• 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

Novel and common BRCA1 mutations in familial breast/ovarian cancer patients from Lithuania.

作者信息

Janavicius Ramūnas, Pepalyte Ingrida, Kucinskas Vaidutis

机构信息

Hematology, Oncology and Transfusion Medicine Center, Department of Molecular and Regenerative Medicine, Vilnius University Hospital Santariskiu Clinics, Santariskiu 2, Vilnius LT-08661, Lithuania.

出版信息

Breast Cancer Res Treat. 2009 Sep;117(2):467-9. doi: 10.1007/s10549-008-0166-3. Epub 2008 Sep 2.

DOI:10.1007/s10549-008-0166-3
PMID:18763032
Abstract
摘要

相似文献

1
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.
2
The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania.BRCA1 种系突变在立陶宛乳腺癌和卵巢癌发病中的作用。
Clin Genet. 2010 Oct;78(4):373-6. doi: 10.1111/j.1399-0004.2010.01404.x.
3
Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.X染色体失活偏倚与乳腺癌和卵巢癌状态:BRCA1的X连锁修饰因子的证据
J Natl Cancer Inst. 2008 Nov 5;100(21):1519-29. doi: 10.1093/jnci/djn345. Epub 2008 Oct 28.
4
Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families.丹麦高危乳腺癌-卵巢癌家族中BRCA1和BRCA2基因的大片段重排
Breast Cancer Res Treat. 2009 May;115(2):315-23. doi: 10.1007/s10549-008-0088-0. Epub 2008 Jun 12.
5
Prevalence of BRCA1 founder mutations in western Poland.波兰西部BRCA1始祖突变的患病率。
Hum Mutat. 2001;17(1):75. doi: 10.1002/1098-1004(2001)17:1<75::AID-HUMU15>3.0.CO;2-9.
6
A functional polymorphism in the miR-146a gene and age of familial breast/ovarian cancer diagnosis.miR-146a基因中的功能性多态性与家族性乳腺癌/卵巢癌诊断年龄
Carcinogenesis. 2008 Oct;29(10):1963-6. doi: 10.1093/carcin/bgn172. Epub 2008 Jul 27.
7
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.
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
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.
10
A protein truncating BRCA1 allele with a low penetrance of breast cancer.一种具有低乳腺癌发病风险的截短型BRCA1等位基因。
J Med Genet. 2004 Dec;41(12):e130. doi: 10.1136/jmg.2004.019430.

引用本文的文献

1
Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa.北非乳腺癌和卵巢癌中 BRCA 基因的特定和复发/起始致病性变异的流行率。
BMC Cancer. 2022 Feb 25;22(1):208. doi: 10.1186/s12885-022-09181-4.
2
Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control.欧洲发现 BRCA1/2 基因突变:对遗传性乳腺癌-卵巢癌预防和控制的影响。
EPMA J. 2010 Sep;1(3):397-412. doi: 10.1007/s13167-010-0037-y. Epub 2010 Jun 27.
3
On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations.
BRCA1 c.5266dupC(5382insC)在欧洲人群中的起源和扩散。
Eur J Hum Genet. 2011 Mar;19(3):300-6. doi: 10.1038/ejhg.2010.203. Epub 2010 Dec 1.