• 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

Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?

作者信息

Fonatsch C, Haase D, Freund M, Bartels H, Tesch H

机构信息

Institut für Humangenetik, Medizinische Universität zu Lübeck, Germany.

出版信息

Cancer Genet Cytogenet. 1991 Oct 15;56(2):243-53. doi: 10.1016/0165-4608(91)90177-v.

DOI:10.1016/0165-4608(91)90177-v
PMID:1756470
Abstract

Cytogenetic and clinical data of 11 patients with de novo myelodysplastic syndromes and partial or total trisomy of the long arm of chromosome 1 are presented. In eight of these patients trisomy 1q was the sole karyotypic change and therefore can be classified as a primary chromosome anomaly. A remarkably young median age of 36.5 years was noticed in this patient group.

摘要

相似文献

1
Partial trisomy 1q. A nonrandom primary chromosomal abnormality in myelodysplastic syndromes?
Cancer Genet Cytogenet. 1991 Oct 15;56(2):243-53. doi: 10.1016/0165-4608(91)90177-v.
2
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes.112例未经治疗的骨髓增生异常综合征的细胞遗传学研究。
Cancer Genet Cytogenet. 1992 Nov;64(1):12-20. doi: 10.1016/0165-4608(92)90315-y.
3
Duplication of 1q in a child with down syndrome and myelodysplastic syndrome.
Cancer Genet Cytogenet. 2000 May;119(1):74-6. doi: 10.1016/s0165-4608(99)00209-5.
4
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.8号染色体三体作为髓细胞性恶性肿瘤中的唯一染色体畸变:一项多色和位点特异性荧光原位杂交研究
Cancer Genet Cytogenet. 2003 Jan 1;140(1):66-9. doi: 10.1016/s0165-4608(02)00628-3.
5
Results of chromosome studies and their relation to morphology, course, and prognosis in 120 patients with de novo myelodysplastic syndrome.120例初发性骨髓增生异常综合征患者的染色体研究结果及其与形态学、病程和预后的关系。
Cancer Genet Cytogenet. 1990 Jan;44(1):15-26. doi: 10.1016/0165-4608(90)90193-e.
6
Trisomy 13 and myelodysplastic syndrome.
Cancer Genet Cytogenet. 1990 Sep;48(2):179-82. doi: 10.1016/0165-4608(90)90117-s.
7
[Clinical and cytogenetic study of chromosome 1 abnormality in myelodysplastic syndrome].骨髓增生异常综合征中1号染色体异常的临床与细胞遗传学研究
Zhonghua Xue Ye Xue Za Zhi. 2015 Oct;36(10):818-23. doi: 10.3760/cma.j.issn.0253-2727.2015.10.003.
8
A der(14)t(1;14)(q12;p11) in chronic myelomonocytic leukemia.慢性粒单核细胞白血病中的14号衍生染色体,t(1;14)(q12;p11)
Cancer Genet Cytogenet. 2005 Jul 1;160(1):89-93. doi: 10.1016/j.cancergencyto.2004.12.009.
9
dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.dup(1)(q21q32)作为唯一的细胞遗传学事件与骨髓增生异常综合征的白血病转化相关。
Leuk Res. 2008 Jan;32(1):159-61. doi: 10.1016/j.leukres.2007.03.033. Epub 2007 May 16.
10
Is trisomy 11 another nonrandom chromosomal anomaly in acute nonlymphocytic leukemia and myelodysplastic syndromes?11三体是急性非淋巴细胞白血病和骨髓增生异常综合征中另一种非随机染色体异常吗?
Cancer Genet Cytogenet. 1988 Oct 15;35(2):205-11. doi: 10.1016/0165-4608(88)90242-7.

引用本文的文献

1
Rare cytogenetic abnormalities in myelodysplastic syndromes.骨髓增生异常综合征中的罕见细胞遗传学异常
Mediterr J Hematol Infect Dis. 2015 May 1;7(1):e2015034. doi: 10.4084/MJHID.2015.034. eCollection 2015.
2
Protein tyrosine phosphatases: structure, function, and implication in human disease.蛋白质酪氨酸磷酸酶:结构、功能及在人类疾病中的意义。
Methods Mol Biol. 2013;1053:179-221. doi: 10.1007/978-1-62703-562-0_13.
3
Inhibition of hematopoietic protein tyrosine phosphatase augments and prolongs ERK1/2 and p38 activation.抑制造血蛋白酪氨酸磷酸酶可增强和延长 ERK1/2 和 p38 的激活。
ACS Chem Biol. 2012 Feb 17;7(2):367-77. doi: 10.1021/cb2004274. Epub 2011 Nov 17.
4
Inhibition of the Hematopoietic Protein Tyrosine Phosphatase by Phenoxyacetic Acids.苯氧乙酸对造血蛋白酪氨酸磷酸酶的抑制作用。
ACS Med Chem Lett. 2011 Feb;2(2):113-118. doi: 10.1021/ml100103p.
5
Cytogenetic findings in 179 patients with myelodysplastic syndromes.179例骨髓增生异常综合征患者的细胞遗传学研究结果。
Ann Hematol. 1995 Apr;70(4):171-87. doi: 10.1007/BF01700373.