Structural basis of adhesion-molecule recognition by ERM proteins revealed by the crystal structure of the radixin–ICAM-2 complex

Por Hamada, Keisuke, Shimizu, Toshiyuki, Yonemura, Shigenobu, Tsukita, Shoichiro, Tsukita, Sachiko, Hakoshima, Toshio
Publicado em 2003

Structural basis of the membrane-targeting and unmasking mechanisms of the radixin FERM domain

Por Hamada, Keisuke, Shimizu, Toshiyuki, Matsui, Takeshi, Tsukita, Shoichiro, Tsukita, Sachiko, Hakoshima, Toshio
Publicado em 2000

Crystallization of the Ets1–Runx1–CBFβ–DNA complex formed on the TCRα gene enhancer

Por Shiina, Masaaki, Hamada, Keisuke, Inoue-Bungo, Taiko, Shimamura, Mariko, Baba, Shiho, Sato, Ko, Ogata, Kazuhiro
Publicado em 2014

Structure–Activity Relationship Studies of 3-epi-Deoxynegamycin Derivatives as Potent Readthrough Drug Candidates

Por Hamada, Keisuke, Taguchi, Akihiro, Kotake, Masaya, Aita, Suguru, Murakami, Saori, Takayama, Kentaro, Yakushiji, Fumika, Hayashi, Yoshio
Publicado no ACS Med Chem Lett (2015)

Structural basis for recruitment of human flap endonuclease 1 to PCNA

Por Sakurai, Shigeru, Kitano, Ken, Yamaguchi, Hiroto, Hamada, Keisuke, Okada, Kengo, Fukuda, Kotaro, Uchida, Makiyo, Ohtsuka, Eiko, Morioka, Hiroshi, Hakoshima, Toshio
Publicado em 2005

Structure–Activity Relationship Study of Leucyl-3-epi-deoxynegamycin for Potent Premature Termination Codon Readthrough

Por Taguchi, Akihiro, Hamada, Keisuke, Shiozuka, Masataka, Kobayashi, Misaki, Murakami, Saori, Takayama, Kentaro, Taniguchi, Atsuhiko, Usui, Takeo, Matsuda, Ryoichi, Hayashi, Yoshio
Publicado no ACS Med Chem Lett (2017)

Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy

Por Saitsu, Hirotomo, Osaka, Hitoshi, Sasaki, Masayuki, Takanashi, Jun-ichi, Hamada, Keisuke, Yamashita, Akio, Shibayama, Hidehiro, Shiina, Masaaki, Kondo, Yukiko, Nishiyama, Kiyomi, Tsurusaki, Yoshinori, Miyake, Noriko, Doi, Hiroshi, Ogata, Kazuhiro, Inoue, Ken, Matsumoto, Naomichi
Publicado em 2011

Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay

Por Saitsu, Hirotomo, Tohyama, Jun, Kumada, Tatsuro, Egawa, Kiyoshi, Hamada, Keisuke, Okada, Ippei, Mizuguchi, Takeshi, Osaka, Hitoshi, Miyata, Rie, Furukawa, Tomonori, Haginoya, Kazuhiro, Hoshino, Hideki, Goto, Tomohide, Hachiya, Yasuo, Yamagata, Takanori, Saitoh, Shinji, Nagai, Toshiro, Nishiyama, Kiyomi, Nishimura, Akira, Miyake, Noriko, Komada, Masayuki, Hayashi, Kenji, Hirai, Syu-ichi, Ogata, Kazuhiro, Kato, Mitsuhiro, Fukuda, Atsuo, Matsumoto, Naomichi
Publicado em 2010