-
1
-
-
33645516595
-
The relationships of proteinuria, serum creatinine, glomerular filtration rate with cardiovascular disease mortality in Japanese general population
-
Irie F, Iso H, Sairenchi T et al. The relationships of proteinuria, serum creatinine, glomerular filtration rate with cardiovascular disease mortality in Japanese general population. Kidney Int 2006; 69: 1264-1271.
-
(2006)
Kidney Int
, vol.69
, pp. 1264-1271
-
-
Irie, F.1
Iso, H.2
Sairenchi, T.3
-
2
-
-
4644221457
-
Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization
-
Go AS, Chertow GM, Fan D et al. Chronic kidney disease and the risks of death, cardiovascular events, and hospitalization. N Engl J Med 2004; 351: 1296-1305.
-
(2004)
N Engl J Med
, vol.351
, pp. 1296-1305
-
-
Go, A.S.1
Chertow, G.M.2
Fan, D.3
-
3
-
-
33846229699
-
Risk factors for chronic kidney disease in a community-based population: A 10-year follow-up study
-
Yamagata K, Ishida K, Sairenchi T et al. Risk factors for chronic kidney disease in a community-based population: a 10-year follow-up study. Kidney Int 2007; 71: 159-166.
-
(2007)
Kidney Int
, vol.71
, pp. 159-166
-
-
Yamagata, K.1
Ishida, K.2
Sairenchi, T.3
-
4
-
-
1342322653
-
Increased prevalence of oxidant stress and inflammation in patients with moderate to severe chronic kidney disease
-
Oberg BP, McMenamin E, Lucas FL et al. Increased prevalence of oxidant stress and inflammation in patients with moderate to severe chronic kidney disease. Kidney Int 2004; 65: 1009-1016.
-
(2004)
Kidney Int
, vol.65
, pp. 1009-1016
-
-
Oberg, B.P.1
McMenamin, E.2
Lucas, F.L.3
-
5
-
-
0032537833
-
Mice lacking serum paraoxonase are susceptible to organophosphate toxicity and atherosclerosis
-
Shih DM, Gu L, Xia YR et al. Mice lacking serum paraoxonase are susceptible to organophosphate toxicity and atherosclerosis. Nature 1998; 394: 284-287.
-
(1998)
Nature
, vol.394
, pp. 284-287
-
-
Shih, D.M.1
Gu, L.2
Xia, Y.R.3
-
6
-
-
0037162376
-
Decreased atherosclerotic lesion formation in human serum paraoxonase transgenic mice
-
Tward A, Xia YR, Wang XP et al. Decreased atherosclerotic lesion formation in human serum paraoxonase transgenic mice. Circulation 2002; 106: 484-490.
-
(2002)
Circulation
, vol.106
, pp. 484-490
-
-
Tward, A.1
Xia, Y.R.2
Wang, X.P.3
-
7
-
-
18744364425
-
Paraoxonase 1 192/55 gene polymorphisms in Alzheimer's disease
-
Dantoine TF. Paraoxonase 1 192/55 gene polymorphisms in Alzheimer's disease. Ann NY Acad Sci 2002; 977: 239-244.
-
(2002)
Ann NY Acad Sci
, vol.977
, pp. 239-244
-
-
Dantoine, T.F.1
-
8
-
-
0031757880
-
Decrease of serum paraoxonase activity in chronic renal failure
-
Dantoine TF, Debord J, Charmes JP et al. Decrease of serum paraoxonase activity in chronic renal failure. J Am Soc Nephrol 1998; 9: 2082-2088.
-
(1998)
J Am Soc Nephrol
, vol.9
, pp. 2082-2088
-
-
Dantoine, T.F.1
Debord, J.2
Charmes, J.P.3
-
9
-
-
40949127806
-
Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk
-
Bhattacharyya T, Nicholls SJ, Topol EJ et al. Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk. JAMA 2008; 299: 1265-1276.
