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教室業績 2012年

英文原著 英文総説 英文著書
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英文原著

2012年
Suzuki M, Suzuki T, Nagano A, Hirasawa M, Sakuyama K, Mizuki N: Cyclooxygenase inhibitor improved an exudative lesion of choroidal neovascularization in age-related macular degeneration. Eur J Ophthalmol 22(3): 495-498, 2012.
Uemoto R, Nakasato-Sonn H, Meguro A, Okada E, Mizuki N: Anatomical and functional changes of retina following subretinal injection of high-speed fluid. Graefes Arch Clin Exp Ophthalmol 250(3): 447-450, 2012.
Nakasato S, Uemoto R, Mizuki N: Thermocautery for Inferior Conjunctivochalasis. Cornea 31(5): 514-519, 2012.
Horie Y, Megur A, Kitaichi N, Lee E-B, Kanda A, Noda K, Song Y-W, Park K-S, Namba K, Ota M, Inoko H, Mizuki N, Ishida S, Ohno S: Replication of a microsatellite genome-wide association study of Behcet disease in a Korean population, Rheumatology 51(6): 983-986, 2012.
Uemoto R, Nakasato-Sonn H, Kawagoe T, Akira M, Okada E, Mizuki N: Factors associated with enlargement of chorioretinal atrophy after intravitreal bevacizumab for myopic choroidal neovascularization. Graefes Arch Clin Exp Ophthalmol: 250(7): 989-997, 2012.
Annabelle A. Okada, Hiroshi Goto, Shigeaki Ohno, Manabu Mochizuki for the Ocular Behcet’s Disease Research Group of Japan: Multicenter study 1 of infliximab for refractory uveoretinitis in Behcet’s disease. Arch Ophthalmol 130(5); 592-598, 2012.
Kurihara Y, Arie Y, Iketani M, Ito H, Nishiyama K, Sato Y, Nakamura F, Mizuki N, Goshima Y, Takei K: The carboxyl-terminal region of Crtac1B/LOTUS acts as a functional domain in endogenous antagonism to Nogo receptor-1. Biochem Biophys Res Commun 418(2): 390-395, 2012.
Kawase K, Allingham RR, Meguro A, Mizuki N, Roos, B, Solivan-Timpe FM, Robin A, Ritch R, Fingert J: Confirmation of TBK1 duplication in normal tension glaucoma. Exp Eye Res. 96(1): 178-180, 2012.
Sakuyama K, Meguro A, Ota M, Ishihara M, Uemoto R, Ito H, Okada E, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Yuasa T, Ohno S, Inoko H, Mizuki N: Lack of association between IL10 polymorphisms and sarcoidosis in Japanese patients. Mol Vis 18: 512-518, 2012.
Okada AA, Goto H, Ohno S, Mochizuki M; Ocular Behçet's Disease Research Group Of Japan: Multicenter study of infliximab for refractory uveoretinitis in Behçet disease. Arch Ophthalmol 130(5): 592-598, 2012.
Nakasato H, Uemoto R, Kawagoe T, Okada E, Mizuki N: Immediate removal of posteriorly dislocated lens fragments through sclerocorneal incision during cataract surgery. Br J Ophthalmol. 96(8): 1058-1062, 2012.
Tabara Y, Kohara K, Miki T; Millennium Genome Project for Hypertension: Hunting for genes for hypertension: the Millennium Genome Project for Hypertension. Hypertens Res. 35(6): 567-573, 2012.
Kimura K, Usui Y, Goto H; Japanese Intraocular Lymphoma Study Group. Clinical features and diagnostic significance of the intraocular fluid of 217 patients with intraocular lymphoma. Jpn J Ophthalmol. 56(4): 383-389, 2012.
Horie Y, Meguro A, Kitaichi N, Lee E-M, Kanda A, Noda K, Song Y-W, Park K-S, Namba K, Ota M, Inoko H, Mizuki N, Ishida S, Ohno S: Replication of a microsatellite genome-wide association study of Behçet's disease in a Korean population. Rheumatology 51(6): 983-986, 2012.
