Murata M - Search Results

1

T280M and V249I polymorphisms of fractalkine receptor CX3CR1 and ischemic cerebrovascular disease.

Hattori H, Ito D, Tanahashi N, Murata M, Saito I, Watanabe K, Suzuki N. Hattori H, et al. Among authors: murata m. Neurosci Lett. 2005 Feb 10;374(2):132-5. doi: 10.1016/j.neulet.2004.10.042. Neurosci Lett. 2005. PMID: 15644279

2

[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: murata m. Rinsho Byori. 2002 Mar;50(3):296-300. Rinsho Byori. 2002. PMID: 11985060 Japanese.

3

[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: murata m. Rinsho Byori. 2004 Jan;52(1):22-7. Rinsho Byori. 2004. PMID: 14968555 Japanese.

4

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: murata m. Blood Coagul Fibrinolysis. 2004 Jul;15(5):367-73. doi: 10.1097/01.mbc.0000114447.59147.d1. Blood Coagul Fibrinolysis. 2004. PMID: 15205584

5

High throughput multiple combination extraction from large scale polymorphism data by exact tree method.

Miyaki K, Omae K, Murata M, Tanahashi N, Saito I, Watanabe K. Miyaki K, et al. Among authors: murata m. J Hum Genet. 2004;49(9):455-462. doi: 10.1007/s10038-004-0174-z. Epub 2004 Aug 11. J Hum Genet. 2004. PMID: 15309679

6

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: murata m. Thromb Res. 2005;115(3):191-7. doi: 10.1016/j.thromres.2004.08.027. Thromb Res. 2005. PMID: 15617741

7

Assessment of tailor-made prevention of atherosclerosis with folic acid supplementation: randomized, double-blind, placebo-controlled trials in each MTHFR C677T genotype.

Miyaki K, Murata M, Kikuchi H, Takei I, Nakayama T, Watanabe K, Omae K. Miyaki K, et al. Among authors: murata m. J Hum Genet. 2005;50(5):241-248. doi: 10.1007/s10038-005-0247-7. Epub 2005 May 14. J Hum Genet. 2005. PMID: 15895286 Clinical Trial.

8

Increased risk of obesity resulting from the interaction between high energy intake and the Trp64Arg polymorphism of the beta3-adrenergic receptor gene in healthy Japanese men.

Miyaki K, Sutani S, Kikuchi H, Takei I, Murata M, Watanabe K, Omae K. Miyaki K, et al. Among authors: murata m. J Epidemiol. 2005 Nov;15(6):203-10. doi: 10.2188/jea.15.203. J Epidemiol. 2005. PMID: 16276029 Free PMC article.

9

Salt intake affects the relation between hypertension and the T-786C polymorphism in the endothelial nitric oxide synthase gene.

Miyaki K, Tohyama S, Murata M, Kikuchi H, Takei I, Watanabe K, Omae K. Miyaki K, et al. Among authors: murata m. Am J Hypertens. 2005 Dec;18(12 Pt 1):1556-62. doi: 10.1016/j.amjhyper.2005.06.012. Am J Hypertens. 2005. PMID: 16364825

10

Telomere length of normal leukocytes is affected by a functional polymorphism of hTERT.

Matsubara Y, Murata M, Yoshida T, Watanabe K, Saito I, Miyaki K, Omae K, Ikeda Y. Matsubara Y, et al. Among authors: murata m. Biochem Biophys Res Commun. 2006 Mar 3;341(1):128-31. doi: 10.1016/j.bbrc.2005.12.163. Epub 2006 Jan 6. Biochem Biophys Res Commun. 2006. PMID: 16412982

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