Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Miharu Yabe"'
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:
Mia Fujisawa, Miharu Yabe, Takashi Ueda, Motoki Kaneko, Makiko Monma, Takayoshi Suzuki, Ryutaro Fujimoto, Toshimasa Yabe, Hidekazu Suzuki, Hajime Mizukami, Masaya Sano, Fumio Nakahara, Erika Teramura, Masashi Matsushima
Publikováno v:
Internal Medicine
The risk of carcinogenesis increases after 20 years old in patients with Fanconi anemia (FA). We herein report three rare cases of FA combined with esophageal cancer in women; all patients were diagnosed with FA in early childhood. Patients 1 and 2 w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56eea592c6d151489881417ba6b69768
https://doi.org/10.2169/internalmedicine.6926-20
https://doi.org/10.2169/internalmedicine.6926-20
Autor:
Hiroyuki Shimada, Koji Kato, Nao Yoshida, Yoshiko Atsuta, Maho Sato, Hirotoshi Sakaguchi, Yuko Cho, Daisuke Hasegawa, Katsuyoshi Koh, Motohiro Kato, Kenichiro Watanabe, Yoshiko Hashii, Harumi Kakuda, Yoshiyuki Takahashi, Asahito Hama, Maiko Noguchi, Daiichiro Hasegawa, Kiminori Terui, Miharu Yabe, Atsushi Sato
Publikováno v:
Biology of Blood and Marrow Transplantation. 26:902-910
Hematopoietic stem cell transplantation (HSCT) is the only curative treatment for juvenile myelomonocytic leukemia (JMML), but few large studies of HSCT for JMML exist. Using data from the Japan Society for Hematopoietic Cell Transplantation registry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e916302baa310f109c011f2b94c8004f
https://doi.org/10.1016/j.bbmt.2019.11.029
https://doi.org/10.1016/j.bbmt.2019.11.029
Autor:
Frank X. Donovan, Kenichi Yoshida, Minoru Takata, Agata Smogorzewska, Babu Rao Vundinti, Avani Solanki, Akifumi Takaori-Kondo, Niranjan Chavan, Yusuke Okuno, Selvaa Kumar C, Minako Mori, Settara C. Chandrasekharappa, Seiji Kojima, Merin George, Hiromasa Yabe, Seishi Ogawa, Sheila Mohan, Arleen D. Auerbach, Aruna Rajendran, Miharu Yabe, Hideki Muramastsu, Ramanagouda Ramanagoudr-Bhojappa, Akira Shimamoto
Publikováno v:
Hum Mutat
Fanconi anemia (FA) is a rare genetic disorder characterized by bone marrow failure, predisposition to cancer, and congenital abnormalities. FA is caused by pathogenic variants in any of 22 genes involved in the DNA repair pathway responsible for rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0cf1057a5d78838591eeaf71993515
https://doi.org/10.1002/humu.23914
https://doi.org/10.1002/humu.23914
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 60(6)
Fanconi anemia (FA) is an inherited bone marrow failure syndrome characterized by multiple congenital abnormalities, progressive bone marrow failure, and a predisposition to malignancies, resulting from mutations in one of the 22 known FANC genes (fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b830712fdc5f94e3d77d292df087551
https://pubmed.ncbi.nlm.nih.gov/31281162
https://pubmed.ncbi.nlm.nih.gov/31281162
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:
Kosuke Tsuboi, Naoya Nakamura, Miharu Yabe, Tomoki Kikuchi, Minoru Kojima, Yoshiaki Ogawa, Yara Yukie Kikuti, Kiyoshi Ando, Hiromichi Murayama, Mami Tokunaka, Makiko Moriuchi
Publikováno v:
International Journal of Hematology. 101:520-524
We report a case of HIV-negative Burkitt lymphoma (BL) that relapsed 9 years after complete remission. We performed a polymerase chain reaction analysis of three regions of the VDJ junction of the immunoglobulin heavy chain (IGH) gene and compared th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b37a1bfa82ad8fa6839323d34e874e5
https://doi.org/10.1007/s12185-014-1729-1
https://doi.org/10.1007/s12185-014-1729-1
Autor:
Hiromasa Yabe, S Kato, Takashi Shimizu, Takashi Koike, Hiromitsu Takakura, Miharu Yabe, Tsuyoshi Morimoto, Keisuke Ohtsubo, Akiko Fukumura
Publikováno v:
Bone Marrow Transplantation. 49:921-926
We retrospectively studied 108 marrow harvests from 105 pediatric sibling donors. The median age of donors was 8 years (range: 1-15) and the median body weight was 27 kg (range: 10-100). The volumes of aspirated marrow were 5.0-23.8 mL/kg donor body
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a095ef742703a769692cfd0e79bb1f
https://doi.org/10.1038/bmt.2014.73
https://doi.org/10.1038/bmt.2014.73
Autor:
Xinan Wang, Kenichi Chiba, Hiroki Yamaguchi, Sayoko Doisaki, Masao Kobayashi, Eiichi Ishii, Etsuro Ito, Yinyan Xu, Hideki Muramatsu, Seiji Kojima, Masashi Sanada, Yuichi Shiraishi, Seishi Ogawa, Satoru Miyano, Shinji Kunishima, Minoru Takata, Kenichi Koike, Hiroko Tanaka, Shouichi Ohga, Atsushi Narita, Yoshiyuki Takahashi, Kenichiro Watanabe, Hitoshi Kanno, Miharu Yabe, Kenichi Yoshida, Asahito Hama, Nozomu Kawashima, Hideo Harigae, Hirotoshi Sakaguchi, Yusuke Okuno, Atsushi Manabe
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 19(7)
Precise genetic diagnosis of inherited bone marrow failure syndromes (IBMFS), a heterogeneous group of genetic disorders, is challenging but essential for precise clinical decision making. We analyzed 121 IBMFS patients using a targeted sequencing co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e61a516e4a698eb8ad5a676c67f8676d
https://pubmed.ncbi.nlm.nih.gov/28102861
https://pubmed.ncbi.nlm.nih.gov/28102861