Výsledky vyhledávání - Mineo Ozaki

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  1. 1
    Identification of Candidate miRNA Biomarkers for Glaucoma

    Identification of Candidate miRNA Biomarkers for Glaucoma Autor Allyson G. Hindle, Robrecht Thoonen, Jessica V. Jasien, Robert M. H. Grange, Krishna Amin, Jasen Wise, Mineo Ozaki, Robert Ritch, Rajeev Malhotra, Emmanuel S. Buys

    Vydáno 2019
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  2. 2
    Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1

    Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1 Autor Francesca Pasutto, Matthias Zenkel, Ursula Hoja, Daniel Berner, Steffen Uebe, Fulvia Ferrazzi, Johannes Schödel, Panah Liravi, Mineo Ozaki, Daniela Paoli, Paolo Frezzotti, Takanori Mizoguchi, S Nakano, Toshiaki Kubota, Shin-ichi Manabe, Erika Salvi, Paolo Manunta, Maria Grazia Cusi, Christian Gieger, Heinz‐Erich Wichmann, Tin Aung, Chiea Chuen Khor, Friedrich E. Kruse, André Reis, Ursula Schlötzer‐Schrehardt

    Vydáno 2017
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  3. 3
    Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the<i>LOXL1</i>locus

    Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the<i>LOXL1</i>locus Autor Michael A. Hauser, Inas F. Aboobakar, Yutao Liu, Shiroh Miura, Benjamin T. Whigham, Pratap Challa, Joshua Wheeler, Andrew M. Williams, Cecelia Santiago-Turla, Xuejun Qin, Robyn M. Rautenbach, Ari Ziskind, Michèle Ramsay, Steffen Uebe, Lingyun Song, Alexias Safi, Eranga N. Vithana, Takanori Mizoguchi, S Nakano, Toshiaki Kubota, Ken Hayashi, Shin-ichi Manabe, Shigeyasu Kazama, Yosai Mori, Kazunori Miyata, Nagahisa Yoshimura, André Reis, Gregory E. Crawford, Francesca Pasutto, Trevor Carmichael, Susan Williams, Mineo Ozaki, Tin Aung, Chiea Chuen Khor, W. Daniel Stamer, Allison E. Ashley‐Koch, R. Rand Allingham

    Vydáno 2015
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  4. 4
    Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma

    Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma Autor Yukihiro Shiga, Masato Akiyama, Koji M. Nishiguchi, Kota Sato, Nobuhiro Shimozawa, Atsushi Takahashi, Yukihide Momozawa, Makoto Hirata, Koichi Matsuda, Taiki Yamaji, Motoki Iwasaki, Shoichiro Tsugane, Isao Oze, Haruo Mikami, Mariko Naito, Kenji Wakai, Munemitsu Yoshikawa, Masahiro Miyake, Kenji Yamashiro, Kenji Kashiwagi, Takeshi Iwata, Fumihiko Mabuchi, Mitsuko Takamoto, Mineo Ozaki, Kazuhide Kawase, Makoto Aihara, Makoto Araie, Tetsuya Yamamoto, Yoshiaki Kiuchi, Makoto Nakamura, Yasuhiro Ikeda, Koh‐Hei Sonoda, Tatsuro Ishibashi, Koji Nitta, Aiko Iwase, Shiroaki Shirato, Yoshitaka Oka, Mamoru Satoh, Makoto Sasaki, Nobuo Fuse, Yoichi Suzuki, Ching‐Yu Cheng, Chiea Chuen Khor, Mani Baskaran, Shamira Perera, Tin Aung, Eranga N. Vithana, Jessica N. Cooke Bailey, Jae H. Kang, Louis R. Pasquale, Jonathan L. Haines, Janey L. Wiggs, Kathryn P. Burdon, Puya Gharahkhani, Alex W. Hewitt, David A. Mackey, Stuart MacGregor, Jamie E. Craig, R. Rand Allingham, M.A. Hauser, Adeyinka Ashaye, Donald L. Budenz, Stephan Akafo, Susan Williams, Yoichiro Kamatani, Toru Nakazawa, Michiaki Kubo

    Vydáno 2018
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  5. 5
    ABCC5, a Gene That Influences the Anterior Chamber Depth, Is Associated with Primary Angle Closure Glaucoma

