School personnel information

写真b

SAKAI Norio


Keyword

pediatric neurology, inborn error metabolic disease, birth defect, medical genetics

Mail Address

Mail Address

URL

http://sahswww.med.osaka-u.ac.jp/~mcns/lab_02_01.html

Organization 【 display / non-display

  • 1999.04.01 - 2005.03.31, Graduate School of Medicine, Research Assistant

  • 2005.04.01 - 2009.09.30, Graduate School of Medicine, Associate Professor

  • 2009.10.01 - 2011.03.31, Division of Internal Medicine, Graduate School of Medicine, Associate Professor

  • 2011.04.01 - 2015.03.31, Division of Medicine, Graduate School of Medicine, Associate Professor

  • 2015.04.01 - , Division of Health Sciences, Graduate School of Medicine, Professor

  • 2004.07.01 - 2009.04.01, Division of Medicine, Graduate School of Medicine

  • 2009.04.01 - , Division of Medicine, Graduate School of Medicine

Education 【 display / non-display

The University of Tokyo Faculty of Science  Graduated 1982.03
Osaka University Faculty of Medicine  Graduated 1987.03
Osaka University Graduate School, Division of Medicine  Completed 1994.03

Research topics 【 display / non-display

  • Embryonic medicine and pediatrics-related, Medical biochemistry-related

 

Academic Papers 【 display / non-display

  • Update on Osaka University Twin Registry: An Overview of Multidisciplinary Research Resources and Biobank at Osaka University Center for Twin Research, Honda, C., Watanabe, M., Tomizawa, R., Osaka Twin Research Group, Sakai, N., Twin Res Hum Genet,(in press), 2019.12, Review Papers

  • Enhanced processivity of Dnmt1 by mono-ubiquitinated histone H3, Mishima, Y., Brueckner, L., Takahashi, S., Kawakami, T., Otani, J., Shinohara, A., Takeshita, K., Garvilles, R., Watanabe, M., Sakai, N., Takeshima, H., Nachtegael, C., Nishiyama, A., Nakanishi, M., Arita, K., Nakashima, K., Hojo, H., Suetake, I., Genes to Cells,(in press), 2019.11, Papers

  • The CODATwins Project: The Current Status and Recent Findings of COllaborative Project of Development of Anthropometrical Measures in Twins., Silventoinen K, et al, Twin Res Hum Genet,(in press), 2019.08, Papers

  • A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features., Yuka Murata, Hiroshi Kurosaka, Yasuhisa Ohata, Tomonao Aikawa, Sosuke Takahata, Katsunori Fujii, Toshiyuki Miyashita, Chisato Morita, Toshihiro Inubushi, Takuo Kubota, Norio Sakai, Keiichi Ozono, Mikihiko Kogo, Takashi Yamashiro, Human genome variation,6 16-16, 2019.04, Papers

  • Effect of Enzyme Replacement Therapy on Basilar Artery Diameter in Male Patients With Fabry Disease., Miwa K, Yagita Y, Sakaguchi M, Kitagawa K, Sakai N, Mochizuki H, Stroke,50(4) 1010-1012, 2019.04, Other

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