124. |
Yoshida M, Meguro A, Okada E, Nomura N, Mizuki N. Association study of fibroblast growth factor 10 (FGF10) polymorphisms with susceptibility to extreme myopia in a Japanese population. Mol Vis. 2013;19:2321-2329. |
125. |
Yoshida M, Meguro A, Yoshino A, Nomura N, Okada E, Mizuki N. Association study of IGF1 polymorphisms with susceptibility to high myopia in a Japanese population. Clin Ophthalmol. 2013;7:2057-2062. doi: 10.2147/OPTH.S52726. |
126. |
Cheng CY, Schache M, Ikram MK, Young TL, Guggenheim JA, Vitart V, MacGregor S, Verhoeven VJ, Barathi VA, Liao J, Hysi PG, Bailey-Wilson JE, St Pourcain B, Kemp JP, McMahon G, Timpson NJ, Evans DM, Montgomery GW, Mishra A, Wang YX, Wang JJ, Rochtchina E, Polasek O, Wright AF, Amin N, van Leeuwen EM, Wilson JF, Pennell CE, van Duijn CM, de Jong PT, Vingerling JR, Zhou X, Chen P, Li R, Tay WT, Zheng Y, Chew M; Consortium for Refractive Error and Myopia, Burdon KP, Craig JE, Iyengar SK, Igo RP Jr, Lass JH Jr; Fuchs' Genetics Multi-Center Study Group, Chew EY, Haller T, Mihailov E, Metspalu A, Wedenoja J, Simpson CL, Wojciechowski R, Höhn R, Mirshahi A, Zeller T, Pfeiffer N, Lackner KJ; Wellcome Trust Case Control Consortium 2, Bettecken T, Meitinger T, Oexle K, Pirastu M, Portas L, Nag A, Williams KM, Yonova-Doing E, Klein R, Klein BE, Hosseini SM, Paterson AD; Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group, Makela KM, Lehtimaki T, Kahonen M, Raitakari O, Yoshimura N, Matsuda F, Chen LJ, Pang CP, Yip SP, Yap MK, Meguro A, Mizuki N, Inoko H, Foster PJ, Zhao JH, Vithana E, Tai ES, Fan Q, Xu L, Campbell H, Fleck B, Rudan I, Aung T, Hofman A, Uitterlinden AG, Bencic G, Khor CC, Forward H, Pärssinen O, Mitchell P, Rivadeneira F, Hewitt AW, Williams C, Oostra BA, Teo YY, Hammond CJ, Stambolian D, Mackey DA, Klaver CC, Wong TY, Saw SM, Baird PN. Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet. 2013;93(2):264-277. doi: 10.1016/j.ajhg.2013.06.016. |
127. |
Kanemaki N, Tchedre KT, Imayasu M, Kawarai S, Sakaguchi M, Yoshino A, Itoh N, Meguro A, Mizuki N. Dogs and Humans Share a Common Susceptibility Gene SRBD1 for Glaucoma Risk. PLoS One. 2013;8(9):e74372. doi: 10.1371/journal.pone.0074372. |
128. |
Kato T, Meguro A, Nomura E, Uemoto R, Nomura N, Ota M, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Chin S, Ohno S, Inoko H, Mizuki N. Association study of genetic variants on chromosome 7q31 with susceptibility to normal tension glaucoma in a Japanese population. Eye (Lond). 2013;27(8):979-983. doi: 10.1038/eye.2013.123. |
129. |
Kirino Y, Zhou Q, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Ozyazgan Y, Ugurlu S, Erer B, Abaci N, Ustek D, Meguro A, Ueda A, Takeno M, Inoko H, Ombrello MJ, Satorius CL, Maskeri B, Mullikin JC, Sun HW, Gutierrez-Cruz G, Kim Y, Wilson AF, Kastner DL, Gül A, Remmers EF. Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behcet disease. Proc Natl Acad Sci U S A. 2013;110(20):8134-8139. doi: 10.1073/pnas.1306352110. |
130. |
Yotsumoto S, Meguro A, Ishihara M, Uemoto R, Ota M, Morimoto SI, Kaburaki T, Ando Y, Takenaka S, Ohno S, Inoko H, Mizuki N. Investigation of the Association Between Toll-like Receptor 9 Gene Polymorphisms and Sarcoidosis in Japanese Patients. Ocul Immunol Inflamm. 2013;21(3):234-236. doi: 10.3109/09273948.2012.756114. |
131. |
Mikami T, Meguro A, Teshigawara T, Takeuchi M, Uemoto R, Kawagoe T, Nomura E, Asukata Y, Ishioka M, Iwasaki M, Fukagawa K, Konomi K, Shimazaki J, Nishida T, Mizuki N. Interleukin 1 beta promoter polymorphism is associated with keratoconus in a Japanese population. Mol Vis. 2013;19:845-851. |
132. |
Kirino Y, Bertsias G, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Ozyazgan Y, Sacli FS, Erer B, Inoko H, Emrence Z, Cakar A, Abaci N, Ustek D, Satorius C, Ueda A, Takeno M, Kim Y, Wood GM, Ombrello MJ, Meguro A, Gül A, Remmers EF, Kastner DL. Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. Nat Genet. 2013;45(2):202-207. doi: 10.1038/ng.2520. |
133. |
Nakasato-Sonn H, Uemoto R, Meguro A, Mizuki N. Modification of Swan-Jacobs lens for iridocorneal angle surgery. Graefes Arch Clin Exp Ophthalmol. 2013;251(9):2247-2248. doi: 10.1007/s00417-012-2232-0. |
134. |
Uemoto R, Nakasato-Sonn H, Meguro A, Ito N, Yazama F, Mizuki N. Staining internal limiting membrane with a mixture of BBG and sodium hyaluronate. Br J Ophthalmol. 2013;97(6):690-693. doi: 10.1136/bjophthalmol-2012-302289. |
135. |
Lee YJ, Horie Y, Wallace GR, Choi YS, Park JA, Song R, Kang YM, Kang SW, Baek HJ, Kitaichi N, Meguro A, Mizuki N, Namba K, Ishida S, Kim J, Niemczek E, Lee EY, Song YW, Ohno S, Lee EB. Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. Ann Rheum Dis. 2013;72(9):1510-1516. doi: 10.1136/annrheumdis-2011-200288. |
136. |
Nishide T, Nakanishi M, Hayakawa N, Kimura I, Mizuki N. Cataract surgery for tilted lens in peters' anomaly type 2. Case Rep Ophthalmol. 2013;4(3):134-137. doi: 10.1159/000354611. |
137. |
Miwa M, Iwanami M, Oba MS, Mizuki N, Nishida T. Comparison of LogMAR Eye charts with angular vision for visually impaired: the Berkeley rudimentary vision test vs LogMAR One target Landolt ring Eye chart. Graefes Arch Clin Exp Ophthalmol. 2013;251(12):2761-2767. doi: 10.1007/s00417-013-2469-2. |
138. |
Nishide T, Hayakawa N, Nakanishi M, Ishii M, Okazaki S, Kimura I, Shibuya E, Mizuki N. Reduction in choroidal thickness of macular area in polypoidal choroidal vasculopathy patients after intravitreal ranibizumab therapy. Graefes Arch Clin Exp Ophthalmol. 2013;251(10):2415-2420. doi: 10.1007/s00417-013-2419-z. |
139. |
Nishide T, Hayakawa N, Nakanishi M, Ishii M, Kimura I, Shibuya E, Nomura E, Mizuki N. Preoperative factors associated with improvement in visual acuity after globe rupture treatment. Eur J Ophthalmol. 2013;23(5):718-722. doi: 10.5301/ejo.5000252. |
