Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients
暂无分享,去创建一个
M. Emi | M. Nagano | H. Hattori | M. Ishihara | T. Iwasaki | M. Tsuji | J. Ishii | T. Kujiraoka | M. Takano
[1] M. Nagano,et al. Altered distribution of plasma PAF-AH between HDLs and other lipoproteins in hyperlipidemia and diabetes mellitus Published, JLR Papers in Press, July 16, 2003. DOI 10.1194/jlr.D300021-JLR200 , 2003, Journal of Lipid Research.
[2] C. Packard,et al. Lipoprotein-associated phospholipase A2 (platelet-activating factor acetylhydrolase) and cardiovascular disease , 2003, Current opinion in lipidology.
[3] M. Emi,et al. Hypertriglyceridemia associated with amino acid variation Asn985Tyr of theRP1 gene , 2003, Journal of Human Genetics.
[4] M. Emi,et al. Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred , 2002, Journal of Human Genetics.
[5] M. Emi,et al. Head-to-head juxtaposition of Fas-associated phosphatase-1 (FAP-1) and c-Jun NH2-terminal kinase 3 (JNK3) genes: genomic structure and seven polymorphisms of the FAP-1 gene , 2002, Journal of Human Genetics.
[6] Yusuke Nakamura,et al. Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190 562 genetic variations in the human genome , 2002, Journal of Human Genetics.
[7] M. Emi,et al. Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis , 2002, Journal of Human Genetics.
[8] A. Sekine,et al. Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR) , 2002, Journal of Human Genetics.
[9] Yozo Ohnishi,et al. [A high-throughput SNP typing system for genome-wide association studies]. , 2002, Gan to kagaku ryoho. Cancer & chemotherapy.
[10] M. Emi,et al. Eight novel mutations and functional impairments of the LDL receptor in familial hypercholesterolemia in the north of Japan , 2002, Journal of Human Genetics.
[11] J. Sugatani,et al. Association of a G994 →T Missense Mutation in the Plasma Platelet-Activating Factor Acetylhydrolase Gene With Risk of Abdominal Aortic Aneurysm in Japanese , 2002, Annals of surgery.
[12] J. Manson,et al. A prospective evaluation of lipoprotein-associated phospholipase A(2) levels and the risk of future cardiovascular events in women. , 2001, Journal of the American College of Cardiology.
[13] D. Stengel,et al. N-linked glycosylation of macrophage-derived PAF-AH is a major determinant of enzyme association with plasma HDL. , 2001, Journal of lipid research.
[14] Yusuke Nakamura,et al. A high-throughput SNP typing system for genome-wide association studies , 2001, Journal of Human Genetics.
[15] T. Kodama,et al. Evidence of Macrophage Foam Cell Formation by Very Low-Density Lipoprotein Receptor: Interferon-&ggr; Inhibition of Very Low-Density Lipoprotein Receptor Expression and Foam Cell Formation in Macrophages , 2001, Circulation.
[16] H. Krumholz. Lipoprotein-Associated Phospholipase A , 2001 .
[17] L. Tjoelker,et al. Platelet-activating factor acetylhydrolases in health and disease. , 2000, Biochimica et biophysica acta.
[18] G. Lowe,et al. Lipoprotein-associated phospholipase A2 as an independent predictor of coronary heart disease. West of Scotland Coronary Prevention Study Group. , 2000, The New England journal of medicine.
[19] J. Sugatani,et al. Plasma platelet-activating factor acetylhydrolase deficiency is associated with atherosclerotic occlusive disease in japan. , 2000, Journal of vascular surgery.
[20] C. Packard,et al. Lipoprotein-associated phospholipase A2, platelet-activating factor acetylhydrolase: a potential new risk factor for coronary artery disease , 2000 .
[21] M. Yokota,et al. Correlations between plasma platelet-activating factor acetylhydrolase (PAF-AH) activity and PAF-AH genotype, age, and atherosclerosis in a Japanese population. , 2000, Atherosclerosis.
[22] T. Fukuda,et al. Deficiency of platelet-activating factor acetylhydrolase is a severity factor for asthma. , 1999, The Journal of clinical investigation.
[23] M. Yokota,et al. Identification of the G994--> T missense in exon 9 of the plasma platelet-activating factor acetylhydrolase gene as an independent risk factor for coronary artery disease in Japanese men. , 1998, Metabolism: clinical and experimental.
[24] T. Imaizumi,et al. A mutation in plasma platelet-activating factor acetylhydrolase (Val279-->Phe) is a genetic risk factor for stroke. , 1997, Stroke.
[25] G. Zimmerman,et al. Platelet-activating Factor Acetylhydrolases* , 1997, The Journal of Biological Chemistry.
[26] P. Macfarlane,et al. West of Scotland Coronary Prevention Study: Identification of high-risk groups and comparison with other cardiovascular intervention trials , 1996 .
[27] G. Zimmerman,et al. Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase. , 1996, The Journal of clinical investigation.
[28] G. Zimmerman,et al. Mammalian platelet-activating factor acetylhydrolases. , 1996, Biochimica et biophysica acta.
[29] G. Zimmerman,et al. Anti-inflammatory properties of a platelet-activating factor acetylhydrolase , 1995, Nature.
[30] F. Snyder,et al. Platelet-activating factor and its analogs: metabolic pathways and related intracellular processes. , 1995, Biochimica et biophysica acta.
[31] J. Berliner,et al. Effect of platelet activating factor-acetylhydrolase on the formation and action of minimally oxidized low density lipoprotein. , 1995, The Journal of clinical investigation.
[32] D. Stafforini,et al. Human plasma platelet-activating factor acetylhydrolase. Oxidatively fragmented phospholipids as substrates. , 1991, The Journal of biological chemistry.
[33] G. Zimmerman,et al. An oxidized derivative of phosphatidylcholine is a substrate for the platelet-activating factor acetylhydrolase from human plasma. , 1989, The Journal of biological chemistry.
[34] U. Steinbrecher,et al. Hydrolysis of phosphatidylcholine during LDL oxidation is mediated by platelet-activating factor acetylhydrolase. , 1989, Journal of lipid research.
[35] J. Sugatani,et al. Characterization of serum platelet-activating factor (PAF) acetylhydrolase. Correlation between deficiency of serum PAF acetylhydrolase and respiratory symptoms in asthmatic children. , 1988, The Journal of clinical investigation.
[36] D. Stafforini,et al. Human plasma platelet-activating factor acetylhydrolase. Association with lipoprotein particles and role in the degradation of platelet-activating factor. , 1987, The Journal of biological chemistry.
[37] D. Stafforini,et al. Human plasma platelet-activating factor acetylhydrolase. Purification and properties. , 1987, The Journal of biological chemistry.
[38] A. Goldstein,et al. Purification and properties , 1975 .
[39] R. Levy,et al. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. , 1972, Clinical chemistry.
[40] S. Yamashita,et al. Two novel missense mutations in the CETP gene in Japanese hyperalphalipoproteinemic subjects: high-throughput assay by Invader ® assay , 2002 .
[41] A. Sekine,et al. Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genes , 2002, Journal of Human Genetics.
[42] C. Packard,et al. Lipoprotein-associated phospholipase A(2), platelet-activating factor acetylhydrolase: a potential new risk factor for coronary artery disease. , 2000, Atherosclerosis.
[43] L. Tjoelker,et al. Human plasma platelet-activating factor acetylhydrolase. , 1999, Methods in molecular biology.
[44] G. Zimmerman,et al. The platelet-activating factor acetylhydrolase from human plasma prevents oxidative modification of low-density lipoprotein. , 1992, Transactions of the Association of American Physicians.