Zobrazeno 1 - 10
of 87
pro vyhledávání: '"Kanako Kojima"'
Autor:
Madoka Sakuramachi, Naoya Murakami, Ayaka Nagao, Kanako Kojima, Yusaku Miyata, Tairo Kashihara, Tomoya Kaneda, Kana Takahashi, Koji Inaba, Kae Okuma, Yuko Nakayama, Hiroyuki Okamoto, Mitsuya Ishikawa, Hiroshi Igaki
Publikováno v:
Journal of Contemporary Brachytherapy, Vol 15, Iss 6, Pp 465-469 (2023)
Externí odkaz:
https://doaj.org/article/de599baddb2f47dd864baa87e495958c
Autor:
Kanako Higashi, Yuri Sonoda, Noriyuki Kaku, Fumihiko Fujii, Fumiya Yamashita, Sooyoung Lee, Vlad Tocan, Go Ebihara, Wakato Matsuoka, Kenichi Tetsuhara, Motoshi Sonoda, Pin Fee Chong, Yuichi Mushimoto, Kanako Kojima‐Ishii, Masataka Ishimura, Yuhki Koga, Atsuhisa Fukuta, Nana Akagi Tsuchihashi, Yoshikazu Kikuchi, Takahito Karashima, Takaaki Sawada, Taeko Hotta, Makoto Yoshimitsu, Hideyuki Terazono, Tatsuro Tajiri, Takashi Nakagawa, Yasunari Sakai, Kimitoshi Nakamura, Shouichi Ohga
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Gaucher disease (GD) is a lysosomal storage disorder caused by a deficiency in the GBA1‐encoded enzyme, β‐glucocerebrosidase. Enzyme replacement therapy is ineffective for neuronopathic Gaucher disease (nGD). High‐dose ambroxol has be
Externí odkaz:
https://doaj.org/article/83b9e0bd176a497ca08bdcbe19378101
Autor:
Takaaki Sawada, Jun Kido, Keishin Sugawara, Ken Momosaki, Shinichiro Yoshida, Kanako Kojima-Ishii, Takahito Inoue, Shirou Matsumoto, Fumio Endo, Shouichi Ohga, Shinichi Hirose, Kimitoshi Nakamura
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background Pompe disease is an autosomal recessive inherited metabolic disorder caused by a deficiency of the acid α-glucosidase (GAA). Pompe disease manifests as an accumulation of lysosomal glycogen in the skeletal and heart muscle. We co
Externí odkaz:
https://doaj.org/article/5bcc5203a9df4ca3a5d7188233c212fb
Autor:
Kanako Kojima-Kita, Satomi Kuramochi-Miyagawa, Manabu Nakayama, Haruhiko Miyata, Steven E. Jacobsen, Masahito Ikawa, Haruhiko Koseki, Toru Nakano
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-19 (2021)
Abstract The PIWI (P-element-induced wimpy testis)-interacting-RNA (piRNA) pathway plays a crucial role in the repression of TE (transposable element) expression via de novo DNA methylation in mouse embryonic male germ cells. Various proteins, includ
Externí odkaz:
https://doaj.org/article/e4240d46cf334381916666d84f0183e3
Autor:
Hiroi Eguchi, Toshihiko Kakiuchi, Masanori Nishi, Kanako Kojima-Ishii, Kei Nishiyama, Yuhki Koga, Muneaki Matsuo
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Background:Juvenile myelomonocytic leukemia (JMML), which is predominantly found in infants, is a clonal abnormality of pluripotent hematopoietic stem cells and presents with the symptoms of both myeloproliferative tumors and myelodysplastic syndrome
Externí odkaz:
https://doaj.org/article/6814b427bfff45d0af8efb0324b6924a
Autor:
Jun Kido, Shirou Matsumoto, Tetsuya Ito, Shinichi Hirose, Kaori Fukui, Kanako Kojima-Ishii, Yuichi Mushimoto, Shinobu Yoshida, Mika Ishige, Norio Sakai, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100724- (2021)
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Severe hyperammonemia adversely affects the brain. Therefore, we conducted a nationwide study between January 2000 and March 2018 to understand the present stat
Externí odkaz:
https://doaj.org/article/1d109c7d81b5461b97f720590b122583
Autor:
Kanako Kojima-Kita, Satomi Kuramochi-Miyagawa, Ippei Nagamori, Narumi Ogonuki, Atsuo Ogura, Hidetoshi Hasuwa, Takashi Akazawa, Norimitsu Inoue, Toru Nakano
Publikováno v:
Cell Reports, Vol 16, Iss 11, Pp 2819-2828 (2016)
During the development of mammalian embryonic germ cells, global demethylation and de novo DNA methylation take place. In mouse embryonic germ cells, two PIWI family proteins, MILI and MIWI2, are essential for the de novo DNA methylation of retrotran
Externí odkaz:
https://doaj.org/article/0cb2c79357cb48fb81e9b18f13b830db
Autor:
Kanako Kojima, Sanai Takahashi, Shungo Saito, Yoshihiro Endo, Tadashi Nittami, Tadashige Nozaki, Ranbir Chander Sobti, Masatoshi Watanabe
Publikováno v:
Applied Sciences, Vol 8, Iss 1, p 134 (2018)
Patients with metastatic castration-resistant prostate cancer (mCRPC) have poor outcomes. Docetaxel (DTX)-based therapy is a current standard treatment for patients with mCRPC. Approaches combining conventional chemotherapeutic agents and nanoparticl
Externí odkaz:
https://doaj.org/article/9bc01c3782e34a6cac2a362032796c83
Autor:
Aya Okubo, Shoichi Fukui, Mai Tanigawa, Kanako Kojima, Remi Sumiyoshi, Tomohiro Koga, Satomi Shojinaga, Ryosuke Sakamoto, Maho Nakashima, Atsushi Kawakami
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 17, p2455-2460, 6p
Autor:
Noriko Oyama1, Kanako Kojima-Ishii1 k-kanako@momo.so-net.ne.jp, Naoko Toda1, Terumichi Matsuo1,2, Vlad Tocan1, Kazuhiro Ohkubo1, Utako Oba1, Yuhki Koga1, Nokitaka Setsu3, Yuichi Yamada4, Kenichi Kohashi4, Yasuharu Nakashima3, Yoshinao Oda4, Kenji Ihara5, Shouichi Ohga1
Publikováno v:
Clinical Pediatric Endocrinology. 2020, Vol. 29 Issue 2, p69-75. 7p. 2 Color Photographs, 1 Chart, 1 Graph.