140. |
Ando K, Ishihara M, Kusumoto Y, Shibuya E, Nakamura S, Mizuki N. A case of corneal endotheliitis with mumps virus RNA in aqueous humor detected by rt-PCR. Ocul Immunol Inflamm. 2013;21(2):150-152. doi: 10.3109/09273948.2012.747619. |
141. |
Nakasato H, Uemoto R, Kawagoe T, Okada E, Mizuki N. Authors' response: immediate removal of posteriorly dislocated lens fragments through sclerocorneal incision during cataract surgery. Br J Ophthalmol. 2013;97(2):234-235. doi: 10.1136/bjophthalmol-2012-302704. |
142. |
Iwahashi-Shima C, Azumi A, Ohguro N, Okada AA, Kaburaki T, Goto H, Sonoda KH, Namba K, Mizuki N, Mochizuki M. Acute retinal necrosis: factors associated with anatomic and visual outcomes. Jpn J Ophthalmol. 2013;57(1):98-103. doi: 10.1007/s10384-012-0211-y. |
143. |
Nozawa Y, Umemura T, Joshita S, Katsuyama Y, Shibata S, Kimura T, Morita S, Komatsu M, Matsumoto A, Tanaka E, Ota M. KIR, HLA, and IL28B variant predict response to antiviral therapy in genotype 1 chronic hepatitis C patients in Japan. PLoS One. 2013;8(12):e83381. doi: 10.1371/journal.pone.0083381. |
144. |
Kobayashi N, Hanaoka M, Droma Y, Ito M, Katsuyama Y, Kubo K, Ota M. Polymorphisms of the tissue inhibitor of metalloproteinase 3 gene are associated with resistance to high-altitude pulmonary edema (HAPE) in a Japanese population: a case control study using polymorphic microsatellite markers. PLoS One. 2013;8(8):e71993. doi: 10.1371/journal.pone.0071993. |
145. |
Kita Y, Hosomichi K, Suzuki S, Inoko H, Shiina T, Watanabe M, Tanaka A, Horie T, Ohizumi H, Tanaka S, Iwasaki T, Ota M, Kulski JK. Genetic and family structure in a group of 165 common bottlenose dolphins caught off the Japanese coast. Mar Mamm Sci. 2013;29(3):474-496. doi: 10.1111/j.1748-7692.2012.00581.x. |
146. |
Joshita S, Shirahata K, Yazaki Y, Okaniwa S, Nakamura Y, Kimura T, Noami S, Horigome R, Yagi H, Ito N, Yamazaki A, Akahane Y, Umemura T, Yoshizawa K, Tanaka E, Ota M. Cutaneous sarcoidosis in a chronic hepatitis C patient receiving pegylated interferon and ribavirin therapy. Hepatol Res. 2013;43(7):801-807. doi: 10.1111/hepr.12021. |
147. |
Watanabe T, Maruyama M, Ito T, Kanai K, Oguchi T, Muraki T, Hamano H, Arakura N, Ota M, Kawa S. c Intern Med. 2013;52(8):895-899. |
148. |
Morita S, Joshita S, Umemura T, Katsuyama Y, Kimura T, Komatsu M, Matsumoto A, Yoshizawa K, Kamijo A, Yamamura N, Tanaka E, Ota M. Association analysis of toll-like receptor 4 polymorphisms in Japanese primary biliary cirrhosis. Hum Immunol. 2013;74(2):219-222. doi: 10.1016/j.humimm.2012.10.022. |
149. |
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. 2012;53(11):7109-7115. doi: 10.1167/iovs.12-10491. |
150. |
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. 2012;7(6):e39300. doi: 10.1371/journal.pone.0039300. |
151. |
Fan Q, Barathi VA, Cheng CY, Zhou X, Meguro A, Nakata I, Khor CC, Goh LK, Li YJ, Lim W, Ho CE, 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 ES, Yoshimura N, Aung T, Young TL, Wong TY, Teo YY, Saw SM. Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. PLoS Genet. 2012;8(6):e1002753. doi: 10.1371/journal.pgen.1002753. |
152. |
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. 2012;18:512-518. |
153. |
Kawase K, Allingham RR, Meguro A, Mizuki N, Roos B, Solivan-Timpe FM, Robin AL, Ritch R, Fingert JH. Confirmation of TBK1 duplication in normal tension glaucoma. Exp Eye Res. 2012;96(1):178-180. doi: 10.1016/j.exer.2011.12.021. |
154. |
Uemoto R, Nakasato-Sonn H, Kawagoe T, Meguro A, Okada E, Mizuki N. Factors associated with enlargement of chorioretinal atrophy after intravitreal bevacizumab for myopic choroidal neovascularization. Graefes Arch Clin Exp Ophthalmol. 2012;250(7):989-997. doi: 10.1007/s00417-011-1921-4. |
155. |
Horie Y, Meguro A, Kitaichi N, Lee EB, Kanda A, Noda K, Song YW, Park KS, Namba K, Ota M, Inoko H, Mizuki N, Ishida S, Ohno S. Replication of a microsatellite genome-wide association study of Behcet's disease in a Korean population. Rheumatology (Oxford). 2012;51(6):983-986. doi: 10.1093/rheumatology/ker444. |
156. |
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. 2012;250(3):447-450. doi: 10.1007/s00417-011-1800-z. |
157. |
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. 2012;43(4):303-311. doi: 10.1177/1550059412445608. |
158. |
Nakasato H, Uemoto R, Mizuki N. Treatment of pterygium by ligation and bevacizumab injection. Cornea. 2012;31(11):1339-41. doi: 10.1097/ICO.0b013e3182408bc7. |
159. |
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. 2012;96(8):1058-1062. doi: 10.1136/bjophthalmol-2011-300864. |
160. |
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. 2012;20(3):193-197. doi: 10.3109/09273948.2012.665124. |
161. |
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. 2012;418(2):390-395. doi: 10.1016/j.bbrc.2012.01.033. |
162. |
Nakasato S, Uemoto R, Mizuki N. Thermocautery for inferior conjunctivochalasis. Cornea. 2012;31(5):514-519. doi: 10.1097/ICO.0b013e3181dc81d2. |
163. |
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. 2012;22(3):495-498. doi: 10.5301/ejo.5000032. |
164. |
Ito R, Ota M, Meguro A, Katsuyama Y, Uemoto R, Nomura E, Nishide T, Kitaichi N, Horie Y, Namba K, Ohno S, Inoko H, Mizuki N. Investigation of association between TLR9 gene polymorphisms and VKH in Japanese patients. Ocul Immunol Inflamm. 2011;19(3):202-205. doi: 10.3109/09273948.2011.553981. |
165. |
Yasumura R, Meguro A, Ota M, Nomura E, Uemoto R, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Investigation of the association between SLC1A3 gene polymorphisms and normal tension glaucoma. Mol Vis. 2011;17:792-796. |
