Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Takuya Naruto"'
Autor:
Huan-Ting Lin, Masatoshi Takagi, Kenji Kubara, Kazuto Yamazaki, Fumiko Michikawa, Takashi Okumura, Takuya Naruto, Tomohiro Morio, Koji Miyazaki, Hideki Taniguchi, Makoto Otsu
Publikováno v:
Stem Cell Research & Therapy, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Background Although oncogenic RAS mutants are thought to exert mutagenic effects upon blood cells, it remains uncertain how a single oncogenic RAS impacts non-transformed multipotent hematopoietic stem or progenitor cells (HPCs). Such potent
Externí odkaz:
https://doaj.org/article/41b677ec4b61423aabb1d9bf49e2ae0f
Autor:
Masaaki Mori, Kanako Yoshizaki, Shinichi Watabe, Mika Ishige, Akinari Hinoki, Takuya Kondo, Tomoaki Taguchi, Hisaya Hasegawa, Tomoko Hatata, Naoyuki Tanuma, Kosuke Kirino, Akihiro Hirakawa, Takuya Naruto, Minoru Imai, Ryuji Koike, Kenichiro Hosoi, Satoshi Kusuda
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 39, Iss , Pp 100847- (2023)
Summary: Background: Pediatric patients with certain rare diseases are at increased risk of severe respiratory syncytial virus (RSV) infection. However, the prophylactic use of anti-RSV antibody (palivizumab) in these patients is not indicated at pre
Externí odkaz:
https://doaj.org/article/faeb27805df24a098986fb0ed51c5afa
Autor:
Yoko Saito, Yukiko Kuroda, Dai Keino, Yumi Enomoto, Takuya Naruto, Masakatsu Yanagimachi, Kenji Kurosawa
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100315- (2023)
Externí odkaz:
https://doaj.org/article/710f9884971e4a4f961b5f0909da8093
Autor:
Masakatsu Yanagimachi, Sayaka Fukuda, Fumiko Tanaka, Mari Iwamoto, Chiho Takao, Kunihiro Oba, Natsuko Suzuki, Koji Kiyohara, Dai Kuranobu, Norimasa Tada, Ayako Nagashima, Taku Ishii, Yoko Ino, Yayoi Kimura, Nobutoshi Nawa, Takeo Fujiwara, Takuya Naruto, Tomohiro Morio, Shouzaburo Doi, Masaaki Mori
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0257138 (2021)
ObjectiveKawasaki disease (KD) is a systemic vasculitis in childhood that can lead to coronary artery lesions (CALs). Although early diagnosis and treatment is important for preventing KD patients from development of CALs, diagnosis depends on the cl
Externí odkaz:
https://doaj.org/article/33fca520da7f4368b4cbbac8e4cb3b0f
Autor:
Kenji Kubara, Kazuto Yamazaki, Yasuharu Ishihara, Takuya Naruto, Huan-Ting Lin, Ken Nishimura, Manami Ohtaka, Mahito Nakanishi, Masashi Ito, Kappei Tsukahara, Tomohiro Morio, Masatoshi Takagi, Makoto Otsu
Publikováno v:
Stem Cell Reports, Vol 11, Iss 2, Pp 380-394 (2018)
Summary: Oncogenic KRAS mutations in hematopoietic stem cells cause RAS-associated autoimmune lymphoproliferative syndrome-like disease (RALD). KRAS plays essential roles in stemness maintenance in some types of stem cells. However, its roles in plur
Externí odkaz:
https://doaj.org/article/bec0e0806fec42e48f4d3ad662e1e2de
Autor:
Tomohiro Kohmoto, Nana Okamoto, Takuya Naruto, Chie Murata, Yuya Ouchi, Naoko Fujita, Hidehito Inagaki, Shigeko Satomura, Nobuhiko Okamoto, Masako Saito, Kiyoshi Masuda, Hiroki Kurahashi, Issei Imoto
Publikováno v:
Molecular Cytogenetics, Vol 10, Iss 1, Pp 1-8 (2017)
Abstract Background Complex genomic rearrangements (CGRs) consisting of interstitial triplications in conjunction with uniparental isodisomy (isoUPD) have rarely been reported in patients with multiple congenital anomalies (MCA)/intellectual disabili
Externí odkaz:
https://doaj.org/article/407a5438f6fd40b9b765d03bdeb34368
Autor:
Daiju Fukuda, Sachiko Nishimoto, Kunduziayi Aini, Atsushi Tanaka, Tsuyoshi Nishiguchi, Joo‐ri Kim‐Kaneyama, Xiao‐Feng Lei, Kiyoshi Masuda, Takuya Naruto, Kimie Tanaka, Yasutomi Higashikuni, Yoichiro Hirata, Shusuke Yagi, Kenya Kusunose, Hirotsugu Yamada, Takeshi Soeki, Issei Imoto, Takashi Akasaka, Michio Shimabukuro, Masataka Sata
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 7 (2019)
Background Toll‐like receptor (TLR) 9 recognizes bacterial DNA, activating innate immunity, whereas it also provokes inflammation in response to fragmented DNA released from mammalian cells. We investigated whether TLR9 contributes to the developme
Externí odkaz:
https://doaj.org/article/8f8f8329a3194984af6b247cbd40b84a
Autor:
Kaori Hisa, Masakatsu D Yanagimachi, Takuya Naruto, Takako Miyamae, Masako Kikuchi, Rhoki Hara, Tomoyuki Imagawa, Shumpei Yokota, Masaaki Mori
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171961 (2017)
Both genetic and environmental factors are associated with susceptibility to juvenile idiopathic arthritis (JIA). Many studies have reported that both a 'shared epitope' (SE) encoded by several HLA-DRB1 alleles and the peptidyl arginine deiminase typ
Externí odkaz:
https://doaj.org/article/ed7d1dc0e8c14e34ba534cf29200d425
Autor:
Kei-ichi Morita, Takuya Naruto, Kousuke Tanimoto, Chisato Yasukawa, Yu Oikawa, Kiyoshi Masuda, Issei Imoto, Johji Inazawa, Ken Omura, Hiroyuki Harada
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0140480 (2015)
Gorlin syndrome (GS) is an autosomal dominant disorder that predisposes affected individuals to developmental defects and tumorigenesis, and caused mainly by heterozygous germline PTCH1 mutations. Despite exhaustive analysis, PTCH1 mutations are ofte
Externí odkaz:
https://doaj.org/article/d8231e1ecccc401b8d8fe230d74edf6c
Autor:
Xiaoming Sun, Masumichi Saito, Yoshinori Sato, Takayuki Chikata, Takuya Naruto, Tatsuhiko Ozawa, Eiji Kobayashi, Hiroyuki Kishi, Atsushi Muraguchi, Masafumi Takiguchi
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e40386 (2012)
T-cell receptor (TCR) α/β chains are expressed on the surface of CD8(+) T-cells and have been implicated in antigen recognition, activation, and proliferation. However, the methods for characterization of human TCRα/β chains have not been well es
Externí odkaz:
https://doaj.org/article/d31ba53e2dfc445abba3695229f72706