Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Takaaki Matsuda"'
Autor:
Takaaki Matsuda, Yoshinori Osaki, Kazushi Maruo, Erika Matsuda, Yasuhiro Suzuki, Hiroaki Suzuki, Bryan J. Mathis, Hitoshi Shimano, Masakazu Mizutani
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-13 (2024)
Abstract Background To evaluate the seasonal variability of urinary albumin to creatinine ratio (UACR) and eGFR and these effects on three-year eGFR slope in persons with type 2 diabetes (T2D). Methods A total of 1135 persons with T2D were analyzed i
Externí odkaz:
https://doaj.org/article/9caafa417767407eb09791af0bb43690
Publikováno v:
Geriatrics, Vol 9, Iss 1, p 20 (2024)
This study examined whether SUKUBARA®, a remotely managed training system that we developed, could improve skeletal muscle mass and muscle strength in community-dwelling older adults. SUKUBARA® is a composite exercise program that combines lower-lo
Externí odkaz:
https://doaj.org/article/7a08d328c217465fba71fee5e30cd174
A case of early-onset diabetes with impaired insulin secretion carrying a PAX6 gene Gln135* mutation
Autor:
Motohiro Sekiya, Mikiko Yuhara, Yuki Murayama, Mariko Ohyama Osawa, Rikako Nakajima, Nami Ohuchi, Nako Matsumoto, Daichi Yamazaki, Sayuri Mori, Takaaki Matsuda, Yoko Sugano, Yoshinori Osaki, Hitoshi Iwasaki, Hiroaki Suzuki, Hitoshi Shimano
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-5 (2022)
A paired homeodomain transcription factor, PAX6 (paired-box 6), is essential for the development and differentiation of pancreatic endocrine cells as well as ocular cells. Despite the impairment of insulin secretion observed in PAX6-deficient mice, e
Externí odkaz:
https://doaj.org/article/0eed796393954047a33fa981c92bedff
Autor:
Motohiro Sekiya, Takaaki Matsuda, Yuki Yamamoto, Yasuhisa Furuta, Mariko Ohyama, Yuki Murayama, Yoko Sugano, Yoshinori Ohsaki, Hitoshi Iwasaki, Naoya Yahagi, Shigeru Yatoh, Hiroaki Suzuki, Hitoshi Shimano
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Renal hypouricemia (RHUC) is a hereditary disorder where mutations in SLC22A12 gene and SLC2A9 gene cause RHUC type 1 (RHUC1) and RHUC type 2 (RHUC2), respectively. These genes regulate renal tubular reabsorption of urates while t
Externí odkaz:
https://doaj.org/article/0f0a62fe77bf4e94b6ab63c2550fa253
Autor:
Takaaki Matsuda, Hiroaki Suzuki, Yoko Sugano, Yasuhiro Suzuki, Daisuke Yamanaka, Risa Araki, Naoya Yahagi, Motohiro Sekiya, Yasushi Kawakami, Yoshinori Osaki, Hitoshi Iwasaki, Koichi Hashimoto, Shin-Ichiro Takahashi, Yasushi Hada, Hitoshi Shimano
Publikováno v:
Nutrients, Vol 14, Iss 19, p 3917 (2022)
Although branched-chain amino acids (BCAA) are known to stimulate myofibrillar protein synthesis and affect insulin signaling and kynurenine metabolism (the latter being a metabolite of tryptophan associated with depression and dementia), the effects
Externí odkaz:
https://doaj.org/article/e31f908945104d98839a6c74c0525031
Publikováno v:
Antarctic Record, Vol 47, Iss 1, Pp 1-22 (2003)
Five members of the summer party of the 42nd Japanese Antarctic Research Expedition (JARE-42) stayed in the Mt. Riiser-Larsen area, Amundsen Bay, Enderby Land, Antarctica, from December 18, 2000 to February 18, 2001 for paleomagnetism, geochronology,
Externí odkaz:
https://doaj.org/article/0d705c6627b74e0ba865913ff7588fdb
Publikováno v:
International Journal of Polymer Science, Vol 2012 (2012)
Novel soluble polyimides having long-chain alkyl groups on their side chain were synthesized via polymer reaction with the polyimides having phenolic OH groups and 3,4,5-tris(dodecyloxy)benzoic acid (12GA) using N,N′-dicyclohexylcarbodiimide (DCC)
Externí odkaz:
https://doaj.org/article/647b7e0cbc964abbb5790d5e795d6ece
Autor:
Taisuke Matsumoto, Rihoko Kichise, Naoya Aizawa, Tsutomu Ishi-i, Honoka Tanaka, In Seob Park, Christopher Davin, Takuma Yasuda, Takaaki Matsuda
Publikováno v:
Chemistry – An Asian Journal. 16:2136-2145
The regulation of multicolor fluorescence changes in mechanochromic fluorescence (MCF) remains a challenging task. Herein, we report the regulation of MCF using a donor-acceptor structure. Two crystal polymorphs, BTD-pCHO(O) and BTD-pCHO(R) produced
Autor:
Hitoshi Shimano, Yoko Sugano, Yuki Yamamoto, Naoya Yahagi, Shigeru Yatoh, Yasuhisa Furuta, Takaaki Matsuda, Motohiro Sekiya, Yuki Murayama, Hiroaki Suzuki, Hitoshi Iwasaki, Mariko Ohyama, Yoshinori Ohsaki
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BMC Medical Genetics
BMC Medical Genetics
Background Renal hypouricemia (RHUC) is a hereditary disorder where mutations in SLC22A12 gene and SLC2A9 gene cause RHUC type 1 (RHUC1) and RHUC type 2 (RHUC2), respectively. These genes regulate renal tubular reabsorption of urates while there exis
Autor:
Yoshinori Takeuchi, Takaaki Matsuda, Takafumi Miyamoto, Yoshimi Nakagawa, Hiroaki Suzuki, Hitoshi Shimano, Motohiro Sekiya, Yoko Sugano, Yoshinori Osaki, Takashi Matsuzaka, Kenta Kainoh, Yang Ma, Hitoshi Iwasaki, Naoya Yahagi
Publikováno v:
Biochemical and biophysical research communications. 523(2)
The epithelial to mesenchymal transition (EMT) is a cell intrinsic program controlling cellular morphological and phenotypic remodeling in a wide range of biological processes. Despite the accumulating evidence, the transcriptional networks regulatin