• 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

Absence of the BRCA1 del (exons 9-12) mutation in breast/ovarian cancer families outside of Mexican Hispanics.

作者信息

Torres Diana, Rashid Muhammad U, Seidel-Renkert Antje, Weitzel Jeffrey N, Briceno Ignacio, Hamann Ute

出版信息

Breast Cancer Res Treat. 2009 Oct;117(3):679-81. doi: 10.1007/s10549-009-0383-4. Epub 2009 Mar 31.

DOI:10.1007/s10549-009-0383-4
PMID:19333752
Abstract
摘要

相似文献

1
Absence of the BRCA1 del (exons 9-12) mutation in breast/ovarian cancer families outside of Mexican Hispanics.墨西哥裔西班牙人以外的乳腺癌/卵巢癌家族中不存在BRCA1 del（外显子9 - 12）突变。
Breast Cancer Res Treat. 2009 Oct;117(3):679-81. doi: 10.1007/s10549-009-0383-4. Epub 2009 Mar 31.
2
High proportion of BRCA1/2 founder mutations in Hispanic breast/ovarian cancer families from Colombia.来自哥伦比亚的西班牙裔乳腺癌/卵巢癌家族中BRCA1/2始祖突变的比例很高。
Breast Cancer Res Treat. 2007 Jun;103(2):225-32. doi: 10.1007/s10549-006-9370-1. Epub 2006 Nov 2.
3
BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland.波兰北部乳腺癌和卵巢癌家族中BRCA1和BRCA2基因的点突变及大片段重排
Oncol Rep. 2008 Jan;19(1):263-8.
4
BRCA1 disease-associated haplotypes in Singapore Malay women with early-onset breast/ovarian cancer.
Breast Cancer Res Treat. 2007 Sep;104(3):351-3. doi: 10.1007/s10549-006-9467-6. Epub 2007 Apr 4.
5
Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network.在美国西南部进行遗传癌症风险评估的西班牙裔人群中 BRCA 突变的流行率和类型：来自临床癌症遗传学社区研究网络的报告。
J Clin Oncol. 2013 Jan 10;31(2):210-6. doi: 10.1200/JCO.2011.41.0027. Epub 2012 Dec 10.
6
Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania.立陶宛家族性乳腺癌/卵巢癌患者中的新型及常见BRCA1突变
Breast Cancer Res Treat. 2009 Sep;117(2):467-9. doi: 10.1007/s10549-008-0166-3. Epub 2008 Sep 2.
7
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast Italy.BRCA1基因第1688位缬氨酸缺失是一种有害突变，在意大利东北部的乳腺癌和卵巢癌家族中反复出现。
J Clin Oncol. 2008 Jan 1;26(1):26-31. doi: 10.1200/JCO.2007.13.2118.
8
Founder effect of the BRCA1 5382insC mutation in Brazilian patients with hereditary breast ovary cancer syndrome.巴西遗传性乳腺癌卵巢癌综合征患者中BRCA1基因5382insC突变的奠基者效应。
Cancer Genet Cytogenet. 2008 Jul;184(1):62-6. doi: 10.1016/j.cancergencyto.2008.03.011.
9
[Hereditary cancer of the breast and ovary].[遗传性乳腺癌和卵巢癌]
Med Clin (Barc). 1998 Feb 14;110(5):199.
10
BRCA1 IVS2-2delA: a deleterious mutation in a family of Asian descent.BRCA1基因内含子2第2位碱基A缺失：一个在亚洲裔家族中的有害突变。
Cancer Genet Cytogenet. 2004 Apr 15;150(2):173-5. doi: 10.1016/j.cancergencyto.2003.08.024.

引用本文的文献

1
Genetic epidemiology of BRCA1- and BRCA2-associated cancer across Latin America.拉丁美洲BRCA1和BRCA2相关癌症的遗传流行病学。
NPJ Breast Cancer. 2021 Aug 19;7(1):107. doi: 10.1038/s41523-021-00317-6.
2
Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients.墨西哥 BRCA1 种系突变：缩短遗传性乳腺癌和卵巢癌患者遗传评估中的差距。
PLoS One. 2019 Sep 23;14(9):e0222709. doi: 10.1371/journal.pone.0222709. eCollection 2019.
3
Pathogenic and likely pathogenic variants in PALB2, CHEK2, and other known breast cancer susceptibility genes among 1054 BRCA-negative Hispanics with breast cancer.
1054 例乳腺癌阴性西班牙裔人群中 PALB2、CHEK2 和其他已知乳腺癌易感基因的致病性和可能致病性变异体。
Cancer. 2019 Aug 15;125(16):2829-2836. doi: 10.1002/cncr.32083. Epub 2019 Jun 17.
4
A novel method to detect the Mexican founder mutation BRCA1 ex9‑12del associated with breast and ovarian cancer using quantitative polymerase chain reaction and TaqMan® probes.一种使用定量聚合酶链反应和 TaqMan®探针检测与乳腺癌和卵巢癌相关的墨西哥种系 BRCA1 ex9-12del 突变的新方法。
Mol Med Rep. 2018 Aug;18(2):1531-1537. doi: 10.3892/mmr.2018.9141. Epub 2018 Jun 6.
5
Prevalence and Penetrance of BRCA1 and BRCA2 Germline Mutations in Colombian Breast Cancer Patients.哥伦比亚乳腺癌患者中 BRCA1 和 BRCA2 种系突变的流行率和外显率。
Sci Rep. 2017 Jul 5;7(1):4713. doi: 10.1038/s41598-017-05056-y.
6
Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.对未确诊的高危乳腺癌和卵巢癌患者进行遗传性癌症易感性的多基因检测。
Breast Cancer Res Treat. 2017 Jun;163(2):383-390. doi: 10.1007/s10549-017-4181-0. Epub 2017 Mar 9.
7
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.拉丁裔人群中的遗传性癌症综合征：基因特征与监测指南
Hered Cancer Clin Pract. 2017 Jan 21;15:3. doi: 10.1186/s13053-017-0063-z. eCollection 2017.
8
Genomic Disparities in Breast Cancer Among Latinas.拉丁裔女性乳腺癌的基因组差异
Cancer Control. 2016 Oct;23(4):359-372. doi: 10.1177/107327481602300407.
9
Recurrent BRCA1 and BRCA2 mutations in Mexican women with breast cancer.患有乳腺癌的墨西哥女性中BRCA1和BRCA2基因的复发性突变
Cancer Epidemiol Biomarkers Prev. 2015 Mar;24(3):498-505. doi: 10.1158/1055-9965.EPI-13-0980. Epub 2014 Nov 4.
10
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Peru.秘鲁未筛选乳腺癌患者中BRCA1和BRCA2基因突变的患病率。
Clin Genet. 2015 Oct;88(4):371-5. doi: 10.1111/cge.12505. Epub 2014 Oct 28.