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A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion gene.

作者信息

Fasan A, Haferlach C, Alpermann T, Kern W, Haferlach T, Schnittger S

出版信息

Leukemia. 2013 Jan;27(1):245-8. doi: 10.1038/leu.2012.230. Epub 2012 Aug 14.

DOI:10.1038/leu.2012.230
PMID:22945772
Abstract
摘要

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1
A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98-NSD1 fusion gene.一小部分罕见但特定的成年急性髓系白血病(AML)患者可由细胞遗传学上隐匿的核孔蛋白98(NUP98)-核受体结合SET结构域蛋白1(NSD1)融合基因来定义。
Leukemia. 2013 Jan;27(1):245-8. doi: 10.1038/leu.2012.230. Epub 2012 Aug 14.
2
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Major form of NUP98/HOXC11 fusion in adult AML with t(11;12)(p15;q13) translocation exhibits aberrant trans-regulatory activity.伴有t(11;12)(p15;q13)易位的成人急性髓系白血病中NUP98/HOXC11融合的主要形式表现出异常的反式调节活性。
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Multiplex reverse transcription polymerase chain reaction screening in acute myeloid leukemia detects cytogenetically unrevealed abnormalities of prognostic significance.急性髓系白血病中的多重逆转录聚合酶链反应筛查可检测出具有预后意义但细胞遗传学未揭示的异常情况。
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Clec12a is required for the pathogenesis of NUP98::NSD1 AML.Clec12a是NUP98::NSD1急性髓系白血病发病机制所必需的。
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Targeted gene sequencing and transcriptome sequencing reveal characteristics of NUP98 rearrangement in pediatric acute myeloid leukemia.靶向基因测序和转录组测序揭示儿童急性髓系白血病中 NUP98 重排的特征。
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Clinical features and prognosis of patients with myeloid neoplasms harboring t(7;11)(p15;p15) translocation: a single-center retrospective study.
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Novel Gene Fusion in Acute Myeloid Leukemia Detected by Optical Genome Mapping.通过光学基因组图谱检测急性髓系白血病中的新型基因融合
Cancers (Basel). 2023 May 27;15(11):2942. doi: 10.3390/cancers15112942.
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Targeted Inhibition of the NUP98-NSD1 Fusion Oncogene in Acute Myeloid Leukemia.急性髓系白血病中NUP98-NSD1融合致癌基因的靶向抑制
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Mechanistic insights and potential therapeutic approaches for NUP98-rearranged hematologic malignancies.NUP98 重排血液系统恶性肿瘤的机制见解和潜在治疗方法。
Blood. 2020 Nov 12;136(20):2275-2289. doi: 10.1182/blood.2020007093.
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Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group.分子谱分析确定儿童急性髓系白血病的不同预后亚组:来自法国ELAM02研究组的报告
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Dasatinib and navitoclax act synergistically to target NUP98-NSD1/FLT3-ITD acute myeloid leukemia.达沙替尼和 navitoclax 协同作用靶向 NUP98-NSD1/FLT3-ITD 急性髓系白血病。
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