Fusion of the Nucleoporin Gene, NUP98, and the Putative RNA Helicase Gene, DZXX10, by Inversion 11 (p15q22) Chromosome Translocation in a Patient with Etoposide-related Myelodysplastic Syndrome (vol 39, pg 412, 2000)

Nakao Katsuyuki; Nishino Maki; Takeuchi Kyoko; Iwata Masayasu; Kawano Akira; Arai Yasuhito; Ohki Misao

首页> 外文期刊>Internal medicine. >Fusion of the Nucleoporin Gene, NUP98, and the Putative RNA Helicase Gene, DZXX10, by Inversion 11 (p15q22) Chromosome Translocation in a Patient with Etoposide-related Myelodysplastic Syndrome (vol 39, pg 412, 2000)

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Fusion of the Nucleoporin Gene, NUP98, and the Putative RNA Helicase Gene, DZXX10, by Inversion 11 (p15q22) Chromosome Translocation in a Patient with Etoposide-related Myelodysplastic Syndrome (vol 39, pg 412, 2000)

机译：依托泊苷相关性骨髓增生异常综合征患者中11号位点（p15q22）染色体易位的核蛋白基因NUP98和推定的RNA解旋酶基因DZXX10的融合（第39卷，第412页，2000年）

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《Internal medicine.》 |2015年第5期|共1页
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Nakao Katsuyuki; Nishino Maki; Takeuchi Kyoko; Iwata Masayasu; Kawano Akira; Arai Yasuhito; Ohki Misao;
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1. Fusion of the Nucleoporin Gene, NUP98, and the Putative RNA Helicase Gene, DZXX10, by Inversion 11 (p15q22) Chromosome Translocation in a Patient with Etoposide-related Myelodysplastic Syndrome (vol 39, pg 412, 2000) [J] . Nakao Katsuyuki, Nishino Maki, Takeuchi Kyoko, Internal medicine. . 2015,第5期

机译：依托泊苷相关性骨髓增生异常综合征患者中11号位点（p15q22）染色体易位的核蛋白基因NUP98和推定的RNA解旋酶基因DZXX10的融合（第39卷，第412页，2000年）
2. A Novel Gene, ANKRD28 on 3p25, Is Fused with NUP98 on 11p15 in a Cryptic 3-Way Translocation of t(3;5;11)(p25;q35;p15) in an Adult Patient with Myelodysplastic Syndrome/Acute Myelogenous Leukemia [J] . Maho Ishikawa, Fumiharu Yagasaki, Daisuke Okamura, International Journal of Hematology . 2007,第3期

机译：在成年骨髓增生异常综合征/急性粒细胞性白血病患者的t（3; 5; 11）（p25; q35; p15）的3位隐性三位易位中，将新基因ANKRD28 3p25与11p15 NUP98融合
3. The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9. [J] . Taketani T, Taki T, Ono R, Genes, Chromosomes and Cancer . 2002,第4期

机译：急性髓细胞性白血病中的染色体易位t（7; 11）（p15; p15）导致NUP98基因与HOXA簇基因HOXA13融合，而不与HOXA9融合。
4. Sequence analysis of the MYC oncogene involved in the t(8;14)(q24;q11) chromosome translocation in a human leukemia T-cell line indicates that putative regulatory regions are not altered. [O] . S N Finver, K Nishikura, L R Finger, 1988

机译：参与人类白血病T细胞系中t（8; 14）（q24; q11）染色体易位的MYC癌基因的序列分析表明假定的调控区未改变。
5. The inv(11)(p15q22) Chromosome Translocation of De Novo and Therapy-Related Myeloid Malignancies Results in Fusion of the Nucleoporin Gene, NUP98, With the Putative RNA Helicase Gene, DDX10 [O] . Yasuhito Arai, Fumie Hosoda, Hirofumi Kobayashi, 1997

机译：De Novo和治疗相关骨髓恶性肿瘤的inv（11）（p15q22）染色体易位导致核偶素基因Nup98的融合，具有推定的RNA Helicase基因，DDX10

Fusion of the Nucleoporin Gene, NUP98, and the Putative RNA Helicase Gene, DZXX10, by Inversion 11 (p15q22) Chromosome Translocation in a Patient with Etoposide-related Myelodysplastic Syndrome (vol 39, pg 412, 2000)

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