166. |
Sato M, Kawagoe T, Meguro A, Ota M, Katsuyama Y, Ishihara M, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Ohno S, Inoko H, Mizuki N. Toll-like receptor 2 (TLR2) gene polymorphisms are not associated with sarcoidosis in the Japanese. Mol Vis. 2011;17:731-736. |
167. |
Sada T, Ota M, Katsuyama Y, Meguro A, Nomura E, Uemoto R, Nishide T, Okada E, Ohno S, Inoko H, Mizuki N. Association analysis of Toll-like receptor 7 gene polymorphisms and Behçet's disease in Japanese. Hum Immunol. 2011;72(3):269-272. doi: 10.1016/j.humimm.2010.12.007. |
168. |
Takase H, Okada AA, Goto H, Mizuki N, Namba K, Ohguro N, Sonoda KH, Tomita M, Keino H, Kezuka T, Kubono R, Mizuuchi K, Shibuya E, Takahashi H, Yanai R, Mochizuki M. Development and validation of new diagnostic criteria for acute retinal necrosis. Jpn J Ophthalmol. 2015;59(1):14-20. doi: 10.1007/s10384-014-0362-0. |
169. |
Kawagoe T, Mizuki N. Sarcoidosis. Curr Opin Ophthalmol. 2011;22(6):502-7. doi: 10.1097/ICU.0b013e32834bbd7e. |
170. |
Nishida T, Shibuya E, Asukata Y, Nakamura S, Ishihara M, Hayashi K, Takeno M, Ishigatsubo Y, Mizuki N. Clinical Course before and after Cataract and Glaucoma Surgery under Systemic Infliximab Therapy in Patients with Behçet's Disease. Case Rep Ophthalmol. 2011;2(2):189-192. doi: 10.1159/000329190. |
171. |
Yanagimachi M, Miyamae T, Naruto T, Hara T, Kikuchi M, Hara R, Imagawa T, Mori M, Kaneko T, Goto H, Morita S, Mizuki N, Kimura A, Yokota S. Association of HLA-A*02:06 and HLA-DRB1*04:05 with clinical subtypes of juvenile idiopathic arthritis. J Hum Genet. 2011;56(3):196-199. doi: 10.1038/jhg.2010.159. |
172. |
Meguro A, Inoko H, Ota M, Katsuyama Y, Oka A, Okada E, Yamakawa R, Yuasa T, Fujioka T, Ohno S, Bahram S, Mizuki N. Genetics of Behcet disease inside and outside the MHC. Ann Rheum Dis. 2010;69(4):747-754. doi: 10.1136/ard.2009.108571. |
173. |
Suzuki M, Meguro A, Ota M, Nomura E, Kato T, Nomura N, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Genotyping HLA-DRB1 and HLA-DQB1 alleles in Japanese patients with normal tension glaucoma. Mol Vis. 2010;16:1874-1879. |
174. |
Kurata R, Nakaoka H, Tajima A, Hosomichi K, Shiina T, Meguro A, Mizuki N, Ohono S, Inoue I, Inoko H. TRIM39 and RNF39 are associated with Behcet's disease independently of HLA-B*51 and -A*26. Biochem Biophys Res Commun. 2010;401(4):533-537. doi: 10.1016/j.bbrc.2010.09.088. |
175. |
Mizuki N, Meguro A, Ota M, Ohno S, Shiota T, Kawagoe T, Ito N, Kera J, Okada E, Yatsu K, Song YW, Lee EB, Kitaichi N, Namba K, Horie Y, Takeno M, Sugita S, Mochizuki M, Bahram S, Ishigatsubo Y, Inoko H. Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci. Nat Genet. 2010;42(8):703-706. doi: 10.1038/ng.624. |
176. |
Writing Committee for the Normal Tension Glaucoma Genetic Study Group of Japan Glaucoma Society, Meguro A, Inoko H, Ota M, Mizuki N, Bahram S. Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. Ophthalmology. 2010;117(7):1331-1338. doi: 10.1016/j.ophtha.2009.12.001. |
177. |
Murakami K, Meguro A, Ota M, Shiota T, Nomura N, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Analysis of microsatellite polymorphisms within the GLC1F locus in Japanese patients with normal tension glaucoma. Mol Vis. 2010;16:462-466. |
178. |
Suzuki M, Noda K, Kubota S, Hirasawa M, Ozawa Y, Tsubota K, Mizuki N, Ishida S. Eicosapentaenoic acid suppresses ocular inflammation in endotoxin-induced uveitis. Mol Vis. 2010;16:1382-1388. |
179. |
Yamaguchi Y, Takahashi H, Satoh T, Okazaki Y, Mizuki N, Takahashi K, Ikezawa Z, Kuwana M. Natural killer cells control a T-helper 1 response in patients with Behçet's disease. Arthritis Res Ther. 2010;12(3):R80. doi: 10.1186/ar3005. |
180. |
Omoto S, Kuroiwa Y, Otsuka S, Baba Y, Wang C, Li M, Mizuki N, Ueda N, Koyano S, Suzuki Y. P1 and P2 components of human visual evoked potentials are modulated by depth perception of 3-dimensional images. Clin Neurophysiol. 2010;121(3):386-391. doi: 10.1016/j.clinph.2009.12.005. |
181. |
Nakamura J, Meguro A, Ota M, Nomura E, Nishide T, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Association of toll-like receptor 2 gene polymorphisms with normal tension glaucoma. Mol Vis. 2009;15:2905-2910. |
182. |
Asukata Y, Ota M, Meguro A, Katsuyama Y, Ishihara M, Namba K, Kitaichi N, Morimoto S, Kaburaki T, Ando Y, Takenaka S, Inoko H, Ohno S, Mizuki N. Lack of association between toll-like receptor 4 gene polymorphisms and sarcoidosis-related uveitis in Japan. Mol Vis. 2009;15:2673-2682. |
183. |
Nakamura K, Ota M, Meguro A, Nomura N, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Association of microsatellite polymorphisms of the GPDS1 locus with normal tension glaucoma in the Japanese population. Clin Ophthalmol. 2009;3:307-312. |
184. |
Kamio M, Meguro A, Ota M, Nomura N, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Investigation of the association between the GLC3A locus and normal tension glaucoma in Japanese patients by microsatellite analysis. Clin Ophthalmol. 2009;3:183-188. |
185. |
Horie Y, Meguro A, Ota M, Kitaichi N, Katsuyama Y, Takemoto Y, Namba K, Yoshida K, Song YW, Park KS, Lee EB, Inoko H, Mizuki N, Ohno S. Association of TLR4 polymorphisms with Behcet's disease in a Korean population. Rheumatology (Oxford). 2009;48(6):638-642. doi: 10.1093/rheumatology/kep077. |
186. |
Tomiyama R, Meguro A, Ota M, Katsuyama Y, Nishide T, Uemoto R, Iijima Y, Ohno S, Inoko H, Mizuki N. Investigation of the association between Toll-like receptor 2 gene polymorphisms and Behcet's disease in Japanese patients. Hum Immunol. 2009;70(1):41-44. doi: 10.1016/j.humimm.2008.10.014. |
187. |
