메뉴 건너뛰기




Volumn 210, Issue 2, 2010, Pages 468-473

Association of genetic variants in SEMA3F, CLEC16A, LAMA3, and PCSK2 with myocardial infarction in Japanese individuals

Author keywords

Atherosclerosis; Coronary heart disease; Genetics; Myocardial infarction; Polymorphism

Indexed keywords

GENE PRODUCT; PROPROTEIN CONVERTASE 2; PROTEIN CLEC16A; PROTEIN LAMA3; SEMAPHORIN 3F; UNCLASSIFIED DRUG;

EID: 77953230914     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.atherosclerosis.2009.11.050     Document Type: Article
Times cited : (19)

References (29)
  • 1
    • 4444382796 scopus 로고    scopus 로고
    • Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study
    • Yusuf S., Hawken S., Ounpuu S., et al. Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study. Lancet 2004, 364:937-952.
    • (2004) Lancet , vol.364 , pp. 937-952
    • Yusuf, S.1    Hawken, S.2    Ounpuu, S.3
  • 2
    • 34848815115 scopus 로고    scopus 로고
    • Mechanisms of disease: the genetic basis of coronary heart disease
    • Kullo I.J., Ding K. Mechanisms of disease: the genetic basis of coronary heart disease. Nat Clin Pract Cardiovasc Med 2007, 4:558-569.
    • (2007) Nat Clin Pract Cardiovasc Med , vol.4 , pp. 558-569
    • Kullo, I.J.1    Ding, K.2
  • 3
    • 34249906772 scopus 로고    scopus 로고
    • Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group
    • Arnett D.K., Baird A.E., Barkley R.A., et al. Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Translational Biology Interdisciplinary Working Group. Circulation 2007, 115:2878-2901.
    • (2007) Circulation , vol.115 , pp. 2878-2901
    • Arnett, D.K.1    Baird, A.E.2    Barkley, R.A.3
  • 4
    • 61349177857 scopus 로고    scopus 로고
    • New susceptibility locus for coronary artery disease on chromosome 3q22.3
    • Erdmann J., Grosshennig A., Braund P.S., et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009, 41:280-282.
    • (2009) Nat Genet , vol.41 , pp. 280-282
    • Erdmann, J.1    Grosshennig, A.2    Braund, P.S.3
  • 5
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Wellcome Trust Case Control Consortium
    • Wellcome Trust Case Control Consortium Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007, 447:661-678.
    • (2007) Nature , vol.447 , pp. 661-678
  • 6
    • 70749096913 scopus 로고    scopus 로고
    • Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
    • Myocardial Infarction Genetics Consortium
    • Myocardial Infarction Genetics Consortium Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009, 41:334-341.
    • (2009) Nat Genet , vol.41 , pp. 334-341
  • 7
    • 34547623750 scopus 로고    scopus 로고
    • Genomewide association analysis of coronary artery disease
    • Samani N.J., Erdmann J., Hall A.S., et al. Genomewide association analysis of coronary artery disease. N Engl J Med 2007, 357:443-453.
    • (2007) N Engl J Med , vol.357 , pp. 443-453
    • Samani, N.J.1    Erdmann, J.2    Hall, A.S.3
  • 8
    • 34249996115 scopus 로고    scopus 로고
    • A common allele on chromosome 9 associated with coronary heart disease
    • McPherson R., Pertsemlidis A., Kavaslar N., et al. A common allele on chromosome 9 associated with coronary heart disease. Science 2007, 316:1488-1491.
    • (2007) Science , vol.316 , pp. 1488-1491
    • McPherson, R.1    Pertsemlidis, A.2    Kavaslar, N.3
  • 9
    • 34250010480 scopus 로고    scopus 로고
    • A common variant on chromosome 9p21 affects the risk of myocardial infarction
    • Helgadottir A., Thorleifsson G., Manolescu A., et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007, 316:1491-1493.
    • (2007) Science , vol.316 , pp. 1491-1493
    • Helgadottir, A.1    Thorleifsson, G.2    Manolescu, A.3
  • 10
    • 70350574629 scopus 로고    scopus 로고
    • Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study