    ABCC5, a Gene That Influences the Anterior Chamber Depth, Is Associated with Primary Angle Closure Glaucoma Autor Monisha E. Nongpiur, Chiea Chuen Khor, Hongyan Jia, Belinda K. Cornes, Lijia Chen, Chunyan Qiao, K. Saidas Nair, Ching‐Yu Cheng, Liang Xu, Ronnie George, Tan Do, Khaled K. Abu‐Amero, Shamira Perera, Mineo Ozaki, Takanori Mizoguchi, Yasuo Kurimoto, Sancy Low, Ahmad Tajudin Liza-Sharmini, Ching‐Lin Ho, Clement C. Tham, Ileana Soto, Paul Chew, Hon‐Tym Wong, Shantha Balekudaru, Masako Kuroda, Essam A. Osman, Guangxian Tang, Sujie Fan, Hailin Meng, Hua Wang, Bo Feng, Victor H. K. Yong, Serena M. L. Ting, Yang Li, Ya Xing Wang, Zheng Li, Raghavan Lavanya, Renyi Wu, Yingfeng Zheng, Daniel Su, Seng‐Chee Loon, R. Rand Allingham, Michael A. Hauser, Nagaswamy Soumittra, Vedam L. Ramprasad, Naushin Waseem, Azhany Yaakub, Kee‐Seng Chia, Govindasamy Kumaramanickavel, Tina Wong, Alicia C. How, Tran Nguyen Bich Chau, Cameron P. Simmons, Jin‐Xin Bei, Yi‐Xin Zeng, Shomi S. Bhattacharya, Mingzhi Zhang, Donald Tan, Yik‐Ying Teo, Saleh A. Al‐Obeidan, Do Nhu Hon, E Shyong Tai, Seang‐Mei Saw, Paul J. Foster, Lingam Vijaya, Jost B. Jonas, Tien Yin Wong, Simon W. M. John, Chi‐Pui Pang, Eranga N. Vithana, Ningli Wang, Tin Aung

    Vydáno 2014
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  6. 6
    Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

    Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci Autor Tin Aung, Mineo Ozaki, Mei Lee, Ursula Schlötzer‐Schrehardt, Guðmar Þorleifsson, Takanori Mizoguchi, Robert P. Igo, Aravind Haripriya, Susan Williams, Yury S Astakhov, Andrew Orr, Kathryn P. Burdon, S Nakano, Kazuhiko Mori, Khaled K. Abu‐Amero, Michael A. Hauser, Zheng Li, Prakadeeswari Gopalakrishnan, Jessica N. Cooke Bailey, Alina Popa‐Cherecheanu, Jae H. Kang, Sarah C. Nelson, Ken Hayashi, Shin-ichi Manabe, Shigeyasu Kazama, Tomasz Żarnowski, Kenji Inoue, Murat İrkeç, Miguel Coca‐Prados, Kazuhisa Sugiyama, Irma Järvelä, Patricio G. Schlottmann, S. Lerner, Hasnaa Lamari, Nilgün Yıldırım, Mukharram M. Bikbov, Ki Ho Park, Soon Cheol, Kenji Yamashiro, Juan Carlos Zenteno, Jost B. Jonas, Rajesh S. Kumar, Shamira Perera, Anita Chan, Nino Kobakhidze, Ronnie George, Lingam Vijaya, Tan Do, Deepak P. Edward, Lourdes de Juan Marcos, Mohammad Pakravan, Sasan Moghimi, Ryuichi Ideta, Daniella Bach‐Holm, Per Kappelgaard, Barbara Wirostko, Samuel Thomas, Daniel Gaston, Karen Bedard, Wenda Greer, Zhenglin Yang, Xueyi Chen, Lulin Huang, Jinghong Sang, Hongyan Jia, Liyun Jia, Chunyan Qiao, Hui Zhang, Xuyang Liu, Bowen Zhao, Ya Xing Wang, Liang Xu, Stéphanie Leruez, Pascal Reynier, George Chichua, S Tabagari, Steffen Uebe, Matthias Zenkel, Daniel Berner, Georg Mossböck, Nicole Weisschuh, Ursula Hoja, Ulrich-Christoph Welge-Luessen, Christian Y. Mardin, Panayiota Founti, A. Chatzikyriakidou, Theofanis Pappas, Eleftherios Anastasopoulos, Alexandros Lambropoulos, Arkasubhra Ghosh, Rohit Shetty, Natalia Porporato, Saravanan Vijayan, Rengaraj Venkatesh, Chandrashekaran Shivkumar, Narendran Kalpana, Sripriya Sarangapani, Mozhgan R. Kanavi, Afsaneh Naderi Beni, Shahin Yazdani

