Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Mayuko Shimada"'
Autor:
Okiru Komine, Syuhei Ohnuma, Kunihiko Hinohara, Yuichiro Hara, Mayuko Shimada, Tomohiro Akashi, Seiji Watanabe, Akira Sobue, Noe Kawade, Tomoo Ogi, Koji Yamanaka
Publikováno v:
iScience, Vol 27, Iss 2, Pp 108872- (2024)
Summary: Recent single-cell analyses have revealed the complexity of microglial heterogeneity in brain development, aging, and neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS). Disease-associated microglia (DAMs) have been ident
Externí odkaz:
https://doaj.org/article/d7f739989e174708a15aabfdf39bff50
Autor:
Akiko Tomita, Hiroyuki Sasanuma, Tomoo Owa, Yuka Nakazawa, Mayuko Shimada, Takahiro Fukuoka, Tomoo Ogi, Shinichiro Nakada
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract CRISPR/Cas9-mediated gene editing has great potential utility for treating genetic diseases. However, its therapeutic applications are limited by unintended genomic alterations arising from DNA double-strand breaks and random integration of
Externí odkaz:
https://doaj.org/article/fd19774db06e4eaea5b2aee8e58463e9
Aicardi–Goutières syndrome with SAMHD1 deficiency can be diagnosed by unscheduled DNA synthesis test
Autor:
Chikako Senju, Yuka Nakazawa, Mayuko Shimada, Dai Iwata, Michiko Matsuse, Katsumi Tanaka, Yasushi Miyazaki, Shinichi Moriwaki, Norisato Mitsutake, Tomoo Ogi
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Aicardi–Goutières syndrome (AGS) is a rare genetic disorder characterised by progressive encephalopathy, involving microcephaly, intracranial calcification, and cerebrospinal fluid lymphocytosis with increased interferon-α concentrations. The cli
Externí odkaz:
https://doaj.org/article/74f968cc04b4464687ed046e1824a78b
Autor:
Chikako Senju, Yuka Nakazawa, Taichi Oso, Mayuko Shimada, Kana Kato, Michiko Matsuse, Mariko Tsujimoto, Taro Masaki, Yasushi Miyazaki, Satoshi Fukushima, Satoshi Tateishi, Atsushi Utani, Hiroyuki Murota, Katsumi Tanaka, Norisato Mitsutake, Shinichi Moriwaki, Chikako Nishigori, Tomoo Ogi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 7/4/2023, Vol. 120 Issue 27, p1-12, 24p
Autor:
Yumiko Kasugai, Shinichiro Nakada, Takuya Ichimura, Mutsumi Yamane, Yoshiyuki Takahashi, Katsushi Tokunaga, Keitaro Matsuo, Kotaro Yuge, Hideki Muramatsu, Masao Nagasaki, Seiji Kito, Yuichiro Hara, Koichiro Higasa, Naomichi Matsumoto, Motoharu Hamada, Tomoo Ogi, Takayoshi Suganami, Yuko Kotani, Hirotoshi Sakaguchi, Yusuke Okuno, Shuichi Ozono, Norisato Mitsutake, Yosuke Kawai, Toshiro Kawakita, Yasuyoshi Oka, Fumihiko Matsuda, Taichi Hirano, Noriko Miyake, Yoriko Watanabe, Mayuko Shimada, Miyako Tanaka, Honoka Takeshima, Keiichi Isoyama, Hideo Kaneko, Tomoji Mashimo, Seiji Mizuno, Katsuhiro Hanada, Yuka Nakazawa, Masafumi Onodera, Kohji Kato, Seiji Kojima
Publikováno v:
Science Advances. 6
Rs671 in the aldehyde dehydrogenase 2 gene (ALDH2) is the cause of Asian alcohol flushing response after drinking. ALDH2 detoxifies endogenous aldehydes, which are the major source of DNA damage re...
