Gln192Arg polymorphism in paraoxonase gene is associated with coronary heart disease in Japanese NIDDM.

被引：0
|
作者：
Odawara, M
Tachi, Y
Sasaki, K
Tada, K
Yamashita, K
机构：
来源：
DIABETES | 1996年 / 45卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：235 / 235
页数：1
相关论文
共 50 条
  • [41] An (192)Arg variant of the human paraoxonase (HUMPONA) gene polymorphisms is associated for with the increased risk for coronary artery disease in the Japanese
    Zama, T
    Murata, M
    Matsubara, Y
    Kawano, K
    Aoki, N
    Yoshino, H
    Watanabe, G
    Ishikawa, K
    Ikeda, Y
    [J]. THROMBOSIS AND HAEMOSTASIS, 1997, : P2129 - P2129
  • [42] Paraoxonase (Gln192-Arg) polymorphism in French type 2 diabetics
    Helbecque, N
    Cottel, D
    Meirhaeghe, A
    Dallongeville, J
    Amouyel, P
    Arveiler, D
    Wagner, A
    Ruidavets, JB
    Ferrieres, J
    [J]. ATHEROSCLEROSIS, 1999, 147 (02) : 415 - 416
  • [43] The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in Taiwan
    Ko, YL
    Ko, YS
    Wang, SM
    Hsu, LA
    Chang, CJ
    Chu, PH
    Cheng, NJ
    Chen, WJ
    Chiang, CW
    Lee, YS
    [J]. ATHEROSCLEROSIS, 1998, 141 (02) : 259 - 264
  • [44] The paraoxonase Leu-Met54 and Gln-Arg191 gene polymorphisms are not associated with the risk of coronary heart disease
    Gardemann, A
    Philipp, M
    Hess, K
    Katz, N
    Tillmanns, H
    Haberbosch, W
    [J]. ATHEROSCLEROSIS, 2000, 152 (02) : 421 - 431
  • [45] Paraoxonase Gln-Arg(192) and Leu-Met(55) gene polymorphisms and enzyme activity in a population with a low rate of coronary heart disease
    Ferré, N
    Tous, M
    Paul, A
    Zamora, A
    Vendrell, JJ
    Bardají, A
    Camps, J
    Richart, C
    Joven, J
    [J]. CLINICAL BIOCHEMISTRY, 2002, 35 (03) : 197 - 203
  • [46] Association between paraoxonase 192Gln/Arg genotype and the mortality rate by coronary artery disease in Japanese general population.
    Nakano, S
    Maruyama, T
    Murata, M
    Maruyama, C
    Kyotani, S
    Kasuga, A
    Hirose, H
    Ikeda, Y
    Tsushima, M
    Saruta, T
    [J]. THROMBOSIS AND HAEMOSTASIS, 1999, : 542 - 543
  • [47] Paraoxonase 1 192Gln/Arg polymorphism is associated with the risk of microangiopathy in Type 2 diabetes mellitus
    Murata, M
    Maruyama, T
    Suzuki, Y
    Saruta, T
    Ikeda, Y
    [J]. DIABETIC MEDICINE, 2004, 21 (08) : 837 - 844
  • [48] The GLN-ARG191 polymorphism of the human paraoxonase gene in Korean coronary artery disease patients with/without diabetes
    Cho, Y
    Park, Y
    Ahn, Y
    Kim, T
    Kim, M
    Lee, J
    Kim, K
    Kim, S
    Kim, J
    Lee, B
    Lee, J
    [J]. RECENT ADVANCES ON THE PATHOGENESIS AND MANAGEMENT OF DIABETES MELLITUS: PROCEEDINGS OF THE 9TH KOREA-JAPAN SYMPOSIUM ON DIABETES MELLITUS, KYONGJU, KOREA, 11-12 APRIL 1997, 1998, 1149 : 201 - 204
  • [49] Different pattern of association of paraoxonase Gln192→Arg polymorphism with sporadic late-onset Alzheimer's disease and coronary artery disease
    Scacchi, R
    Gambina, G
    Martini, MC
    Broggio, E
    Vilardo, T
    Corbo, RM
    [J]. NEUROSCIENCE LETTERS, 2003, 339 (01) : 17 - 20
  • [50] Endothelial nitric oxide synthase gene polymorphism and coronary heart disease in Japanese NIDDM
    M. Odawara
    K. Sasaki
    Y. Tachi
    K. Yamashita
    [J]. Diabetologia, 1998, 41 : 365 - 366
12345