Takeshita E - Search Results

1

Cholesteryl ester transfer protein polymorphism associated with macroangiopathy in Japanese patients with type 2 diabetes.

Meguro S, Takei I, Murata M, Hirose H, Takei N, Mitsuyoshi Y, Ishii K, Oguchi S, Shinohara J, Takeshita E, Watanabe K, Saruta T. Meguro S, et al. Among authors: takeshita e. Atherosclerosis. 2001 May;156(1):151-6. doi: 10.1016/s0021-9150(00)00606-7. Atherosclerosis. 2001. PMID: 11369008

2

[Genetic risk factors for ischemic cerebrovascular disease--analysis on fifteen candidate prothrombotic gene polymorphisms in the Japanese population].

Ishii K, Murata M, Oguchi S, Takeshita E, Ito D, Tanahashi N, Fukuuchi Y, Saitou I, Ikeda Y, Watanabe K. Ishii K, et al. Among authors: takeshita e. Rinsho Byori. 2004 Jan;52(1):22-7. Rinsho Byori. 2004. PMID: 14968555 Japanese.

3

Angiotensin converting enzyme insertion/deletion polymorphism is associated with plasma antigen levels of plasminogen activator inhibitor-1 in healthy Japanese population.

Matsubara Y, Hayakawa T, Tsuda T, Takeshita E, Watanabe G, Murata M, Watanabe K, Ikeda Y. Matsubara Y, et al. Among authors: takeshita e. Blood Coagul Fibrinolysis. 2000 Mar;11(2):115-20. Blood Coagul Fibrinolysis. 2000. PMID: 10759003

4

Activated factor XII levels are dependent on factor XII 46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects.

Ishii K, Oguchi S, Murata M, Mitsuyoshi Y, Takeshita E, Ito D, Tanahashi N, Fukuuchi Y, Oosumi K, Matsumoto K, Kitajima M, Yamamoto M, Watanabe G, Ikeda Y, Watanabe K. Ishii K, et al. Among authors: takeshita e. Blood Coagul Fibrinolysis. 2000 Apr;11(3):277-84. Blood Coagul Fibrinolysis. 2000. PMID: 10870808

5

[Study of genotype frequencies of ANP 664G/A polymorphism in normal subjects and CVD patients, and its association with plasma ANP levels].

Ohta A, Sonoda A, Yatabe Y, Takeshita E, Saito I, Ito D, Tanahashi N, Fukuuchi Y, Kikuchi H, Murata M, Watanabe K. Ohta A, et al. Among authors: takeshita e. Rinsho Byori. 2002 Mar;50(3):296-300. Rinsho Byori. 2002. PMID: 11985060 Japanese.

6

Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency.

Ishii K, Oguchi S, Moriki T, Yatabe Y, Takeshita E, Murata M, Ikeda Y, Watanabe K. Ishii K, et al. Among authors: takeshita e. Blood Coagul Fibrinolysis. 2004 Jul;15(5):367-73. doi: 10.1097/01.mbc.0000114447.59147.d1. Blood Coagul Fibrinolysis. 2004. PMID: 15205584

7

Factor XII Shizuoka, a novel mutation (Ala392Thr) identified and characterized in a patient with congenital coagulation factor XII deficiency.

Oguchi S, Ishii K, Moriki T, Takeshita E, Murata M, Ikeda Y, Watanabe K. Oguchi S, et al. Among authors: takeshita e. Thromb Res. 2005;115(3):191-7. doi: 10.1016/j.thromres.2004.08.027. Thromb Res. 2005. PMID: 15617741

8

Insulin resistance syndrome in adolescents and adults.

Saito I, Kawabe H, Takeshita E, Wainai H, Murata K, Saruta T. Saito I, et al. Among authors: takeshita e. Hypertens Res. 1996 Jun;19 Suppl 1:S19-22. doi: 10.1291/hypres.19.supplementi_s19. Hypertens Res. 1996. PMID: 9240758 Free article.

9

Association between platelet glycoprotein Ibalpha genotype and ischemic cerebrovascular disease.

Sonoda A, Murata M, Ito D, Tanahashi N, Ohta A, Tada Y, Takeshita E, Yoshida T, Saito I, Yamamoto M, Ikeda Y, Fukuuchi Y, Watanabe K. Sonoda A, et al. Among authors: takeshita e. Stroke. 2000 Feb;31(2):493-7. doi: 10.1161/01.str.31.2.493. Stroke. 2000. PMID: 10657428

10

Serum cortisol in the white-coat phenomenon.

Saito I I, Takeshita E, Murata K, Kawabe H, Saruta T. Saito I I, et al. Among authors: takeshita e. Blood Press Monit. 1996 Aug;1(4):381-383. Blood Press Monit. 1996. PMID: 10226263

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