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Volumn 39, Issue 3, 2012, Pages 2723-2731

Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease

Author keywords

Coronary artery disease; Diabetes mellitus; Genetic polymorphism; Lipid profile; Paraoxonase; Vessel stenosis

Indexed keywords

ANGIOTENSIN CONVERTING ENZYME D; ARGININE; ARYLDIALKYLPHOSPHATASE; DIPEPTIDYL CARBOXYPEPTIDASE; UNCLASSIFIED DRUG;

EID: 84863837572     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-011-1027-4     Document Type: Article
Times cited : (4)

References (54)
  • 1
    • 33745197993 scopus 로고    scopus 로고
    • Association between apolipoprotein e polymorphism and coronary artery disease in the Kermanshah population in Iran
    • Kharrazi H, Vaisi-Raygani A, Sabokroh AR, Pourmotabbed T (2006) Association between apolipoprotein E polymorphism and coronary artery disease in the Kermanshah population in Iran. Clin Biochem 39:613-616
    • (2006) Clin Biochem , vol.39 , pp. 613-616
    • Kharrazi, H.1    Vaisi-Raygani, A.2    Sabokroh, A.R.3    Pourmotabbed, T.4
  • 2
    • 34548478363 scopus 로고    scopus 로고
    • The presence of apolipoprotein e4 and e2 alleles augments the risk of coronary artery disease in type 2 diabetic patients
    • Vaisi-Raygani A, Rahimi Z, Nomani H, Tavilani H, Pourmotabbed T (2007) The presence of apolipoprotein e4 and e2 alleles augments the risk of coronary artery disease in type 2 diabetic patients. Clin Biochem 40:1150-1156
    • (2007) Clin Biochem , vol.40 , pp. 1150-1156
    • Vaisi-Raygani, A.1    Rahimi, Z.2    Nomani, H.3    Tavilani, H.4    Pourmotabbed, T.5
  • 3
    • 79951580660 scopus 로고    scopus 로고
    • Association between apolipoprotein e4 allele, factor v leiden, and plasma lipid and lipoprotein levels with sickle cell disease in Southern Iran
    • Rahimi Z, Vaisi-Raygani A, Pourmotaabed T (2011) Association between apolipoprotein e4 allele, factor V leiden, and plasma lipid and lipoprotein levels with sickle cell disease in Southern Iran. Mol Biol Reports 38(2):703-710
    • (2011) Mol Biol Reports , vol.38 , Issue.2 , pp. 703-710
    • Rahimi, Z.1    Vaisi-Raygani, A.2    Pourmotaabed, T.3
  • 5
    • 77953165868 scopus 로고    scopus 로고
    • Butyrylcholinesterase K variant and the APOE-e4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients
    • Vaisi Raygani A, Rahimi Z, Tavilani H, Pourmotabbed T (2010) Butyrylcholinesterase K variant and the APOE-e4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients. Mol Bio Rep 37(4):2083-2091
    • (2010) Mol Bio Rep , vol.37 , Issue.4 , pp. 2083-2091
    • Vaisi Raygani, A.1    Rahimi, Z.2    Tavilani, H.3    Pourmotabbed, T.4
  • 8
    • 0031748660 scopus 로고    scopus 로고
    • Clinical and epidemiological characteristics of juvenile myocardial infarction in Italy: The GISSI experience
    • Imazio M, Bobbio M, Bergerone S, Barlera S, Maggioni AP (1998) Clinical and epidemiological characteristics of juvenile myocardial infarction in Italy: the GISSI experience. J Ital Cardiol 28(5):505-512
    • (1998) J Ital Cardiol , vol.28 , Issue.5 , pp. 505-512
    • Imazio, M.1    Bobbio, M.2    Bergerone, S.3    Barlera, S.4    Maggioni, A.P.5
  • 9
    • 0029788728 scopus 로고    scopus 로고
    • The Gln-Arg 191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns
    • Antikainen M, Murtomaki S, Syvanne M, Pahlman R, Tahvanainen E, Jauhi-ainen M (1996) The Gln-Arg 191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns. J Clin Invest 98:883-885