Nishizaki R, Ota M, Inoko H, Meguro A, Shiota T, Okada E, Mok J, Oka A, Ohno S, Mizuki N. New susceptibility locus for high myopia is linked to the uromodulin-like 1 (UMODL1) gene region on chromosome 21q22.3. Eye (Lond). 2009;23(1):222-229. doi: 10.1038/eye.2008.152. |
188. |
Uemoto R, Mizuki N. Ocular rupture after accidental intraocular injection of bupivacaine. Retin Cases Brief Rep. 2009;3(4):340-342. doi: 10.1097/ICB.0b013e31817f2e2e. |
189. |
Albuquerque RJ, Hayashi T, Cho WG, Kleinman ME, Dridi S, Takeda A, Baffi JZ, Yamada K, Kaneko H, Green MG, Chappell J, Wilting J, Weich HA, Yamagami S, Amano S, Mizuki N, Alexander JS, Peterson ML, Brekken RA, Hirashima M, Capoor S, Usui T, Ambati BK, Ambati J. Alternatively spliced vascular endothelial growth factor receptor-2 is an essential endogenous inhibitor of lymphatic vessel growth. Nat Med. 2009;15(9):1023-1030. doi: 10.1038/nm.2018. |
190. |
Uemoto R, Nakasato S, Mizuki N. New technique for inserting 27-gauge twinlight chandelier illumination fibers into the eye using intravenous cannula. Retina. 2009;29(7):1040-102. doi: 10.1097/IAE.0b013e3181a3b946. |
191. |
Horie Y, Kitaichi N, Katsuyama Y, Yoshida K, Miura T, Ota M, Asukata Y, Inoko H, Mizuki N, Ishida S, Ohno S. Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients. Mol Vis. 2009;15:1115-1119. |
192. |
Hayashi T, Yamagami S, Tanaka K, Yokoo S, Usui T, Amano S, Mizuki N. Immunologic mechanisms of corneal allografts reconstituted from cultured allogeneic endothelial cells in an immune-privileged site. Invest Ophthalmol Vis Sci. 2009;50(7):3151-3158. doi: 10.1167/iovs.08-2530. |
193. |
Meguro A, Ota M, Katsuyama Y, Oka A, Ohno S, Inoko H, Mizuki N. Association of the toll-like receptor 4 gene polymorphisms with Behcet's disease. Ann Rheum Dis. 2008;67(5):725-727. doi: 10.1136/ard.2007.079871. |
194. |
Shibuya E, Meguro A, Ota M, Kashiwagi K, Mabuchi F, Iijima H, Kawase K, Yamamoto T, Nakamura M, Negi A, Sagara T, Nishida T, Inatani M, Tanihara H, Aihara M, Araie M, Fukuchi T, Abe H, Higashide T, Sugiyama K, Kanamoto T, Kiuchi Y, Iwase A, Ohno S, Inoko H, Mizuki N. Association of toll-like receptor 4 gene polymorphisms with normal tension glaucoma. Invest Ophthalmol Vis Sci. 2008;49(10):4453-4457. doi: 10.1167/iovs.07-1575. |
195. |
Kamiishi T, Itoh Y, Meguro A, Nishida T, Sasaki S, Nanba K, Ohno S, Inoko H, Mizuki N. Four-digit allele genotyping of HLA-A and HLA-B genes in Japanese patients with Behçet's disease. Nippon Ganka Gakkai Zasshi. 2008;112(5):451-458. |
196. |
Nomura N, Nomura M, Mizuki N, Hamada J. Rac1 mediates phorbol 12-myristate 13-acetate-induced migration of glioblastoma cells via paxillin. Oncol Rep. 2008;20(4):705-711. |
197. |
Hayashi T, Yamagami S, Tanaka K, Yokoo S, Usui T, Amano S, Mizuki N. A mouse model of allogeneic corneal endothelial cell transplantation. Cornea. 2008;27(6):699-705. doi: 10.1097/QAI.0b013e31815e722b. |
198. |
Asukata Y, Ishihara M, Hasumi Y, Nakamura S, Hayashi K, Ohno S, Mizuki N. Guidelines for the diagnosis of ocular sarcoidosis. Ocul Immunol Inflamm. 2008;16(3):77-81. doi: 10.1080/09273940802051100. |
199. |
Hayashi T, Ishioka M, Ito N, Kato Y, Nakagawa H, Hatano H, Mizuki N. Bilateral herpes simplex keratitis in a patient with chronic graft-versus-host disease. Clin Ophthalmol. 2008;2(2):457-459. |
200. |
Kirino Y, Takeno M, Watanabe R, Murakami S, Kobayashi M, Ideguchi H, Ihata A, Ohno S, Ueda A, Mizuki N, Ishigatsubo Y. Association of reduced heme oxygenase-1 with excessive Toll-like receptor 4 expression in peripheral blood mononuclear cells in Behçet's disease. Arthritis Res Ther. 2008;10(1):R16. doi: 10.1186/ar2367. |
201. |
Mizuki N, Meguro A, Tohnai I, Gül A, Ohno S, Mizuki N. Association of major histocompatibility complex class I chain-related gene A and HLA-B alleles with Behçet's disease in Turkey. Jpn J Ophthalmol. 2007;51(6):431-436. |
202. |
Yamane T, Mok J, Oka A, Okada E, Nishizaki R, Meguro A, Yonemoto J, Kulski JK, Ohno S, Inoko H, Mizuki N. Lack of association with high myopia and the MYP2 locus in the Japanese population by high resolution microsatellite analysis on chromosome 18. Clin Ophthalmol. 2007;1(3):311-316. |
203. |
Sasaki S, Ota M, Meguro A, Nishizaki R, Okada E, Mok J, Kimura T, Oka A, Katsuyama Y, Ohno S, Inoko H, Mizuki N. A single nucleotide polymorphism analysis of the LAMA1 gene in Japanese patients with high myopia. Clin Ophthalmol. 2007;1(3):289-295. |
204. |
Horie Y, Kitaichi N, Takemoto Y, Namba K, Yoshida K, Hirose S, Hasumi Y, Ota M, Inoko H, Mizuki N, Ohno S. Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease. Mol Vis. 2007;13:2334-2338. |
205. |
Omoto S, Kuroiwa Y, Wang C, Li M, Mizuki N, Hakii Y. The effect of attended color on the P1/N1 component of visual event-related potentials. Neurosci Lett. 2007;429(1):22-27. |
206. |
Teshigawara T, Hata S, Hayashi T, Watanabe Y, Itoh Y, Hitoi K, Mizuki N. Penetration of gatifloxacin eye drops into the aqueous humor in humans. Ocul Immunol Inflamm. 2007;15(4):309-313. |
207. |
Katsuyama Y, Ota M, Mizuki N, Ito A, Okada E, Ohno S, Matsunaga T, Fukushima H, Ohmori S. MDR1 polymorphisms effect cyclosporine AUC0-4 values in Behçet's disease patients. Clin Ophthalmol. 2007 Sep;1(3):297-303. |
208. |
Inamori Y, Ota M, Inoko H, Okada E, Nishizaki R, Shiota T, Mok J, Oka A, Ohno S, Mizuki N. The COL1A1 gene and high myopia susceptibility in Japanese. Hum Genet. 2007;122(2):151-157. |
209. |
Hayashi T, Inoko H, Nishizaki R, Ohno S, Mizuki N. Exclusion of transforming growth factor-beta1 as a candidate gene for myopia in the Japanese. Jpn J Ophthalmol. 2007;51(2):96-99. |
210. |
Matsuda A, Ebihara N, Kumagai N, Fukuda K, Ebe K, Hirano K, Sotozono C, Tei M, Hasegawa K, Shimizu M, Tamari M, Namba K, Ohno S, Mizuki N, Ikezawa Z, Shirakawa T, Hamuro J, Kinoshita S. Genetic polymorphisms in the promoter of the interferon gamma receptor 1 gene are associated with atopic cataracts. Invest Ophthalmol Vis Sci. 2007;48(2):583-589. |
