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TBI, etoposide, and cyclophosphamide conditioning for intermediate-risk relapsed childhood acute lymphoblastic leukemia.
Ueki H, Ogawa C, Goto H, Nishi M, Yamanaka J, Mochizuki S, Nishikawa T, Kumamoto T, Nishiuchi R, Kikuta A, Yamamoto S, Igarashi S, Sato A, Hori T, Saito AM, Watanabe T, Deguchi T, Manabe A, Horibe K, Toyoda H. Ueki H, et al. Among authors: nishiuchi r. Int J Hematol. 2024 Apr;119(4):450-458. doi: 10.1007/s12185-024-03710-6. Epub 2024 Jan 25. Int J Hematol. 2024. PMID: 38267673
PAX5 alterations in an infant case of KMT2A-rearranged leukemia with lineage switch.
Nakajima K, Kubota H, Kato I, Isobe K, Ueno H, Kozuki K, Tanaka K, Kawabata N, Mikami T, Tamefusa K, Nishiuchi R, Saida S, Umeda K, Hiramatsu H, Adachi S, Takita J. Nakajima K, et al. Among authors: nishiuchi r. Cancer Sci. 2022 Jul;113(7):2472-2476. doi: 10.1111/cas.15380. Epub 2022 May 31. Cancer Sci. 2022. PMID: 35467057 Free PMC article.
Prolyl oligopeptidase participates in the cytosine arabinoside-induced nuclear translocation of glyceraldehyde 3-phosphate dehydrogenase in a human neuroblastoma cell line.
Sakaguchi M, Nishiuchi R, Bando M, Yamada Y, Kondo R, Mitsumori M, Shiokawa A, Kanazawa M, Ikeguchi S, Kikyo F, Tanaka S. Sakaguchi M, et al. Among authors: nishiuchi r. Biochem Biophys Res Commun. 2021 Oct 1;572:65-71. doi: 10.1016/j.bbrc.2021.07.094. Epub 2021 Jul 30. Biochem Biophys Res Commun. 2021. PMID: 34358965
Survey of patients with spinal muscular atrophy on the island of Shikoku, Japan.
Okamoto K, Motoki T, Saito I, Urate R, Aibara K, Jogamoto T, Fukuda M, Wakamoto H, Maniwa S, Kondo Y, Toda Y, Goji A, Mori T, Soga T, Konishi Y, Nagai S, Takami Y, Tokorodani C, Nishiuchi R, Usui D, Ando R, Tada S, Yamanishi Y, Nagai M, Arakawa R, Saito K, Nishio H, Ishii E, Eguchi M. Okamoto K, et al. Among authors: nishiuchi r. Brain Dev. 2020 Sep;42(8):594-602. doi: 10.1016/j.braindev.2020.05.004. Epub 2020 Jun 3. Brain Dev. 2020. PMID: 32505480
A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).
Tozawa Y, Abdrabou SSMA, Nogawa-Chida N, Nishiuchi R, Ishida T, Suzuki Y, Sano H, Kobayashi R, Kishimoto K, Ohara O, Imai K, Naruto T, Kobayashi K, Ariga T, Yamada M. Tozawa Y, et al. Among authors: nishiuchi r. Clin Immunol. 2019 Nov;208:108256. doi: 10.1016/j.clim.2019.108256. Epub 2019 Sep 5. Clin Immunol. 2019. PMID: 31494288
Barth Syndrome: Different Approaches to Diagnosis.
Imai-Okazaki A, Kishita Y, Kohda M, Yatsuka Y, Hirata T, Mizuno Y, Harashima H, Hirono K, Ichida F, Noguchi A, Yoshida M, Tokorodani C, Nishiuchi R, Takeda A, Nakaya A, Sakata Y, Murayama K, Ohtake A, Okazaki Y. Imai-Okazaki A, et al. Among authors: nishiuchi r. J Pediatr. 2018 Feb;193:256-260. doi: 10.1016/j.jpeds.2017.09.075. Epub 2017 Dec 15. J Pediatr. 2018. PMID: 29249525
48 results