    • (1996) J Clin Invest , vol.98 , pp. 883-885
    • Antikainen, M.1    Murtomaki, S.2    Syvanne, M.3    Pahlman, R.4    Tahvanainen, E.5    Jauhi-Ainen, M.6
  • 10
    • 71449093018 scopus 로고    scopus 로고
    • Paraoxonases: Structure, gene polymorphism &role in coronary artery disease
    • Gupta N, Gill K, Singh S (2009) Paraoxonases: structure, gene polymorphism &role in coronary artery disease. Indian J Med Res 130:361-368
    • (2009) Indian J Med Res , vol.130 , pp. 361-368
    • Gupta, N.1    Gill, K.2    Singh, S.3
  • 11
    • 0031283145 scopus 로고    scopus 로고
    • A 192Arg variant of the human paraoxonase (HUMPONA) gene polymorphism is associated with an increased risk for coronary artery disease in Japanese
    • Zama T, Murata M, Matsubara Y, Kawano K, Aoki N, Yoshina H et al (1997) A 192Arg variant of the human paraoxonase (HUMPONA) gene polymorphism is associated with an increased risk for coronary artery disease in Japanese. Arterioscler Thromb Vasc Biol 17:3565-3569
    • (1997) Arterioscler Thromb Vasc Biol , vol.17 , pp. 3565-3569
    • Zama, T.1    Murata, M.2    Matsubara, Y.3    Kawano, K.4    Aoki, N.5    Yoshina, H.6
  • 12
    • 0032974874 scopus 로고    scopus 로고
    • Paraoxonase 192 Gln/Arg gene polymorphism, coronary artery disease, and myocardial infarction in type 2 diabetes
    • Pfohl M, Koch M, Enderle MD, Kuhn R, Fullhase J, Karsch KR, Haring HU (1999) Paraoxonase 192 Gln/Arg gene polymorphism, coronary artery disease, and myocardial infarction in type 2 diabetes. Diabetes 48:623-627
    • (1999) Diabetes , vol.48 , pp. 623-627
    • Pfohl, M.1    Koch, M.2    Enderle, M.D.3    Kuhn, R.4    Fullhase, J.5    Karsch, K.R.6    Haring, H.U.7
  • 13
    • 67349235526 scopus 로고    scopus 로고
    • Association of homocysteine thiolactonase activity and PON1 polymorphisms with the severity of acute coronary syndrome
    • Koubaa N, Nakbi A, Hammami S, Attia N, Mehri S, Hamda K, Farhat M, Miled A, Hammami M (2009) Association of homocysteine thiolactonase activity and PON1 polymorphisms with the severity of acute coronary syndrome. Clin Biochem 42:771-776
    • (2009) Clin Biochem , vol.42 , pp. 771-776
    • Koubaa, N.1    Nakbi, A.2    Hammami, S.3    Attia, N.4    Mehri, S.5    Hamda, K.6    Farhat, M.7    Miled, A.8    Hammami, M.9
  • 14
    • 0030293198 scopus 로고    scopus 로고
    • The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin
    • Davies HG (1996) The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin. Nat Genet 14:334-336
    • (1996) Nat Genet , vol.14 , pp. 334-336
    • Davies, H.G.1
  • 15
    • 0029905656 scopus 로고    scopus 로고
    • Structural, functional diversity of paraoxonases
    • La Du BN (1996) Structural, functional diversity of paraoxonases. Nat Med 2:1186-1187
    • (1996) Nat Med , vol.2 , pp. 1186-1187
    • La Du, B.N.1
  • 16
    • 0032784986 scopus 로고    scopus 로고
    • Does paraoxonase play a role in susceptibility to cardiovascular disease?
    • Aviram M (1999) Does paraoxonase play a role in susceptibility to cardiovascular disease? Mole Medici Today 5:66-78
    • (1999) Mole Medici Today , vol.5 , pp. 66-78
    • Aviram, M.1
  • 17
    • 0034985074 scopus 로고    scopus 로고
    • Coronary artery disease risk in Chinese type 2 diabetics: Is there a role for paraoxonase 1 gene (Q192R polymorphism?)