    Vydáno 2017
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  7. 7
    New loci and coding variants confer risk for age-related macular degeneration in East Asians

    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 2015
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  8. 8
    A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

    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 2015
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  9. 9
    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome Autor Najim Lahrouchi, Rafik Tadros, Lia Crotti, Yuka Mizusawa, Pieter G. Postema, Leander Beekman, Roddy Walsh, Kanae Hasegawa, Julien Barc, Marko Ernsting, Kari L. Turkowski, Andrea Mazzanti, Britt M. Beckmann, Keiko Shimamoto, Ulla-Britt Diamant, Yanushi D. Wijeyeratne, Yu Kucho, Tomas Robyns, Taisuke Ishikawa, Elena Arbelo, Michael Christiansen, Annika Winbo, Reza Jabbari, Steven A. Lubitz, Johannes Steinfurt, Boris Rudic, Bart Loeys, Moore B. Shoemaker, Peter Weeke, Ryan Pfeiffer, Brianna Davies, Antoine Andorin, Nynke Hofman, Federica Dagradi, Matteo Pedrazzini, David J. Tester, J. Martijn Bos, Geòrgia Sarquella-Brugada, Òscar Campuzano, Pyotr G. Platonov, Birgit Stallmeyer, Sven Zumhagen, Eline A. Nannenberg, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Christopher E. Shaw, Pamela J. Shaw, Karen Morrison, Peter M. Andersen, Martina Müller‐Nurasyid, Daniele Cusi, Cristina Barlassina, Pilar Galán, Mark Lathrop, Markus Munter, Thomas Werge, Marta Ribasés, Tin Aung, Chiea Chuen Khor, Mineo Ozaki, Peter Lichtner, Thomas Meitinger, J. Peter van Tintelen, Yvonne M. Hoedemaekers, Isabelle Denjoy, Antoine Leenhardt, Carlo Napolitano, Wataru Shimizu, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Andrew D. Krahn, Charles Antzelevitch, Dan M. Roden, Johan Saenen, Martin Borggrefe, Katja E. Odening, Patrick T. Ellinor, Jacob Tfelt‐Hansen, Jonathan R. Skinner, Maarten P. van den Berg, Morten S. Olesen, Josép Brugada, Ramón Brugada, Naomasa Makita, Jeroen Breckpot, Masao Yoshinaga, Elijah R. Behr, Annika Rydberg, Takeshi Aiba, Stefan Kääb, Silvia G. Priori, Pascale Guicheney, Hanno L. Tan, Christopher Newton‐Cheh, Michael Ackerman, Peter J. Schwartz

    Vydáno 2020
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  10. 10
    A common variant near TGFBR3 is associated with primary open angle glaucoma

