Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Hiroki Shimogawa"'
Autor:
Yutaka Kondo, Yoshitaka Sekido, Jean-Pierre J. Issa, Toshihiko Wakabayashi, Seung U. Kim, Hideyuki Okano, Motonari Uesugi, Hiroki Shimogawa, Ichiro Takeuchi, Yuta Ishikawa, Satoru Takahashi, Shinya Sato, Keiko Shinjo, Akira Hatanaka, Fumiharu Ohka, Keisuke Katsushima, Motokazu Ito, Atsushi Natsume
PDF - 157KB, Figure S1. Characterization of GSCs. Figure S2. Significance of EZH2/PRC2 in GBMs and GSCs. Figure S3. ChIP-chip analysis and MCAM analysis in GSCs. Figure S4. Effects of Wnt1-KD and BMP5-overexpression in GSCs. Figure S5. Downregulation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e189c5fd111ab30bc30a63c660b56b6
https://doi.org/10.1158/0008-5472.22396394
https://doi.org/10.1158/0008-5472.22396394
Autor:
Kouhei Yamada, Motonari Uesugi, Lutfi Abu-Elheiga, Hiroki Shimogawa, Takashi Shirakawa, Shinji Kamisuki, Akira Kugimiya, Salih J. Wakil, Hea-Young Park Choo
Publikováno v:
Journal of Medicinal Chemistry. 54:4923-4927
Fatostatin, a recently discovered small molecule that inhibits activation of sterol regulatory element-binding protein (SREBP), blocks biosynthesis and accumulation of fat in obese mice. The present study synthesized and evaluated a series of fatosta
Autor:
Norio Nakatsuji, Kayoko Tsukita, Kazuhiro Aiba, Yasuyuki Asai, Gaku Murakami, Yuji Amagai, Haruhisa Inoue, Hiroki Shimogawa, Ryosuke Takahashi, Motonari Uesugi
Publikováno v:
SLAS Discovery. 16:405-414
Familial amyotrophic lateral sclerosis (fALS) accounts for 10% of ALS cases, and about 25% of fALS cases are due to mutations in superoxide dismutase 1 (SOD1). Mutant SOD1-mediated ALS is caused by a gain of toxic function of the mutant protein, and
Autor:
Hiroki Shimogawa, Shinichi Sato, Qian Mao, Hideo Kigoshi, Shinji Kamisuki, Dongju Jung, Youngjoo Kwon, Motonari Uesugi
Publikováno v:
Journal of the American Chemical Society. 131:4774-4782
Naturally occurring transcription factors usually have two independent domains, a DNA-binding domain and an activation domain. In designing a synthetic small molecule that mimics a transcription factor, each of the two domains needs to be replaced by
Autor:
Motonari Uesugi, Hiroki Shimogawa, Yongmun Choi, Jun Qin, Latha Ramdas, Wei Zhang, Koji Murakami
Publikováno v:
Chemistry & Biology. 13:241-249
SummaryInsulin-like growth factor 2 (IGF2) is a potent mitogen whose deregulation plays a role in developing liver, breast, and prostate cancers. Here, we take a small-molecule approach to investigate molecular pathways that modulate IGF2 signaling,
Publikováno v:
Tetrahedron. 60:7067-7075
To obtain information on the chemical modification of biomolecules with jolkinolide D, a bioactive diterpenoid of plant origin, jolkinolide D pharmacophore was synthesized, and its reactivity toward amino acids, nucleosides, and DNA was investigated.
Autor:
Shinichi Asada, Yongmun Choi, Youngjoo Kwon, Yoshinori Kawazoe, Hideo Kigoshi, Hiroki Shimogawa, Motonari Uesugi, Qian Mao
Publikováno v:
Journal of the American Chemical Society. 126:3461-3471
Development of synthetic molecules that provide external control over the transcription of a given gene represents a challenge in medicinal and bioorganic chemistry. Here we report design and analysis of wrenchnolol, a wrench-shaped synthetic molecul
Autor:
Yasuhisa Kimura, Eihachiro Kawase, Norio Nakatsuji, Di Mao, Hiroki Shimogawa, Kazumitsu Ueda, Nao Hirata, Bilon Khambu, Ting-Fang Kuo, Makoto Ojika, Motonari Uesugi
Publikováno v:
Journal of the American Chemical Society. 136(28)
One of the current obstacles to stem cell therapy is the tumorigenic potential of residual undifferentiated stem cells. The present study reports rediscovery of a synthetic derivative of okadaic acid, a marine polyether toxin, as a reagent that selec
Publikováno v:
Tetrahedron Letters. 47:1409-1411
The trifluoroacetate salt of cinachyramine (1) was isolated from the Okinawan sponge Cinachyrella sp. This structure was determined by the spectroscopic analysis and the degradation under acidic conditions. Cinachyramine (1) is a novel alkaloid with
Publikováno v:
Bulletin of the Chemical Society of Japan. 78:1345-1347
New 13-epi-neoverrucosane-type diterpenes 1 and 2 were isolated from the marine sponge Axinyssa tethyoides. Their structures were elucidated by 2D-NMR spectroscopy, the modified Mosher’s method, an...