    • Yamada Y., Fuku N., Tanaka M., et al. Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Atherosclerosis 2009, 207:144-149.
    • (2009) Atherosclerosis , vol.207 , pp. 144-149
    • Yamada, Y.1    Fuku, N.2    Tanaka, M.3
  • 11
    • 0037069779 scopus 로고    scopus 로고
    • Prediction of the risk of myocardial infarction from polymorphisms in candidate genes
    • Yamada Y., Izawa H., Ichihara S., et al. Prediction of the risk of myocardial infarction from polymorphisms in candidate genes. N Engl J Med 2002, 347:1916-1923.
    • (2002) N Engl J Med , vol.347 , pp. 1916-1923
    • Yamada, Y.1    Izawa, H.2    Ichihara, S.3
  • 12
    • 42049084137 scopus 로고    scopus 로고
    • Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population
    • Yamada Y., Kato K., Oguri M., et al. Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population. J Med Genet 2008, 45:216-221.
    • (2008) J Med Genet , vol.45 , pp. 216-221
    • Yamada, Y.1    Kato, K.2    Oguri, M.3
  • 13
    • 33747117971 scopus 로고    scopus 로고
    • Assessment of genetic risk for myocardial infarction
    • Yamada Y., Matsuo H., Segawa T., et al. Assessment of genetic risk for myocardial infarction. Thromb Haemost 2006, 96:220-227.
    • (2006) Thromb Haemost , vol.96 , pp. 220-227
    • Yamada, Y.1    Matsuo, H.2    Segawa, T.3
  • 14
    • 27744456947 scopus 로고    scopus 로고
    • High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population
    • Itoh Y., Mizuki N., Shimada T., et al. High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population. Immunogenetics 2005, 57:717-729.
    • (2005) Immunogenetics , vol.57 , pp. 717-729
    • Itoh, Y.1    Mizuki, N.2    Shimada, T.3
  • 15
    • 0001677717 scopus 로고
    • Controlling the false discovery rate: a practical and powerful approach to multiple testing
    • Benjamini Y., Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Royal Stat Soc Ser B 1995, 57:289-300.
    • (1995) J Royal Stat Soc Ser B , vol.57 , pp. 289-300
    • Benjamini, Y.1    Hochberg, Y.2
  • 16
    • 36148984168 scopus 로고    scopus 로고
    • Targeting endothelial and tumor cells with semaphorins
    • Bielenberg D.R., Klagsbrun M. Targeting endothelial and tumor cells with semaphorins. Cancer Metastasis Rev 2007, 26:421-431.
    • (2007) Cancer Metastasis Rev , vol.26 , pp. 421-431
    • Bielenberg, D.R.1    Klagsbrun, M.2
  • 17
    • 36348990716 scopus 로고    scopus 로고
    • Control of intracellular localization and function of Cx43 by SEMA3F
    • Kawasaki Y., Kubomoto A., Yamasaki H. Control of intracellular localization and function of Cx43 by SEMA3F. J Membr Biol 2007, 217:53-61.
    • (2007) J Membr Biol , vol.217 , pp. 53-61
    • Kawasaki, Y.1    Kubomoto, A.2    Yamasaki, H.3
  • 18
    • 0035252340 scopus 로고    scopus 로고
    • Immunocytochemical analysis of connexin expression in the healthy and diseased cardiovascular system
    • Severs N.J., Rothery S., Dupont E., et al. Immunocytochemical analysis of connexin expression in the healthy and diseased cardiovascular system. Microsc Res Tech 2001, 52:301-322.
    • (2001) Microsc Res Tech , vol.52 , pp. 301-322
    • Severs, N.J.1    Rothery, S.2    Dupont, E.3
  • 19
    • 0029161009 scopus 로고
    • Upregulation of connexin43 gap junctions during early stages of human coronary atherosclerosis
    • Blackburn J.P., Peters N.S., Yeh H.I., et al. Upregulation of connexin43 gap junctions during early stages of human coronary atherosclerosis. Arterioscler Thromb Vasc Biol 1995, 15:1219-1228.
    • (1995) Arterioscler Thromb Vasc Biol , vol.15 , pp. 1219-1228
    • Blackburn, J.P.1    Peters, N.S.2    Yeh, H.I.3
  • 20
    • 51749098572 scopus 로고    scopus 로고
    • Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
