写真:内子の白壁

論文集
Collected Papers

2014年以前の記事一覧

  • Masuyama T, Matsuo M, Jing JJ, Tabara Y, Kitsuki K, Yamagata H, Kan Y, Miki T, Ishii K, Kondo I.
    Classic Rett syndrome in a boy with R133C mutation of MECP2.
    Brain Dev 2014以前; 27:439-442.

  • Zhong, W, Yamagata H, Taguchi K, Akatsu H, Kamino K, Yamamoto T, Kosaka K, Takeda M, Kondo K, Miki T.
    Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease.
    J Neurol Sci 2014以前; 238:53-57.

  • Osawa H, Onuma H, Ochi M, Murakami A, Yamauchi J, Takasuka T, Tanabe F, Shimizu I, Kato K, Nishida W, Yamada K, Tabara Y, Yasukawa M, Fujii Y, Ohashi J, Miki T, Makino H.
    Resistin SNP-420 determines its monocyte mRNA and serum levels inducing type 2 diabetes.
    Biochem Biophys Res Commun 2014以前; 335:596-602.

  • Abe M, Wu Z, Yamamoto M, Jin JJ, Tabara Y, Mogi M, Kohara K, Miki T, Nakura J.
    Association of dopamine beta-hydroxylase polymorphism with hypertension through interaction with fasting plasma glucose in Japanese.
    Hypertens Res 2014以前; 28:215-221.

  • Ogimoto A, Hamada M, Miki T, Higaki J.
    Angiotensin I-converting enzyme insertion/insertion genotype as a genetic risk factor for cardiovascular disease.
    Am Heart J 2014以前; 150:1

  • Kohara K, Tabara Y, Oshiumi A, Miyawaki Y, Kobayashi T, Miki T.
    Radial augmentation index: a useful and easily obtainable parameter for vascular aging.
    Am J Hypertens 2014以前; 18:11S-14S.

  • Ogimoto A, Shigematsu Y, Nakura J, Hara Y, Ohtsuka T, Kohara K, Hamada M, Miki T, Higaki J.
    Endothelial nitric oxide synthase gene polymorphism (Glu298Asp) in patients with coexistent hypertrophic cardiomyopathy and coronary spastic angina.
    J Mol Med 2014以前; 83:619-625.

  • Takemura Y, Sakurai Y, Yokoya S, Otaki J, Matsuoka T, Ban N, Hirata I, Miki T, Tsuda T.
    Open-ended questions: are they really beneficial for gathering medical information from patients?
    Tohoku J Exp Med 2014以前; 206:151-154.

  • Fukuda T, Yamashita Y, Nagamitsu S, Miyamoto K, Jin JJ, Ohmori I, Ohtsuka Y, Kuwajima K, Endo S, Iwai T, Yamagata H, Tabara Y, Miki T, Matsuishi T, Kondo I.
    Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
    Brain Dev 2014以前; 27:211-217.

  • Taguchi K, Yamagata HD, Zhong W, Kamino K, Akatsu H, Hata R, Yamamoto T, Kosaka K, Takeda M, Kondo, Miki T.
    Identification of hippocampus-related candidate genes for Alzheimer’s disease.
    Ann Neurol 2014以前; 57:585-588.

  • Yamamoto M, Abe M, Jin JJ, Wu Z, Tabara Y, Mogi M, Kohara K, Miki T, Nakura J.
    Association of a GNAS1 gene variant with hypertension and diabetes mellitus.
    Hypertens Res 2014以前; 27:919-924.

  • Tachibana R, Tabara Y, Kondo I, Miki T, Kohara K.
    Home blood pressure is a better predictor of carotid atherosclerosis than office blood pressure in community-dwelling subjects.
    Hypertens Res 2014以前; 27:633-639.