Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Makiko Nakagawa"'
Autor:
Motoi Tobiume, Shigeyuki Aoki, Genya Nishikawa, Hiroyuki Muramatsu, Kenzo Ono, Shingo Morinaga, Koji Hara, Natsuko Ando, Keiko Ono, Chie Nishibata, Ayumi Hidano, Makiko Nakagawa, Ikumi Takahashi, Kanae Matsubara, Yoshiaki Yamada
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-7 (2021)
Abstract Background Extragonadal germ cell tumor (EGCT) is a relatively rare condition, reportedly representing 3–7% of all germ cell tumors. We report a patient who had metachronous testicular tumor with uncommon metastases 20 years after primary
Externí odkaz:
https://doaj.org/article/e0c30670f2ce4c1eafd15644268382b7
Autor:
Tadashi Nakagawa, Akane Morohoshi, Yuko Nagasawa, Makiko Nakagawa, Masaki Hosogane, Yasuhiro Noda, Toru Hosoi, Keiko Nakayama
Publikováno v:
Cell Reports, Vol 38, Iss 12, Pp 110541- (2022)
Summary: The histone chaperone complex FACT comprises SPT16 and SSRP1 and contributes to DNA replication, transcription, and repair, but how it plays such various roles is unclear. Here, we show that human SPT16 is ubiquitylated at lysine-674 (K674)
Externí odkaz:
https://doaj.org/article/acc2ec7278fc475baaf6a4baafc163bc
Autor:
Yasuaki Watanabe, Tadashi Nakagawa, Tetsuya Akiyama, Makiko Nakagawa, Naoki Suzuki, Hitoshi Warita, Masashi Aoki, Keiko Nakayama
Publikováno v:
iScience, Vol 23, Iss 9, Pp 101491- (2020)
Summary: C21ORF2 and NEK1 have been identified as amyotrophic lateral sclerosis (ALS)-associated genes. Both genes are also mutated in certain ciliopathies, suggesting that they might contribute to the same signaling pathways. Here we show that FBXO3
Externí odkaz:
https://doaj.org/article/ac28b87d59564ffa9eb3a02133e43da7
Autor:
Tadashi Nakagawa, Satoko Hattori, Risa Nobuta, Ryuichi Kimura, Makiko Nakagawa, Masaki Matsumoto, Yuko Nagasawa, Ryo Funayama, Tsuyoshi Miyakawa, Toshifumi Inada, Noriko Osumi, Keiichi I. Nakayama, Keiko Nakayama
Publikováno v:
iScience, Vol 23, Iss 4, Pp - (2020)
Summary: Haploinsufficiency of SETD5 is implicated in syndromic autism spectrum disorder (ASD), but the molecular mechanism underlying the pathological role of this protein has remained unclear. We have now shown that Setd5+/– mice manifest ASD-rel
Externí odkaz:
https://doaj.org/article/e94f71749c494d6d8151cc398653ff33
Autor:
Tadashi Nakagawa, Akane Morohoshi, Yuko Nagasawa, Makiko Nakagawa, Masaki Hosogane, Yasuhiro Noda, Toru Hosoi, Keiko Nakayama
Publikováno v:
Cell reports. 38(12)
The histone chaperone complex FACT comprises SPT16 and SSRP1 and contributes to DNA replication, transcription, and repair, but how it plays such various roles is unclear. Here, we show that human SPT16 is ubiquitylated at lysine-674 (K674) by the DC
Autor:
Makiko Nakagawa, Keiko Nakayama, Yujiao Yu, Noriko Ishida, Akane Morohoshi, Naoki Suzuki, Tadashi Nakagawa, Masashi Aoki
Publikováno v:
Human Molecular Genetics. 28:3486-3497
Amyotrophic lateral sclerosis (ALS) is an adult-onset motor neuron disease characterized by a progressive decline in motor function. Genetic analyses have identified several genes mutated in ALS patients, and one of them is Cyclin F gene (CCNF), the
Autor:
Mika Nashimoto, Yoshitomo Koshida, Eisuke Fukuma, Yurie Haruyama, Makiko Nakagawa, Naomi Sakamoto
Publikováno v:
Breast cancer (Tokyo, Japan). 28(2)
Locally advanced breast cancer sometimes results in a large chest wall defect at mastectomy. When closing the wound horizontally, the skin tension is usually severe in the middle of the wound, while the skin of the lateral area tends to make a dog-ea
Autor:
Ryuichi Kimura, Keiichi I. Nakayama, Keiko Nakayama, Yuko Nagasawa, Toshifumi Inada, Masaki Matsumoto, Makiko Nakagawa, Noriko Osumi, Ryo Funayama, Satoko Hattori, Tadashi Nakagawa, Risa Nobuta, Tsuyoshi Miyakawa
Publikováno v:
iScience
iScience, Vol 23, Iss 4, Pp-(2020)
iScience, Vol 23, Iss 4, Pp-(2020)
Summary Haploinsufficiency of SETD5 is implicated in syndromic autism spectrum disorder (ASD), but the molecular mechanism underlying the pathological role of this protein has remained unclear. We have now shown that Setd5+/– mice manifest ASD-rela
Autor:
Naoki Suzuki, Hitoshi Warita, Yasuaki Watanabe, Makiko Nakagawa, Masashi Aoki, Tadashi Nakagawa, Keiko Nakayama, Tetsuya Akiyama
Publikováno v:
iScience, Vol 23, Iss 9, Pp 101491-(2020)
iScience
iScience
Summary C21ORF2 and NEK1 have been identified as amyotrophic lateral sclerosis (ALS)-associated genes. Both genes are also mutated in certain ciliopathies, suggesting that they might contribute to the same signaling pathways. Here we show that FBXO3,
Autor:
Teng Zhang, Makiko Nakagawa, Noriko Yanagihara, Ryo Kushi, Seiji Nakano, Takahiro Endo, Tadashi Nakagawa, David Zarkower, Keiko Nakayama
Publikováno v:
Development.
The mitosis-meiosis transition is essential for spermatogenesis. Specific and timely down-regulation of the transcription factor DMRT1, and consequent induction of Stra8 expression, is required for this process in mammals, but the molecular mechanism