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Are PU.1 mutations frequent genetic events in acute myeloid leukemia (AML)?

作者信息

Lamandin Charlotte, Sagot Christophe, Roumier Christophe, Lepelley Pascale, De Botton Stéphane, Cosson Alain, Fenaux Pierre, Preudhomme Claude

出版信息

Blood. 2002 Dec 15;100(13):4680-1. doi: 10.1182/blood-2002-08-2563.

DOI:10.1182/blood-2002-08-2563
PMID:12453885
Abstract
摘要

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1
Are PU.1 mutations frequent genetic events in acute myeloid leukemia (AML)?
Blood. 2002 Dec 15;100(13):4680-1. doi: 10.1182/blood-2002-08-2563.
2
Heterozygous PU.1 mutations are associated with acute myeloid leukemia.杂合型PU.1突变与急性髓系白血病相关。
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Mutation analysis of the transcription factor PU.1 in younger adults (16 to 60 years) with acute myeloid leukemia: a study of the AML Study Group Ulm (AMLSG ULM).16至60岁急性髓系白血病年轻成人中转录因子PU.1的突变分析:乌尔姆急性髓系白血病研究组(AMLSG ULM)的一项研究
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Heterozygous PU.1 mutations are associated with acute myeloid leukemia.杂合型PU.1突变与急性髓系白血病相关。
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AML-1 mutations outside the RUNT domain: description of two cases in myeloid malignancies.RUNT结构域外的AML-1突变:两例髓系恶性肿瘤病例描述
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Novel FLT3 point mutations within exon 14 found in patients with acute myeloid leukaemia.在急性髓系白血病患者中发现的位于第14外显子内的新型FLT3点突变。
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Suppression of myeloid transcription factors and induction of STAT response genes by AML-specific Flt3 mutations.急性髓系白血病特异性Flt3突变对髓系转录因子的抑制及STAT反应基因的诱导
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C/EBP-epsilon: chromosomal mapping and mutational analysis of the gene in leukemia and preleukemia.C/EBP-ε:白血病和白血病前期该基因的染色体定位及突变分析
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Down-regulation of Notch-1 expression decreases PU.1-mediated myeloid differentiation signaling in acute myeloid leukemia.Notch-1表达的下调降低了急性髓系白血病中PU.1介导的髓系分化信号。
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PU.1 is a suppressor of myeloid leukemia, inactivated in mice by gene deletion and mutation of its DNA binding domain.PU.1是一种髓系白血病抑制因子,在小鼠中因DNA结合结构域的基因缺失和突变而失活。
Blood. 2004 Dec 1;104(12):3437-44. doi: 10.1182/blood-2004-06-2234. Epub 2004 Aug 10.

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Genome-scale definition of the transcriptional programme associated with compromised PU.1 activity in acute myeloid leukaemia.急性髓系白血病中与PU.1活性受损相关的转录程序的全基因组规模定义
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Frequency of acute myeloid leukaemia-associated mouse chromosome 2 deletions in X-ray exposed immature haematopoietic progenitors and stem cells.
X 射线照射未成熟造血祖细胞和干细胞后急性髓性白血病相关的小鼠染色体 2 缺失的频率。
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RUNX1 regulates corepressor interactions of PU.1.RUNX1 调节 PU.1 的核心抑制因子相互作用。
Blood. 2011 Jun 16;117(24):6498-508. doi: 10.1182/blood-2010-10-312512. Epub 2011 Apr 25.
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Inactivation of PU.1 in adult mice leads to the development of myeloid leukemia.成年小鼠中PU.1的失活会导致髓系白血病的发生。
Proc Natl Acad Sci U S A. 2006 Jan 31;103(5):1486-91. doi: 10.1073/pnas.0510616103. Epub 2006 Jan 23.
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Effect of transcription-factor concentrations on leukemic stem cells.转录因子浓度对白血病干细胞的影响。
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A pilot study of high-throughput, sequence-based mutational profiling of primary human acute myeloid leukemia cell genomes.一项关于原代人类急性髓系白血病细胞基因组的高通量、基于序列的突变分析的初步研究。
Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14275-80. doi: 10.1073/pnas.2335924100. Epub 2003 Nov 12.