• 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

Screening for genomic rearrangements at BRCA1 locus in Iranian women with breast cancer using multiplex ligation-dependent probe amplification.

作者信息

Yassaee Vahid R, Emamalizadeh Babak, Omrani Mir Davood

机构信息

Genomic Research Center, Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

J Genet. 2013 Apr;92(1):131-4. doi: 10.1007/s12041-013-0223-5.

DOI:10.1007/s12041-013-0223-5
PMID:23640417
Abstract
摘要

相似文献

1
Screening for genomic rearrangements at BRCA1 locus in Iranian women with breast cancer using multiplex ligation-dependent probe amplification.利用多重连接依赖探针扩增技术对伊朗乳腺癌女性患者BRCA1基因座的基因组重排进行筛查。
J Genet. 2013 Apr;92(1):131-4. doi: 10.1007/s12041-013-0223-5.
2
Identification of a novel BRCA1 large genomic rearrangement in a Spanish breast/ovarian cancer family.在一个西班牙乳腺癌/卵巢癌家族中鉴定出一种新型BRCA1大基因组重排。
Breast Cancer Res Treat. 2008 Nov;112(1):63-7. doi: 10.1007/s10549-007-9839-6. Epub 2007 Dec 1.
3
Multiplex ddPCR assay for screening copy number variations in BRCA1 gene.多重数字 PCR 检测法用于筛查 BRCA1 基因的拷贝数变异。
Breast Cancer Res Treat. 2019 Dec;178(3):545-555. doi: 10.1007/s10549-019-05425-3. Epub 2019 Sep 3.
4
Screening for genomic rearrangements in BRCA1 and BRCA2 genes in Czech high-risk breast/ovarian cancer patients: high proportion of population specific alterations in BRCA1 gene.在捷克高危乳腺癌/卵巢癌患者的 BRCA1 和 BRCA2 基因中筛查基因组重排：BRCA1 基因中存在高比例的群体特异性改变。
Breast Cancer Res Treat. 2010 Nov;124(2):337-47. doi: 10.1007/s10549-010-0745-y. Epub 2010 Feb 5.
5
Identification of novel large genomic rearrangements at the BRCA1 locus in Malaysian women with breast cancer.鉴定马来西亚乳腺癌妇女中 BRCA1 基因座的新型大片段基因组重排。
Cancer Epidemiol. 2010 Aug;34(4):442-7. doi: 10.1016/j.canep.2010.04.010. Epub 2010 May 6.
6
Genomic large rearrangement screening of BRCA1 and BRCA2 genes in high-risk Turkish breast/ovarian cancer patients by using multiplex ligation-dependent probe amplification assay.采用多重连接依赖探针扩增检测法对高危土耳其乳腺癌/卵巢癌患者的 BRCA1 和 BRCA2 基因进行基因组大片段重排筛查。
Cancer Invest. 2011 Jan;29(1):73-7. doi: 10.3109/07357907.2010.512599. Epub 2010 Oct 5.
7
Evaluation of BRCA1 Large Genomic Rearrangements in Group of Egyptian Female Breast Cancer Patients Using MLPA.使用多重连接探针扩增技术评估埃及女性乳腺癌患者群体中BRCA1基因的大片段基因组重排
Gulf J Oncolog. 2017 Sep;1(25):64-69.
8
Prevalence of BRCA1 and BRCA2 large genomic rearrangements in Tunisian high risk breast/ovarian cancer families: Implications for genetic testing.突尼斯高危乳腺癌/卵巢癌家族中BRCA1和BRCA2大基因组重排的患病率：对基因检测的影响。
Cancer Genet. 2017 Jan;210:22-27. doi: 10.1016/j.cancergen.2016.11.002. Epub 2016 Nov 18.
9
Detection of large genomic rearrangements in breast and ovarian cancer patients: an overview of the current methods.检测乳腺癌和卵巢癌患者的大片段基因组重排：当前方法概述。
Expert Rev Mol Diagn. 2019 Sep;19(9):795-802. doi: 10.1080/14737159.2019.1657011. Epub 2019 Aug 28.
10
Complex Characterization of Germline Large Genomic Rearrangements of the and Genes in High-Risk Breast Cancer Patients-Novel Variants from a Large National Center.高危乳腺癌患者中 和 基因种系大片段基因组重排的复杂特征——来自大型国家中心的新变异。
Int J Mol Sci. 2020 Jun 30;21(13):4650. doi: 10.3390/ijms21134650.

引用本文的文献

1
The neuroscience in breast cancer: Current insights and clinical opportunities.乳腺癌中的神经科学：当前见解与临床机遇
Heliyon. 2025 Jan 27;11(3):e42293. doi: 10.1016/j.heliyon.2025.e42293. eCollection 2025 Feb 15.
2
Male Breast Cancer: Results of the Application of Multigene Panel Testing to an Italian Cohort of Patients.男性乳腺癌：多基因检测在意大利患者队列中的应用结果
Diagnostics (Basel). 2020 Apr 30;10(5):269. doi: 10.3390/diagnostics10050269.

本文引用的文献

1
Genomic rearrangements in BRCA1 and BRCA2: A literature review.BRCA1 和 BRCA2 中的基因组重排：文献综述。
Genet Mol Biol. 2009 Jul;32(3):437-46. doi: 10.1590/S1415-47572009005000049. Epub 2009 Sep 1.
2
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.PALB2编码一种与BRCA2相互作用的蛋白质，是一种乳腺癌易感基因。
Nat Genet. 2007 Feb;39(2):165-7. doi: 10.1038/ng1959. Epub 2006 Dec 31.
3
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.
范可尼贫血J基因BRIP1中的截短突变是低外显率的乳腺癌易感等位基因。
Nat Genet. 2006 Nov;38(11):1239-41. doi: 10.1038/ng1902. Epub 2006 Oct 8.
4
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.导致共济失调毛细血管扩张症的ATM突变是乳腺癌易感等位基因。
Nat Genet. 2006 Aug;38(8):873-5. doi: 10.1038/ng1837. Epub 2006 Jul 9.
5
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.乳腺癌高危家族中BRCA1、BRCA2、CHEK2和TP53的突变谱。
JAMA. 2006 Mar 22;295(12):1379-88. doi: 10.1001/jama.295.12.1379.
6
Genomic rearrangements in the BRCA1 and BRCA2 genes.BRCA1和BRCA2基因中的基因组重排。
Hum Mutat. 2005 May;25(5):415-22. doi: 10.1002/humu.20169.
7
Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.在3%的德国高危乳腺癌家族中发现了大面积的BRCA1基因缺失。
Hum Mutat. 2004 Dec;24(6):534. doi: 10.1002/humu.9291.
8
Dosage analysis of cancer predisposition genes by multiplex ligation-dependent probe amplification.通过多重连接依赖探针扩增技术对癌症易感基因进行剂量分析。
Br J Cancer. 2004 Sep 13;91(6):1155-9. doi: 10.1038/sj.bjc.6602121.
9
CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.CHEK2基因1100位密码子C缺失与乳腺癌易感性：一项涉及来自10项研究的10860例乳腺癌病例和9065例对照的协作分析。
Am J Hum Genet. 2004 Jun;74(6):1175-82. doi: 10.1086/421251. Epub 2004 Apr 30.
10
Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi-quantitative multiplex PCR method.使用半定量多重聚合酶链反应方法对德国乳腺癌或卵巢癌家族中的BRCA1基因大重排进行筛查。
Hum Mutat. 2003 Jul;22(1):103-4. doi: 10.1002/humu.9154.