Literature DB >> 17215856

Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia.

A Attarbaschi, G Mann, S Strehl, M König, M Steiner, V Jeitler, Th Lion, M N Dworzak, H Gadner, O A Haas.   

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Year:  2007        PMID： 17215856     DOI： 10.1038/sj.leu.2404507

Source DB:  PubMed          Journal:  Leukemia        ISSN： 0887-6924            Impact factor:   11.528


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  4 in total

1.  ETV6 mutation in a cohort of 970 patients with hematologic malignancies.

Authors:  Qinrong Wang; Shasha Dong; Hong Yao; Lijun Wen; Huiying Qiu; Llili Qin; Liang Ma; Suning Chen
Journal:  Haematologica       Date:  2014-07-04       Impact factor: 9.941

2.  11q23 abnormalities in adult Chinese patients with hematological malignancies.

Authors:  Xiaoli Zhao; Shuang Li; Nianyi Li; Rong Fan; Guowei Lin; Xiaoqin Wang
Journal:  Med Oncol       Date:  2014-07-10       Impact factor: 3.064

Review 3.  Pathogenesis of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia and mechanisms underlying its relapse.

Authors:  Congcong Sun; Lixian Chang; Xiaofan Zhu
Journal:  Oncotarget       Date:  2017-05-23

4.  Outcome and Prognostic Factors for ETV6/RUNX1 Positive Pediatric Acute Lymphoblastic Leukemia Treated at a Single Institution in Korea.

Authors:  Jae Wook Lee; Seong-Koo Kim; Pil-Sang Jang; Nack-Gyun Chung; Dae-Chul Jeong; Myungshin Kim; Bin Cho; Hack-Ki Kim
Journal:  Cancer Res Treat       Date:  2016-08-10       Impact factor: 4.679
  4 in total

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