Výsledky vyhledávání - Norimoto Gotoh
- Zobrazuji výsledky 1 - 19 z 19
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Comprehensive Molecular Diagnosis of a Large Cohort of Japanese Retinitis Pigmentosa and Usher Syndrome Patients by Next-Generation Sequencing Autor Maho Oishi, Akio Oishi, Norimoto Gotoh, Ken Ogino, Koichiro Higasa, Kei Iida, Yukiko Makiyama, Satoshi Morooka, Fumihiko Matsuda, Nagahisa Yoshimura
Vydáno 2014Artigo -
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Quantification of Oxygen Consumption in Retina Ex Vivo Demonstrates Limited Reserve Capacity of Photoreceptor Mitochondria Autor Keshav Kooragayala, Norimoto Gotoh, Tiziana Cogliati, Jacob Nellissery, Talia R. Kaden, Stephanie French, Robert S. Balaban, Wei Li, Raúl Covián, Anand Swaroop
Vydáno 2015Artigo -
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Developing Rods Transplanted into the Degenerating Retina of Crx-Knockout Mice Exhibit Neural Activity Similar to Native Photoreceptors Autor Kohei Homma, Satoshi Okamoto, Michiko Mandai, Norimoto Gotoh, Harsha Rajasimha, Yi-Sheng Chang, Shan Chen, Wei Li, Tiziana Cogliati, Anand Swaroop, Masayo Takahashi
Vydáno 2013Artigo -
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Comprehensive Replication of the Relationship Between Myopia-Related Genes and Refractive Errors in a Large Japanese Cohort Autor Munemitsu Yoshikawa, Kenji Yamashiro, Masahiro Miyake, Maho Oishi, Yumiko Akagi-Kurashige, Kyoko Kumagai, Isao Nakata, Hideo Nakanishi, Akio Oishi, Norimoto Gotoh, Ryo Yamada, Fumihiko Matsuda, Nagahisa Yoshimura
Vydáno 2014Artigo -
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Optical Coherence Tomography Angiography to Estimate Retinal Blood Flow in Eyes with Retinitis Pigmentosa Autor Masako Sugahara, Manabu Miyata, Kenji Ishihara, Norimoto Gotoh, Satoshi Morooka, Ken Ogino, Tomoko Hasegawa, Takako Hirashima, Munemitsu Yoshikawa, Masayuki Hata, Yuki Muraoka, Sotaro Ooto, Kenji Yamashiro, Nagahisa Yoshimura
Vydáno 2017Artigo -
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A Genome-Wide Association Analysis Identified a Novel Susceptible Locus for Pathological Myopia at 11q24.1 Autor Hideo Nakanishi, Ryo Yamada, Norimoto Gotoh, Hisako Hayashi, Kenji Yamashiro, Noriaki Shimada, Kyoko Ohno-Matsui, Manabu Mochizuki, Masaaki Saito, Tomohiro Iida, Keitaro Matsuo, Kazuo Tajima, Nagahisa Yoshimura, Fumihiko Matsuda
Vydáno 2009Artigo -
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Reduction of lipid accumulation rescues Bietti’s crystalline dystrophy phenotypes Autor Masayuki Hata, Hanako Ohashi Ikeda, Sachiko Iwai, Yuto Iida, Norimoto Gotoh, Isao Asaka, Kazutaka Ikeda, Yosuke Isobe, Aya Hori, Saori Nakagawa, Susumu Yamato, Makoto Arita, Nagahisa Yoshimura, Akitaka Tsujikawa
Vydáno 2018Artigo -
