Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Masatake Araki"'
Autor:
Takuya Nagai, Tomohisa Sekimoto, Syuji Kurogi, Tomomi Ohta, Shihoko Miyazaki, Yoichiro Yamaguchi, Takuya Tajima, Etsuo Chosa, Mai Imasaka, Kumiko Yoshinobu, Kimi Araki, Masatake Araki, Narantsog Choijookhuu, Katsuaki Sato, Yoshitaka Hishikawa, Taro Funamoto
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Bone remodeling is an extraordinarily complex process involving a variety of factors, such as genetic, metabolic, and environmental components. Although genetic factors play a particularly important role, many have not been identified. In th
Externí odkaz:
https://doaj.org/article/0e6015e1753c41daacaf7b76f7d2d5ac
Autor:
Michio Sato, Tsuyoshi Kadomatsu, Keishi Miyata, Junco S. Warren, Zhe Tian, Shunshun Zhu, Haruki Horiguchi, Aman Makaju, Anna Bakhtina, Jun Morinaga, Taichi Sugizaki, Kaname Hirashima, Kumiko Yoshinobu, Mai Imasaka, Masatake Araki, Yoshihiro Komohara, Tomohiko Wakayama, Shinichi Nakagawa, Sarah Franklin, Koichi Node, Kimi Araki, Yuichi Oike
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-21 (2021)
Long noncoding RNAs (lncRNAs) have been shown to play a role in cardiac physiology and disease. Here the authors identify the lncRNA Caren as a cytoplasmic RNA that decreases the translation of a distant gene encoding Hint1, thereby maintaining cardi
Externí odkaz:
https://doaj.org/article/c7569bc158f84c42902d65025ac3c85c
Autor:
Kazuhito Naka, Ryosuke Ochiai, Eriko Matsubara, Chie Kondo, Kyung-Min Yang, Takayuki Hoshii, Masatake Araki, Kimi Araki, Yusuke Sotomaru, Ko Sasaki, Kinuko Mitani, Dong-Wook Kim, Akira Ooshima, Seong-Jin Kim
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
How lipid metabolism can affect cancer recurrence is still unclear. Here, the authors show that the lysophospholipase D Gdpd3 maintains self-renewal capacity of CML stem cells by regulating the quiescence, and AKT/mTORC1 and Foxo3a/β-catenin signall
Externí odkaz:
https://doaj.org/article/73aca2b556d542e499ca1a950b353d8d
Autor:
Aki Sugano, Yutaka Takaoka, Haruyuki Kataguchi, Mika Ohta, Shigemi Kimura, Masatake Araki, Yoshitomo Morinaga, Yoshihiro Yamamoto
Publikováno v:
Microorganisms, Vol 10, Iss 10, p 2090 (2022)
Previously, we developed a mathematical model via molecular simulation analysis to predict the infectivity of six SARS-CoV-2 variants. In this report, we aimed to predict the relative risk of the recent new variants of SARS-CoV-2 based on our previou
Externí odkaz:
https://doaj.org/article/0024f18bd8a745ac97e5fa2fe8dfb9b3
Autor:
Ryoko Tsukahara, Shinji Yamamoto, Keisuke Yoshikawa, Mari Gotoh, Tamotsu Tsukahara, Hiroyuki Neyama, Satoshi Ishii, Noriyuki Akahoshi, Keisuke Yanagida, Hayakazu Sumida, Masatake Araki, Kimi Araki, Ken-ichi Yamamura, Kimiko Murakami-Murofushi, Hiroshi Ueda
Publikováno v:
Journal of Pharmacological Sciences, Vol 136, Iss 2, Pp 93-96 (2018)
Lysophosphatidic acid (LPA) and LPA1 receptor signaling play a crucial role in the initiation of peripheral nerve injury-induced neuropathic pain through the alternation of pain-related genes/proteins expression and demyelination. However, LPA and it
Externí odkaz:
https://doaj.org/article/ca0e3644ed2d4ffcb3e2a11f4629bdbc
Autor:
Vladimir Camarena, Lei Cao, Clemer Abad, Alexander Abrams, Yaima Toledo, Kimi Araki, Masatake Araki, Katherina Walz, Juan I Young
Publikováno v:
EMBO Molecular Medicine, Vol 6, Iss 8, Pp 1003-1015 (2014)
Abstract 2q23.1 microdeletion syndrome is characterized by intellectual disability, motor delay, autistic‐like behaviors, and a distinctive craniofacial phenotype. All patients carry a partial or total deletion of methyl‐CpG‐binding domain prot
Externí odkaz:
https://doaj.org/article/6a29e32a66ae4c0086b628af9aefa3f3
Autor:
Kei Semba, Kimi Araki, Ken-ichirou Matsumoto, Hiroko Suda, Takashi Ando, Akira Sei, Hiroshi Mizuta, Katsumasa Takagi, Mai Nakahara, Mayumi Muta, Gen Yamada, Naomi Nakagata, Aritoshi Iida, Shiro Ikegawa, Yusuke Nakamura, Masatake Araki, Kuniya Abe, Ken-ichi Yamamura
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003204 (2013)
Danforth's short tail (Sd) is a semidominant mutation on mouse chromosome 2, characterized by spinal defects, urogenital defects, and anorectal malformations. However, the gene responsible for the Sd phenotype was unknown. In this study, we identifie
Externí odkaz:
https://doaj.org/article/9a64bfd6856e4cb1bcb46aa784c64ad0
Autor:
Shihoko, Miyazaki, Taro, Funamoto, Tomohisa, Sekimoto, Syuji, Kurogi, Tomomi, Ohta, Takuya, Nagai, Takuya, Tajima, Mai, Imasaka, Kumiko, Yoshinobu, Kimi, Araki, Masatake, Araki, Narantsog, Choijookhuu, Yoshitaka, Hishikawa, Etsuo, Chosa
Publikováno v:
ACTA HISTOCHEMICA ET CYTOCHEMICA. 55:99-110
Epithelial protein lost in neoplasm (EPLIN) is an actin-associated cytoskeletal protein that plays an important role in epithelial cell adhesion. EPLIN has two isoforms: EPLINα and EPLINβ. In this study, we investigated the role of EPLINβ in osteo
Autor:
Shingo Kawano, Kimi Araki, Jie Bai, Imari Furukawa, Keigo Tateishi, Kumiko Yoshinobu, Shingo Usuki, Rachael A. Nimmo, Tadashi Kaname, Masaharu Yoshihara, Satoru Takahashi, Goro Sashida, Masatake Araki
Publikováno v:
Cancer Science.
Autor:
XingLiang Zhu, Yuyoung Joo, Simone Bossi, Ross McDevitt, Aoji Xie, Yue Wang, Yutong Xue, Shuaikun Su, Seung Kyu Lee, Nirnath Sah, Shiliang Zhang, Rong Ye, Alejandro Pinto, Yongqing Zhang, Kimi Araki, Masatake Araki, Marisela Morales, Mark Mattson, Henriette van Praag, Weidong Wang
The Topoisomerase 3B (Top3b) - Tudor domain containing 3 (Tdrd3) protein complex is the only dual-activity topoisomerase complex in animals that can alter the topology of both DNA and RNA. TOP3B mutations in humans are associated with schizophrenia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69022459718596e4dfdaefa3b7fb42ed
https://doi.org/10.21203/rs.3.rs-2597043/v1
https://doi.org/10.21203/rs.3.rs-2597043/v1