Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Ryosuke Tanaka"'
Autor:
Kenta Shigemura, Kaori Kuribayashi-Shigetomi, Ryosuke Tanaka, Haruka Yamasaki, Takaharu Okajima
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 11 (2023)
As epithelial cells in vitro reach a highly confluent state, the cells often form a microscale dome-like architecture that encloses a fluid-filled lumen. The domes are stabilized by mechanical stress and luminal pressure. However, the mechanical prop
Externí odkaz:
https://doaj.org/article/3c89be2b4d77482f84f555cb7f09bf45
Autor:
Omer Mano, Minseung Choi, Ryosuke Tanaka, Matthew S Creamer, Natalia CB Matos, Joseph W Shomar, Bara A Badwan, Thomas R Clandinin, Damon A Clark
Publikováno v:
eLife, Vol 12 (2023)
Locomotor movements cause visual images to be displaced across the eye, a retinal slip that is counteracted by stabilizing reflexes in many animals. In insects, optomotor turning causes the animal to turn in the direction of rotating visual stimuli,
Externí odkaz:
https://doaj.org/article/4ae68f9a5d4643fc8931dd8bc53af950
Autor:
Rina Imanishi, Kouichi Nakau, Sorachi Shimada, Hideharu Oka, Ryo Takeguchi, Ryosuke Tanaka, Tatsutoshi Sugiyama, Mitsumaro Nii, Toshio Okamoto, Ken Nagaya, Yoshio Makita, Kumiko Yanagi, Tadashi Kaname, Satoru Takahashi
Publikováno v:
Human Genome Variation, Vol 10, Iss 1, Pp 1-3 (2023)
Abstract Pathogenic variants of HECW2 have been reported in cases of neurodevelopmental disorder with hypotonia, seizures, and absent language (NDHSAL; OMIM #617268). A novel HECW2 variant (NM_001348768.2:c.4343 T > C,p.Leu1448Ser) was identified in
Externí odkaz:
https://doaj.org/article/759a403f14234af1881497e323c091ca
Autor:
Hirofumi Tsuru, Chika Yoshihara, Hidehiro Suginobe, Mizuki Matsumoto, Yoichiro Ishii, Jun Narita, Ryo Ishii, Renjie Wang, Atsuko Ueyama, Kazutoshi Ueda, Masaki Hirose, Kazuhisa Hashimoto, Hiroki Nagano, Ryosuke Tanaka, Takaharu Okajima, Keiichi Ozono, Hidekazu Ishida
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 13 (2023)
Background Dilated cardiomyopathy (DCM) is a major cause of heart failure in children. Despite intensive genetic analyses, pathogenic gene variants have not been identified in most patients with DCM, which suggests that cardiomyocytes are not solely
Externí odkaz:
https://doaj.org/article/e6039d40fe46452c8bcddb63e277baf4
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 3, Pp 763-771 (2021)
Hereditary spastic paraplegias (HSPs) are rare neurological disorders caused by degeneration of the corticospinal tract. Among the 79 causative genes involved in HSPs, variants in SPAST on chromosome 2p22, which encodes the microtubule-severing prote
Externí odkaz:
https://doaj.org/article/ad7956db9301452a839dc2ffeee685f8
Autor:
Ryosuke Tanaka, Ryo Takeguchi, Mami Kuroda, Nao Suzuki, Yoshio Makita, Kumiko Yanagi, Tadashi Kaname, Satoru Takahashi
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-3 (2022)
Abstract Leigh syndrome is the most genetically heterogenous phenotype of mitochondrial disease. We describe a patient with Leigh syndrome whose diagnosis had not been confirmed because of normal metabolic screening results at the initial presentatio
Externí odkaz:
https://doaj.org/article/7459aae1a95642c9b3b6c6719db94e34
Autor:
Yuichi Akaba, Satoru Takahashi, Ryo Takeguchi, Ryosuke Tanaka, Shin Nabatame, Hirotomo Saitsu, Naomichi Matsumoto
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1711-1715 (2021)
Abstract Pyruvate dehydrogenase complex (PDHC) deficiency is a mitochondrial disorder. We report two cases of PDHC deficiency with clinical symptoms and brain imaging findings reminiscent of FOXG1 syndrome, suggesting a phenotypic overlap of these di
Externí odkaz:
https://doaj.org/article/b8641c670ef84b60a248b4e5009efd26
Autor:
Mizuki Matsumoto, Hirofumi Tsuru, Hidehiro Suginobe, Jun Narita, Ryo Ishii, Masaki Hirose, Kazuhisa Hashimoto, Renjie Wang, Chika Yoshihara, Atsuko Ueyama, Ryosuke Tanaka, Keiichi Ozono, Takaharu Okajima, Hidekazu Ishida
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0275296 (2022)
Restrictive cardiomyopathy (RCM) is a rare disease characterized by increased ventricular stiffness and preserved ventricular contraction. Various sarcomere gene variants are known to cause RCM; however, more than a half of patients do not harbor suc
Externí odkaz:
https://doaj.org/article/a09914d7287c4c10bded7af8db472da0
Autor:
Ryosuke Tanaka, Tatsuya Sakamaki, Eiji Ohtani, Hiroshi Fukui, Seiji Kamada, Akio Suzuki, Satoshi Tsutsui, Hiroshi Uchiyama, Alfred Q. R. Baron
Publikováno v:
Progress in Earth and Planetary Science, Vol 7, Iss 1, Pp 1-7 (2020)
Abstract The longitudinal sound velocity (V P ) and the density (ρ) of wüstite, FeO, were measured at pressures of up to 112.3 GPa and temperatures of up to 1700 K using both inelastic X-ray scattering and X-ray diffraction combined with a laser-he
Externí odkaz:
https://doaj.org/article/118e62cbe01946089df02a5ba00dc7db
Autor:
Masakazu Nagamatsu, Praful Maste, Masato Tanaka, Yoshihiro Fujiwara, Shinya Arataki, Taro Yamauchi, Yoshiyuki Takeshita, Rika Takamoto, Tsukasa Torigoe, Ryosuke Tanaka, Shinsuke Moriue
Publikováno v:
Diagnostics, Vol 12, Iss 4, p 956 (2022)
Study design: Prospective study. Objective: The aim of this study is to visualize the morphology of a lumbar herniated disc and Kambin’s triangle in three dimensions (3D) based on preoperative CT/MRI fusion images. Methods: CT/MRI fusion images of
Externí odkaz:
https://doaj.org/article/a6f5f3a097ca45689eac8392fa3a8e8c