    • Osei-Hyiaman D, Hou L, Mengbai F, Zhiyin R, Zhiming Z, Kano K (2001) Coronary artery disease risk in Chinese type 2 diabetics: is there a role for paraoxonase 1 gene (Q192R) polymorphism? Euro J Endocrin 144:639-644
    • (2001) Euro J Endocrin , vol.144 , pp. 639-644
    • Osei-Hyiaman, D.1    Hou, L.2    Mengbai, F.3    Zhiyin, R.4    Zhiming, Z.5    Kano, K.6
  • 19
    • 20444375456 scopus 로고    scopus 로고
    • Renin-angiotensin system gene polymorphisms and premature coronary heart disease
    • Sekuri C, Cam FS, Ercan E, Tengiz I, Sagcan A, Eser E et al (2005) Renin-angiotensin system gene polymorphisms and premature coronary heart disease. JRAAS 6:38-42
    • (2005) JRAAS , vol.6 , pp. 38-42
    • Sekuri, C.1    Cam, F.S.2    Ercan, E.3    Tengiz, I.4    Sagcan, A.5    Eser, E.6
  • 20
    • 0036799681 scopus 로고    scopus 로고
    • Angiotensin i converting enzyme, angiotensin II type i receptor and angiotensinogen polymorphisms and early myocardial infarction in Turkish population
    • Ermis C, Tsai MY, Hanson NQ, Akar N, Aras O (2002) Angiotensin I converting enzyme, angiotensin II type I receptor and angiotensinogen polymorphisms and early myocardial infarction in Turkish population. Thromb Haemost 88:693-694
    • (2002) Thromb Haemost , vol.88 , pp. 693-694
    • Ermis, C.1    Tsai, M.Y.2    Hanson, N.Q.3    Akar, N.4    Aras, O.5
  • 21
    • 0032212736 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: Association with early coronary disease
    • Alvarez R, Reguero JR, Batalla A (1998) Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: association with early coronary disease. Cardiovasc Res 40:375-379
    • (1998) Cardiovasc Res , vol.40 , pp. 375-379
    • Alvarez, R.1    Reguero, J.R.2    Batalla, A.3
  • 22
    • 0034088388 scopus 로고    scopus 로고
    • Angiotensinconverting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population
    • Dzimiri N, Basco C, Moorji A, Meyer BF (2000) Angiotensinconverting enzyme polymorphism and the risk of coronary heart disease in the Saudi male population. Arch Pathol Lab Med 124(4):531-534
    • (2000) Arch Pathol Lab Med , vol.124 , Issue.4 , pp. 531-534
    • Dzimiri, N.1    Basco, C.2    Moorji, A.3    Meyer, B.F.4
  • 23
    • 0035814784 scopus 로고    scopus 로고
    • Increased angiotensin-converting enzyme activity in coronary artery specimens from patients with acute coronary syndrome
    • Hoshida S, Kato J, Nishino M, Egami Y, Takeda T, Kawabata M et al (2001) Increased angiotensin-converting enzyme activity in coronary artery specimens from patients with acute coronary syndrome. Circulation 103(5):630-633
    • (2001) Circulation , vol.103 , Issue.5 , pp. 630-633
    • Hoshida, S.1    Kato, J.2    Nishino, M.3    Egami, Y.4    Takeda, T.5    Kawabata, M.6
  • 26
    • 33749066121 scopus 로고    scopus 로고
    • Association between apolipoprotein e polymorphism and serum lipid and apolipoprotein levels with Alzheimer's disease
    • Raygani AV, Rahimi Z, Kharazi H, Tavilani H, Pourmotabbed T (2006) Association between apolipoprotein E polymorphism and serum lipid and apolipoprotein levels with Alzheimer's disease. Neurosci Lett 6 408(1):68-72
    • (2006) Neurosci Lett 6 , vol.408 , Issue.1 , pp. 68-72
    • Raygani, A.V.1    Rahimi, Z.2    Kharazi, H.3    Tavilani, H.4    Pourmotabbed, T.5
  • 27
    • 0026651907 scopus 로고
    • Evidance, from combined segregation and linkage analaysis, that a variant of the angiotensin converting enzyme(ACE) gene controls plasma ACE level
    • Tiret L, Rigat B, Visvikis S, Breda C, Corovol P, Cambien F, Soubrier F (1992) Evidance, from combined segregation and linkage analaysis, that a variant of the angiotensin converting enzyme(ACE) gene controls plasma ACE level. Am J Hum Genet 51:197-205
    • (1992) Am J Hum Genet , vol.51 , pp. 197-205
    • Tiret, L.1    Rigat, B.2    Visvikis, S.3    Breda, C.4    Corovol, P.5    Cambien, F.6    Soubrier, F.7
  • 28
    • 77950859888 scopus 로고    scopus 로고
    • The relationship between paraoxonase1-192 polymorphism and activity with coronary artery disease
    • Mohamed RH, Mohamed RH, Karam RA, Abd El-Aziz TA (2010) The relationship between paraoxonase1-192 polymorphism and activity with coronary artery disease. Clin Biochem 43:553-558
    • (2010) Clin Biochem , vol.43 , pp. 553-558
    • Mohamed, R.H.1    Mohamed, R.H.2    Karam, R.A.3    Abd El-Aziz, T.A.4
  • 29
