Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Yuki Miyasaka"'
Autor:
Ruchen Zhang, Paniz Farshadyeganeh, Bisei Ohkawara, Kazuki Nakajima, Jun-ichi Takeda, Mikako Ito, Shaochuan Zhang, Yuki Miyasaka, Tamio Ohno, Madoka Mori-Yoshimura, Akio Masuda, Kinji Ohno
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 8 (2024)
Externí odkaz:
https://doaj.org/article/dd1d6d2ad7d74c9db299f98aace79c6f
Autor:
Misato Kobayashi, Fumi Kanbe, Reika Ishii, Hiroki Tsubouchi, Kana Hirai, Yuki Miyasaka, Tamio Ohno, Hiroaki Oda, Saiko Ikeda, Hirokazu Katoh, Kenji Ichiyanagi, Akira Ishikawa, Atsushi Murai, Fumihiko Horio
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract High serum levels of triglycerides (TG) and low levels of high-density lipoprotein cholesterol (HDL-C) increase the risk of coronary heart disease in humans. Herein, we first reported that the C3H/HeNSlc (C3H-S) mouse, a C3H/HeN-derived subs
Externí odkaz:
https://doaj.org/article/5f8aa6917a3d4aa692c883570dd21b94
Autor:
Paniz Farshadyeganeh, Mohammad Nazim, Ruchen Zhang, Bisei Ohkawara, Kazuki Nakajima, Mohammad Alinoor Rahman, Farhana Nasrin, Mikako Ito, Jun-ichi Takeda, Kenji Ohe, Yuki Miyasaka, Tamio Ohno, Akio Masuda, Kinji Ohno
Publikováno v:
iScience, Vol 26, Iss 10, Pp 107746- (2023)
Summary: Glutamine:fructose-6-phosphate transaminase 1 (GFPT1) is the rate-limiting enzyme of the hexosamine biosynthetic pathway (HBP). A 54-bp exon 9 of GFPT1 is specifically included in skeletal and cardiac muscles to generate a long isoform of GF
Externí odkaz:
https://doaj.org/article/3389bd93cb9e4caaa6d1fa76afe19c00
Autor:
Yuya Murase, Takuya Takeichi, Jun Koseki, Yuki Miyasaka, Yoshinao Muro, Tamio Ohno, Teppei Shimamura, Masashi Akiyama
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
NLRP1 (NACHT and leucine-rich repeat-containing protein family, pyrin domain-containing protein 1) is an innate immune sensor that is involved in the formation of inflammasome complexes. NLRP1 hyperactivity has been reported to cause inherited autoin
Externí odkaz:
https://doaj.org/article/a7793bfa579245f3b02b72a2cc501531
Autor:
Takuya Takeichi, John Y. W. Lee, Yusuke Okuno, Yuki Miyasaka, Yuya Murase, Takenori Yoshikawa, Kana Tanahashi, Emi Nishida, Tatsuya Okamoto, Komei Ito, Yoshinao Muro, Kazumitsu Sugiura, Tamio Ohno, John A. McGrath, Masashi Akiyama
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
Heterozygous mutations in JAK1 which result in JAK-STAT hyperactivity have been implicated in an autosomal dominant disorder that features multi-organ immune dysregulation. This study identifies another previously unreported heterozygous missense JAK
Externí odkaz:
https://doaj.org/article/6391e3e6db344fdea31bbf01dd88d1ad
Autor:
Shumpei P. Yasuda, Yuki Miyasaka, Xuehan Hou, Yo Obara, Hiroshi Shitara, Yuta Seki, Kunie Matsuoka, Ai Takahashi, Eri Wakai, Hiroshi Hibino, Toyoyuki Takada, Toshihiko Shiroishi, Ryo Kominami, Yoshiaki Kikkawa
Publikováno v:
Biomedicines, Vol 10, Iss 9, p 2221 (2022)
An MSM/Ms strain was established using Japanese wild mice, which exhibit resistance to several phenotypes associated with aging, such as obesity, inflammation, and tumorigenesis, compared to common inbred mouse strains. MSM/Ms strain is resistant to
Externí odkaz:
https://doaj.org/article/b75c825ab039479b8e28c8ba546586f6
Autor:
Ding Li, Yuki Miyasaka, Arisa Kubota, Takuma Kozono, Yoshikazu Kitano, Nobumitsu Sasaki, Tadashi Fujii, Takumi Tochio, Yoshihiro Kadota, Atsushi Nishikawa, Takashi Tonozuka
Publikováno v:
Bioscience, Biotechnology & Biochemistry; Sep2023, Vol. 87 Issue 9, p981-990, 10p
Autor:
Yuki Miyasaka, Takeshi Kobayashi, Naoya Gotoh, Masako Kuga, Misato Kobayashi, Fumihiko Horio, Katsunori Hashimoto, Tsutomu Kawabe, Tamio Ohno
Publikováno v:
Mammalian Genome. 34:32-43
Autor:
Tomomi Masuya, Miyako Suzuki, Junko Tsujimura, Shinsaku Kanamori, Yuki Miyasaka, Tamio Ohno, Atsushi Murai, Fumihiko Horio, Misato Kobayashi
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233087 (2020)
Nonalcoholic fatty liver disease (NAFLD) is a pathological condition caused by excess triglyceride deposition in the liver. The SMXA-5 severe fatty liver mouse model has been established from the SM/J and A/J strains. To explore the genetic factors i
Externí odkaz:
https://doaj.org/article/4dcac94e2d4e4f19bd44115ad1c0000f
Autor:
Takenori Yoshikawa, Takuya Takeichi, Tetsuya Hirabayashi, Yoshinao Muro, Yuki Miyasaka, Tamio Ohno, Masashi Akiyama
Pityriasis rubra pilaris (PRP) is a rare inflammatory keratinization disorder with perifollicular erythema, and most autosomal dominant familial cases of atypical juvenile (type V) PRP are caused by gain-of-function mutations in CARD14, which encodes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25f20cba988c9da331424f01a02032fa
https://doi.org/10.21203/rs.3.rs-2513325/v1
https://doi.org/10.21203/rs.3.rs-2513325/v1