211. |
Yatsu K, Mizuki N, Hirawa N, Oka A, Itoh N, Yamane T, Ogawa M, Shiwa T, Tabara Y, Ohno S, Soma M, Hata A, Nakao K, Ueshima H, Ogihara T, Tomoike H, Miki T, Kimura A, Mano S, Kulski JK, Umemura S, Inoko H. High-resolution mapping for essential hypertension using microsatellite markers. Hypertension. 2007;49(3):446-452. |
212. |
Itoh Y, Inoko H, Kulski JK, Sasaki S, Meguro A, Takiyama N, Nishida T, Yuasa T, Ohno S, Mizuki N. Four-digit allele genotyping of the HLA-A and HLA-B genes in Japanese patients with Behcet’s disease by a PCR-SSOP-Luminex method. Tissue Antigens. 2006;67(5):390-394. |
213. |
Horie Y, Takemoto Y, Miyazaki A, Namba K, Kase S, Yoshida K, Ota M, Hasumi Y, Inoko H, Mizuki N, Ohno S. Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients. Mol Vis. 2006;12:1601-1605. |
214. |
Matsui K, Saha S, Saitoh M, Mizuki N, Itoh N, Okada E, Yoshida A, Xin KQ, Nishio O, Okuda K. Isolation and identification of adenovirus from conjunctival scrapings over a two-year period (between 2001 and 2003) in Yokohama, Japan. J Med Virol. 2007;79(2):200-205. |
215. |
Hasumi Y, Inoko H, Mano S, Ota M, Okada E, Kulski JK, Nishizaki R, Mok J, Oka A, Kumagai N, Nishida T, Ohno S, Mizuki N. Analysis of single nucleotide polymorphisms at 13 loci within the transforming growth factor-induced factor gene shows no association with high myopia in Japanese subjects. Immunogenetics. 2006;58(12):947-953. |
216. |
Chen X, Katoh Y, Nakamura K, Oyama N, Kaneko F, Endo Y, Fujita T, Nishida T, Mizuki N. Single nucleotide polymorphisms of Ficolin 2 gene in Behçet's disease. J Dermatol Sci. 2006;43(3):201-205. |
217. |
Asukata Y, Ishihara M, Nakamura S, Hayashi K, Itoh Y, Takiyama N, Mizuki N. The reevaluation of categorization for ocular manifestation of sarcoidosis in the "Guidelines for Diagnosis of Ocular Sarcoidosis". Nippon Ganka Gakkai Zasshi. 2006;110(5):391-397. |
218. |
Yanagihori H, Oyama N, Nakamura K, Mizuki N, Oguma K, Kaneko F. Role of IL-12B promoter polymorphism in Adamantiades-Behcet's disease susceptibility: An involvement of Th1 immunoreactivity against Streptococcus Sanguinis antigen. J Invest Dermatol. 2006;126(7):1534-1540. |
219. |
Itoh Y, Mizuki N, Shimada T, Azuma F, Itakura M, Kashiwase K, Kikkawa E, Kulski JK, Satake M, Inoko H. High-throughput DNA typing of HLA-A, -B, -C, and -DRB1 loci by a PCR-SSOP-Luminex method in the Japanese population. Immunogenetics. 2005;57(10):717-729. |
220. |
Kato Y, Saito H, Nishizaki R, Shiota T, Matsuda T, Mizuki N, Okada E. Contact lens user statistics in Okada eye clinic. Eye Contact Lens. 2005;31(5):231-237. |
221. |
Saitou H, Kato Y, Nishizaki R, Shiota T, Matsuda T, Iyanaga K, Mizuki N, Okada E. An investigation of the actual conditions of use of daily-disposable soft contact lenses and two-week disposable soft contact lenses. Eye Contact Lens. 2005;31(5):225-320. |
222. |
Mizuki N, Watanabe Y, Miyamoto M, Iijima Y, Takiyama N, Ito Y, Ito N, Nishida T, Iwata S, Endo Y, Ito D. Flomoxef sodium and levofloxacin concentrations in aqueous humor. Ocul Immunol Inflamm. 2005;13(2-3):229-234. |
223. |
Kobayashi T, Sudo Y, Okamura S, Ohashi S, Urano F, Hosoi T, Segawa K, Mizuki N, Ota M. Monozygotic twins concordant for intestinal Behçet's disease. J Gastroenterol. 2005;40(4):421-425. |
224. |
Teuchner B, Nagl M, Schidlbauer A, Ishiko H, Dragosits E, Ulmer H, Aoki K, Ohno S, Mizuki N, Gottardi W, Larcher C. Tolerability and efficacy of N-chlorotaurine in epidemic keratoconjunctivitis--a double-blind, randomized, phase-2 clinical trial. J Ocul Pharmacol Ther. 2005;21(2):157-165. |
225. |
Yamaki K, Takiyama N, Itho N, Mizuki N, Seiya M, Sinsuke W, Hayakawa K, Kotani T. Experimentally induced Vogt-Koyanagi-Harada disease in two Akita dogs. Exp Eye Res. 2005;80(2):273-280. |
226. |
Mitani N, Aihara M, Yamakawa Y, Yamada M, Itoh N, Mizuki N, Ikezawa Z. Drug-induced hypersensitivity syndrome due to cyanamide associated with multiple reactivation of human herpesviruses. J Med Virol. 2005;75(3):430-434. |
227. |
Wang H, Nakamura K, Inoue T, Yanagihori H, Kawakami Y, Hashimoto S, Oyama N, Kaneko F, Fujita T, Nishida T, Mizuki N. Mannose-binding lectin polymorphisms in patients with Behçet's disease. J Dermatol Sci. 2004;36(2):115-117. |
228. |
Nishida T, Miyata S, Itoh Y, Mizuki N, Ohgami K, Shiratori K, Ilieva IB, Ohno S, Taylor AW. Anti-inflammatory effects of alpha-melanocyte-stimulating hormone against rat endotoxin-induced uveitis and the time course of inflammatory agents in aqueous humor. Int Immunopharmacol. 2004;4(8):1059-1066. |
229. |
Yanagihori H, Tojo M, Inoue T, Nakamura K, Kaneko F, Nishida T, Mizuki N. Lack of association of interleukin-12 p40 gene (IL12B) polymorphism with Behçet's disease in the Japanese population. J Dermatol Sci. 2004;34(2):112-114. |
230. |
Cheng Q, Sasaki Y, Shoji M, Sugiyama Y, Tanaka H, Nakayama T, Mizuki N, Nakamura F, Takei K, Goshima Y. Cdk5/p35 and Rho-kinase mediate ephrin-A5-induced signaling in retinal ganglion cells. Mol Cell Neurosci. 2003;24(3):632-645. |
231. |
Ohgami K, Ilieva IB, Shiratori K, Isogai E, Yoshida K, Kotake S, Nishida T, Mizuki N, Ohno S. Effect of human cationic antimicrobial protein 18 Peptide on endotoxin-induced uveitis in rats. Invest Ophthalmol Vis Sci. 2003;44(10):4412-4418. |
232. |
Ohgami K, Shiratori K, Kotake S, Nishida T, Mizuki N, Yazawa K, Ohno S. Effects of astaxanthin on lipopolysaccharide-induced inflammation in vitro and in vivo. Invest Ophthalmol Vis Sci. 2003;44(6):2694-2701. |
233. |