    • 64249104818 scopus 로고    scopus 로고
    • Association of genetic variants in methylenetetrahydrofolate reductase and paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease
    • Aydin M, Gokkusu C, Ozkok E, Tulubas F, Unlucerci Y, Pamukcu B, Ozbek Z, Umman B (2009) Association of genetic variants in methylenetetrahydrofolate reductase and paraoxonase-1 genes with homocysteine, folate and vitamin B12 in coronary artery disease. Mol Cell Biochem 325:199-208
    • (2009) Mol Cell Biochem , vol.325 , pp. 199-208
    • Aydin, M.1    Gokkusu, C.2    Ozkok, E.3    Tulubas, F.4    Unlucerci, Y.5    Pamukcu, B.6    Ozbek, Z.7    Umman, B.8
  • 30
    • 85047677146 scopus 로고    scopus 로고
    • Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus
    • Odawara M, Tachi Y, Yamashitya K (1997) Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab 82:2257-2260
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 2257-2260
    • Odawara, M.1    Tachi, Y.2    Yamashitya, K.3
  • 31
    • 0028809494 scopus 로고
    • A variant of human paraoxonase/ arylesterase (HUMPONA) gene is a risk factor for coronary artery disease
    • Serrato M, Marian AJ (1995) A variant of human paraoxonase/ arylesterase (HUMPONA) gene is a risk factor for coronary artery disease. J Clin Invest 96:3005-3008
    • (1995) J Clin Invest , vol.96 , pp. 3005-3008
    • Serrato, M.1    Marian, A.J.2
  • 32
    • 1542331537 scopus 로고    scopus 로고
    • Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: Meta-analysis of 43 studies
    • Wheeler JG, Keavney BD, Watkins H, Collins R, Danesh J (2004) Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies. Lancet 28:363(9410):686-695
    • (2004) Lancet 28 , vol.363 , Issue.9410 , pp. 686-695
    • Wheeler, J.G.1    Keavney, B.D.2    Watkins, H.3    Collins, R.4    Danesh, J.5
  • 33
    • 23644439454 scopus 로고    scopus 로고
    • The association of the PON1 Q192R polymorphism with coronary heart disease: Findings from the British Women's heart and health cohort study and a meta-analysis
    • Debbie T, Lawlor A, Day INM, Gaunt TR, Hinks LJ, Briggs PJ, Kiessling M, Timpson N, Smith GD, Ebrahim S (2004) The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's heart and health cohort study and a meta-analysis. BMC Genet 5(17):1-13
    • (2004) BMC Genet , vol.5 , Issue.17 , pp. 1-13
    • Debbie, T.1    Lawlor, A.2    Inm, D.3    Gaunt, T.R.4    Hinks, L.J.5    Briggs, P.J.6    Kiessling, M.7    Timpson, N.8    Smith, G.D.9    Ebrahim, S.10
  • 34
    • 75649118616 scopus 로고    scopus 로고
    • The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease
    • Task?ran P, Cam SF, Sekuri C, Tuzun N, Alioglu E, Alt?ntas N, Berdeli A (2009) The relationship between paraoxanase gene Leu-Met (55) and Gln-Arg (192) polymorphisms and coronary artery disease. Arch Turk Soc Cardiol 37(7):473-478
    • (2009) Arch Turk Soc Cardiol , vol.37 , Issue.7 , pp. 473-478
    • Taskran, P.1    Cam, S.F.2    Sekuri, C.3    Tuzun, N.4    Alioglu, E.5    Altntas, N.6    Berdeli, A.7
  • 39
    • 0032512704 scopus 로고    scopus 로고
    • Effect of the human serum PON1 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification
    • Mackness B, Mackness MI, Arrol S, Turkie W, Durrington PN (1998) Effect of the human serum PON1 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification. FEBS Lett 423:57-60
    • (1998) FEBS Lett , vol.423 , pp. 57-60
    • MacKness, B.1    MacKness, M.I.2    Arrol, S.3    Turkie, W.4    Durrington, P.N.5
  • 40
    • 0031757519 scopus 로고    scopus 로고
    • LDL oxidation by arterial wall macrophages depends on the oxidative status in the lipoprotein and in the cells: Role of prooxidants vs. antioxidants
    • Aviram M, Fuhrman B (1998) LDL oxidation by arterial wall macrophages depends on the oxidative status in the lipoprotein and in the cells: role of prooxidants vs. antioxidants. Mol Cell Biochem 188:149-159
    • (1998) Mol Cell Biochem , vol.188 , pp. 149-159
    • Aviram, M.1    Fuhrman, B.2
  • 41
    • 0031696245 scopus 로고    scopus 로고
    • Paraoxonase and coronary heart disease
    • Mackness MI (1998) Paraoxonase and coronary heart disease. Curr Opin Lipidol 9:319-324
    • (1998) Curr Opin Lipidol , vol.9 , pp. 319-324
    • MacKness, M.I.1
  • 42
    • 0031939725 scopus 로고    scopus 로고
    • Paraoxonase-gene polymorphisms associated with coronary heart disease support for the oxidative damage hypothesis?
