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Three Cases of Esophageal Cancer Related to Fanconi Anemia.
Fujisawa M, Matsushima M, Ueda T, Kaneko M, Fujimoto R, Sano M, Teramura E, Monma M, Mizukami H, Nakahara F, Suzuki H, Suzuki T, Yabe M, Yabe T. Fujisawa M, et al. Among authors: yabe t, yabe m. Intern Med. 2021 Sep 15;60(18):2953-2959. doi: 10.2169/internalmedicine.6926-20. Epub 2021 Apr 5. Intern Med. 2021. PMID: 33814498 Free PMC article.
Long-term outcome in patients with Fanconi anemia who received hematopoietic stem cell transplantation: a retrospective nationwide analysis.
Yabe M, Morio T, Tabuchi K, Tomizawa D, Hasegawa D, Ishida H, Yoshida N, Koike T, Takahashi Y, Koh K, Okamoto Y, Sano H, Kato K, Kanda Y, Goto H, Takita J, Miyamura T, Noguchi M, Kato K, Hashii Y, Astuta Y, Yabe H. Yabe M, et al. Among authors: yabe h. Int J Hematol. 2021 Jan;113(1):134-144. doi: 10.1007/s12185-020-02991-x. Epub 2020 Sep 19. Int J Hematol. 2021. PMID: 32949371
Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.
Hira A, Yoshida K, Sato K, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Shimamoto A, Tahara H, Ito E, Kojima S, Kurumizaka H, Ogawa S, Takata M, Yabe H, Yabe M. Hira A, et al. Among authors: yabe m, yabe h. Am J Hum Genet. 2015 Jun 4;96(6):1001-7. doi: 10.1016/j.ajhg.2015.04.022. Am J Hum Genet. 2015. PMID: 26046368 Free PMC article.
Associations of complementation group, ALDH2 genotype, and clonal abnormalities with hematological outcome in Japanese patients with Fanconi anemia.
Yabe M, Koike T, Ohtsubo K, Imai E, Morimoto T, Takakura H, Koh K, Yoshida K, Ogawa S, Ito E, Okuno Y, Muramatsu H, Kojima S, Matsuo K, Mori M, Hira A, Takata M, Yabe H. Yabe M, et al. Among authors: yabe h. Ann Hematol. 2019 Feb;98(2):271-280. doi: 10.1007/s00277-018-3517-0. Epub 2018 Oct 27. Ann Hematol. 2019. PMID: 30368588
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients.
Mori M, Hira A, Yoshida K, Muramatsu H, Okuno Y, Shiraishi Y, Anmae M, Yasuda J, Tadaka S, Kinoshita K, Osumi T, Noguchi Y, Adachi S, Kobayashi R, Kawabata H, Imai K, Morio T, Tamura K, Takaori-Kondo A, Yamamoto M, Miyano S, Kojima S, Ito E, Ogawa S, Matsuo K, Yabe H, Yabe M, Takata M. Mori M, et al. Among authors: yabe m, yabe h. Haematologica. 2019 Oct;104(10):1962-1973. doi: 10.3324/haematol.2018.207241. Epub 2019 Feb 21. Haematologica. 2019. PMID: 30792206 Free PMC article. Clinical Trial.
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India.
Donovan FX, Solanki A, Mori M, Chavan N, George M, C SK, Okuno Y, Muramastsu H, Yoshida K, Shimamoto A, Takaori-Kondo A, Yabe H, Ogawa S, Kojima S, Yabe M, Ramanagoudr-Bhojappa R, Smogorzewska A, Mohan S, Rajendran A, Auerbach AD, Takata M, Chandrasekharappa SC, Vundinti BR. Donovan FX, et al. Among authors: yabe m, yabe h. Hum Mutat. 2020 Jan;41(1):122-128. doi: 10.1002/humu.23914. Epub 2019 Sep 26. Hum Mutat. 2020. PMID: 31513304 Free PMC article.
319 results