• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Subclonal evolution involving SF3B1 mutations in chronic lymphocytic leukemia.

作者信息

Schwaederlé M, Ghia E, Rassenti L Z, Obara M, Dell'Aquila M L, Fecteau J F, Kipps T J

出版信息

Leukemia. 2013 Apr;27(5):1214-7. doi: 10.1038/leu.2013.22. Epub 2013 Jan 22.

DOI:10.1038/leu.2013.22
PMID:23337928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3650490/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e40/3650490/c7288e409249/leu201322f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e40/3650490/c7288e409249/leu201322f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e40/3650490/c7288e409249/leu201322f1.jpg

相似文献

1
Subclonal evolution involving SF3B1 mutations in chronic lymphocytic leukemia.慢性淋巴细胞白血病中涉及SF3B1突变的亚克隆进化。
Leukemia. 2013 Apr;27(5):1214-7. doi: 10.1038/leu.2013.22. Epub 2013 Jan 22.
2
SF3B1 mutations in chronic lymphocytic leukemia.SF3B1 突变与慢性淋巴细胞白血病。
Blood. 2013 Jun 6;121(23):4627-34. doi: 10.1182/blood-2013-02-427641. Epub 2013 Apr 8.
3
Genetic characterization of SF3B1 mutations in single chronic lymphocytic leukemia cells.单个慢性淋巴细胞白血病细胞中SF3B1突变的遗传学特征分析
Leukemia. 2013 Nov;27(11):2264-7. doi: 10.1038/leu.2013.155. Epub 2013 May 20.
4
Chronic lymphocytic leukemia with SF3B1 mutation.伴有SF3B1突变的慢性淋巴细胞白血病
N Engl J Med. 2012 Jun 28;366(26):2530. doi: 10.1056/NEJMc1204033.
5
Different impact of NOTCH1 and SF3B1 mutations on the risk of chronic lymphocytic leukemia transformation to Richter syndrome.NOTCH1和SF3B1突变对慢性淋巴细胞白血病转化为 Richter 综合征风险的不同影响。
Br J Haematol. 2012 Aug;158(3):426-9. doi: 10.1111/j.1365-2141.2012.09155.x. Epub 2012 May 10.
6
Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia.慢性淋巴细胞白血病中克隆性和亚克隆性TP53、SF3B1、BIRC3、NOTCH1和ATM突变的临床影响
Blood. 2016 Apr 28;127(17):2122-30. doi: 10.1182/blood-2015-07-659144. Epub 2016 Feb 2.
7
NOTCH1, SF3B1, BIRC3 and TP53 mutations in patients with chronic lymphocytic leukemia undergoing first-line treatment: correlation with biological parameters and response to treatment.接受一线治疗的慢性淋巴细胞白血病患者的NOTCH1、SF3B1、BIRC3和TP53突变:与生物学参数及治疗反应的相关性
Leuk Lymphoma. 2014 Dec;55(12):2785-92. doi: 10.3109/10428194.2014.898760.
8
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.外显子组测序鉴定出慢性淋巴细胞白血病中剪接因子 SF3B1 基因的反复突变。
Nat Genet. 2011 Dec 11;44(1):47-52. doi: 10.1038/ng.1032.
9
Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: association with progression and fludarabine-refractoriness.SF3B1 剪接因子在慢性淋巴细胞白血病中的突变:与进展和氟达拉滨耐药性相关。
Blood. 2011 Dec 22;118(26):6904-8. doi: 10.1182/blood-2011-08-373159. Epub 2011 Oct 28.
10
A common alternative splicing signature is associated with SF3B1 mutations in malignancies from different cell lineages.一种常见的可变剪接特征与来自不同细胞谱系的恶性肿瘤中的SF3B1突变相关。
Leukemia. 2014 Jun;28(6):1355-7. doi: 10.1038/leu.2014.28. Epub 2014 Jan 17.

引用本文的文献

1
Aberrant spliceosome activity via elevated intron retention and upregulation and phosphorylation of SF3B1 in chronic lymphocytic leukemia.慢性淋巴细胞白血病中,通过内含子保留增加以及SF3B1的上调和磷酸化导致剪接体活性异常。
Mol Ther Nucleic Acids. 2024 Apr 26;35(2):102202. doi: 10.1016/j.omtn.2024.102202. eCollection 2024 Jun 11.
2
Dielectrophoretic recovery of DNA from plasma for the identification of chronic lymphocytic leukemia point mutations.用于鉴定慢性淋巴细胞白血病点突变的从血浆中通过介电泳回收DNA的方法
Int J Hematol Oncol. 2016 May;5(1):27-35. doi: 10.2217/ijh-2015-0009. Epub 2016 May 5.
3
Identification of potential therapeutic target genes and miRNAs for primary myelofibrosis with microarray analysis.