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Transcriptional Regulation of Rod Photoreceptor Homeostasis Revealed by In Vivo NRL Targetome Analysis Autor Hong Hao, Douglas S. Kim, Bernward Klocke, Kory R. Johnson, Kairong Cui, Norimoto Gotoh, Chongzhi Zang, Janina Gregorski, Linn Gieser, Weiqun Peng, Yang C. Fann, Martin Seifert, Keji Zhao, Anand Swaroop
Vydáno 2012Artigo -
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Preservation of Cone Photoreceptors after a Rapid yet Transient Degeneration and Remodeling in Cone-Only<i>Nrl</i><sup>−/−</sup>Mouse Retina Autor Jérôme E. Roger, Keerthi Ranganath, Lian Zhao, Radu Cojocaru, Matthew Brooks, Norimoto Gotoh, Shobi Veleri, Avinash Hiriyanna, Rivka A. Rachel, Maria M Campos, Robert N. Fariss, Wai T. Wong, Anand Swaroop
Vydáno 2012Artigo -
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CEP290 alleles in mice disrupt tissue-specific cilia biogenesis and recapitulate features of syndromic ciliopathies Autor Rivka A. Rachel, Erin Yamamoto, Mrinal K. Dewanjee, Helen May‐Simera, Yuri V. Sergeev, Alice N. Hackett, Katherine Pohida, Jeeva Munasinghe, Norimoto Gotoh, Bill Wickstead, Robert N. Fariss, Lijin Dong, Tiansen Li, Anand Swaroop
Vydáno 2015Artigo -
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NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors Autor Jung-Woong Kim, Hyun‐Jin Yang, Matthew J. Brooks, Lina Zelinger, Gökhan Karakülah, Norimoto Gotoh, Alexis Boleda, Linn Gieser, Felipe Giuste, D. Thad Whitaker, Ashley Walton, Rafael Villasmil, Jennifer J. Barb, Peter J. Munson, Koray Dogan Kaya, Vijender Chaitankar, Tiziana Cogliati, Anand Swaroop
Vydáno 2016Artigo -
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Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis Autor Rivka A. Rachel, Helen May‐Simera, Shobi Veleri, Norimoto Gotoh, Byung Yoon Choi, Carlos Murga‐Zamalloa, Jeremy C. McIntyre, Jonah Marek, Irma López, Alice N. Hackett, Matthew Brooks, Anneke I. den Hollander, Philip L. Beales, Tiansen Li, Samuel G. Jacobson, Raman Sood, Jeffrey R. Martens, Paul Liu, Thomas B. Friedman, Hemant Khanna, Robert K. Koenekoop, Matthew W. Kelley, Anand Swaroop
Vydáno 2012Artigo -
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Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia Autor Masahiro Miyake, Kenji Yamashiro, Yasuharu Tabara, K. Suda, Satoshi Morooka, Hideo Nakanishi, Chiea Chuen Khor, Peng Chen, Qiao Fan, Isao Nakata, Yumiko Akagi-Kurashige, Norimoto Gotoh, Akitaka Tsujikawa, Akira Meguro, Sentaro Kusuhara, Ozren Polašek, Caroline Hayward, Alan F. Wright, Harry Campbell, Andrea J. Richardson, Maria Schäche, Masaki Takeuchi, David A. Mackey, Alex W. Hewitt, Gabriel Cuéllar-Partida, Yi Shi, Luling Huang, Zhenglin Yang, Kim Hung Leung, Patrick Y.P. Kao, Maurice Yap, Shea Ping Yip, Muka Moriyama, Kyoko Ohno-Matsui, Nobuhisa Mizuki, Stuart MacGregor, Véronique Vitart, Tin Aung, Seang‐Mei Saw, E Shyong Tai, Tien Yin Wong, Ching‐Yu Cheng, Paul N. Baird, Ryo Yamada, Fumihiko Matsuda, Takeo Nakayama, Akihiro Sekine, Shinji Kosugi, Nagahisa Yoshimura
