• 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

A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia.

作者信息

Sakai H, Hosono N, Nakazawa H, Przychodzen B, Polprasert C, Carraway H E, Sekeres M A, Radivoyevitch T, Yoshida K, Sanada M, Yoshizato T, Kataoka K, Nakagawa M M, Ueno H, Nannya Y, Kon A, Shiozawa Y, Takeda J, Shiraishi Y, Chiba K, Miyano S, Singh J, Padgett R A, Ogawa S, Maciejewski J P, Makishima H

机构信息

Department of Translational Hematology and Oncology Research, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH, USA.

Division of Hematology, Department of Internal Medicine, Shinshu University, Matsumoto, Japan.

出版信息

Leukemia. 2018 Mar;32(3):839-843. doi: 10.1038/leu.2017.319. Epub 2017 Nov 3.

DOI:10.1038/leu.2017.319
PMID:29099495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8694071/
Abstract
摘要

相似文献

1
A novel genetic and morphologic phenotype of ARID2-mediated myelodysplasia.ARID2介导的骨髓发育异常的一种新型遗传和形态学表型。
Leukemia. 2018 Mar;32(3):839-843. doi: 10.1038/leu.2017.319. Epub 2017 Nov 3.
2
First Korean case of Emberger syndrome (primary lymphedema with myelodysplasia) with a novel GATA2 gene mutation.首例伴有新型GATA2基因突变的韩国恩贝格尔综合征(原发性淋巴水肿伴骨髓发育异常)病例。
Korean J Intern Med. 2016 Jan;31(1):188-90. doi: 10.3904/kjim.2016.31.1.188. Epub 2015 Dec 28.
3
Clinical and functional characterization of telomerase variants in patients with pediatric acute myeloid leukemia/myelodysplastic syndrome.儿童急性髓系白血病/骨髓增生异常综合征患者端粒酶变体的临床和功能特征
Leukemia. 2021 Jan;35(1):269-273. doi: 10.1038/s41375-020-0835-8. Epub 2020 Apr 21.
4
A novel t(3;9)(q21.2; p24.3) associated with SMARCA2 and ZNF148 genes rearrangement in myelodysplastic syndrome.
Leuk Lymphoma. 2018 Apr;59(4):996-999. doi: 10.1080/10428194.2017.1352093. Epub 2017 Jul 18.
5
Germ line tissues for optimal detection of somatic variants in myelodysplastic syndromes.用于最佳检测骨髓增生异常综合征体细胞变异的生殖系组织。
Blood. 2018 May 24;131(21):2402-2405. doi: 10.1182/blood-2018-01-827881. Epub 2018 Apr 16.
6
Myelodysplasia.骨髓发育异常
Curr Opin Oncol. 1994 Jan;6(1):32-40. doi: 10.1097/00001622-199401000-00005.
7
Myelodysplastic syndromes: dissecting the heterogeneity.骨髓增生异常综合征:剖析其异质性
J Clin Oncol. 2011 May 20;29(15):1937-8. doi: 10.1200/JCO.2011.35.2211. Epub 2011 Apr 25.
8
Myelodysplasia in younger adults: outlier or unique molecular entity?年轻成年人的骨髓发育异常:异常情况还是独特的分子实体?
Haematologica. 2017 Jun;102(6):967-968. doi: 10.3324/haematol.2017.165993.
9
GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia.GATA-2 异常与散发性淋巴水肿、树突状细胞、单核细胞、B 细胞和自然杀伤(NK)细胞(DCML)缺陷和骨髓增生异常的临床表型
Eur J Pediatr. 2012 Aug;171(8):1273-6. doi: 10.1007/s00431-012-1715-7. Epub 2012 Mar 21.
10
Patient with anomalous skin pigmentation expands the phenotype of ARID2 loss-of-function disorder, a SWI/SNF-related intellectual disability.具有异常皮肤色素沉着的患者扩展了 ARID2 功能丧失障碍的表型,这是一种与 SWI/SNF 相关的智力障碍。
Am J Med Genet A. 2019 May;179(5):808-812. doi: 10.1002/ajmg.a.61075. Epub 2019 Mar 5.

引用本文的文献

1
Revealing the clinical impact of MTOR and ARID2 gene mutations on MALT lymphoma of the alimentary canal using targeted sequencing.利用靶向测序揭示 MTOR 和 ARID2 基因突变对消化道黏膜相关淋巴组织淋巴瘤的临床影响。
Diagn Pathol. 2024 Jul 25;19(1):102. doi: 10.1186/s13000-024-01525-x.
2
BCL7A is silenced by hypermethylation to promote acute myeloid leukemia.BCL7A因高甲基化而沉默,从而促进急性髓系白血病的发生。
Biomark Res. 2023 Mar 20;11(1):32. doi: 10.1186/s40364-023-00472-x.
3
SWI/SNF complexes in hematological malignancies: biological implications and therapeutic opportunities.

