Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Yuka Takezawa"'
Autor:
Katsuya Nakamura, Saki Mukai, Yuka Takezawa, Yuika Natori, Akari Miyazaki, Yuichiro Ide, Mayu Takebuchi, Kana Nanato, Mizuki Katoh, Harue Suzuki, Akiko Sakyu, Tomomi Kojima, Emiko Kise, Hiroaki Hanafusa, Tomoki Kosho, Koichiro Kuwahara, Yoshiki Sekijima
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 36, Iss , Pp 100983- (2023)
Introduction: Variants in the galactosidase alpha (GLA) gene cause Fabry disease (FD), an X-linked lysosomal storage disorder caused by α-galactosidase A (α-GAL) deficiency. Recently, disease-modifying therapies have been developed, and simple diag
Externí odkaz:
https://doaj.org/article/119d97007211468bbaeab2995a8ed9ad
Publikováno v:
Bioscience, Biotechnology, and Biochemistry. 87:314-319
This study investigates the mechanisms governing experience-dependent tolerance of bitter compounds in Caenorhabditis elegans. The nematodes showed an aversion to nicotinamide, MgCl2, isoleucine, and arginine in a Gα-dependent manner. Worms furtherm
Autor:
Jun Kobayashi, Yuka Takezawa, Shoji Saito, Noriko Kubota, Kazuo Sakashita, Yozo Nakazawa, Yumiko Higuchi, Minoru Tozuka, Fumihiro Ishida
Publikováno v:
Journal of Pediatric Hematology/Oncology. 45:e249-e253
Thrombocytopenia is a common abnormality encountered in the neonatal period, and immature platelet fraction (IPF) may be an informative indicator of thrombopoiesis; however, data on IPF in neonates are scarce. To define reference intervals (RIs) and
Autor:
Keisuke Oshimi, Yushi Nishimura, Tsutomu Matsubara, Masuaki Tanaka, Eiji Shikoh, Li Zhao, Yajuan Zou, Naoki Komatsu, Yuta Ikado, Yuka Takezawa, Eriko Kage-Nakadai, Yumi Izutsu, Katsutoshi Yoshizato, Saho Morita, Masato Tokunaga, Hiroshi Yukawa, Yoshinobu Baba, Yoshio Teki, Masazumi Fujiwara
Publikováno v:
Quantum Sensing, Imaging, and Precision Metrology.
We report a notch-shaped coplanar microwave waveguide antenna on a glass plate designed for on-chip detection of optically detected magnetic resonance (ODMR) of fluorescent nanodiamonds (NDs). A lithographically patterned thin wire at the center of t
Publikováno v:
Bioscience, Biotechnology & Biochemistry; Mar2023, Vol. 87 Issue 3, p314-319, 6p
Autor:
Yuka Takezawa, Hideyuki Nakazawa, Ryu Yanagisawa, Shinpei Arai, Tomu Kamijo, Takeshi Uehara, Mitsutoshi Sugano, Nobuo Okumura, Takayuki Honda
Publikováno v:
International Journal of Hematology. 112:96-104
Article
International journal of hematology. 112(1): 96-104. (2020)
International journal of hematology. 112(1): 96-104. (2020)
Autor:
Saki Mukai, Nobuo Okumura, Mitsutoshi Sugano, Shinpei Arai, Takayuki Honda, Naoko Ogiwara, Yuka Takezawa
Publikováno v:
International Journal of Hematology. 105:758-768
Fibrinogen storage disease (FSD) is a rare disorder that is characterized by the accumulation of fibrinogen in hepatocytes and induces liver injury. Six mutations in the γC domain (γG284R, γT314P, γD316N, the deletion of γG346-Q350, γG366S, and
Autor:
Keisuke Oshimi, Oliver Benson, Yuka Takezawa, Nikola Sadzak, Simo Sun, Eriko Kage-Nakadai, Yumi Umehara, Yushi Nishimura, Naoki Komatsu, Li Zhao, Yoshio Teki, Yutaka Shikano, Masazumi Fujiwara, Alexander Dohms, Ken Suto
Publikováno v:
Science Advances
Real-time temperature monitoring inside living organisms provides a direct measure of their biological activities. However, it is challenging to reduce the size of biocompatible thermometers down to submicrometers, despite their potential application
Autor:
Shinpei Arai, Mai Nanya, Fumiko Terasawa, Nobuo Okumura, Naoko Ogiwara, Yuka Takezawa, Tamaki Kobayashi
Publikováno v:
Thrombosis Research. 133:101-107
Background Hepatic endoplasmic reticulum (ER) storage disease (HERSD) associated with hypofibrinogenemia has been reported in patients with four types of heterozygous γ-chain variant fibrinogen in the C terminal region. Of interest, substitution of
Publikováno v:
Thrombosis Research. 132:465-470
We report two novel hypofibrinogenemias, Shizuoka III and Kanazawa II, which are caused by heterozygous mutations in FGG. Shizuoka III showed c.147delT and 147_149insACA in FGG exon 3 and a subsequent frameshift mutation, resulting in mature protein