Vydáno 2015Artigo -
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New loci and coding variants confer risk for age-related macular degeneration in East Asians Autor Ching‐Yu Cheng, Kenji Yamashiro, Li Jia Chen, Jeeyun Ahn, Lulin Huang, Lvzhen Huang, Chui Ming Gemmy Cheung, Masahiro Miyake, Peter Cackett, Ian Yeo, Augustinus Laude, Ranjana Mathur, Junxiong Pang, Kar Seng Sim, Adrian H. Koh, Peng Chen, Shu Yen Lee, Damon Wing Kee Wong, Choi Mun Chan, Boon Kwang Loh, Yaoyao Sun, Sonia Dávila, Isao Nakata, Hideo Nakanishi, Yumiko Akagi-Kurashige, Norimoto Gotoh, Akitaka Tsujikawa, Fumihiko Matsuda, Keisuke Mori, Shin Yoneya, Yoichi Sakurada, Hiroyuki Iijima, Tomohiro Iida, Shigeru Honda, Timothy Y. Y. Lai, Pancy Oi Sin Tam, Haoyu Chen, Shibo Tang, Xiaoyan Ding, Feng Wen, Fang Lü, Xiongze Zhang, Yi Shi, Peiquan Zhao, Bowen Zhao, Jinghong Sang, Bo Gong, Rajkumar Dorajoo, Jian‐Min Yuan, Woon‐Puay Koh, Rob M. van Dam, Yechiel Friedlander, Ying Lin, Martin L. Hibberd, Jia Nee Foo, Ningli Wang, Chang Hua Wong, Gavin Tan, Sang Jun Park, Mayuri Bhargava, Lingam Gopal, Thet Naing, Jiemin Liao, Peng Guan Ong, Paul Mitchell, Peng Zhou, Xuefeng Xie, Jinlong Liang, Junpu Mei, Xin Jin, Seang‐Mei Saw, Mineo Ozaki, Takanori Mizoguchi, Yasuo Kurimoto, Se Joon Woo, Hum Chung, Hyeong Gon Yu, Joo Young Shin, Dong Ho Park, In Taek Kim, Woohyok Chang, Min Sagong, Sang Joon Lee, Hyun Woong Kim, Ji Eun Lee, Yi Li, Jianjun Liu, Yik Ying Teo, Chew‐Kiat Heng, Tock Han Lim, Suk‐Kyun Yang, Kyuyoung Song, Eranga N. Vithana, Tin Aung, Jin Bei, Yi Zeng, E Shyong Tai, Xiao Xin Li, Zhenglin Yang, Kyu-Hyung Park
Vydáno 2015Artigo -
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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome Autor Tin Aung, Mineo Ozaki, Takanori Mizoguchi, R. Rand Allingham, Zheng Li, Aravind Haripriya, S Nakano, Steffen Uebe, Jeffrey M. Harder, Anita Chan, Mei Lee, Kathryn P. Burdon, Yury S. Astakhov, Khaled K. Abu‐Amero, Juan Carlos Zenteno, Nilgün Yıldırım, Tomasz Żarnowski, Mohammad Pakravan, Leen Abu Safieh, Liyun Jia, Ya Xing Wang, Susan Williams, Daniela Paoli, Patricio G. Schlottmann, Lulin Huang, Kar Seng Sim, Jia Nee Foo, Masakazu Nakano, Yoko Ikeda, Rajesh S. Kumar, Morio Ueno, Shin-ichi Manabe, Ken Hayashi, Shigeyasu Kazama, Ryuichi Ideta, Yosai Mori, Kazunori Miyata, Kazuhisa Sugiyama, Tomomi Higashide, Etsuo Chihara, Kenji Inoue, Satoshi Ishiko, Akitoshi Yoshida, Masahide Yanagi, Yoshiaki Kiuchi, Makoto Aihara, Tsutomu Ōhashi, Toshiya Sakurai, Takako Sugimoto, Hideki Chuman, Fumihiko Matsuda, Kenji Yamashiro, Norimoto Gotoh, Masahiro Miyake, Sergei Astakhov, Essam A. Osman, Saleh A. Al‐Obeidan, Ohoud Owaidhah, Leyla Ali Aljasim, Sami Al Shahwan, Rhys A Fogarty, Paul Leo, Yetkin Yaz, Oğuz Çilingir, Mozhgan Rezaei Kanavi, Afsaneh Naderi Beni, Shahin Yazdani, Evgeny