本文引用的文献

1
NOTCH1 and SF3B1 mutations can be added to the hierarchical prognostic classification in chronic lymphocytic leukemia.NOTCH1和SF3B1突变可添加到慢性淋巴细胞白血病的分层预后分类中。
Leukemia. 2013 Feb;27(2):512-4. doi: 10.1038/leu.2012.307. Epub 2012 Nov 6.
2
Chronic lymphocytic leukemia with SF3B1 mutation.伴有SF3B1突变的慢性淋巴细胞白血病
N Engl J Med. 2012 Jun 28;366(26):2530. doi: 10.1056/NEJMc1204033.
3
SF3B1 in chronic lymphocytic leukemia.慢性淋巴细胞白血病中的SF3B1
通过微阵列分析鉴定原发性骨髓纤维化的潜在治疗靶基因和微小RNA
Exp Ther Med. 2017 Oct;14(4):2743-2750. doi: 10.3892/etm.2017.4912. Epub 2017 Aug 9.
4
The splicing modulator sudemycin induces a specific antitumor response and cooperates with ibrutinib in chronic lymphocytic leukemia.剪接调节剂苏地霉素可诱导特异性抗肿瘤反应,并在慢性淋巴细胞白血病中与依鲁替尼协同作用。
Oncotarget. 2015 Sep 8;6(26):22734-49. doi: 10.18632/oncotarget.4212.
5
Targeting the spliceosome in chronic lymphocytic leukemia with the macrolides FD-895 and pladienolide-B.使用大环内酯类药物FD - 895和普拉地诺醇B靶向慢性淋巴细胞白血病中的剪接体。
Haematologica. 2015 Jul;100(7):945-54. doi: 10.3324/haematol.2014.122069. Epub 2015 Apr 10.
6
Transcriptome sequencing reveals potential mechanism of cryptic 3' splice site selection in SF3B1-mutated cancers.转录组测序揭示了SF3B1突变癌症中隐匿性3'剪接位点选择的潜在机制。
PLoS Comput Biol. 2015 Mar 13;11(3):e1004105. doi: 10.1371/journal.pcbi.1004105. eCollection 2015 Mar.
7
Recurrent mutations refine prognosis in chronic lymphocytic leukemia.反复出现的突变可改善慢性淋巴细胞白血病的预后。
Leukemia. 2015 Feb;29(2):329-36. doi: 10.1038/leu.2014.196. Epub 2014 Jun 19.
8
Clinical application of targeted and genome-wide technologies: can we predict treatment responses in chronic lymphocytic leukemia?靶向技术和全基因组技术的临床应用:我们能否预测慢性淋巴细胞白血病的治疗反应?
Per Med. 2013 Jun 1;10(4):361-376. doi: 10.2217/pme.13.33.
9
SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients.在 1160 例未经治疗的 CLL 患者中,SF3B1 突变与细胞遗传学以及 NOTCH1、FBXW7、MYD88、XPO1 和 TP53 的突变相关。
Leukemia. 2014 Jan;28(1):108-17. doi: 10.1038/leu.2013.263. Epub 2013 Sep 12.
10
The pathogenesis of chronic lymphocytic leukemia.慢性淋巴细胞白血病的发病机制。
Annu Rev Pathol. 2014;9:103-18. doi: 10.1146/annurev-pathol-020712-163955. Epub 2013 Aug 26.
N Engl J Med. 2012 Mar 15;366(11):1057; author reply 1057-8. doi: 10.1056/NEJMc1201040.
4
Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes.骨髓增生异常综合征患者中 SRSF2、U2AF1 和 ZRSR2 突变的频率及其预后影响。
Blood. 2012 Apr 12;119(15):3578-84. doi: 10.1182/blood-2011-12-399337. Epub 2012 Mar 2.
5
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia.外显子组测序鉴定出慢性淋巴细胞白血病中剪接因子 SF3B1 基因的反复突变。
Nat Genet. 2011 Dec 11;44(1):47-52. doi: 10.1038/ng.1032.
6
SF3B1 and other novel cancer genes in chronic lymphocytic leukemia.SF3B1 及其他慢性淋巴细胞白血病中的新型癌症基因。
N Engl J Med. 2011 Dec 29;365(26):2497-506. doi: 10.1056/NEJMoa1109016. Epub 2011 Dec 12.
7
SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications.骨髓增生异常综合征中的SF3B1突变:临床关联及预后意义
Leukemia. 2012 May;26(5):1137-40. doi: 10.1038/leu.2011.321. Epub 2011 Nov 8.
8
Mutations of the SF3B1 splicing factor in chronic lymphocytic leukemia: association with progression and fludarabine-refractoriness.SF3B1 剪接因子在慢性淋巴细胞白血病中的突变:与进展和氟达拉滨耐药性相关。
Blood. 2011 Dec 22;118(26):6904-8. doi: 10.1182/blood-2011-08-373159. Epub 2011 Oct 28.
9
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.环形铁幼粒细胞性难治性贫血伴多系发育异常中的体细胞 SF3B1 突变。
N Engl J Med. 2011 Oct 13;365(15):1384-95. doi: 10.1056/NEJMoa1103283. Epub 2011 Sep 26.
10
A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL).B 细胞慢性淋巴细胞白血病(B-CLL)的高分辨率等位基因型
Blood. 2002 Sep 1;100(5):1787-94.