Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Shigeaki Miyabayashi"'
Autor:
Toshihiro Ohura, Shigeaki Miyabayashi, Kei Murayama, Junji Takeyama, Daiki Abukawa, Shigeo Kure, Osamu Sakamoto, Kazuhiro Haginoya, Akira Ohtake, Hiroko Harashima
Publikováno v:
Pediatrics International. 53:921-925
Background: Succinyl-coenzyme A ligase (SUCL) is a mitochondrial enzyme that catalyses the reversible conversion of succinyl-coenzyme A to succinate. SUCL consists of an α subunit, encoded by SUCLG1, and a β subunit, encoded by either SUCLA2 or SUC
Autor:
Makoto Kameda, Miki Morikawa, Mayumi Tamari, Tomomitsu Hirota, Yoichi Suzuki, Hiroshi Fujiwara, Chifuyu Nakazawa, Kimie Fujita, Hiroko Endo, Fumiaki Kamada, Yasushi Chiba, Toshio Morikawa, Taro Shirakawa, Tadao Enomoto, Hiroki Inoue, Chenchen Shao, Satoru Doi, Gen Tamura, Shigeaki Miyabayashi, Yoichi Mashimo, Akira Hata, Sei Sasaki, Yoichi Matsubara, Reiko Takayanagi
Publikováno v:
International Archives of Allergy and Immunology. 144:275-286
Background: Bronchial asthma is a chronic airway disorder characterized by bronchial inflammation. Oxidative stress is a key component of inflammation. Glutathione S-transferase P1 (GSTP1), the abundant isoform of glutathione S-transferases (GSTs) in
Publikováno v:
Journal of Pediatric Hematology/Oncology. 26:279-583
The identification of a mutation in the MYH9 gene in hereditary macrothrombocytopenia has established a distinct entity proposed as "MYH9 disorders," which previously have often been misdiagnosed as chronic immune thrombocytopenic purpura. The author
Autor:
Taro Shirakawa, Koichi Hasegawa, Chenchen Shao, Yasushi Chiba, Seichi Saito, Gen Tamura, Mayumi Tamari, Yoko Aoki, Shigeaki Miyabayashi, Yoichi Suzuki, Kiyoshi Kanno, Miki Morikawa, Chifuyu Nakazawa, Reiko Takayanagi, Hiroko Endo, Minoru Karahashi, Yoichi Matsubara, Fumiaki Kamada, Toshio Morikawa, Xue Yang, Shigeo Kure
Publikováno v:
Journal of Human Genetics. 49:115-122
Several studies have shown linkage of chromosome region 12q13-24 to bronchial asthma and related phenotypes in ethnically diverse populations. In the Japanese population, a genome-wide study failed to show strong evidence of linkage of this region. C
Autor:
Masashi Tanaka, Harm-Jan Borgeld, Jin Zhang, Shin-ichi Muramatsu, Jian-Sheng Gong, Makoto Yoneda, Wakako Maruyama, Makoto Naoi, Tohru Ibi, Ko Sahashi, Masayo Shamoto, Noriyuki Fuku, Miyuki Kurata, Yoshiji Yamada, Kumi Nishizawa, Yukihiro Akao, Nobuko Ohishi, Shigeaki Miyabayashi, Hiraku Umemoto, Tatsuo Muramatsu, Koichi Furukawa, Akihiko Kikuchi, Imaharu Nakano, Keiya Ozawa, Kunio Yagi
Publikováno v:
Journal of Biomedical Science. 9:534-541
Autor:
