The Distinct Roles of Class I and II RPD3-Like Histone Deacetylases in Salinity Stress Response von Ueda, Minoru, Matsui, Akihiro, Tanaka, Maho, Nakamura, Tomoe, Abe, Takahiro, Sako, Kaori, Sasaki, Taku, Kim, Jong-Myong, Ito, Akihiro, Nishino, Norikazu, Shimada, Hiroaki, Yoshida, Minoru, Seki, Motoaki

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Real-time imaging of histone H4 hyperacetylation in living cells von Sasaki, Kazuki, Ito, Tamaki, Nishino, Norikazu, Khochbin, Saadi, Yoshida, Minoru

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Potent histone deacetylase inhibitors built from trichostatin A and cyclic tetrapeptide antibiotics including trapoxin von Furumai, Ryohei, Komatsu, Yasuhiko, Nishino, Norikazu, Khochbin, Saadi, Yoshida, Minoru, Horinouchi, Sueharu

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Bone Morphogenetic Protein-2 Stimulates Runx2 Acetylation von Jeon, Eun-Joo, Lee, Kwang-Youl, Choi, Nam-Sook, Lee, Mi-Hye, Kim, Hyun-Nam, Jin, Yun-Hye, Ryoo, Hyun-Mo, Choi, Je-Yong, Yoshida, Minoru, Nishino, Norikazu, Oh, Byung-Chul, Lee, Kyeong-Sook, Lee, Yong Hee, Bae, Suk-Chul

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Identification of novel molecular targets regulated by tumor suppressive miR-375 induced by histone acetylation in esophageal squamous cell carcinoma von ISOZAKI, YUKA, HOSHINO, ISAMU, NOHATA, NIJIRO, KINOSHITA, TAKASHI, AKUTSU, YASUNORI, HANARI, NAOYUKI, MORI, MIKITO, YONEYAMA, YASUO, AKANUMA, NAOKI, TAKESHITA, NOBUYOSHI, MARUYAMA, TETSURO, SEKI, NAOHIKO, NISHINO, NORIKAZU, YOSHIDA, MINORU, MATSUBARA, HISAHIRO

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Potent Histone Deacetylase Inhibitors Built from Trichostatin A and Cyclic Tetrapeptide Antibiotics Including Trapoxin von Furumai, Ryohei, Komatsu, Yasuhiko, Nishino, Norikazu, Khochbin, Saadi, Yoshida, Minoru, Horinouchi, Sueharu

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Live imaging of H3K9 acetylation in plant cells von Kurita, Kazuki, Sakamoto, Takuya, Yagi, Noriyoshi, Sakamoto, Yuki, Ito, Akihiro, Nishino, Norikazu, Sako, Kaori, Yoshida, Minoru, Kimura, Hiroshi, Seki, Motoaki, Matsunaga, Sachihiro

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Epoxy amino acids produced from allylglycines intramolecularly cyclised to yield four stereoisomers of 4-hydroxyproline derivatives von Krishnamurthy, Suvratha, Arai, Toru, Nakanishi, Kanae, Nishino, Norikazu

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Histone deacetylase inhibitors block nuclear factor‐κB‐dependent transcription by interfering with RNA polymerase II recruitment von Furumai, Ryohei, Ito, Akihiro, Ogawa, Kenji, Maeda, Satoko, Saito, Akiko, Nishino, Norikazu, Horinouchi, Sueharu, Yoshida, Minoru

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Histone deacetylation regulates de novo shoot regeneration von Temman, Haruka, Sakamoto, Takuya, Ueda, Minoru, Sugimoto, Kaoru, Migihashi, Masako, Yamamoto, Kazunari, Tsujimoto-Inui, Yayoi, Sato, Hikaru, Shibuta, Mio K, Nishino, Norikazu, Nakamura, Tomoe, Shimada, Hiroaki, Taniguchi, Yukimi Y, Takeda, Seiji, Aida, Mitsuhiro, Suzuki, Takamasa, Seki, Motoaki, Matsunaga, Sachihiro

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The role of class I histone deacetylase (HDAC) on gluconeogenesis in liver von Oiso, Hiroshi, Furukawa, Noboru, Suefuji, Mihoshi, Shimoda, Seiya, Ito, Akihiro, Furumai, Ryohei, Nakagawa, Junichi, Yoshida, Minoru, Nishino, Norikazu, Araki, Eiichi

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Bicyclic tetrapeptides as potent HDAC inhibitors: Effect of aliphatic loop position and hydrophobicity on inhibitory activity von Islam, Md. Nurul, Islam, Md. Shahidul, Hoque, Md. Ashraful, Kato, Tamaki, Nishino, Norikazu, Ito, Akihiro, Yoshida, Minoru

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Histone deacetylases control neurogenesis in embryonic brain by inhibition of BMP2/4 signaling von Shakèd, Maya, Weissmüller, Kathrin, Svoboda, Hanno, Hortschansky, Peter, Nishino, Norikazu, Wölfl, Stefan, Tucker, Kerry L

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Mechanisms of G1 cell cycle arrest and apoptosis in myeloma cells induced by hybrid-compound histone deacetylase inhibitor von Fujii, Seiko, Okinaga, Toshinori, Ariyoshi, Wataru, Takahashi, Osamu, Iwanaga, Kenjiro, Nishino, Norikazu, Tominaga, Kazuhiro, Nishihara, Tatsuji

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Dynamics and regulation of lysine-acetylation during one-cell stage mouse embryos von Matsubara, Keigo, Lee, Ah Reum, Kishigami, Satoshi, Ito, Akio, Matsumoto, Kazuya, Chi, Hongfang, Nishino, Norikazu, Yoshida, Minoru, Hosoi, Yoshihiko

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Histone deacetylase as a new target for cancer chemotherapy von YOSHIDA, Minoru, FURUMAI, Ryohei, NISHIYAMA, Akoto, KOMATSU, Yasuhiko, NISHINO, Norikazu, HORINOUCHI, Sueharu

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High-resolution structures of collagen-like peptides [(Pro-Pro-Gly)4-Xaa-Yaa-Gly-(Pro-Pro-Gly)4]: Implications for triple-helix hydration and Hyp(X) puckering von Okuyama, Kenji, Hongo, Chizuru, Wu, Guanghan, Mizuno, Kazunori, Noguchi, Keiichi, Ebisuzaki, Shutoku, Tanaka, Yuji, Nishino, Norikazu, Bächinger, Hans Peter

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Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework von Shivashimpi, Gururaj M., Amagai, Satoshi, Kato, Tamaki, Nishino, Norikazu, Maeda, Satoko, Nishino, Tomonori G., Yoshida, Minoru

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Design and synthesis of mono and bicyclic tetrapeptides thioester as potent inhibitor of histone deacetylases von Hoque, Md. Ashraful, Islam, Md. Shahidul, Islam, Md. Nurul, Kato, Tamaki, Nishino, Norikazu, Ito, Akihiro, Yoshida, Minoru

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Chlamydocin analogs bearing carbonyl group as possible ligand toward zinc atom in histone deacetylases von Bhuiyan, Mohammed P.I., Kato, Tamaki, Okauchi, Tatsuo, Nishino, Norikazu, Maeda, Satoko, Nishino, Tomonori G., Yoshida, Minoru

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