    • Heinecke JW, Lusis AJ (1998) Paraoxonase-gene polymorphisms associated with coronary heart disease: support for the oxidative damage hypothesis? Am J Hum Genet 62:20-24
    • (1998) Am J Hum Genet , vol.62 , pp. 20-24
    • Heinecke, J.W.1    Lusis, A.J.2
  • 43
    • 0032522985 scopus 로고    scopus 로고
    • Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions: A possible peroxidative role for PON1
    • Aviram M, Rosenblat M, Bisgaier CL, Newton RS, Primo-Parmo SL, La Du BN (1998) Paraoxonase inhibits high-density lipoprotein oxidation and preserves its functions: a possible peroxidative role for PON1. J Clin Invest 101:1581-1590
    • (1998) J Clin Invest , vol.101 , pp. 1581-1590
    • Aviram, M.1    Rosenblat, M.2    Bisgaier, C.L.3    Newton, R.S.4    Primo-Parmo, S.L.5    La Du, B.N.6
  • 44
    • 78149469153 scopus 로고    scopus 로고
    • Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia
    • Ajmal M, Ahmed W, Sadeque A, Ali SH, Bokhari SH, Ahmed N, Qamar R (2010) Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia. Mol Biol Rep 37(8):3869-3875
    • (2010) Mol Biol Rep , vol.37 , Issue.8 , pp. 3869-3875
    • Ajmal, M.1    Ahmed, W.2    Sadeque, A.3    Ali, S.H.4    Bokhari, S.H.5    Ahmed, N.6    Qamar, R.7
  • 45
    • 77949263616 scopus 로고    scopus 로고
    • Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians
    • AshokKumar M, Subhashini NG, SaiBabu R, Ramesh A, Cherian KM, Emmanuel C (2010) Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians. Mol Biol Rep 37(1):521-527
    • (2010) Mol Biol Rep , vol.37 , Issue.1 , pp. 521-527
    • Ashokkumar, M.1    Subhashini, N.G.2    Saibabu, R.3    Ramesh, A.4    Cherian, K.M.5    Emmanuel, C.6
  • 46
    • 39049118376 scopus 로고    scopus 로고
    • Association of angiotensin-converting enzyme gene insertion/ deletion polymorphism with metabolic syndrome in Iranians with type 2 diabetes mellitus
    • Nikzamir A, Nakhjavani M, Golmohamadi T, Dibai L (2008) Association of angiotensin-converting enzyme gene insertion/ deletion polymorphism with metabolic syndrome in Iranians with type 2 diabetes mellitus. Arch Iranian Med 11(1):3-9
    • (2008) Arch Iranian Med , vol.11 , Issue.1 , pp. 3-9
    • Nikzamir, A.1    Nakhjavani, M.2    Golmohamadi, T.3    Dibai, L.4
  • 47
    • 79951577923 scopus 로고    scopus 로고
    • DD genotype of ace gene I/D polymorphism is associated in a Turkish study population with osteoarthritis
    • Bayram B, Say?n E, Gunes HV, Deg?irmenci I, Turkog?lu Z, Doganer F, Cosan DT (2011) DD genotype of ace gene I/D polymorphism is associated in a Turkish study population with osteoarthritis. Mol Biol 38(3):1713-1716
    • (2011) Mol Biol , vol.38 , Issue.3 , pp. 1713-1716
    • Bayram, B.1    Sayn, E.2    Gunes, H.V.3    Degirmenci, I.4    Turkoglu, Z.5    Doganer, F.6    Cosan, D.T.7
  • 48
    • 79951581875 scopus 로고    scopus 로고
    • The frequency of factor v Leiden mutation, ACE gene polymorphism, serum ACE activity and response to ACE inhibitor and angiotensin II receptor antagonist drugs in Iranians type II diabetic patients with microalbuminuria
    • Rahimi Z, Felehgari V, Rahimi M, Mozafari H, Yari K, Vaisi-Raygani A, Rezaei M, Malek-Khosravi S, Khazaie H (2011) The frequency of factor V Leiden mutation, ACE gene polymorphism, serum ACE activity and response to ACE inhibitor and angiotensin II receptor antagonist drugs in Iranians type II diabetic patients with microalbuminuria. Mol Biol Rep 38(3):2117-2123
    • (2011) Mol Biol Rep , vol.38 , Issue.3 , pp. 2117-2123