    • Skinningsrud B., Husebye E.S., Pearce S.H., et al. Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. J Clin Endocrinol Metab 2008, 93:3310-3317.
    • (2008) J Clin Endocrinol Metab , vol.93 , pp. 3310-3317
    • Skinningsrud, B.1    Husebye, E.S.2    Pearce, S.H.3
  • 21
    • 34347341846 scopus 로고    scopus 로고
    • Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
    • Todd J.A., Walker N.M., Cooper J.D., et al. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nat Genet 2007, 39:857-864.
    • (2007) Nat Genet , vol.39 , pp. 857-864
    • Todd, J.A.1    Walker, N.M.2    Cooper, J.D.3
  • 22
    • 34547621758 scopus 로고    scopus 로고
    • A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
    • Hakonarson H., Grant S.F., Bradfield J.P., et al. A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. Nature 2007, 448:591-594.
    • (2007) Nature , vol.448 , pp. 591-594
    • Hakonarson, H.1    Grant, S.F.2    Bradfield, J.P.3
  • 23
    • 0033553883 scopus 로고    scopus 로고
    • Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells
    • Ryan M.C., Lee K., Miyashita Y., et al. Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells. J Cell Biol 1999, 145:1309-1323.
    • (1999) J Cell Biol , vol.145 , pp. 1309-1323
    • Ryan, M.C.1    Lee, K.2    Miyashita, Y.3
  • 24
    • 36249022091 scopus 로고    scopus 로고
    • Bridging structure with function: structural, regulatory, and developmental role of laminins
    • Tzu J., Marinkovich M.P. Bridging structure with function: structural, regulatory, and developmental role of laminins. Int J Biochem Cell Biol 2008, 40:199-214.
    • (2008) Int J Biochem Cell Biol , vol.40 , pp. 199-214
    • Tzu, J.1    Marinkovich, M.P.2
  • 25
    • 0027965348 scopus 로고
    • The family of subtilisin/kexin like pro-protein and pro-hormone convertases: divergent or shared functions
    • Seidah N.G., Chretien M., Day R. The family of subtilisin/kexin like pro-protein and pro-hormone convertases: divergent or shared functions. Biochimie 1994, 76:197-209.
    • (1994) Biochimie , vol.76 , pp. 197-209
    • Seidah, N.G.1    Chretien, M.2    Day, R.3
  • 26
    • 0028294866 scopus 로고
    • Proglucagon is processed to glucagon by prohormone convertase PC2 in alpha TC1-6 cells
    • Rouille Y., Westermark G., Martin S.K., et al. Proglucagon is processed to glucagon by prohormone convertase PC2 in alpha TC1-6 cells. Proc Natl Acad Sci USA 1994, 91:3242-3246.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 3242-3246
    • Rouille, Y.1    Westermark, G.2    Martin, S.K.3
  • 27
    • 0026726773 scopus 로고
    • Proinsulin processing by the subtilisin-related proprotein convertases furin PC2, and PC3
    • Smeekens S.P., Montag A.G., Thomas G., et al. Proinsulin processing by the subtilisin-related proprotein convertases furin PC2, and PC3. Proc Natl Acad Sci USA 1992, 89:8822-8826.
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 8822-8826
    • Smeekens, S.P.1    Montag, A.G.2    Thomas, G.3
  • 28
    • 0028952108 scopus 로고
    • Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects
    • Yoshida H., Ohagi S., Sanke T., et al. Association of the prohormone convertase 2 gene (PCSK2) on chromosome 20 with NIDDM in Japanese subjects. Diabetes 1995, 44:389-393.
    • (1995) Diabetes , vol.44 , pp. 389-393
    • Yoshida, H.1    Ohagi, S.2    Sanke, T.3
  • 29
    • 34548403935 scopus 로고    scopus 로고
    • Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population
    • Leak T.S., Keene K.L., Langefeld C.D., et al. Association of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population. Mol Genet Metab 2007, 92:145-150.
    • (2007) Mol Genet Metab , vol.92 , pp. 145-150
    • Leak, T.S.1    Keene, K.L.2    Langefeld, C.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.