1 - 25 of 37 results for author:"Kuno S." in Literature citations
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| Levels of the oxidative stress marker gamma-glutamyltranspeptidase at different stages of nonalcoholic fatty liver disease. Irie M., Sohda T., Iwata K., Kunimoto H., Fukunaga A., Kuno S., Yotsumoto K., Sakurai K., Iwashita H., Hirano G. et al. J. Int. Med. Res. 40:924-933(2012) · Mapped (9) |
| Diurnal infection patterns and impact of Microcystis cyanophages in a Japanese pond. Kimura S., Yoshida T., Hosoda N., Honda T., Kuno S., Kamiji R., Hashimoto R., Sako Y. Appl. Environ. Microbiol. 78:5805-5811(2012) · UniProtKB (87) |
| Effects of anti-beta2-glycoprotein I antibody on PlGF, VEGF and sVEGFR1 production from cultured choriocarcinoma cell line. Ichikawa G., Yamamoto T., Chishima F., Nakamura A., Kuno S., Murase T., Suzuki M. J. Obstet. Gynaecol. Res. 37:1076-1083(2011) · Mapped (6) |
| ACTN3 polymorphism affects thigh muscle area. Zempo H., Tanabe K., Murakami H., Iemitsu M., Maeda S., Kuno S. Int J Sports Med 31:138-142(2010) · Mapped (5) |
| Positive association of common variants in CD36 with neovascular age-related macular degeneration. Kondo N., Honda S., Kuno S., Negi A. Aging (Albany NY) 1:266-274(2009) · Mapped (19) |
| Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology. Kondo N., Honda S., Kuno S., Negi A. Ophthalmology 116:1502-1509(2009) · Mapped (35) |
| Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy. Bessho H., Kondo N., Honda S., Kuno S., Negi A. Mol. Vis. 15:1107-1114(2009) · Mapped (1) |
| Combination of polymorphisms in the beta2-adrenergic receptor and nitric oxide synthase 3 genes increases the risk for hypertension. Misono M., Maeda S., Iemitsu M., Nakata Y., Otsuki T., Sugawara J., Zempo H., Yoshizawa M., Miyaki A., Kuno S. et al. J. Hypertens. 27:1377-1383(2009) · Mapped (9) |
| Effect of moderate exercise training on T-helper cell subpopulations in elderly people. Shimizu K., Kimura F., Akimoto T., Akama T., Tanabe K., Nishijima T., Kuno S., Kono I. Exerc Immunol Rev 14:24-37(2008) · Mapped (3) |
| Coding variant I62V in the complement factor H gene is strongly associated with polypoidal choroidal vasculopathy. Kondo N., Honda S., Kuno S., Negi A. Ophthalmology 116:304-310(2009) · Mapped (5) |
| Arterial stiffness, physical activity, and atrial natriuretic Peptide gene polymorphism in older subjects. Iemitsu M., Maeda S., Otsuki T., Sugawara J., Kuno S., Ajisaka R., Matsuda M. Hypertens. Res. 31:767-774(2008) · Mapped (1) |
| Male-specific cardiac pathologies in mice lacking either the A or B subunit of factor XIII. Souri M., Koseki-Kuno S., Takeda N., Yamakawa M., Takeishi Y., Degen J.L., Ichinose A. Thromb. Haemost. 99:401-408(2008) · Mapped (9) |
| Estrogen receptor-alpha genotype affects exercise-related reduction of arterial stiffness. Hayashi K., Maeda S., Iemitsu M., Otsuki T., Sugawara J., Tanabe T., Miyauchi T., Kuno S., Ajisaka R., Matsuda M. Med Sci Sports Exerc 40:252-257(2008) · Mapped (58) |
| Influence of adiponectin gene polymorphism SNP276 (G/T) on adiponectin in response to exercise training. Huang H., Tada Iida K., Murakami H., Saito Y., Otsuki T., Iemitsu M., Maeda S., Sone H., Kuno S., Ajisaka R. Endocr. J. 54:879-886(2007) · Mapped (3) |