Omoto S, Kuroiwa Y, Otsuka S, Wang C, Mizuki N, Nagatani H, Hirayama Y: Modulation of human visual evoked potentials in 3-dimensional perception after stimuli produced with an integral imaging method. Clin EEG Neurosci. 43(4): 303-311, 2012.
Fan Q, Barathi VA, Cheng C-Y, Zhou X, Meguro A, Nakata I, Khor C-C, Goh L-K, Li Y-J, Lim W, Ho CEH , Hawthorne F, Zheng Y, Chua D, Inoko H, Yamashiro K , Ohno-Matsui K, Matsuo K, Matsuda F, Vithana E, Seielstad M , Mizuki N, Beuerman RW, Tai E-S, Yoshimura N, Aung T, Young TL, Wong T-Y, Teo Y-Y, Saw S-W: Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. PLoS Genet 8(6): e1002753, 2012.
Meguro A, Ideta H, Ota M, Ito N, Ideta R, Yonemoto J, Takeuchi M, Uemoto R, Nishide T, Iijima Y, Kawagoe T, Okada E, Shiota T, Hagihara Y, Oka A, Inoko H, Mizuki N: Common variants in the COL4A4 gene confer susceptibility to lattice degeneration of the retina. PLoS One 7(6): e39300, 2012.
Takeuchi M, Asukata Y, Kawagoe T, Ito N, Nishide T, Mizuki N: Infliximab monotherapy versus infliximab and colchicine combination therapy in patients with Behçet's disease. Ocul Immunol Inflamm. 20(3): 193-197, 2012.
Suzuki H, Ota M, Meguro A, Katsuyama Y, Kawagoe T, Ishihara M, Asukata Y, Takeuchi M, Ito N, Shibuya E, Nomura E, Uemoto R, Nishide T, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Nakamura J, Saeki K, Ohno S, Inoko H, Mizuki N: Genetic characterization and susceptibility for sarcoidosis in Japanese patients: Risk factors of BTNL2 gene polymorphisms and HLA class II alleles. Invest Ophthalmol Vis Sci 53(11): 7109-7115, 2012.
Hanaoka M, Droma Y, Basnyat B, Ito M, Kobayashi N, Katsuyama Y, Kubo K, Ota M. Genetic Variants in EPAS1 Contribute to Adaptation to High-Altitude Hypoxia in Sherpas. PLoS One. 7(12): e50566, 2012.
Shiina T, Suzuki S, Ozaki Y, Taira H, Kikkawa E, Shigenari A, Oka A, Umemura T, Joshita S, Takahashi O, Hayashi Y, Paumen M, Katsuyama Y, Mitsunaga S, Ota M, Kulski JK, Inoko H. Super high resolution for single molecule-sequence-based typing of classical HLA loci at the 8-digit level using next generation sequencers. Tissue Antigens. 80: 305-316, 2012.
Blancher A, Aarnink A, Tanaka K, Ota M, Inoko H, Yamanaka H, Nakagawa H, Apoil PA, Shiina T. Study of cynomolgus monkey (Macaca fascicularis) Mhc DRB gene polymorphism in four populations. Immunogenetics. 64(8): 605-614, 2012.
Yoshizawa K, Matsumoto A, Ichijo T, Umemura T, Joshita S, Komatsu M, Tanaka N, Tanaka E, Ota M, Katsuyama Y, Kiyosawa K, Abe M, Onji M. Long-term outcome of japanese patients with type 1 autoimmune hepatitis. Hepatology. 56: 668-676, 2012
Ito M, Hanaoka M, Droma Y, Kobayashi N, Yasuo M, Kitaguchi Y, Horiuchi T, Ikegawa K, Katsuyama Y, Kubo K, Ota M. The association of Toll-like receptor 4 gene polymorphisms with the development of emphysema in Japanese subjects: a case control study. BMC Res Notes. 5(1): 36, 2012
Oki T, Hayashi T, Ota M, Asamura H. Development of multiplex assay with 16 SNPs on X chromosome for degraded samples. Leg Med (Tokyo), 14(1):11-16, 2012.
Joshita S, Umemura T, Katsuyama Y, Ichikawa Y, Kimura T, Morita S, Kamijo A, Komatsu M, Ichijo T, Matsumoto A, Yoshizawa K, Kamijo N, Ota M, Tanaka E. Association of IL28B gene polymorphism with development of hepatocellular carcinoma in Japanese patients with chronic hepatitis C virus infection. Hum Immunol. 73(3): 298-300, 2012.

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