Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Asuka Hira"'
Autor:
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Externí odkaz:
https://doaj.org/article/1e27fb0a8ca04310ab6bda480ec5592e
Autor:
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata
Publikováno v:
Haematologica, Vol 104, Iss 10 (2019)
Fanconi anemia is a rare recessive disease characterized by multiple congenital abnormalities, progressive bone marrow failure, and a predisposition to malignancies. It results from mutations in one of the 22 known FANC genes. The number of Japanese
Externí odkaz:
https://doaj.org/article/d3c2fd958fd54b47ac29c05a214c04da
Autor:
Megumu K. Saito, Kazuko Inoue, Keitaro Matsuo, Minoru Takata, Seishi Ogawa, Akira Niwa, Tatsutoshi Nakahata, Keita Kondo, Mitsujiro Osawa, Anfeng Mu, Yusuke Okamoto, Kenichi Yoshida, Masato T. Kanemaki, Etsuro Ito, Seiji Kojima, Keigo Tanaka, Tomonari Matsuda, Minako Mori, Asuka Hira
Publikováno v:
Blood. 137:2021-2032
We have recently discovered Japanese children with a novel Fanconi anemia–like inherited bone marrow failure syndrome (IBMFS). This disorder is likely caused by the loss of a catabolic system directed toward endogenous formaldehyde due to biallelic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd9222a688f45d4711b6ff5cdfaf0fee
https://doi.org/10.1182/blood.2020009111
https://doi.org/10.1182/blood.2020009111
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 62(6)
We have recently described the identification of a novel inherited bone marrow failure syndrome. The first set of patients was diagnosed through the exome analysis of cells from Japanese patients with hypoplastic anemia, which have been deposited to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::41a736c490d5c4c7ef35145bbe22392a
https://pubmed.ncbi.nlm.nih.gov/34219079
https://pubmed.ncbi.nlm.nih.gov/34219079
Autor:
Mami Matsuda, Asuka Hirai-Yuki, Osamu Kotani, Michiyo Kataoka, Xin Zheng, Daisuke Yamane, Masaru Yokoyama, Koji Ishii, Masamichi Muramatsu, Ryosuke Suzuki
Publikováno v:
PLoS Pathogens, Vol 20, Iss 3, p e1012091 (2024)
No antiviral drugs currently are available for treatment of infection by hepatitis A virus (HAV), a causative agent of acute hepatitis, a potentially life-threatening disease. Chemical screening of a small-compound library using nanoluciferase-expres
Externí odkaz:
https://doaj.org/article/21dadf4bf2934359b841214f73051e83
Autor:
Etsuro Ito, Seiji Kojima, Kenichi Yoshida, Rui Yu, Camille Nadler, Paul S. Monks, Asuka Hira, Nicola K. Wilson, Motohiro Kato, Ashley N. Kamimae-Lanning, Satoru Miyano, Hiromasa Yabe, Tomoo Osumi, Minako Mori, Miharu Yabe, Michael R. G. Hodskinson, Minoru Takata, Hideki Muramatsu, Lucas B. Pontel, Seishi Ogawa, Toshinori Moriguchi, Christopher L. Millington, Yusuke Okamoto, Masayuki Kobayashi, Yuichi Shiraishi, Meng Wang, Ketan J. Patel, Frederic Langevin, Berthold Göttgens, Yusuke Okuno, Sam Watcham, Felix A. Dingler, Rebecca Cordell, Keitaro Matsuo, Nina Oberbeck, Anfeng Mu
Publikováno v:
Molecular Cell
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Summary Reactive aldehydes arise as by-products of metabolism and are normally cleared by multiple families of enzymes. We find that mice lacking two aldehyde detoxifying enzymes, mitochondrial ALDH2 and cytoplasmic ADH5, have greatly shortened lifes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d65d6f96b03ddf58df2484332f40f7
http://hdl.handle.net/2433/255881
http://hdl.handle.net/2433/255881
Autor:
Yohei Otaka, Shin Kitamura, Megumi Suzuki, Akiko Maeda, Chinami Kato, Rena Ito, Asuka Hirano, Yuki Okochi, Koji Mizutani, Hiroshi Yoshino, Hajime Takechi
Publikováno v:
Journal of Rehabilitation Medicine - Clinical Communications, Vol 6 (2023)
Objective: To evaluate the effectiveness of a dyadic outpatient rehabilitation program focused on improving the real-life daily activities of patients with mild cognitive impairments or dementia and their caregivers. Design: Retrospective study. Su
Externí odkaz:
https://doaj.org/article/fd25eb94ec734f60a9858c8284d8ceb8
Autor:
Kenichi Chiba, Seiji Kojima, Tomohiro Morio, Yusuke Okuno, Hiromasa Yabe, Satoru Miyano, Kohsuke Imai, Minoru Takata, Hideki Muramatsu, Kenichi Yoshida, Seishi Ogawa, Ayako Arai, Kanako Mitsui-Sekinaka, Hiroko Tanaka, Kenichi Honma, Miharu Yabe, Yuichi Shiraishi, Osamu Ohara, Shigeaki Nonoyama, Masatoshi Takagi, Noriko Mitsuiki, Asuka Hira, Yujin Sekinaka
Publikováno v:
Journal of clinical immunology. 37(5)
Common variable immunodeficiency (CVID) is the most common adult-onset primary antibody deficiency disease due to various causative genes. Several genes, which are known to be the cause of different diseases, have recently been reported as the cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f87129aa9a09053fcb71ee419a9e7f8
https://pubmed.ncbi.nlm.nih.gov/28493158
https://pubmed.ncbi.nlm.nih.gov/28493158
Autor:
Akifumi Takaori-Kondo, Miharu Yabe, Asuka Hira, Kazuo Tamura, Minako Mori, Hiroshi Kawabata, Michiko Anmae, Tomoo Osumi, Yusuke Okuno, Hiromasa Yabe, Seiji Kojima, Kenichi Yoshida, Minoru Takata, Yasushi Noguchi, Hideki Muramatsu, Seishi Ogawa, Jun Yasuda, Souichi Adachi
Publikováno v:
Blood. 132:3860-3860
Objective: Fanconi anemia (FA) is the most common inherited bone marrow failure syndrome associated with multiple congenital abnormalities and predisposition to malignancies, resulting from mutations in one of the 22 known FA genes (FANCA to W). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::548ce32d0c54effd4ac408557861bcfa
https://doi.org/10.1182/blood-2018-99-110362
https://doi.org/10.1182/blood-2018-99-110362
Autor:
Tatsutoshi Nakahata, Kenichiro Watanabe, Minoru Takata, Megumu K. Saito, Akira Niwa, Naoya M. Suzuki, Toshio Heike, Asuka Hira, Naoki Amano, Chihiro Okada, Akira Watanabe, Miharu Yabe
Publikováno v:
Stem cells translational medicine. 4(4)
Fanconi anemia (FA) is a disorder of genomic instability characterized by progressive bone marrow failure (BMF), developmental abnormalities, and an increased susceptibility to cancer. Although various consequences in hematopoietic stem/progenitor ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2125c5802725c897522c5c99bb505e62
https://pubmed.ncbi.nlm.nih.gov/25762002
https://pubmed.ncbi.nlm.nih.gov/25762002