Autor:
Yasuyoshi, Oka, Motoharu, Hamada, Yuka, Nakazawa, Hideki, Muramatsu, Yusuke, Okuno, Koichiro, Higasa, Mayuko, Shimada, Honoka, Takeshima, Katsuhiro, Hanada, Taichi, Hirano, Toshiro, Kawakita, Hirotoshi, Sakaguchi, Takuya, Ichimura, Shuichi, Ozono, Kotaro, Yuge, Yoriko, Watanabe, Yuko, Kotani, Mutsumi, Yamane, Yumiko, Kasugai, Miyako, Tanaka, Takayoshi, Suganami, Shinichiro, Nakada, Norisato, Mitsutake, Yuichiro, Hara, Kohji, Kato, Seiji, Mizuno, Noriko, Miyake, Yosuke, Kawai, Katsushi, Tokunaga, Masao, Nagasaki, Seiji, Kito, Keiichi, Isoyama, Masafumi, Onodera, Hideo, Kaneko, Naomichi, Matsumoto, Fumihiko, Matsuda, Keitaro, Matsuo, Yoshiyuki, Takahashi, Tomoji, Mashimo, Seiji, Kojima, Tomoo, Ogi
Publikováno v:
Science advances. 6(51)
Rs671 in the aldehyde dehydrogenase 2 gene (
Autor:
Mayu Isono, Satoru Hashimoto, Kana Kato, Okiru Komine, Yuko Kotani, Akio Masuda, Takayoshi Suganami, Nan Jia, Yuichiro Hara, Norisato Mitsutake, Shinichiro Nakada, Yuxi He, Yasukazu Daigaku, Yasuyoshi Oka, Koji Yamanaka, Tomoji Mashimo, Tomoo Ogi, Yuka Miyoshi, Akira Sobue, Mayuko Shimada, Chaowan Guo, Miyako Tanaka, Diana van den Heuvel, Kinji Ohno, Martijn S. Luijsterburg, Yuka Nakazawa
Publikováno v:
Cell, 180(6), 1228-1244.e24. CELL PRESS
Transcription-coupled nucleotide excision repair (TC-NER) is initiated by the stalling of elongating RNA polymerase II (RNAPIIo) at DNA lesions. The ubiquitination of RNAPIIo in response to DNA damage is an evolutionarily conserved event, but its fun
Autor:
Jun-ichi Kawada, Kazuhiro Horiba, Takako Suzuki, Hideki Muramatsu, Suguru Takeuchi, Yuka Torii, Mayuko Shimada, Yuichiro Hara, Yoshinori Ito, Toshihiko Okumura, Yoshiyuki Takahashi, Tomoo Ogi
Publikováno v:
Open Forum Infectious Diseases
Background Febrile neutropenia (FN) is a common complication in patients with solid tumors and hematologic malignancies. Identification of the causative microorganisms would contribute to optimization of antimicrobial treatment and thus improve the o
Autor:
Shunichi Yamashita, Alan R. Lehmann, Akira Kinoshita, Shinji Ono, Kaname Ohyama, Norisato Mitsutake, Michiko Matsuse, Katsuya Takenaka, Tomoo Ogi, Hiroyuki Mishima, Yuka Nakazawa, Kensaku Sasaki, Ritsuko Masuyama, Satoshi Tateishi, Yoshito Takahashi, Koh-ichiro Yoshiura, Takashi Kudo, Atsushi Utani, Miria Stefanini, Masayo Nomura, Kosei Ito, Tiziana Nardo, Mayuko Shimada, Hanoch Slor
Publikováno v:
Nature Genetics. 44:586-592
UV-sensitive syndrome (UV SS) is a genodermatosis characterized by cutaneous photosensitivity without skin carcinoma. Despite mild clinical features, cells from individuals with UV SS, like Cockayne syndrome cells, are very UV sensitive and are defic
Autor:
Norisato Mitsutake, Tao-Sheng Li, Mayuko Shimada, Andrea Björkman, Qiang Pan-Hammarström, Yuji Nagayama, Nan Jia, Guo Chaowan, Heather Fawcett, Lisa Woodbine, Kaname Ohyama, Penny A. Jeggo, Tomoo Ogi, Andrew R. Gennery, Alan R. Lehmann, Yuka Nakazawa
Background\ud \ud Nonhomologous end-joining (NHEJ) is the major DNA double-strand break (DSB) repair mechanism in human cells. The final rejoining step requires DNA ligase IV (LIG4) together with the partner proteins X-ray repair cross-complementing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dad67a5bf93081e490c114a695afe058