| Sex differences in the relationship between estrogen receptor alpha gene polymorphisms and arterial stiffness in older humans. Hayashi K., Maeda S., Iemitsu M., Otsuki T., Sugawara J., Tanabe T., Miyauchi T., Kuno S., Ajisaka R., Matsuda M. Am. J. Hypertens. 20:650-656(2007) · Mapped (58) |
| Lack of association of CPT1A polymorphisms or haplotypes on hepatic lipid content or insulin resistance in Japanese individuals with type 2 diabetes mellitus. Hirota Y., Ohara T., Zenibayashi M., Kuno S., Fukuyama K., Teranishi T., Kouyama K., Miyake K., Maeda E., Kasuga M. Metab. Clin. Exp. 56:656-661(2007) · Mapped (3) |
| Combination of multiple genetic risk factors is synergistically associated with carotid atherosclerosis in Japanese subjects with type 2 diabetes. Yamasaki Y., Katakami N., Sakamoto K., Kaneto H., Matsuhisa M., Sato H., Hori M., Haneda M., Kashiwagi A., Tanaka Y. et al. Diabetes Care 29:2445-2451(2006) · Mapped (23) |
| Polymorphism in endothelin-related genes limits exercise-induced decreases in arterial stiffness in older subjects. Iemitsu M., Maeda S., Otsuki T., Sugawara J., Tanabe T., Jesmin S., Kuno S., Ajisaka R., Miyauchi T., Matsuda M. Hypertension 47:928-936(2006) · Mapped (9) |
| Association of the -112A>C polymorphism of the uncoupling protein 1 gene with insulin resistance in Japanese individuals with type 2 diabetes. Fukuyama K., Ohara T., Hirota Y., Maeda K., Kuno S., Zenibayashi M., Teranishi T., Kouyama K., Maeda E., Sakamoto N. et al. Biochem. Biophys. Res. Commun. 339:1212-1216(2006) · Mapped (3) |
| The effect of tau genotype on clinical features in FTDP-17. Baba Y., Tsuboi Y., Baker M.C., Uitti R.J., Hutton M.L., Dickson D.W., Farrer M., Putzke J.D., Woodruff B.K., Ghetti B. et al. Parkinsonism Relat. Disord. 11:205-208(2005) · Mapped (6) |
| Brain-derived neurotrophic factor gene polymorphisms in Japanese patients with sporadic Alzheimer's disease, Parkinson's disease, and multiple system atrophy. Nishimura M., Kuno S., Kaji R., Kawakami H. Mov. Disord. 20:1031-1033(2005) · Mapped (6) |
| Glutathione-S-transferase-1 and interleukin-1beta gene polymorphisms in Japanese patients with Parkinson's disease. Nishimura M., Kuno S., Kaji R., Yasuno K., Kawakami H. Mov. Disord. 20:901-902(2005) · Mapped (5) |
| Influence of a tumor necrosis factor gene polymorphism in Japanese patients with multiple system atrophy. Nishimura M., Kuno S., Kaji R., Kawakami H. Neurosci. Lett. 374:218-221(2005) · Mapped (27) |
| A naturally occurring E30Q mutation in the Gla domain of protein Z causes its impaired secretion and subsequent deficiency. Souri M., Koseki-Kuno S., Iwata H., Kemkes-Matthes B., Ichinose A. Blood 105:3149-3154(2005) · Mapped (1) |
| Identification of two novel mutations in adenine phosphoribosyltransferase gene in patients with 2,8-dihydroxyadenine urolithiasis. Taniguchi A., Tsuchida S., Kuno S., Mita M., Machida T., Ioritani N., Terai C., Yamanaka H., Kamatani N. Nucleosides Nucleotides Nucleic Acids 23:1141-1145(2004) · UniProtKB (1) · Mapped (3) |