Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia

Ogawa Shinichi; Yokoyama Yasuhisa; Suzukawa Kazumi; Nanmoku Toru; Kurita Naoki; Seki Masanori; Maie Koichiro; Suyama Takuya; Takaiwa Naoko; Sakata-Yanagimoto Mamiko; Obara Naoshi; Hasegawa Yuichi; Chiba Shigeru

首页> 外文期刊>Annals of hematology >Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia

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Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia

机译：在急性髓样白血病的复发易位t（8; 12）（q22; p13）中鉴定由河马途径基因MST2和共同易位伴侣ETV6组成的融合基因

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来源
《Annals of hematology》 |2015年第8期|共3页
作者
Ogawa Shinichi; Yokoyama Yasuhisa; Suzukawa Kazumi; Nanmoku Toru; Kurita Naoki; Seki Masanori; Maie Koichiro; Suyama Takuya; Takaiwa Naoko; Sakata-Yanagimoto Mamiko; Obara Naoshi; Hasegawa Yuichi; Chiba Shigeru;
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正文语种 eng
中图分类血液及淋巴系疾病;
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1. Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia [J] . Ogawa Shinichi, Yokoyama Yasuhisa, Suzukawa Kazumi, Annals of hematology . 2015,第8期

机译：在急性髓样白血病的复发易位t（8; 12）（q22; p13）中鉴定由河马途径基因MST2和共同易位伴侣ETV6组成的融合基因
2. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene. [J] . Penas EM, Cools J, Algenstaedt P, Genes, Chromosomes and Cancer . 2003,第1期

机译：在继发性急性髓细胞性白血病中的新型隐性易位t（12; 17）（p13; p12-p13）导致ETV6基因与PER1基因的反义链融合。
3. Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation. [J] . Hosoya N, Qiao Y, Hangaishi A, Genes, Chromosomes and Cancer . 2005,第3期

机译：在携带t（6; 12）（q21; p13）易位的急性骨髓性白血病患者中鉴定SRC样酪氨酸激酶基因FRK与ETV6融合。
4. The t(14;21)(q11.2;q22) chromosomal translocation associated with T-cell acute lymphoblastic leukemia activates the BHLHB1 and BHLHB2 genes. [D] . Wang, Junjie. 2003

机译：与T细胞急性淋巴细胞白血病相关的t（14; 21）（q11.2; q22）染色体易位激活了BHLHB1和BHLHB2基因。
5. Characteristics of translocation (16;16)(p13;q22) acute myeloid leukemia [O] . Alireza Eghtedar, Gautam Borthakur, Farhad Ravandi, -1

机译：（p13; Q22）急性髓性白血病;易位（16 16）的特性
6. SIGNIFICANCE OF ETV6-RUNX1 FUSION GENE TRANSCRIPT DETECTION IN PEDIATRIC B-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA WITH TRANSLOCATION t(12;21)(p13;q22) [O] . G. A. Tsaur, Т. О. Riger, A. M. Popov, 2018

机译：具有易位T（12; 21）的etV6-runx1融合基因转录物检测在儿科B细胞前体急性淋巴细胞白血病（P13; Q22）中的意义

Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia

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