Zobrazeno 1 - 10
of 106
pro vyhledávání: '"KATSUYA MIYAKE"'
Autor:
Wataru Masuda, Tomoko Yamakawa, Rieko Ajima, Katsuya Miyake, Toshifumi Umemiya, Kazuhiko Azuma, Jun-ichi Tamaru, Makoto Kiso, Puspa Das, Yumiko Saga, Kenji Matsuno, Motoo Kitagawa
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-16 (2023)
Abstract Notch signaling is an evolutionarily conserved mechanism required for numerous types of cell fate decisions in metazoans. It mediates short-range communication between cells with receptors and ligands, both of which are expressed on the cell
Externí odkaz:
https://doaj.org/article/db8e41c628a4412e85d3d2da141b5a7e
Autor:
Yuko Kokubu, Tomoko Nagino, Katsunori Sasa, Tatsuo Oikawa, Katsuya Miyake, Akiko Kume, Mikiko Fukuda, Hiromitsu Fuse, Ryuichi Tozawa, Hidetoshi Sakurai
Publikováno v:
Stem Cells Translational Medicine, Vol 8, Iss 10, Pp 1017-1029 (2019)
Abstract Dysferlinopathy is a progressive muscle disorder that includes limb‐girdle muscular dystrophy type 2B and Miyoshi myopathy (MM). It is caused by mutations in the dysferlin (DYSF) gene, whose function is to reseal the muscular membrane. Tre
Externí odkaz:
https://doaj.org/article/b07e2c3175334def8fbba6cc177a30d7
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e106721 (2014)
Defects in dystroglycan glycosylation are associated with a group of muscular dystrophies, termed dystroglycanopathies, that include Fukuyama congenital muscular dystrophy (FCMD). It is widely believed that abnormal glycosylation of dystroglycan lead
Externí odkaz:
https://doaj.org/article/c73c1d1fd80a487a8d5eaf3e138f2643
Autor:
Akihito Tanaka, Knut Woltjen, Katsuya Miyake, Akitsu Hotta, Makoto Ikeya, Takuya Yamamoto, Tokiko Nishino, Emi Shoji, Atsuko Sehara-Fujisawa, Yasuko Manabe, Nobuharu Fujii, Kazunori Hanaoka, Takumi Era, Satoshi Yamashita, Ken-ichi Isobe, En Kimura, Hidetoshi Sakurai
Publikováno v:
PLoS ONE, Vol 8, Iss 12 (2013)
Externí odkaz:
https://doaj.org/article/fb247d6028b74f0592fd3875603622c6
Autor:
Akihito Tanaka, Knut Woltjen, Katsuya Miyake, Akitsu Hotta, Makoto Ikeya, Takuya Yamamoto, Tokiko Nishino, Emi Shoji, Atsuko Sehara-Fujisawa, Yasuko Manabe, Nobuharu Fujii, Kazunori Hanaoka, Takumi Era, Satoshi Yamashita, Ken-Ichi Isobe, En Kimura, Hidetoshi Sakurai
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e61540 (2013)
The establishment of human induced pluripotent stem cells (hiPSCs) has enabled the production of in vitro, patient-specific cell models of human disease. In vitro recreation of disease pathology from patient-derived hiPSCs depends on efficient differ
Externí odkaz:
https://doaj.org/article/a53a2e125cb94ca9862365174625ce99
Publikováno v:
PLoS ONE, Vol 2, Iss 8, p e687 (2007)
BACKGROUND: Ingestion of the lectins present in certain improperly cooked vegetables can result in acute GI tract distress, but the mechanism of toxicity is unknown. In vivo, gut epithelial cells are constantly exposed to mechanical and other stresse
Externí odkaz:
https://doaj.org/article/8061df6d13e84a5399a5950015fc1407
Autor:
Akiko Kume, Tomoko Nagino, Katsunori Sasa, Hidetoshi Sakurai, Katsuya Miyake, Mikiko Fukuda, Ryuichi Tozawa, Tatsuo Oikawa, Yuko Kokubu, Hiromitsu Fuse
Publikováno v:
Stem Cells Translational Medicine, Vol 8, Iss 10, Pp 1017-1029 (2019)
Stem Cells Translational Medicine
Stem Cells Translational Medicine
Dysferlinopathy is a progressive muscle disorder that includes limb-girdle muscular dystrophy type 2B and Miyoshi myopathy (MM). It is caused by mutations in the dysferlin (DYSF) gene, whose function is to reseal the muscular membrane. Treatment with
Autor:
Md. Golam Mostofa, Tomotake Kanki, Takashi Ushimaru, Katsuya Miyake, Talukdar Muhammad Waliullah, Mashu Terasawa, Islam Nafisa, Akter Mst Yeasmin, Akihiro Kondo
Publikováno v:
Journal of Molecular Biology. 430:1671-1684
Cdc14 protein phosphatase is critical for late mitosis progression in budding yeast, although its orthologs in other organisms, including mammalian cells, function as stress-responsive phosphatases. We found herein unexpected roles of Cdc14 in autoph
Autor:
KATSUYA MIYAKE1,2 miyakek@bz-csp.tepm.jp
Publikováno v:
Number Theory: Plowing & Starring Through High Wave Forms - Proceedings of the 7th China-Japan Seminar. 2015, p145-167. 23p.
Autor:
Nobukazu Araki, Masashi Aoki, Naoki Suzuki, Hiroya Ono, Katsuya Miyake, Kensuke Ikeda, Naoko Nakamura, Hitoshi Warita, Yukiko K. Hayashi, Tomomi Shijo, Shio Mitsuzawa, Tetsuya Akiyama, Yasuo Kitajima, Ryoichi Nagatomi, Shin Ichiro Kanno, Akira Yasui, Genri Kawahara, Toshiaki Takahashi, Shion Osana, Rumiko Izumi
Publikováno v:
Molecular Therapy
Mutations in dysferlin are responsible for a group of progressive, recessively inherited muscular dystrophies known as dysferlinopathies. Using recombinant proteins and affinity purification methods combined with liquid chromatography-tandem mass spe