Toshiyuki Yamamoto

J-GLOBAL         Last updated: Sep 21, 2018 at 12:56
 
Avatar
Name
Toshiyuki Yamamoto
Affiliation
Tokyo Women's Medical University Faculty of Medicine
ORCID ID
0000-0002-9484-3505

Research Interests

 
 

Research Areas

 
 

Academic & Professional Experience

 
Apr 2002
 - 
Jan 2003
Visiting fellow, Adelaide University, Centre for Medical Genetics
 

Published Papers

 
Toshiyuki Yamamoto, Keiko Yamamoto-Shimojima, Yuki Ueda, Katsumi Imai, Yukitoshi Takahashi, Eri Imagawa, Noriko Miyake, Naomichi Matsumoto
Human Genome Variation   5(1) 18   Dec 2018   [Refereed]
Yoshika Akizawa, Toshiyuki Yamamoto, Kazuo Tamura, Toshiyuki Kanno, Nobuko Takahashi, Takeshi Ohki, Teppei Omori, Katsutoshi Tokushige, Masakazu Yamamoto, Kayoko Saito
Human Genome Variation   5(1) 13   Dec 2018   [Refereed]
Shimada S, Oguni H, Otani Y, Nishikawa A, Ito S, Eto K, Nakazawa T, Yamamoto-Shimojima K, Takanashi JI, Nagata S, Yamamoto T
Brain & development   40(9) 813-818   Oct 2018   [Refereed]
Shimada S, Hirasawa K, Takeshita A, Nakatsukasa H, Yamamoto-Shimojima K, Imaizumi T, Nagata S, Yamamoto T
American Journal of Medical Genetics Part A      Aug 2018   [Refereed]
Akahoshi K, Yamamoto T
Neuropsychiatric Disease and Treatment   14 1773-1778   Jul 2018   [Refereed]

Misc

 
YAMAMOTO Toshiyuki, AKASAKA Yuko, OHTANI Kyoichi, HAYASHI Takashi, KASHIWAGI Shiro, ICHIYAMA Takashi, NISHIKAWA Miki, KATO Mitsuhiro, MAEGAKI Yoshihiro, OKA Akira, OHNO Kousaku
脳と発達 = OFFICIAL JOURNAL OF THE JAPANESE SOCIETY OF CHILD NEUROLOGY   37(1) 15-19   Jan 2005
YAMAMOTO Toshiyuki, AKASAKA Yuko, OHTANI Kyoichi, HAYASHI Takashi, KASHIWAGI Shiro, ICHIYAMA Takashi, NISHIKAWA Miki, KATO Mitsuhiro, MAEGAKI Yoshihiro, OKA Akira, OHNO Kousaku
脳と発達 = OFFICIAL JOURNAL OF THE JAPANESE SOCIETY OF CHILD NEUROLOGY   37(1) 20-25   Jan 2005
TOMINAGA R, NANBA E, INADA A, YAMAMOTO T, TAKESHIMA T, KITAMURA Y, TANIGUCHI M, OHNO K, OSHIMA A, MATSUDA J, SUZUKI Y
日本先天代謝異常学会雑誌   14(2)    Oct 1998

Books etc

 
ベン・ポリス (Part:Single Translation)
三輪書店   Jun 2003   ISBN:4895901947

Research Grants & Projects

 
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(C))
Project Year: 2007 - 2008    Investigator(s): Toshiyuki YAMAMOTO
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(基盤研究(B))
Project Year: 2001 - 2003    Investigator(s): Eiji NANBA
The chemical chaperon therapy for inherited metabolic diseases including GM1-gangliosidois have been developed in the study. GM1-gangliosidosis which caused by deficiency of β-galactosidase in lysosome, is manifested by central nervous involvement...
Ministry of Education, Culture, Sports, Science and Technology: Grants-in-Aid for Scientific Research(一般研究(B), 基盤研究(B))
Project Year: 1994 - 1996    Investigator(s): Kenzo TAKESHITA
The fragile X syndrome is the most common cause of inherited mental retardation. Recently, a genomic locus was identified and the CGG trinucleotide rerepeat expansion has been found. We reported a rapid screening test by a non-radioisotope PCR tec...