Zobrazeno 1 - 10
of 383
pro vyhledávání: '"Toshio Heike"'
Autor:
Takuya Hirata, Shiro Baba, Kentaro Akagi, Koichi Matsuda, Katsutsugu Umeda, Souichi Adachi, Toshio Heike, Junko Takita
Publikováno v:
PLoS ONE, Vol 19, Iss 1, p e0297083 (2024)
BackgroundDuchenne muscular dystrophy (DMD), a severe degenerative skeletal and cardiac muscle disease, has a poor prognosis, and no curative treatments are available. Because decreased autophagy has been reported to contribute to skeletal muscle deg
Externí odkaz:
https://doaj.org/article/cadc9586ab94407ab04694f3e8f5fa6d
Publikováno v:
eJHaem, Vol 4, Iss 3, Pp 852-853 (2023)
Externí odkaz:
https://doaj.org/article/348d0b061efe4086a4ee43d47ffbab18
Autor:
Takayuki Hamabata, Katsutsugu Umeda, Kagehiro Kouzuki, Takayuki Tanaka, Tomoo Daifu, Seishiro Nodomi, Satoshi Saida, Itaru Kato, Shiro Baba, Hidefumi Hiramatsu, Mitsujiro Osawa, Akira Niwa, Megumu K. Saito, Yasuhiko Kamikubo, Souichi Adachi, Yoshiko Hashii, Akira Shimada, Hiroyoshi Watanabe, Kenji Osafune, Keisuke Okita, Tatsutoshi Nakahata, Kenichiro Watanabe, Junko Takita, Toshio Heike
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-4 (2021)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/b950f5eee1ed4eed9297ec002e679c2f
Publikováno v:
eJHaem, Vol 3, Iss 2, Pp 543-544 (2022)
Externí odkaz:
https://doaj.org/article/fc865730a5d34cf98fbfa3e3ca2e1000
Autor:
Daisuke Yoshinaga, Shiro Baba, Takeru Makiyama, Hirofumi Shibata, Takuya Hirata, Kentaro Akagi, Koichi Matsuda, Hirohiko Kohjitani, Yimin Wuriyanghai, Katsutsugu Umeda, Yuta Yamamoto, Bruce R. Conklin, Minoru Horie, Junko Takita, Toshio Heike
Publikováno v:
Stem Cell Reports, Vol 13, Iss 2, Pp 394-404 (2019)
Summary: For long QT syndrome (LQTS), recent progress in genome-sequencing technologies enabled the identification of rare genomic variants with diagnostic, prognostic, and therapeutic implications. However, pathogenic stratification of the identifie
Externí odkaz:
https://doaj.org/article/b189b2413cc34770b097f88d43dcd361
Autor:
Manabu Nakayama, Hirotsugu Oda, Kenji Nakagawa, Takahiro Yasumi, Tomoki Kawai, Kazushi Izawa, Ryuta Nishikomori, Toshio Heike, Osamu Ohara
Publikováno v:
Biochemistry and Biophysics Reports, Vol 9, Iss C, Pp 146-152 (2017)
Autoinflammatory diseases occupy one of a group of primary immunodeficiency diseases that are generally thought to be caused by mutation of genes responsible for innate immunity, rather than by acquired immunity. Mutations related to autoinflammatory
Externí odkaz:
https://doaj.org/article/35a8440b7674454a8818c90977402da6
Autor:
Fumitoshi Tsurumi, Shiro Baba, Daisuke Yoshinaga, Katsutsugu Umeda, Takuya Hirata, Junko Takita, Toshio Heike
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0213768 (2019)
Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy. The major symptoms of this condition are walking difficulties, dyspnea caused by progressive skeletal muscle weakness, and cardiomyopathy. Recent advances in
Externí odkaz:
https://doaj.org/article/29b85971eff04020995f78b63298ae80
Autor:
Ryo Kimura, Yuko Ishii, Kiyotaka Tomiwa, Tomonari Awaya, Masatoshi Nakata, Takeo Kato, Shin Okazaki, Toshio Heike, Masatoshi Hagiwara
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Williams–Beuren syndrome (WBS) is a multisystemic neurodevelopmental disorder caused by a hemizygous deletion on chromosome 7q11.23. Though at present there is a limited number of reports on WBS patients with tumors, most cases are related to blood
Externí odkaz:
https://doaj.org/article/53c7fed34ca64f7ab935c60947b44e90
Autor:
Tomoyuki Iwasaki, Naoe Kaneko, Yuki Ito, Hiroyuki Takeda, Tatsuya Sawasaki, Toshio Heike, Kiyoshi Migita, Kazunaga Agematsu, Atsushi Kawakami, Shinnosuke Morikawa, Sho Mokuda, Mie Kurata, Junya Masumoto
Publikováno v:
The Scientific World Journal, Vol 2016 (2016)
Nucleotide-binding oligomerization domain-containing protein (Nod) 2 is an intracellular pattern recognition receptor, which recognizes muramyl dipeptide (N-Acetylmuramyl-L-Alanyl-D-Isoglutamine: MDP), a bacterial peptidoglycan component, and makes a
Externí odkaz:
https://doaj.org/article/725b492ae4d440729c24225fda611f23
Publikováno v:
Allergology International, Vol 61, Iss 2, Pp 207-217 (2012)
Anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) is characterized according to its various manifestations, which include ectodermal dysplasia, vascular anomalies, osteopetrosis, and diverse immunological abnormalities such as susceptibi
Externí odkaz:
https://doaj.org/article/a096a91d295f4b90b49406330d8ed387