    • Rahimi, Z.1    Felehgari, V.2    Rahimi, M.3    Mozafari, H.4    Yari, K.5    Vaisi-Raygani, A.6    Rezaei, M.7    Malek-Khosravi, S.8    Khazaie, H.9
  • 49
    • 33846870739 scopus 로고    scopus 로고
    • Angiotensin-converting enzyme gene polymorphism and allele frequencies in the Lebanese population: Prevalence and review of the literature
    • Sabbagh AS, Otrock ZK, Mahfoud ZR, Zaatari GS, Mahfouz RA (2007) Angiotensin-converting enzyme gene polymorphism and allele frequencies in the Lebanese population: prevalence and review of the literature. Mol Biol Rep 34(1):47-52
    • (2007) Mol Biol Rep , vol.34 , Issue.1 , pp. 47-52
    • Sabbagh, A.S.1    Otrock, Z.K.2    Mahfoud, Z.R.3    Zaatari, G.S.4    Mahfouz, R.A.5
  • 50
    • 0027968353 scopus 로고
    • Synergistic effects of angiotensin-converting enzyme and angiotensin II type 1 receptor DD genotype of the gene polymorphisms on risk of myocardial infarction
    • Tiret L, Bonnardeaux A, Poirier (1994) Synergistic effects of angiotensin-converting enzyme and angiotensin II type 1 receptor DD genotype of the gene polymorphisms on risk of myocardial infarction. Lancet 344:910-913
    • (1994) Lancet , vol.344 , pp. 910-913
    • Tiret, L.1    Poirier, B.A.2
  • 51
    • 0026675062 scopus 로고
    • Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction
    • Cambien F, Poirier O, Lecerf L et al (1992) Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction. Nature 359:641-644
    • (1992) Nature , vol.359 , pp. 641-644
    • Cambien, F.1    Poirier, O.2    Lecerf, L.3
  • 52
    • 77952674755 scopus 로고    scopus 로고
    • Angiotensin converting enzyme DD genotype not associated with increased risk of coronary artery disease in the Iranian population
    • Shafiee SM, Firoozrai M, Salimi S, Zand H, Hesabi B, Mohebbi A (2010) Angiotensin converting enzyme DD genotype not associated with increased risk of coronary artery disease in the Iranian population. Pathophysiology 17(3):163-167
    • (2010) Pathophysiology , vol.17 , Issue.3 , pp. 163-167
    • Shafiee, S.M.1    Firoozrai, M.2    Salimi, S.3    Zand, H.4    Hesabi, B.5    Mohebbi, A.6
  • 53
    • 0034606897 scopus 로고    scopus 로고
    • Largescale test of hypothesized associations between the angiotensinconverting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 control subjects: International studies of infarct survival (ISIS) collaborators
    • Keavney B, McKenzie C, Parish S, Palmer A, Clark S, Youngman L, Delepine M, Lathrop M, Peto R, Collins R (2000) Largescale test of hypothesized associations between the angiotensinconverting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 control subjects: international studies of infarct survival (ISIS) collaborators. Lancet 355:434-442
    • (2000) Lancet , vol.355 , pp. 434-442
    • Keavney, B.1    McKenzie, C.2    Parish, S.3    Palmer, A.4    Clark, S.5    Youngman, L.6    Delepine, M.7    Lathrop, M.8    Peto, R.9    Collins, R.10
  • 54
    • 78651082840 scopus 로고    scopus 로고
    • Angiotensin converting enzyme I/D, angiotensinogen M235T and AT1-R A/C1166 gene polymorphisms in patients with acromegaly
    • Turgut S, Ak?n F, Akc?lar R, Ayada C, Turgut G (2011) Angiotensin converting enzyme I/D, angiotensinogen M235T and AT1-R A/C1166 gene polymorphisms in patients with acromegaly. Mol Biol Rep 38(1):569-576
    • (2011) Mol Biol Rep , vol.38 , Issue.1 , pp. 569-576
    • Turgut, S.1    Akn, F.2    Akclar, R.3    Ayada, C.4    Turgut, G.5


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