অনুসন্ধান ফলাফলগুলি - Kazuhiro Ogata
- প্রদর্শন 1 - 20 ফলাফল এর 37
- পরবর্তী পৃষ্ঠায় যান
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Solution structure of a DNA-binding unit of Myb: a helix-turn-helix-related motif with conserved tryptophans forming a hydrophobic core. অনুযায়ী Kazuhiro Ogata, Hironobu Hojo, Saburo Aimoto, Toshiki Nakai, Haruki Nakamura, Akinori Sarai, Shunsuke Ishii, Yoshifumi Nishimura
প্রকাশিত 1992Artigo -
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A <i>PLK4</i> mutation causing azoospermia in a man with Sertoli cell‐only syndrome অনুযায়ী Toshinobu Miyamoto, Yoshio Bandô, E. Koh, Akira Tsujimura, Yasushi Miyagawa, Masashi Iijima, Mikio Namiki, Masaaki Shiina, Kazuhiro Ogata, Nobuyuki Matsumoto, Kazuo Sengoku
প্রকাশিত 2015Artigo -
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Structural basis of the regulation of the normal and oncogenic methylation of nucleosomal histone H3 Lys36 by NSD2 অনুযায়ী Ko Sato, Amarjeet Kumar, Keisuke Hamada, Chikako Okada, Asako Oguni, Ayumi Machiyama, Shun Sakuraba, Tomohiro Nishizawa, Osamu Nureki, Hidetoshi Kono, Kazuhiro Ogata, Toru Sengoku
প্রকাশিত 2021Artigo -
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De novo <i><scp>DNM1</scp></i> mutations in two cases of epileptic encephalopathy অনুযায়ী Mitsuko Nakashima, Takeshi Kouga, Charles Marques Lourenço, Masaaki Shiina, Tomohide Goto, Yoshinori Tsurusaki, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Kazuhiro Ogata, Hitoshi Osaka, Naomichi Matsumoto
প্রকাশিত 2015Artigo -
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LimF is a versatile prenyltransferase for histidine-C-geranylation on diverse non-natural substrates অনুযায়ী Yuchen Zhang, Keisuke Hamada, Dinh Thanh Nguyen, Sumika Inoue, Masayuki Satake, Shunsuke Kobayashi, Chikako Okada, Kazuhiro Ogata, Masahiro Okada, Toru Sengoku, Yuki Goto, Hiroaki Suga
প্রকাশিত 2022Artigo -
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Structural Analyses of DNA Recognition by the AML1/Runx-1 Runt Domain and Its Allosteric Control by CBFβ অনুযায়ী T.H. Tahirov, Taiko Inoue-Bungo, Hisayuki Morii, Atsushi Fujikawa, Motoko Sasaki, Kazumi Kimura, Masaaki Shiina, Ko Sato, Takashi Kumasaka, Masaki Yamamoto, Shunsuke Ishii, Kazuhiro Ogata
প্রকাশিত 2001Artigo -
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De Novo Discovery of Thiopeptide Pseudo-natural Products Acting as Potent and Selective TNIK Kinase Inhibitors অনুযায়ী Alexander A. Vinogradov, Yue Zhang, Keisuke Hamada, Jun Shi Chang, Chikako Okada, Hirotaka Nishimura, Naohiro Terasaka, Yuki Goto, Kazuhiro Ogata, Toru Sengoku, Hiroyasu Onaka, Hiroaki Suga
প্রকাশিত 2022Artigo -
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Missense mutations in the DNA-binding/dimerization domain of NFIX cause Sotos-like features অনুযায়ী Yuriko Yoneda, Hirotomo Saitsu, Mayumi Touyama, Yoshio Makita, Akie Miyamoto, Keisuke Hamada, Naohiro Kurotaki, Hiroaki Tomita, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kazuhiro Ogata, Kenji Naritomi, Naomichi Matsumoto
প্রকাশিত 2012Artigo -
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Mechanism of c-Myb–C/EBPβ Cooperation from Separated Sites on a Promoter অনুযায়ী T.H. Tahirov, Ko Sato, Emi Ichikawa-Iwata, Motoko Sasaki, Taiko Inoue-Bungo, Masaaki Shiina, Kazumi Kimura, Shioka Takata, Atsushi Fujikawa, Hisayuki Morii, Takashi Kumasaka, Masaki Yamamoto, Shunsuke Ishii, Kazuhiro Ogata
প্রকাশিত 2002Artigo -
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Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy অনুযায়ী Hirotomo Saitsu, Hitoshi Osaka, Masayuki Sasaki, Jun‐ichi Takanashi, Keisuke Hamada, Akio Yamashita, Hidehiro Shibayama, Masaaki Shiina, Yukiko Kondo, Kiyomi Nishiyama, Yoshinori Tsurusaki, Noriko Miyake, Hiroshi Doi, Kazuhiro Ogata, Ken Inoue, Naomichi Matsumoto
প্রকাশিত 2011Artigo -
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Mitochondrial Complex III Deficiency Caused by a Homozygous<i>UQCRC2</i>Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation অনুযায়ী Noriko Miyake, Shoji Yano, Chika Sakai, Hideyuki Hatakeyama, Yuichi Matsushima, Masaaki Shiina, Yoriko Watanabe, James Bartley, José E. Abdenur, Raymond Wang, Richard Chang, Yoshinori Tsurusaki, Hiroshi Doi, Mitsuko Nakashima, Hirotomo Saitsu, Kazuhiro Ogata, Yu-ichi Goto, Naomichi Matsumoto
প্রকাশিত 2012Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Biology
Gene
Genetics
Mutation
Medicine
Missense mutation
Biochemistry
Cell biology
DNA
Transcription factor
Chemistry
Epilepsy
Exome sequencing
Internal medicine
Phenotype
Computational biology
Neuroscience
Amino acid
DNA-binding domain
Encephalopathy
Intellectual disability
MYB
Molecular biology
Psychiatry
DNA-binding protein
Endocrinology
Enzyme
Gene expression
Kinase
Myopathy