    A common variant near TGFBR3 is associated with primary open angle glaucoma Autor Zheng Li, R. Rand Allingham, Masakazu Nakano, Liyun Jia, Yuhong Chen, Yoko Ikeda, Mani Baskaran, Lijia Chen, Changwon Kee, David F. Garway‐Heath, Sarangapani Sripriya, Nobuo Fuse, Khaled K. Abu‐Amero, Chukai Huang, Prasanthi Namburi, Kathryn P. Burdon, Shamira Perera, Puya Gharahkhani, Ying Lin, Morio Ueno, Mineo Ozaki, Takanori Mizoguchi, Subbiah R. Krishnadas, Essam A. Osman, Mei Lee, Anita Chan, Ahmad Tajudin Liza-Sharmini, Tan Do, Aurélien Goncalves, Pascal Reynier, Hong Zhang, Rupert Bourne, David Goh, David C. Broadway, Rahat Husain, Anil Negi, Daniel Su, Ching‐Lin Ho, Augusto Azuara‐Blanco, Christopher Kai-Shun Leung, Tina Wong, Azhany Yakub, Yutao Liu, Monisha E. Nongpiur, Jong Chul Han, Do Nhu Hon, Shantha Balekudaru, Bowen Zhao, Jinghong Sang, Nihong Zhang, Ryuichi Sato, Kengo Yoshii, Songhomita Panda-Jonas, Allison E. Ashley‐Koch, Leon W. Herndon, Sayoko E. Moroi, Pratap Challa, Jia Nee Foo, Jin‐Xin Bei, Yi-Xin Zeng, Cameron P. Simmons, Tran Nguyen Bich Chau, Ferdinamarie Sharmila, Merwyn Chew, Blanche Lim, Pansy O.S. Tam, Elaine Chua, Xiao Yu Ng, Victor H. K. Yong, Yaan Fun Chong, Wee Yang Meah, Saravanan Vijayan, Seongsoo Sohn, Wanghong Xu, Yik Ying Teo, Jessica N. Cooke Bailey, Jae H. Kang, Jonathan L. Haines, Ching‐Yu Cheng, Seang‐Mei Saw, E Shyong Tai, Julia E. Richards, Robert Ritch, Douglas Gaasterland, Louis R. Pasquale, Jianjun Liu, Jost B. Jonas, Dan Milea, Ronnie George, Saleh A. Al‐Obeidan, Kazuhiko Mori, Stuart MacGregor, Alex W. Hewitt, Christopher A. Girkin, Mingzhi Zhang, Periasamy Sundaresan, Lingam Vijaya, David A. Mackey, Tien Yin Wong, Jamie E. Craig

    Vydáno 2015
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  11. 11
    Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma

    Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma Autor Chiea Chuen Khor, Tan Do, Hongyan Jia, Masakazu Nakano, Ronnie George, Khaled K. Abu‐Amero, Roopam Duvesh, Li Jia Chen, Zheng Li, Monisha E. Nongpiur, Shamira Perera, Chunyan Qiao, Hon‐Tym Wong, Hiroshi Sakai, Mônica Barbosa de Melo, Mei Lee, Anita Chan, Azhany Yaakub, Thi Lam Huong Dao, Yoko Ikeda, Rodolfo A. Perez-Grossmann, Tomasz Żarnowski, Alexander Day, Jost B. Jonas, Pancy O. S. Tam, Tuan Anh Tran, Humaira Ayub, Farah Akhtar, Shazia Micheal, Paul Chew, Leyla Ali Aljasim, Tanuj Dada, Tam Thi Luu, Mona S. Awadalla, Naris Kitnarong, Boonsong Wanichwecharungruang, Yee Yee Aung, Jelinar Mohamed-Noor, Saravanan Vijayan, Sripriya Sarangapani, Rahat Husain, Aliza Jap, Mani Baskaran, David Goh, Daniel Su, Huaizhou Wang, Vernon K. Yong, Leonard Wei Leon Yip, Tuyet Bach Trinh, Manchima Makornwattana, Thanh Thu Nguyen, Edgar U. Leuenberger, Ki-Ho Park, Widya Artini Wiyogo, Rajesh S. Kumar, Celso Tello, Yasuo Kurimoto, Suman Thapa, Kessara Pathanapitoon, John F. Salmon, Yongho Sohn, Antonio Maria Fea, Mineo Ozaki, Jimmy S.M. Lai, Visanee Tantisevi, Chaw Chaw Khaing, Takanori Mizoguchi, S Nakano, Chan-Yun Kim, Guangxian Tang, Sujie Fan, Renyi Wu, Hailin Meng, Thi Thuy Giang Nguyen, Dat T. Tran, Morio Ueno, Jose Maria D. Martinez, Norlina Ramli, Yin Mon Aung, Rigo Daniel Reyes, S A Vernon, Seng Kheong Fang, Zhicheng Xie, Xiao Yin Chen, Jia Nee Foo, Kar Seng Sim, Tina Wong, Desmond Quek, Rengaraj Venkatesh, Srinivasan Kavitha, Subbiah R. Krishnadas, Nagaswamy Soumittra, Shantha Balekudaru, Boon-Ang Lim, Jeanne J. Ogle, José Paulo Cabral de Vasconcellos, Vital Paulino Costa, Ricardo Y. Abe, Bruno Batista de Souza, Chelvin C. A. Sng

    Vydáno 2016
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