Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Nao Nakamura"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract The α-helical antimicrobial peptide Kn2-7 enhances the activation of mouse macrophage-like RAW264.7 induced by DNA containing unmethylated cytosine-guanine motifs (CpG DNA). This enhancement is related to increased cellular uptake of DNA by
Externí odkaz:
https://doaj.org/article/b0e292b4eefe4539b52cd6ac482ef70d
Autor:
Nao Shiraishi, Tsuyoshi Konuma, Yoshie Chiba, Sayaka Hokazono, Nao Nakamura, Md Hadiul Islam, Makoto Nakanishi, Atsuya Nishiyama, Kyohei Arita
Publikováno v:
Communications Biology, Vol 7, Iss 1, Pp 1-11 (2024)
Abstract DNA methylation maintenance is essential for cell fate inheritance. In differentiated cells, this involves orchestrated actions of DNMT1 and UHRF1. In mice, the high-affinity binding of DPPA3 to the UHRF1 PHD finger regulates UHRF1 chromatin
Externí odkaz:
https://doaj.org/article/92681e5b48734fd3a2dd131edcc20335
Autor:
Yuka Kurokawa, Yusuke Kaida, Takuma Hazama, Yosuke Nakayama, Takaomi Otome, Ryo Shibata, Sakuya Ito, Goh Kodama, Nao Nakamura, Takatoshi Kambe, Tomofumi Moriyama, Akiko Nagata, Aki Minami, Ryotaro Ando, Yoshifumi Wada, Miki Sugiyama, Michiaki Usui, Michio Chiba, Atsuo Moriyama, Atsuko Ohara, Hiroshi Miyazaki, Tatsuyuki Kakuma, Kei Fukami
Publikováno v:
Renal Replacement Therapy, Vol 6, Iss 1, Pp 1-10 (2020)
Abstract Background Etelcalcetide is the first intravenously administered calcimimetic agent used to manage secondary hyperparathyroidism (SHPT) in hemodialysis (HD) patients. We evaluated the safety and efficacy of replacing cinacalcet with etelcalc
Externí odkaz:
https://doaj.org/article/44fc4637fec249aab21820b2c2f391c2
Autor:
Hironobu Fujisawa, Yosuke Nakayama, Shoichiro Nakao, Ryo Yamamoto, Yuka Kurokawa, Nao Nakamura, Akiko Nagata, Takahiro Tsukimura, Tadayasu Togawa, Hitoshi Sakuraba, Kei Fukami
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-8 (2019)
Abstract Background Fabry disease (FD) is an X-linked lysosomal storage disorder caused by mutations of the GLA gene, followed by deficiency in α-galactosidase A (α-gal) activity. Nephrotic syndrome, as the renal phenotype of FD, is unusual. Here,
Externí odkaz:
https://doaj.org/article/53d75e63bc8449fc985fddea2f46b27d
Autor:
Giorgia Graells, Nao Nakamura, Juan L. Celis-Diez, Nelson A. Lagos, Pablo A. Marquet, Patricio Pliscoff, Stefan Gelcich
Publikováno v:
Frontiers in Marine Science, Vol 8 (2021)
Coastal urban areas have dramatically increased during the last decades, however, coastal research integrating the impacts and challenges facing urban areas is still scarce. To examine research advances and critical gaps, a review of the literature o
Externí odkaz:
https://doaj.org/article/ea4a73c5ff1a4a258e94d85afda31b24
Autor:
Junko Yano, Yusuke Kaida, Yosuke Nakayama, Sakuya Ito, Yuka Kurokawa, Nao Nakamura, Takuma Hazama, Takashi Maeda, Ryuki Hashida, Kyoko Tashiro, Takahiro Inokuchi, Hiroo Matsuse, Kei Fukami
Publikováno v:
Renal Replacement Therapy, Vol 5, Iss 1, Pp 1-6 (2019)
Abstract Background and aim Carnitine deficiency is common and associated with muscle atrophy in hemodialysis (HD) patients. We investigated whether carnitine levels could be an independent predictor for exercise capacity in these patients. Method A
Externí odkaz:
https://doaj.org/article/eac2bde917854560ad959c7a8dc950d4
Autor:
Yuna Amemiya, Nao Nakamura, Nao Ikeda, Risa Sugiyama, Chiaki Ishii, Masatoshi Maki, Hideki Shibata, Terunao Takahara
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 6897 (2021)
Mechanistic target of rapamycin complex 1 (mTORC1) is a master growth regulator by controlling protein synthesis and autophagy in response to environmental cues. Amino acids, especially leucine and arginine, are known to be important activators of mT
Externí odkaz:
https://doaj.org/article/e21d571a140e4fdfaa4fa7a5ae4efc25
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0190095 (2017)
Mucosal barrier formed by cationic antimicrobial peptides (CAMPs) is believed to be crucial for host protection from pathogenic gut infection. However, some pathogens can develop resistance to the CAMPs to survive in hosts. Salmonella enterica is a c
Externí odkaz:
https://doaj.org/article/ed597804a89d4d85bfd7523a03f960c0
Autor:
Makoto, Nasu, Naoki, Nakagawa, Shigeo, Hara, Junko, Yano, Yuka, Kurokawa, Nao, Nakamura, Hitoshi, Yokoyama, Akira, Shimizu, Hitoshi, Sugiyama, Hiroshi, Sato, Kei, Fukami
Publikováno v:
Clinical and Experimental Nephrology. 27:141-150
Background Fabry disease (FD) is an X-linked inherited disease where renal complications are associated with a poor prognosis. However, little is known about the prevalence of Fabry nephropathy (FN) in patients with chronic kidney disease (CKD). We e
Autor:
Tadayasu Togawa, Yosuke Nakayama, Yusuke Kaida, Yuka Kurokawa, Takahiro Tsukimura, Takuma Hazama, Makoto Nasu, Hitoshi Sakuraba, Ryo Shibata, Kei Fukami, Akiko Nagata, Nao Nakamura, Seiji Saito
Publikováno v:
Nephrology Dialysis Transplantation
Fabry disease (FD), an X-linked lysosomal storage disorder caused by a deficiency in alfa-galactosidase A (α-Gal A) activity due to mutations in the GLA gene, has a prevalence of 0-1.69% in patients undergoing haemodialysis; however, its prevalence