-
(2008)
JAMA
, vol.299
, pp. 1265-1276
-
-
Bhattacharyya, T.1
Nicholls, S.J.2
Topol, E.J.3
-
11
-
-
4444307712
-
The role of paraoxonase 1 activity in cardiovascular disease: Potential for therapeutic intervention
-
Mackness MI, Durrington PN, Mackness B. The role of paraoxonase 1 activity in cardiovascular disease: potential for therapeutic intervention. Am J Cardiovasc Drugs 2004; 4: 211-217.
-
(2004)
Am J Cardiovasc Drugs
, vol.4
, pp. 211-217
-
-
Mackness, M.I.1
Durrington, P.N.2
Mackness, B.3
-
12
-
-
0027486997
-
Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: Glutamine or arginine at position 191, for the respective A or B allozymes
-
Adkins S, Gan KN, Mody M et al. Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes. Am J Hum Genet 1993; 52: 598-608.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 598-608
-
-
Adkins, S.1
Gan, K.N.2
Mody, M.3
-
13
-
-
1542331537
-
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 et al. Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies. Lancet 2004; 363: 689-695.
-
(2004)
Lancet
, vol.363
, pp. 689-695
-
-
Wheeler, J.G.1
Keavney, B.D.2
Watkins, H.3
-
14
-
-
0141790176
-
Role of the endothelin-1 gene locus for renal impairment in the general nondiabetic population
-
Pinto-Sietsma SJ, Herrmann SM, Schmidt-Petersen K et al. Role of the endothelin-1 gene locus for renal impairment in the general nondiabetic population. J Am Soc Nephrol 2003; 14: 2596-2602.
-
(2003)
J Am Soc Nephrol
, vol.14
, pp. 2596-2602
-
-
Pinto-Sietsma, S.J.1
Herrmann, S.M.2
Schmidt-Petersen, K.3
-
15
-
-
40049100295
-
Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: The Takahata study
-
Konta T, Emi M, Toriyama S et al. Association of CC chemokine ligand 5 genotype with urinary albumin excretion in the non-diabetic Japanese general population: the Takahata study. J Hum Genet 2008; 53: 267-274.
-
(2008)
J Hum Genet
, vol.53
, pp. 267-274
-
-
Konta, T.1
Emi, M.2
Toriyama, S.3
-
16
-
-
0027396833
-
The molecular basis of the human serum paraoxonase activity polymorphism
-
Humbert R, Adler DA, Disteche CM et al. The molecular basis of the human serum paraoxonase activity polymorphism. Nat Genet 1993; 3: 73-76.
-
(1993)
Nat Genet
, vol.3
, pp. 73-76
-
-
Humbert, R.1
Adler, D.A.2
Disteche, C.M.3
-
17
-
-
33845572689
-
The 192R/Q polymorphs of serum paraoxonase PON1 differ in HDL binding, lipolactonase stimulation, and cholesterol efflux
-
Gaidukov L, Rosenblat M, Aviram M et al. The 192R/Q polymorphs of serum paraoxonase PON1 differ in HDL binding, lipolactonase stimulation, and cholesterol efflux. J Lipid Res 2006; 47: 2492-2502.
-
(2006)
J Lipid Res
, vol.47
, pp. 2492-2502
-
-
Gaidukov, L.1
Rosenblat, M.2
Aviram, M.3
-
19
-
-
0034673981
-
Smoking is associated with reduced serum paraoxonase activity and concentration in patients with coronary artery disease
-
James RW, Leviev I, Righetti A. Smoking is associated with reduced serum paraoxonase activity and concentration in patients with coronary artery disease. Circulation 2000; 101: 2252-2257.
-
(2000)
Circulation
, vol.101
, pp. 2252-2257
-
-
James, R.W.1
Leviev, I.2
Righetti, A.3
-
20
-
-
0037219558
-
WISE Study Group. Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study
-
Chen Q, Reis SE, Kammerer CM et al. WISE Study Group. Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study. Am J Hum Genet 2003; 72: 13-22.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 13-22
-
-
Chen, Q.1
Reis, S.E.2
Kammerer, C.M.3
-
21
-
-
85047677146
-
Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus
-
Odawara M, Tachi Y, Yamashita K. Paraoxonase polymorphism (Gln192-Arg) is associated with coronary heart disease in Japanese noninsulin-dependent diabetes mellitus. J Clin Endocrinol Metab 1997; 82: 2257-2260.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 2257-2260
-
-
Odawara, M.1
Tachi, Y.2
Yamashita, K.3
-
22
-
-
0028809494
-
A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease
-
Serrato M, Marian AJ. A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease. J Clin Invest 1995; 96: 3005-3008.