Nomura E, Sato M, Suemizu H, Watanabe T, Kimura T, Yabuki K, Goto K, Ito N, Mizuki N, Ohno S, Kimura M. Hyperkaratosis and leukocytosis in transgenic mice carrying MHC class I related gene B (MICB). Tissue Antigens. 2003;61(4):300-307. |
234. |
Mizuki N, Yabuki K, Ota M, Katsuyama Y, Ando H, Nomura E, Funakoshi K, Davatchi F, Chams H, Nikbin B, Ghaderi AA, Ohno S, Inoko H. Analysis of microsatellite polymorphism around the HLA-B locus in Iranian patients with Behcet's disease.Tissue Antigens. 2002;60(5):396-399. |
235. |
Mizuki N, Ota M, Katsuyama Y, Yabuki K, Ando H, Shiina T, Palimeris GD, Kaklamani E, Ohno S, Inoko H. Sequenced-based typing of HLA-B*51 alleles and the significant association of HLA-B*5101 and -B*5108 with Behçet's disease in Greek patients. Tissue Antigens. 2002;59(2):118-121. |
236. |
Sano K, Yabuki K, Imagawa Y, Shiina T, Mizuki N, Ohno S, Kuiski JK, Inoko H. The absence of disease-specific polymorphisms within the HLA-B51 gene that is the susceptible locus for Behçet's disease. Tissue Antigens. 2001;58(2):77-82. |
237. |
Seki SS, Sugimura K, Ota M, Matsuzawa J, Katsuyama Y, Ishizuka K, Mochizuki T, Suzuki K, Yoneyama O, Mizuki N, Honma T, Inoko H, Asakura H. Strafication analysis of MICA triplet repeat polymorphisms and HLA antigens associated with ulcerative colitis in Japanese. Tissue Antigens. 2001;58(2):71-76. |
238. |
Yoshida M, Mizuki N, Okada E, Kokaze A, Sekine Y, Uchida Y, Harada N, Takashima Y. Age-specific prevalence of open-angle glaucoma among more than 60,000 asymptomatic Japanese population. J Clin Epidemiol. 2001;54(11):1151-1158. |
239. |
Shina T, Suto Y, Kasai F, Shigrnari A, Takishima N, Kikkawa E, Iwata K, Kuwano Y, Kitamura Y, Matsuzawa Y, Sano K, Nogami M, Kawata H, Li S, Fukuzumi Y, Yamazaki M, Tashiro H, Tamiya G, Kohda A, Okumura K, Ikemura T, Soeda E, Mizuki N, Kimura M, Bahram S, Inoko H. Genomic anatomy of a premiar Major Histocompatibility Complex paralogous region on chromosome 1q21-22. Genome Res. 2001;11(5):789-802. |
240. |
Ota M, Katsuyama Y, Kimura A, Tsuchiya K, Kondo M, Naruse T, Mizuki N, Itoh K, Sasazuki T, Inoko H. A second susceptibility gene for developing rheumatoid arthritis in the human MHC is localized within a 70-kb interval telomeric of the TNF genes in the HLAclass III region. Genomics. 2001;71(3):263-270. |
241. |
Sugimura K, Ota M, Matsuzawa J, Katsuyama Y, Ishizuka K, Mochizuki T, Mizuki N, Seki S, Honma T, Inoko H. A cloase relationship of triplet repeat polymorphism in MHC class I chain-related gene A (MICA) to the disease susceptibility and behavior in ulcerative colitis. Tissue Antigens. 2001;57(1):9-14. |
242. |
Mizuki N, Ota M, Katsuyama Y, Yabuki K, Ando H, Nikbin B, Davatchi F, Chams H, Ghaderi AA, Ohno S, Inoko H. HLA class I genotyping including HLA-B*51 allele typing in the Iranian patients with Behçet's disease. Tissue Antigens. 2001;57(5):457-462. |
243. |
Mizuki N, Yabuki K, Ota M, Verity D, Katsuyama Y, Ando H, Goto K, Nomura E, Imagawa Y, Madanat W, Fayyad F, Stanford M, Ohno S, Inoko H. Microsatellite mapping of a susceptibility locus within the HLA region for Behçet's disease using Jordanian patients. Hum Immunol. 2001;62(2):186-190. |
244. |
Mizuki N, Ota M, Katsuyama Y, Yabuki K, Ando H, Nomura E, Ohno S, Inoko H. HLA-B*51 allele analysis by the PCR-SBT method and a strong association of HLA-B*5101 with Japanese patients with Behçet's disease. Tissue Antigens. 2001;58(3):181-184. |
245. |
Mizuki N, Ota M, Katsuyama Y, Ando H, Yabuki K, Goto k, Palimeris G, Kaklamani E, Pivetti-Pezzi P, Ohno S, Inoko H. Localization of the pathogenic gene of Behçet's disease onto the HLA-B locus by investigation of microsatellite polymorphism in three different populations. Invest Ophthalmol Visual Sci. 2000;41(12):3702-3708. |
246. |
Kera J, Mizuki N, Ota M, katsuyama Y, Pivetti-Pezzi P, Ohno S, Inoko H. Significant associations of HLA-B*5101 and B*5108, and lack of association of class II alleles with Behçet's disease in Italian patients. Tissue Antigens. 1999;54(6):565-571. |
247. |
Katsuyama Y, Ota M, Ando H, Saito S, Mizuki N, Kera J, Bahram S, Nose Y, Inoko H. Sequencing based typing for genetic polymorphisms in exon 2, 3 and 4 of the MICA gene. Tissue Antigens. 1999;54(2):178-184. |
248. |
Yabuki K, Ohno S, Mizuki N, Ando H, Tabbara KF, Goto K, Nomura E, Nakamura S, Ito N, Ota M, Katsuyama Y, Inoko H. HLA class I and class II typing of the patients with Behçet's disease in Saudi Arabia. Tissue Antigens. 1999;54(3):273-277. |
249. |
Wallace GR, Verity DH, Delamaine LJ, Ohno S, Inoko H, Ota M, Mizuki N, Yabuki K,Kondiatis E, Stephens HA, Madanat W, Kanawati CA, Stanford MR, Vaughan RW. MICA allele profiles and HLA class I associations in Behçet's disease. Immunogenetics. 1999;49(7-8):613-617. |
250. |
Yabuki K, Mizuki N, Ota M, Katsuyama Y, Palimeris G, Stavropoulos C, Koumantaki Y, Spyropoulou M, Giziaki E, Kaklamani V, Kaklamani E, Inoko H, Ohno S. Association of MICA Gene and HLA-B*5101 with Behçet's disease in Greece. Invest Ophthalmol Visual Sci. 1999;40(9):1921-1926. |
251. |
Ota M, Mizuki N, Katsuyama Y, Tamiya G, Takashi S, Oka A, Ando H, Kimura M, Goto K, Ohno S, Inoko H. The critical region for Behçet disease in the human major histo-compatibility complex is reduced to a 46-kb segment centromeric of HLA-B by association analysis using refined microsatellite mapping. Am J Hum Genet. 1999;64(5):1406-1410. |
252. |
Yabuki K, Ota M, Goto K, Kimura M, Nomura E, Ohno S, Mizuki N, Katsuyama Y, Makysymowych WP, Bahram S, Kimura M, Inoko H. Triplet repeat polymorphism in the MICA gene in HLA-B27 positive and negative patients with ankylosing spondylitis. Hum Immunol. 1999;60(1):83-86. |
253. |
