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CHEK2*1100delC and male breast cancer risk in Israel.

作者信息

Ohayon Tal, Gal Inbar, Baruch Ruth Gershoni, Szabo Csilla, Friedman Eitan

出版信息

Int J Cancer. 2004 Jan 20;108(3):479-80. doi: 10.1002/ijc.11603.

DOI:10.1002/ijc.11603
PMID:14648719
Abstract
摘要

相似文献

1
CHEK2*1100delC and male breast cancer risk in Israel.以色列CHEK2*1100delC与男性乳腺癌风险
Int J Cancer. 2004 Jan 20;108(3):479-80. doi: 10.1002/ijc.11603.
2
Role of CHEK2*1100delC in unselected series of non-BRCA1/2 male breast cancers.CHEK2*1100delC在未经选择的非BRCA1/2男性乳腺癌系列中的作用。
Int J Cancer. 2004 Jan 20;108(3):477-8. doi: 10.1002/ijc.11385.
3
CHEK2 1100delC is not a risk factor for male breast cancer population.CHEK2基因1100delC不是男性乳腺癌人群的风险因素。
Int J Cancer. 2004 Jan 20;108(3):475-6. doi: 10.1002/ijc.11384.
4
BRCA1/BRCA2 rearrangements and CHEK2 common mutations are infrequent in Italian male breast cancer cases.在意大利男性乳腺癌病例中,BRCA1/BRCA2重排和CHEK2常见突变并不常见。
Breast Cancer Res Treat. 2008 Jul;110(1):161-7. doi: 10.1007/s10549-007-9689-2. Epub 2007 Jul 28.
5
CHEK2 1100delC and male breast cancer in the Netherlands.荷兰的 CHEK2 1100delC 与男性乳腺癌
Breast Cancer Res Treat. 2009 Jul;116(2):397-400. doi: 10.1007/s10549-008-0162-7. Epub 2008 Aug 31.
6
CHEK2:1100delC and female breast cancer in the United States.CHEK2基因1100delC与美国女性乳腺癌
Int J Cancer. 2004 Nov 10;112(3):541-3. doi: 10.1002/ijc.20439.
7
The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families.CHEK2*1100delC变异体在非BRCA1/BRCA2多病例家族中作为乳腺癌风险修饰因子发挥作用。
Cancer Res. 2003 Dec 1;63(23):8153-7.
8
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations.在 BRCA1 或 BRCA2 基因无突变的个体中,CHEK2(*)1100delC 导致的乳腺癌低外显率易感性。
Nat Genet. 2002 May;31(1):55-9. doi: 10.1038/ng879. Epub 2002 Apr 22.
9
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.多基因检测队列中的男性乳腺癌:见解与意外结果
Breast Cancer Res Treat. 2017 Feb;161(3):575-586. doi: 10.1007/s10549-016-4085-4. Epub 2016 Dec 22.
10
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.CHEK2 c.1100delC 突变与芬兰患者群体中男性乳腺癌风险增加相关。
BMC Cancer. 2017 Sep 5;17(1):620. doi: 10.1186/s12885-017-3631-8.

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1
Gender-Specific Genetic Predisposition to Breast Cancer: Genes and Beyond.乳腺癌的性别特异性遗传易感性:基因及其他因素
Cancers (Basel). 2024 Jan 30;16(3):579. doi: 10.3390/cancers16030579.
2
Genetic predisposition to male breast cancer in Poland.波兰男性乳腺癌的遗传易感性。
BMC Cancer. 2021 Aug 30;21(1):975. doi: 10.1186/s12885-021-08718-3.
3
Genetic Landscape of Male Breast Cancer.男性乳腺癌的基因图谱
Cancers (Basel). 2021 Jul 15;13(14):3535. doi: 10.3390/cancers13143535.
4
Association Between CHEK2*1100delC and Breast Cancer: A Systematic Review and Meta-Analysis.CHEK2*1100delC 与乳腺癌的关联:系统评价和荟萃分析。
Mol Diagn Ther. 2018 Aug;22(4):397-407. doi: 10.1007/s40291-018-0344-x.
5
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population.CHEK2 c.1100delC 突变与芬兰患者群体中男性乳腺癌风险增加相关。
BMC Cancer. 2017 Sep 5;17(1):620. doi: 10.1186/s12885-017-3631-8.
6
Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.多基因检测队列中的男性乳腺癌:见解与意外结果
Breast Cancer Res Treat. 2017 Feb;161(3):575-586. doi: 10.1007/s10549-016-4085-4. Epub 2016 Dec 22.
7
BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review.与男性乳腺癌相关的BRCA1基因变体p.P142H:一项两代系谱研究及文献综述
Fam Cancer. 2015 Dec;14(4):515-9. doi: 10.1007/s10689-015-9819-7.
8
Inherited and acquired alterations in development of breast cancer.乳腺癌发生过程中的遗传和后天改变。
Appl Clin Genet. 2011 Nov 14;4:145-58. doi: 10.2147/TACG.S13226. Print 2011.
9
Strictly defined familial male breast cancer.严格定义的家族性男性乳腺癌。
Fam Cancer. 2011 Mar;10(1):73-7. doi: 10.1007/s10689-010-9400-3.
10
Male Breast Cancer.男性乳腺癌
Breast Care (Basel). 2008;3(3):183-189. doi: 10.1159/000136825. Epub 2008 Jun 24.