-
(1995)
J Clin Invest
, vol.96
, pp. 3005-3008
-
-
Serrato, M.1
Marian, A.J.2
-
23
-
-
0031284880
-
The Arg192 isoform of paraoxonase with low sarin-hydrolyzing activity is dominant in the Japanese
-
Yamasaki Y, Sakamoto K, Watada H et al. The Arg192 isoform of paraoxonase with low sarin-hydrolyzing activity is dominant in the Japanese. Hum Genet 1997; 101: 67-68.
-
(1997)
Hum Genet
, vol.101
, pp. 67-68
-
-
Yamasaki, Y.1
Sakamoto, K.2
Watada, H.3
-
24
-
-
33747036671
-
Prevalence and risk factor analysis of microalbuminuria in Japanese general population: The Takahata study
-
Konta T, Hao Z, Abiko H et al. Prevalence and risk factor analysis of microalbuminuria in Japanese general population: the Takahata study. Kidney Int 2006; 70: 751-756.
-
(2006)
Kidney Int
, vol.70
, pp. 751-756
-
-
Konta, T.1
Hao, Z.2
Abiko, H.3
-
25
-
-
23044448585
-
Definition and classification of chronic kidney disease: A position statement from Kidney Disease: Improving Global Outcomes (KDIGO)
-
Levey AS, Eckardt KU, Tsukamoto Y et al. Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO). Kidney Int 2005; 67: 2089-2100.
-
(2005)
Kidney Int
, vol.67
, pp. 2089-2100
-
-
Levey, A.S.1
Eckardt, K.U.2
Tsukamoto, Y.3
-
26
-
-
36248970058
-
Modification of the Modification of Diet in Renal Disease (MDRD) Study equation for Japan
-
Imai E, Horio M, Nitta K et al. Modification of the Modification of Diet in Renal Disease (MDRD) Study equation for Japan. Am J Kidney Dis 2007; 50: 927-937.
-
(2007)
Am J Kidney Dis
, vol.50
, pp. 927-937
-
-
Imai, E.1
Horio, M.2
Nitta, K.3
-
27
-
-
0020534463
-
The human serum paraoxonase polymorphism: Identification of phenotypes by their response to salts
-
Eckerson HW, Romson J, Wyte C et al. The human serum paraoxonase polymorphism: identification of phenotypes by their response to salts. Am J Hum Genet 1983; 35: 214-227.
-
(1983)
Am J Hum Genet
, vol.35
, pp. 214-227
-
-
Eckerson, H.W.1
Romson, J.2
Wyte, C.3
-
28
-
-
0032998425
-
Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes
-
Lyamichev V, Mast AL, Hall JG et al. Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes. Nat Biotechnol 1997; 17: 292-296.
-
(1997)
Nat Biotechnol
, vol.17
, pp. 292-296
-
-
Lyamichev, V.1
Mast, A.L.2
Hall, J.G.3
-
29
-
-
17344387757
-
Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation
-
Mein CA, Barratt BJ, Dunn MG et al. Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation. Genome Res 2000; 10: 330-343.
-
(2000)
Genome Res
, vol.10
, pp. 330-343
-
-
Mein, C.A.1
Barratt, B.J.2
Dunn, M.G.3
-
30
-
-
0033006003
-
Allelic discrimination using fluorogenic probes and the 50 nuclease assay
-
Livak KJ. Allelic discrimination using fluorogenic probes and the 50 nuclease assay. Genet Anal 1999; 14: 143-149.
-
(1999)
Genet Anal
, vol.14
, pp. 143-149
-
-
Livak, K.J.1
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