携带BRCA1基因突变的三阴性乳腺癌患者的发病率：常见阿什肯纳兹犹太突变与其他突变的比较。 - Suppr

Suppr

超能文献

Frequency of triple-negative breast cancer in BRCA1 mutation carriers: comparison between common Ashkenazi Jewish and other mutations.

作者信息

Tung Nadine, Garber Judy E, Lincoln Anne, Domchek Susan M

出版信息

J Clin Oncol. 2012 Dec 10;30(35):4447-8. doi: 10.1200/JCO.2012.44.5635. Epub 2012 Oct 22.

DOI:10.1200/JCO.2012.44.5635

PMID:23091104

Abstract

摘要

相似文献

Frequency of triple-negative breast cancer in BRCA1 mutation carriers: comparison between common Ashkenazi Jewish and other mutations.携带BRCA1基因突变的三阴性乳腺癌患者的发病率：常见阿什肯纳兹犹太突变与其他突变的比较。

J Clin Oncol. 2012 Dec 10;30(35):4447-8. doi: 10.1200/JCO.2012.44.5635. Epub 2012 Oct 22.

Germ-line BRCA1 mutation is an adverse prognostic factor in Ashkenazi Jewish women with breast cancer.种系BRCA1突变是患乳腺癌的阿什肯纳兹犹太妇女的不良预后因素。

Clin Cancer Res. 1997 Dec;3(12 Pt 1):2465-9.

Germline BRCA1-2 mutations in non-Ashkenazi families with double primary breast and ovarian cancer.非阿什肯纳兹族双原发性乳腺癌和卵巢癌家族中的种系BRCA1-2突变

Gynecol Oncol. 2001 Nov;83(2):383-7. doi: 10.1006/gyno.2001.6431.

Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.阿什肯纳兹犹太人群中BRCA1和BRCA2突变与范可尼贫血和布卢姆综合征突变的共遗传：对癌症发生风险修正的可能作用。

Am J Hematol. 2005 Mar;78(3):203-6. doi: 10.1002/ajh.20310.

Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer.BRCA1和BRCA2对早发性乳腺癌的不同贡献。

N Engl J Med. 1997 May 15;336(20):1416-21. doi: 10.1056/NEJM199705153362003.

HER-2/neu status and tumor morphology of invasive breast carcinomas in Ashkenazi women with known BRCA1 mutation status in the Ontario Familial Breast Cancer Registry.安大略省家族性乳腺癌登记处中已知BRCA1突变状态的德系犹太妇女浸润性乳腺癌的HER-2/neu状态和肿瘤形态。

Cancer. 2002 Nov 15;95(10):2068-75. doi: 10.1002/cncr.10949.

Recurrent germline mutations in BRCA1 and BRCA2 genes in high risk families in Israel.以色列高危家族中 BRCA1 和 BRCA2 基因的种系突变复发。

Breast Cancer Res Treat. 2012 Jun;133(3):1153-7. doi: 10.1007/s10549-012-2006-8. Epub 2012 Mar 8.

Prevalence of BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and pancreatic cancer.BRCA1 和 BRCA2 突变在具有乳腺癌和胰腺癌的阿什肯纳兹犹太家族中的流行率。

Cancer. 2012 Jan 15;118(2):493-9. doi: 10.1002/cncr.26191. Epub 2011 May 19.

Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from India.印度乳腺癌患者中乳腺癌易感基因BRCA1、BRCA2和p53基因的新型种系突变。

Breast Cancer Res Treat. 2004 Nov;88(2):177-86. doi: 10.1007/s10549-004-0593-8.

Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer.犹太和非犹太早发性乳腺癌女性中的种系BRCA1突变

N Engl J Med. 1996 Jan 18;334(3):143-9. doi: 10.1056/NEJM199601183340302.

引用本文的文献

Randomized phase II comparison of single-agent carboplatin versus combination of carboplatin and everolimus for advanced triple negative breast cancer.单药卡铂与卡铂联合依维莫司治疗晚期三阴性乳腺癌的随机II期比较

Breast Cancer Res Treat. 2025 Aug 16. doi: 10.1007/s10549-025-07802-7.

Economic Evaluation of Population-Based Mutation Testing across Multiple Countries and Health Systems.多个国家和卫生系统基于人群的突变检测的经济评估。

Cancers (Basel). 2020 Jul 17;12(7):1929. doi: 10.3390/cancers12071929.

Microfluidics: Rapid Diagnosis for Breast Cancer.微流控技术：乳腺癌的快速诊断

Nanomicro Lett. 2016;8(3):204-220. doi: 10.1007/s40820-015-0079-8. Epub 2016 Jan 8.

The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.乳腺癌易感基因中的致病变异对家族性乳腺癌风险的影响。

NPJ Breast Cancer. 2017 Jun 9;3:22. doi: 10.1038/s41523-017-0024-8. eCollection 2017.

Cost-effectiveness of population screening for BRCA mutations in Ashkenazi jewish women compared with family history-based testing.与基于家族史检测相比，对阿什肯纳兹犹太妇女进行BRCA突变群体筛查的成本效益。

J Natl Cancer Inst. 2014 Nov 30;107(1):380. doi: 10.1093/jnci/dju380. Print 2015 Jan.

Phase 2 trial of everolimus and carboplatin combination in patients with triple negative metastatic breast cancer.厄洛替尼联合卡铂治疗三阴性转移性乳腺癌的Ⅱ期临床试验。

Breast Cancer Res. 2014 Mar 31;16(2):R32. doi: 10.1186/bcr3634.

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