research communications.
[10] Jennifer L. Harris,et al. Secreted PCSK9 promotes LDL receptor degradation independently of proteolytic activity. , 2007, The Biochemical journal.
[11] J. Horton,et al. Catalytic Activity Is Not Required for Secreted PCSK9 to Reduce Low Density Lipoprotein Receptors in HepG2 Cells* , 2007, Journal of Biological Chemistry.
[12] R. De Francesco,et al. Effects of pH and Low Density Lipoprotein (LDL) on PCSK9-dependent LDL Receptor Regulation* , 2007, Journal of Biological Chemistry.
[13] Y. Qian,et al. Secreted PCSK9 downregulates low density lipoprotein receptor through receptor-mediated endocytosis Published, JLR Papers in Press, April 20, 2007. , 2007, Journal of Lipid Research.
[14] Jonathan C. Cohen,et al. Binding of Proprotein Convertase Subtilisin/Kexin Type 9 to Epidermal Growth Factor-like Repeat A of Low Density Lipoprotein Receptor Decreases Receptor Recycling and Increases Degradation* , 2007, Journal of Biological Chemistry.
[15] G. Lambert. Unravelling the functional significance of PCSK9 , 2007, Current opinion in lipidology.
[16] Annik Prat,et al. The Cellular Trafficking of the Secretory Proprotein Convertase PCSK9 and Its Dependence on the LDLR , 2007, Traffic.
[17] N. Walker,et al. The crystal structure of PCSK9: a regulator of plasma LDL-cholesterol. , 2007, Structure.
[18] Xiayang Qiu,et al. Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia , 2007, Nature Structural &Molecular Biology.
[19] B. Monia,et al. Antisense inhibition of proprotein convertase subtilisin/kexin type 9 reduces serum LDL in hyperlipidemic mice Published, JLR Papers in Press, January 22, 2007. , 2007, Journal of Lipid Research.
[20] Jonathan C. Cohen,et al. Molecular biology of PCSK9: its role in LDL metabolism. , 2007, Trends in biochemical sciences.
[21] T. Ranheim,et al. Degradation of the LDL receptors by PCSK9 is not mediated by a secreted protein acted upon by PCSK9 extracellularly , 2007, BMC Cell Biology.
[22] R. Hammer,et al. Secreted PCSK9 decreases the number of LDL receptors in hepatocytes and in livers of parabiotic mice. , 2006, The Journal of clinical investigation.
[23] M. Krempf,et al. Fasting induces hyperlipidemia in mice overexpressing proprotein convertase subtilisin kexin type 9: lack of modulation of very-low-density lipoprotein hepatic output by the low-density lipoprotein receptor. , 2006, Endocrinology.
[24] M. Krempf,et al. Hepatic PCSK9 Expression Is Regulated by Nutritional Status via Insulin and Sterol Regulatory Element-binding Protein 1c* , 2006, Journal of Biological Chemistry.
[25] P Glasziou,et al. Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial , 2005, The Lancet.
[26] H. McIntyre,et al. Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study: baseline characteristics and short-term effects of fenofibrate [ISRCTN64783481]. , 2005 .
[27] A. Keech,et al. Fenofibrate Intervention and Event Lowering in Diabetes ( FIELD ) study : baseline characteristics and short-term effects of fenofibrate [ ISRCTN 64783481 ] The FIELD Study Investigators * , 2022 .
[28] R. Hammer,et al. Decreased plasma cholesterol and hypersensitivity to statins in mice lacking Pcsk9. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[29] Jay D. Horton,et al. Post-transcriptional Regulation of Low Density Lipoprotein Receptor Protein by Proprotein Convertase Subtilisin/Kexin Type 9a in Mouse Liver* , 2004, Journal of Biological Chemistry.
[30] L. Bernier,et al. Statins Upregulate PCSK9, the Gene Encoding the Proprotein Convertase Neural Apoptosis-Regulated Convertase-1 Implicated in Familial Hypercholesterolemia , 2004, Arteriosclerosis, thrombosis, and vascular biology.
[31] G. Barish,et al. PPARs and the complex journey to obesity , 2004, Nature Medicine.