L. Akopov, Kai Yee Toh, Gareth R. Howell, Andrew Orr, Yufen Goh, Wee Yang Meah, Su Qin Peh, Ewa Kosior‐Jarecka, Urszula Łukasik, Mandy Krumbiegel, Eranga N. Vithana, Tien Yin Wong, Yutao Liu, Allison E Ashley Koch, Pratap Challa, Robyn M. Rautenbach, David A. Mackey, Alex W. Hewitt, Paul Mitchell, Jie Jin Wang, Ari Ziskind, Trevor Carmichael, Ramakrishnan Rangappa, Kalpana Narendran, Rangaraj Venkatesh, Saravanan Vijayan, Peiquan Zhao, Xueyi Chen, Dalia Guadarrama-Vallejo, Ching‐Yu Cheng, Shamira Perera, Rahat Husain, Su-Ling Ho
Vydáno 2015Artigo -
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Genetic variants near <i>TIMP3</i> and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration Autor Wei Chen, Dwight Stambolian, Albert O. Edwards, Kari Branham, Mohammad Othman, Jóhanna Jakobsdóttir, Nirubol Tosakulwong, Margaret A. Pericak‐Vance, Peter A. Campochiaro, Michael L. Klein, Perciliz L. Tan, Yvette P. Conley, Atsuhiro Kanda, Laura J. Kopplin, Yanming Li, Katherine J. Augustaitis, Athanasios J. Karoukis, William K. Scott, Anita Agarwal, Jaclyn L. Kovach, Stephen G. Schwartz, Eric A. Postel, Matthew Brooks, Keith H. Baratz, William L. Brown, Alexander J. Brucker, Anton Orlin, Gary C. Brown, Allen C. Ho, Carl D. Regillo, Larry A. Donoso, Lifeng Tian, Brian Kaderli, Dexter Hadley, Stephanie A. Hagstrom, Neal S. Peachey, Ronald Klein, Barbara E.K. Klein, Norimoto Gotoh, Kenji Yamashiro, Frederick L. Ferris, Jesen Fagerness, Robyn Reynolds, Lindsay A. Farrer, Ivana K. Kim, Joan W. Miller, Marta Cortón, Ãngel Carracedo, Manuel Sánchez‐Salorio, Elizabeth Pugh, Kimberly F. Doheny, Marı́a Brión, Margaret M. DeAngelis, Daniel E. Weeks, Donald J. Zack, Emily Y. Chew, John R. Heckenlively, Nagahisa Yoshimura, Sudha K. Iyengar, Peter J. Francis, Nicholas Katsanis, Johanna M. Seddon, Jonathan L. Haines, Michael B. Gorin, Gonçalo R. Abecasis, Anand Swaroop, Robert N. Johnson, Everett Ai, H. Richard McDonald, Margaret Stolarczuk, Peter R. Pavan, Karina K. Billiris, Mohan Iyer, Matthew M. Menosky, Scott E. Pautler, Sharon M. Millard, G. Baker Hubbard, Thomas Aaberg, Lindy DuBois, Alice T. Lyon, Susan Anderson-Nelson, Lee M. Jampol, David V. Weinberg, Annie Muñana, Zuzanna Rozenbajgier, David H. Orth, Jack Cohen, Matthew MacCumber, Matthew MacCumber, Celeste Figliulo, Liz Porcz, James C. Folk, H. Culver Boldt, Stephen R. Russell, Rachel Ivins, Connie J. Hinz, Charles C. Barr, Steve Bloom, Ken Jaegers, Brian Kritchman
Vydáno 2010Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Cell biology
Medicine
Neuroscience
Phenotype
Ophthalmology
Retina
Biochemistry
Gene expression
Locus (genetics)
Pathology
Transcription factor
Anatomy
Environmental health
Genetic association
Genome-wide association study
Genotype
Internal medicine
Mutation
Population
Regulation of gene expression
Retinal
Single-nucleotide polymorphism
Allele
Ciliogenesis
Ciliopathies
Ciliopathy
Cilium