Hiraku Umemoto, Liangmei He, Ya-Ling Chang, Mei-Chiao Wu, Chi-Hung Lin, H. Yee, Tatsuo Muramatsu, Tohru Ibi, Fernando Augusto Proietti, Hsiu-Yu Lai, Koichi Furukawa, Shin-ichi Muramatsu, Binh N. Tran, Alice Y.W. Chang, Hung-Chou Kuo, Hung-Ming Chen, Imaharu Nakano, Wen-Fang Cheng, Shiow-Lin Pan, Chungming Chang, Kumi Nishizawa, Harm-Jan Borgeld, Ren-Bin Tang, Young-Chau Liu, Hal F. Yee, S. Chan, Pisit Tangkijvanich, Andrew M. James, Jan M. Orenstein, Steven P. Tam, Yukihiro Akao, Chen-Che Chu, Jin-Lian Tsai, Nobuko Ohishi, Elizabeth A. Rich, I. Bravo, May-Ghee Lum, Xavier Roucou, Paik-Seong Lim, Ta-Chen Lin, Chun-Ching Lin, J.A. Marshall, C.H. Lai, Samuel H.H. Chan, E. Gutiérrez-Reyes, Julie Y.H. Chan, Mei-Jie Jou, James K V Willson, Hsing I. Chen, Chuen Miin Leu, T.-C. Wu, Shigeaki Miyabayashi, Chia-Wei Liou, Pen-Hui Yin, Yueh-Mei Cheng, Che-Ming Teng, Fen-Hwa Wong, D.K.Y. Shum, Kunio Yagi, Catherine Transy, Jian-Sheng Gong, Keiya Ozawa, Horng-Der Shen, Ying-Wen Huang, Chai-Wei Liou, David Wang, Chien-Min Yang, Françoise Bergametti, Helen Wong, Sheng-Chu Kuo, June L. Traicoff, Y.S. Chan, Masayo Shamoto, J.-Y. Lee, Shuo-Bin Jou, Hong Chou, J.A. Moreno-Yanes, Stefanie N. Vogel, Keng-Fu Hsu, Anna Bárbara F. Carneiro-Proietti, M. Shehu-Xhilaga, S. Campbell, J. Mak, Hsin-Chen Lee, M.S. Cho, Cheng-po Hu, Tania M. Hansen, Chiung-Yun Chang, Ming F. Tam, Herbert C. Morse rd, John S. Cowdery, Akihiko Kikuchi, R. Bonfante-Cabarcas, Miyuki Kurata, Shan-Chun Chen, Ru Ping Lee, Julie Bianchi, Ching-Yun Chang, Chien-Fu Hung, Yi-Shing Ma, Cheng-Feng Lee, Arin J. Schroeder, Makoto Yoneda, Bernadette Catalan-Soares, Yao-Chung Chuang, Sammy Saab, Tsung-I Peng, Ko Sahashi, Henry Chai, Sanford D. Markowitz, Hsin-Su Yu, Kuan-Teh Jeang, Makoto Naoi, Hua-Yew Cheng, Ching-jang Huang, Michael P. Murphy, C. Nello, Phillip Nagley, Noriyuki Fuku, Sara I. Pai, Tzu-Ling Chen, Wan-Shung Fong, Yau-Huei Wei, Chin-Wen Chi, Maria L.R. Lim, Andrew C. Melton, Jin Zhang, Morris Ling, Yoshiji Yamada, Mary Bradford, Li-Jiau Huang, S.M. Crowe, N.E. Loureiro Dos Santos, Masashi Tanaka, Wakako Maruyama, Chin-Chang Huang, Jih-Hwa Guh, Nien Tsung Lin
Publikováno v:
Journal of Biomedical Science. 9:741-744
Gene Therapy for Mitochondrial Disease by Delivering Restriction Endonuclease SmaI into Mitochondria
Autor:
Hiraku Umemoto, Makoto Naoi, Tohru Ibi, Masashi Tanaka, Nobuko Ohishi, Kunio Yagi, Ko Sahashi, Jian-Sheng Gong, Imaharu Nakano, Wakako Maruyama, Shin-ichi Muramatsu, Akihiko Kikuchi, Koichi Furukawa, Miyuki Kurata, Yukihiro Akao, Jin Zhang, Masayo Shamoto, Shigeaki Miyabayashi, Tatsuo Muramatsu, Noriyuki Fuku, Keiya Ozawa, Kumi Nishizawa, Harm-Jan Borgeld, Makoto Yoneda, Yoshiji Yamada
Publikováno v:
Journal of Biomedical Science. 9:534-541
The restriction endonuclease Sma I has been used for the diagnosis of neurogenic muscle weakness, ataxia and retinitis pigmentosa disease or Leigh’s disease, caused by the Mt8993T→G
Autor:
Young-Chau Liu, Michael P. Murphy, C. Nello, S. Campbell, Cheng-po Hu, Chiung-Yun Chang, Shin-ichi Muramatsu, Pisit Tangkijvanich, John S. Cowdery, Hal F. Yee, Jan M. Orenstein, Phillip Nagley, Hung-Ming Chen, J.A. Moreno-Yanes, Anna Bárbara F. Carneiro-Proietti, M. Shehu-Xhilaga, Chen-Che Chu, M.S. Cho, Bernadette Catalan-Soares, Paik-Seong Lim, Tatsuo Muramatsu, Morris Ling, Fernando Augusto Proietti, Steven P. Tam, T.-C. Wu, Ren-Bin Tang, May-Ghee Lum, Chun-Ching Lin, Tsung-I Peng, Ko Sahashi, Henry Chai, Sanford D. Markowitz, Shuo-Bin Jou, Akihiko Kikuchi, Chi-Hung Lin, Tohru Ibi, H. Yee, Li-Jiau Huang, Pen-Hui Yin, C.H. Lai, Chin-Chang Huang, Jih-Hwa Guh, S. Chan, Andrew M. James, Nien Tsung Lin, Keng-Fu Hsu, Shiow-Lin Pan, Nobuko Ohishi, Elizabeth A. Rich, Samuel H.H. Chan, J.A. Marshall, Julie Y.H. Chan, Hsing I. Chen, Ying-Wen Huang, Jin-Lian Tsai, I. Bravo, Mei-Jie Jou, Chuen Miin Leu, Hsiu-Yu Lai, Noriyuki Fuku, Sara I. Pai, Hung-Chou Kuo, Tania M. Hansen, Xavier Roucou, Chungming Chang, Shan-Chun Chen, Ru Ping Lee, Imaharu Nakano, Fen-Hwa Wong, Ta-Chen Lin, Catherine Transy, Kuan-Teh Jeang, Wen-Fang Cheng, Yao-Chung Chuang, S.M. Crowe, Chien-Fu Hung, R. Bonfante-Cabarcas, Chai-Wei Liou, E. Gutiérrez-Reyes, Horng-Der Shen, Françoise Bergametti, Chien-Min Yang, Herbert C. Morse rd, Masayo Shamoto, Helen Wong, Sheng-Chu Kuo, Y.S. Chan, Julie Bianchi, Ching-jang Huang, Koichi Furukawa, Ching-Yun Chang, Ming F. Tam, Kumi Nishizawa, Harm-Jan Borgeld, Hiraku Umemoto, Yi-Shing Ma, Binh N. Tran, Alice Y.W. Chang, Stefanie N. Vogel, Hsin-Su Yu, Shigeaki Miyabayashi, Jian-Sheng Gong, Makoto Naoi, Hua-Yew Cheng, Wan-Shung Fong, Maria L.R. Lim, Liangmei He, Chin-Wen Chi, Wakako Maruyama, Jin Zhang, Tzu-Ling Chen, Yau-Huei Wei, Mary Bradford, Andrew C. Melton, Ya-Ling Chang, David Wang, Kunio Yagi, Mei-Chiao Wu, Chia-Wei Liou, June L. Traicoff, Yueh-Mei Cheng, Che-Ming Teng, Yukihiro Akao, James K V Willson, Hong Chou, J. Mak, Sammy Saab, Masashi Tanaka, D.K.Y. Shum, Keiya Ozawa, Cheng-Feng Lee, Arin J. Schroeder, J.-Y. Lee, Hsin-Chen Lee, Miyuki Kurata, Makoto Yoneda, Yoshiji Yamada, N.E. Loureiro Dos Santos
Publikováno v:
Journal of Biomedical Science. 9:730-739
Autor:
Yoichi Suzuki, Kunihiro Fujii, Osamu Sakamoto, Jun Akanuma, Toshihiro Ohura, Shigeaki Miyabayashi, Kazutoshi Takahashi, Kaoru Wataya, Yoko Aoki, Masahito Ogasawara, Yoichi Matsubara, Kuniaki Narisawa, Shigeo Kure
Publikováno v:
American Journal of Medical Genetics. 92:90-94
Glycogen storage disease type Ia (GSD-Ia) is an autosomal recessive disorder of glycogen metabolism caused by glucose-6-phosphatase (G6Pase) deficiency. It is characterized by short stature, hepatomegaly, hypoglycemia, hyperuricemia, and lactic acide
Autor:
Hiroshi Shitara, Shigeaki Miyabayashi, Makiko Yamaoka, Kotoyo Isobe, Jun-Ichi Hayashi, Hiromichi Yonekawa
Publikováno v:
Genetics. 155:301-307
By the fusion of mtDNA-less (ρ0) cells of Mus musculus domesticus with platelets from different species, mtDNA repopulated cybrids were obtained for finding the mtDNA species that could induce mitochondrial abnormalities. Expression of mitochondrial