Mizuki N, Ota M, Katsuyama Y, Ando H, Yabuki K, Goto K, Nakamura S, Ohno S, Inoko H. Association analysis between the MICA and HLA-B alleles in the Japanese patients with Behçet's disease. Arthritis Rheumatism. 1999;42(9):1961-1966. |
254. |
Katsuyama Y, Inoko H, Imanishi T, Mizuki N, Gojobori T, Ota M. Genetic relationships among Japanese, northern Han, Hui, Uygur, Kazakh, Greek, Saudi Arabian, and Italian populations based on allelic frequencies at four VNTR (D1S80, D4S43, COL2A1, D17S5) and one STR (ACTBP2) loci. Hum Hered. 1998;48(3):126-137. |
255. |
Kimura T, Goto K, Yabuki K, Mizuki N, Tamiya G, Sato M, Kimura M, Inoko H, Ohno S. Microsatellite polymorphism within the MICB gene among Japanese patients with Behçet's disease. Hum Immunol. 1998;59(8):500-502. |
256. |
Goto K, Ota M, Maksymowych WP, Mizuki N, Yabuki K, Katsuyama Y, Kimura M, Inoko H, Ohno S. Association between MICA gene A4 allele and acute anterior uveitis in White patients with and without HLA-B27. Am J Ophthalmol. 1998;126(3):436-441. |
257. |
Goto K, Ota M, Ando H, Mizuki N, Nakamura S, Inoue K, Yabuki K, Kotake S, Katsuyama Y, Kimura M, Inoko H, Ohno S. MICA gene polymorphisms and HLA-B27 subtypes in Japanese patients with HLA-B27-associated acute anterior uveitis. Invest Ophthalmol Vis Sci. 1998;39(3):634-637. |
258. |
Shiina T, Tamiya G, Oka A, Yamagata T, Yamagata N, Kikkawa E, Goto K, Mizuki N, Watanabe K, Fukuzumi Y, Taguchi S, Sugawara C, Ono A, Chen L, Yamazaki M, TashiroH, Ando A, Ikemura T, Kimura M, Inoko H. Nucleotide sequencing analysis of the 146 kb segment around the IkBL and MICA genes at the centromeric end of the HLA class I region. Genomics. 1998;47(3):372-382. |
259. |
Mizuki N, Ohno S, Ando H, Sato T, Imanishi T, Gojobori T, Ishihara M, Goto K, Ota M, Geng Z, Geng L, Li G, Inoko H. Major histocompatibility complex class II alleles in an Uygur population in the Silk Route of northwest China. Tissue Antigens. 1998;51(3):287-292. |
260. |
Ishihara M, Ohno S, Ishida T, Naruse T, Kagiya M, Mizuki N, Naruya E, Saji H, Inoko H. Analysis of allelic variation of the TAP2 gene in sarcoidosis. Tissue Antigens. 1997;49(2):107-110. |
261. |
Imai H, Motegi M, Mizuki N, Ohtani H, Komatsuda A, Hamai K, Miura AB. Mouth and genital ulcers with inflamed cartilage (MAGIC syndrome): A case report and literature review. Am J Med Sci. 1997;314(5):330-332. |
262. |
Ando H, Mizuki N, Ota M, Yamazaki M, Ohno S, Goto K, Miyata Y, Wakisaka K, Bahram S, Inoko H. Allelic variants of the human MHC class I-related B gene (MICB). Immunogenetics. 1997;46(6):499-508. |
263. |
Goto K, Ota M, Ohno S, Mizuki N, Ando H, Katsuyama Y, Kimura M, Inoko H. Polymorphism in the MICA gene in the patients with ankylosing spondylitis. Tissue Antigens. 1997;49(5):503-507. |
264. |
Ota M, Katsuyama K, Mizuki N, Ando H, Furihata K, Ono S, Pivetti-Pezzi P, Tabbara KF, Palimeris GP, Nikbin B, Davatchi F, Chams H, Geng Z, Bahram S, Inoko H. Trinucleotide repeat polymorphism within exon 5 of the MICA gene (MHC class I chain- related gene A): Allele frequency data in the nine population groups Japanese, Northern Han, Hui, Uygur, Kazakhstan, Iranian, Saudi Arabian, Greek, Italian. Tissue Antigens. 1997;49(5):448-454. |
265. |
Ando H, Mizuki N, Ohno S, Tabbara KF, Taguchi S, Yamazaki M, Miyata Y, Wakisaka K, Inoko H. Identification of a novel HLA-B allele (B*4202) from a Saudi Arabian family with Behçet's disease. Tissue Antigens. 1997;49(5):526-528. |
266. |
Mizuki N, Ohno S, Ando H, Sato T, Ishihara M, Imanishi T, Geng Z, Geng L, Li G, Inoko H. Major histocompatibility complex class II alleles in Kazak and Han populations in the Silk Route of northwest China. Tissue Antigens. 1997;50(5):527-534. |
267. |
Mizuki N, Ohno S, Ando H, Palimeris GD, Stavropoulos-Gikas C, Ishihara M, Nakamura S, Isobe K, Shindo Y, Ito N, Inoko H. A strong association of HLA-B*5101 with Behçet's disease in Greek patients. Tissue Antigens. 1997;50(1):57-60. |
268. |
Mizuki N, Ando H, Kimura M, Ohno S, Miyata S, Yamazaki M, Tashiro H, Watanabe K, Ono A, Taguchi S, Sugawara C, Fukuzumi Y, Okumura K, Goto K, Ishihara M, Nakamura S, Yonemoto J, Kikuti YY, Shiina T, Chen L, Ando A, Ikemura T, Inoko H. Nucleotide sequence analysis of the HLA class I region spanning the 237 kb segment around the HLA-B and -C genes. Genomics. 1997;42(1):55-66. |
269. |
Mizuki N, Ota M, Kimura M, Ohno S, Ando H, Katsuyama Y, Yamazaki M, Watanabe K, Goto K, Nakamura S, Bahram S, Inoko H. Triplet repeat polymorphism in the transmembrane region of the MICA gene: A strong association of six GCT repetitions with Behçet's disease. Proc Natl Acad Sci U S A. 1997;94(4):1298-1303. |
270. |
Ishihara M, Yamagata N, Ohno S, Naruse T, Ando A, Kawata H, Ozawa A, Ohkido M, Mizuki N, Shiina T, Ando H, Inoko H. Genetic polymorphisms in the keratin-like S gene within the human major histocompatibility complex and association analysis on the susceptibility to psoriasis vulgaris. Tissue Antigens. 1996;48(3):182-186. |
271. |
Fodil N, Laloux L, Wanner V, Pellet P, Hauptmann G, Mizuki N, Inoko H, Spies T, Theodorou I, Bahram S. Allelic repertoire of the human MHC class I MICA gene. Immunogenetics. 1996;44(5):351-357. |
272. |
Ishihara M, Naruse T, Ohno S, Kawata H, Mizuki N, Yamagata N, Ishida T, Nose Y, Inoko H. Analysis of HLA-DM polymorphisms in sarcoidosis. Hum Immunol. 1996;49(2):144-146. |
273. |
Ishihara M, Ohno S, Mizuki N, Yamagata N, Ishida T, Naruse T, Ando A, Inoko H. LMP7 polymorphism in Japanese patients with sarcoidosis and Behçet's disease. Hum Immunol. 1996;51(2):103-105. |
274. |
Ishihara M, Ohno S, Mizuki N, Yamagata N, Naruse T, Shiina T, Kawata H, Kuwata S, Inoko H. Allelic variations in the TAP2 and LMP2 genes in Behçet's disease. Tissue Antigens. 1996;47(3):249-252. |
