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المؤلفون: Fairoozy, Roaa Hani, Cooper, Jackie, White, Jon, Giambartolomei, Claudia, Folkersen, Lasse Westergaard, Wannamethee, S. Goya, Jefferis, Barbara J., Whincup, Peter H., Ben-Shlomo, Yoav, Kumari, Meena, Kivimaki, Mika, Wong, Andrew, Hardy, Rebecca, Kuh, Diana, Gaunt, Tom R., Casas, Juan P., McLachlan, Stela, Price, Jackie F., Hingorani, Aroon D, Franco-Cereceda, Anders, Grewal, Thomas, Kalea, Anastasia Z., Humphries, Steve E
المصدر: Atherosclerosis
Fairoozy, R H, Cooper, J A, White, J, Giambartolomei, C, Folkersen, L, Wannamethee, S G, Jefferis, B J, Whincup, P H, Ben-shlomo, Y, Kumari, M, Kivimaki, M, Wong, A, Hardy, R, Kuh, D, Gaunt, T R, Casas, J P, McLachlan, S, Price, J, Hingorani, A D, Franco-Cereceda, A, Grewal, T & Kalea, A Z & Humphries, S E 2017, ' Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene ', Atherosclerosis . https://doi.org/10.1016/j.atherosclerosis.2017.04.010
Fairoozy, R H, Cooper, J A, White, J, Giambartolomei, C, Folkersen, L, Wannamethee, SG, Jefferis, B J, Whincup, P H, Ben-Shlomo, Y, Kumari, M, Kivimaki, M, Wong, A, Hardy, R, Kuh, D, Gaunt, T, Casas, JP, McLachlan, S, Price, J F, Hingorani, A D, Franco-Cereceda, A, Grewal, T, Kalea, A Z & Humphries, S E 2017, ' Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene ', Atherosclerosis, vol. 261, pp. 60-68 . https://doi.org/10.1016/j.atherosclerosis.2017.04.010
Fairoozy, R H, Cooper, J, White, J, Giambartolomei, C, Folkersen, L W, Wannamethee, S G, Jefferis, B J, Whincup, P H, Ben-Shlomo, Y, Kumari, M, Kivimaki, M, Wong, A, Hardy, R, Kuh, D, Gaunt, T R, Casas, J P, McLachlan, S, Price, J F, Hingorani, A D, Franco-Cereceda, A, Grewal, T, Kalea, A Z & Humphries, S E 2017, ' Identifying low density lipoprotein cholesterol associated variants in the Annexin A2 (ANXA2) gene ', Atherosclerosis, vol. 261, pp. 60-68 . https://doi.org/10.1016/j.atherosclerosis.2017.04.010مصطلحات موضوعية: Male, CTCF, CTC-binding factor, Heterozygote, LDLR, low-density lipoprotein cholesterol-receptor, Quantitative Trait Loci, Coronary Disease, UCLEB, UCL-LSHTM-Edinburgh-Bristol consortium, Transfection, Polymorphism, Single Nucleotide, Article, Linkage Disequilibrium, Low-density lipoprotein cholesterol-receptor, AnxA2, annexin A2, Gene Frequency, Genes, Reporter, NPHSII, Second-Northwick-Park Heart Study, Databases, Genetic, Humans, Low-density lipoprotein cholesterol, Genetic Predisposition to Disease, Annexin A2, Genetic Association Studies, Homozygote, Computational Biology, PCSK9, proprotein convertase subtilisin/kexin type-9, Cholesterol, LDL, Hep G2 Cells, Middle Aged, FAIRE, formaldehyde assisted isolation of regulatory elements, United Kingdom, Single nucleotide polymorphism, CHRD, cysteine-histidine-rich domain of PCSK9, Coronary heart disease, Phenotype, LDL-C, low-density lipoprotein cholesterol, Female, Proprotein Convertase 9, K562 Cells, Proprotein convertase subtilisin/kexin type-9, Biomarkers
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