本文引用的文献

1
Dynamics of clonal evolution in myelodysplastic syndromes.骨髓增生异常综合征的克隆进化动力学
Nat Genet. 2017 Feb;49(2):204-212. doi: 10.1038/ng.3742. Epub 2016 Dec 19.
2
Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia.初发及复发急性早幼粒细胞白血病的全面突变分析
Leukemia. 2016 Aug;30(8):1672-81. doi: 10.1038/leu.2016.69. Epub 2016 Apr 11.
3
Biallelic germline and somatic mutations in malignant mesothelioma: multiple mutations in transcription regulators including mSWI/SNF genes.
SWI/SNF 复合物在血液系统恶性肿瘤中的作用:生物学意义和治疗机会。
Mol Cancer. 2023 Feb 21;22(1):39. doi: 10.1186/s12943-023-01736-8.
4
Inferring cancer common and specific gene networks via multi-layer joint graphical model.通过多层联合图形模型推断癌症常见和特定基因网络。
Comput Struct Biotechnol J. 2023 Jan 18;21:974-990. doi: 10.1016/j.csbj.2023.01.017. eCollection 2023.
5
The Impact of Clonal Hierarchy and Heterogeneity on Phenotypic Manifestations of Myelodysplastic Neoplasms.克隆层次结构和异质性对骨髓增生异常肿瘤表型表现的影响
Cancers (Basel). 2022 Nov 19;14(22):5690. doi: 10.3390/cancers14225690.
6
Mutational profile of ZBTB16-RARA-positive acute myeloid leukemia.ZBTB16-RARA 阳性急性髓系白血病的突变特征。
Cancer Med. 2021 Jun;10(12):3839-3847. doi: 10.1002/cam4.3904. Epub 2021 May 27.
7
Myeloid/lymphoid neoplasms with eosinophilia/ basophilia and ETV6-ABL1 fusion: cell-of-origin and response to tyrosine kinase inhibition.伴有嗜酸性粒细胞增多/嗜碱性粒细胞增多及ETV6-ABL1融合的髓系/淋系肿瘤:起源细胞及对酪氨酸激酶抑制的反应
Haematologica. 2021 Feb 1;106(2):614-618. doi: 10.3324/haematol.2020.249649.
8
Genetics of MDS.骨髓增生异常综合征的遗传学。
Blood. 2019 Mar 7;133(10):1049-1059. doi: 10.1182/blood-2018-10-844621. Epub 2019 Jan 22.
9
The chromatin remodeling subunit Baf200 promotes normal hematopoiesis and inhibits leukemogenesis.染色质重塑亚基 Baf200 促进正常造血并抑制白血病发生。
J Hematol Oncol. 2018 Feb 26;11(1):27. doi: 10.1186/s13045-018-0567-7.
恶性间皮瘤中的双等位基因种系和体细胞突变:转录调节因子中的多个突变,包括mSWI/SNF基因。
Int J Cancer. 2015 Feb 1;136(3):560-71. doi: 10.1002/ijc.29015. Epub 2014 Jun 19.
4
Essential role of BRG, the ATPase subunit of BAF chromatin remodeling complexes, in leukemia maintenance.BRG,即 BAF 染色质重塑复合物的 ATP 酶亚基,在白血病维持中起关键作用。
Blood. 2014 Mar 13;123(11):1720-8. doi: 10.1182/blood-2013-02-483495. Epub 2014 Jan 29.
5
Primary urethral clear-cell adenocarcinoma: comprehensive analysis by surgical pathology, cytopathology, and next-generation sequencing.原发性尿道透明细胞腺癌:通过外科病理学、细胞病理学和下一代测序进行的综合分析
Am J Pathol. 2014 Mar;184(3):584-91. doi: 10.1016/j.ajpath.2013.11.023. Epub 2014 Jan 3.
6
Role of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation.SWI/SNF 在急性白血病维持和增强子介导的 Myc 调控中的作用。
Genes Dev. 2013 Dec 15;27(24):2648-62. doi: 10.1101/gad.232710.113. Epub 2013 Nov 27.
7
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes.944例骨髓增生异常综合征患者的基因损伤图谱
Leukemia. 2014 Feb;28(2):241-7. doi: 10.1038/leu.2013.336. Epub 2013 Nov 13.
8
Clinical and biological implications of driver mutations in myelodysplastic syndromes.骨髓增生异常综合征中驱动突变的临床和生物学意义。
Blood. 2013 Nov 21;122(22):3616-27; quiz 3699. doi: 10.1182/blood-2013-08-518886. Epub 2013 Sep 12.
9
Recurrent inactivating mutations of ARID2 in non-small cell lung carcinoma.非小细胞肺癌中 ARID2 的反复失活突变。
Int J Cancer. 2013 May 1;132(9):2217-21. doi: 10.1002/ijc.27900. Epub 2012 Nov 20.
10
A landscape of driver mutations in melanoma.黑色素瘤中的驱动基因突变全景。
Cell. 2012 Jul 20;150(2):251-63. doi: 10.1016/j.cell.2012.06.024.