275. |
Ishihara M, Ohno S, Mizuki N, Yamagata N, Ishida T, Naruse T, Kawata S, Inoko H. Genetic polymorphisms of the MHC-encoded antigen processing gene (TAP, LMP) in sarcoidosis. Hum Immunol. 1996;45(2):105-110. |
276. |
Inoko H, Mizuki N, Shiina T, Ando A, Kimura M, Kikuchi YY, Kawata H, Sugaya K, Fukagawa T, Matsumoto K, Nagata T, Taketo M, Okumura K, Kasahara M, Ikemura T: Cloning, sequencing and evolutionary analyses of the human major histocompatibility complex (MHC) region. DNA Seq. 1996;7(1):31-32. |
277. |
Bahram S, Mizuki N, Inoko H, Spies T. Nucleotide sequence of the human MHC class I MICA gene. Immunogenetics. 1996;44(1):80-81. |
278. |
Ando H, Mizuki N, Ando R, Miyata Y, Miyata S, Wakisaka K, Inoko H. HLA-C genotyping in the Japanese population by the PCR-SSP method. Tissue Antigens. 1996;48(1):55-58. |
279. |
Mizuki N, Inoko H, Ando H, Kiyosawa K, Seki T, Geng Z, Geng L, Li G, Ishihara M, Shindo Y, Onishi H, Onoe K, Ohno S. Seroepidemiological studies on Silk Route ethnic groups. Tokai Exp Clin Med. 1996;21(3):117-120. |
280. |
Mizuki N, Ando H, Ohno S, Kimura M, Ishihara M, Miyata S, Nakamura S, Mizuki N, Inoko H. HLA-C genotyping of patients with Behçet's disease in the Japanese population. Hum Immunol. 1996;50(1):47-53. |
281. |
Mizuki N, Kimura M, Ohno S, Miyata S, Sato M, Ishihara M, Ono A, Taguchi S, Yamazaki M, Ando H, Okumura K, Nogami M, Taguchi H, Ando A, Inoko H. Isolation of cDNA and genomic clones of a human ras-related GTP-binding protein (Rheb) and its chromosomal localization to the long arm of chromosome 7, 7q36. Genomics. 1996;34(1):114-118. |
282. |
Geng L, Imanishi T, Tokunaga K, Zhu D, Mizuki N, Xu S, Geng Z Gojobori T, Tsuji K, Inoko H. Determination of HLA class II alleles by genotyping in a Manchu population in the northern part of China and its relationship with Han and Japanese populations. Tissue Antigens. 1995;46(2):111-116. |
283. |
Ishihara M, Ohno S, Ishida T, Mizuki N, Ando H, Naruse T, Inoko H. Genetic polymorphisms of the TNFB and HSP70 genes located in the human major histocompatibility complex in sarcoidosis. Tissue Antigens. 1995;46(1):59-62. |
284. |
Ishihara M, Ishida T, Mizuki N, Inoko H, Ando H, Ohno S. Clinical features of sarcoidosis in relation to HLA distribution and HLA-DRB3 genotyping by PCR-RFLP. Br J Ophthalmol. 1995;79(4):322-325. |
285. |
Mizuki N, Ohno S, Sato T, Ishihara M, Miyata S, Nakamura S, Naruse T, Mizuki H, Tsuji K, Inoko H. Microsatellite polymorphism located between the TNF and HLA-B genes in Behçet's disease. Hum Immunol. 1995;43(2):129-135. |
286. |
Ishihara M, Ishida T, Mizuki N, Inoko H, Kagiya M, Ando H, Ohno S. A case study of sibling relationship in sarcoidosis by HLA-DNA genotyping. Graef Arch Clin Exp Ophthalmol. 1994;232(12):761-762. |
287. |
Niizeki H, Inoko H, Mizuki N, Inamoto N, Watanabe K, Hashimoto T, Nishikawa T. HLA-DQA1, -DQB1 and -DRB1 genotyping in Japanese pemphigus vulgaris by PCR-RFLP method. Tissue Antigens. 1994;44(4):248-251. |
288. |
Mizuki N, Inoko H, Ishihara M, Ando H, Nakamura S, Nishio M, Ohno S. A complete type patient with Behçet's disease associated with HLA-B*5102. Acta Ophthalmologica. 1994;72(6): 757-758. |
289. |
Seki T, Kiyosawa K, Ota M, Fukushima H, Tanaka E, Yoshizawa K, Furuta S, Kumagai T, Mizuki N, Ando A, Inoko H. Association of primary biliary cirrhosis with human leukocyte antigen-DPB1*0501 in Japanese. Hepatology 1993;18(1):73-78. |
290. |
Sugimura K, Asakura H, Mizuki N, Inoue M, Hibi T, Yagita A, Tsuji K, Inoko H. Analysis of genes within the HLA region affecting susceptibility to Ulcerative Colitis. Hum Immunol. 1993;36(2):112-118. |
291. |
Mizuki N, Inoko H, Ando H, Nakamura S, Kashiwae K, Akaza T, Fujino Y, Masuda K, Takiguchi M, Ohno S. Behçet's disease associated with one of the HLA-B51 subantigens, HLA-B*5101. Am J Ophthalmol. 1993;116(4):406-409. |
292. |
Mizuki N, Ohno S, Sugimura K, Seki T, Mizuki N, Ishioka M, Inoko H. Identification of a new HLA-DPB1 allele detected by PCR-RFLP and its nucleotide sequence determination by direct sequencing after PCR amplification. Tissue Antigens. 1993;41(5):259-262. |
293. |
Seki T, Ota M, Furuta S, Fukushima H, Kondo T, Hino K, Mizuki N, Ando A, Tsuji K,Inoko H, Kiyosawa K. HLA class II molecules associated autoimmune hepatitis susceptibility in Japanese patients. Gastroenterology. 1992;103(3):1041-1047. |
294. |
Mizuki N, Ohno S, Nakamura S, Mizuki N, Mizuki H, Sugimura K, Tanaka H, Kera J, Tsuji K, Inoko H. Searching for the gene(s) within the HLA region responsible for the susceptibility to Behçet's disease. Chibret Int J Ophthalmol. 1992;9:10-24. |
295. |
Mizuki N, Inoko H, Sugimura K, Nishimura K, Nakamura S, Tanaka H, Mizuki N, Mizuki H, Inaba G, Tsuji K, Ohno S. RFLP analysis in the TNFβgene and the susceptibility to NK cells in Behçet's disease. Invest Ophthalmol Vis Sci. 1992;33(11):3084-3090. |
296. |
Mizuki N, Inoko H, Mizuki N, Tanaka H, Kera J, Tsuji K, Ohno S. Human leukocyte antigen serologic and DNA typing of Behçet's disease and its primary association with B51. Invest Ophthalmol Vis Sci. 1992;33(12):3332-3340. |
297. |
Mizuki N, Ohno S, Sugimura K, Seki T, Kikuti YY, Ando A, Tsuji K, Inoko H. PCR-RFLP is as sensitive and reliable as PCR-SSO in HLA class II genotyping. Tissue Antigens. 1992;40(2):100-103. |
298. |
Mizuki N, Ohno S, Tanaka H, Sugimura K, Seki T, Ando A, Kera J, Inaba G, Tsuji K, Inoko H. Association of HLA-B51 and lack of association of class II alleles with Behçet's disease. Tissue Antigens. 1992;40(1):22-30. |
299. |
Ota M, Seki T, Nomura N, Sugimura K, Mizuki N, Fukushima H, Tsuji K, Inoko H. Modifie PCR-RFLP method for HLA DPB1 and -DQA1 genotyping. Tissue Antigenes. 1991;38(2):60-71. |