JP2010527603A5 - - Google Patents

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Publication number
JP2010527603A5
JP2010527603A5 JP2010508970A JP2010508970A JP2010527603A5 JP 2010527603 A5 JP2010527603 A5 JP 2010527603A5 JP 2010508970 A JP2010508970 A JP 2010508970A JP 2010508970 A JP2010508970 A JP 2010508970A JP 2010527603 A5 JP2010527603 A5 JP 2010527603A5
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JP
Japan
Prior art keywords
breast cancer
individual
allele
seq
marker
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2010508970A
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English (en)
Japanese (ja)
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JP2010527603A (ja
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Priority claimed from PCT/IS2008/000012 external-priority patent/WO2008146309A2/en
Publication of JP2010527603A publication Critical patent/JP2010527603A/ja
Publication of JP2010527603A5 publication Critical patent/JP2010527603A5/ja
Pending legal-status Critical Current

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JP2010508970A 2007-05-25 2008-05-21 乳癌のリスクアセスメント、診断、予後診断および治療における使用のためのマーカーとしてのCHR5p12および10q26上の遺伝的変異 Pending JP2010527603A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IS8647 2007-05-25
IS8700 2007-12-21
PCT/IS2008/000012 WO2008146309A2 (en) 2007-05-25 2008-05-21 Genetic variants on chr 5pl2 and 10q26 as markers for use in breast cancer risk assessment, diagnosis, prognosis and treatment

Publications (2)

Publication Number Publication Date
JP2010527603A JP2010527603A (ja) 2010-08-19
JP2010527603A5 true JP2010527603A5 (enExample) 2011-07-07

Family

ID=39661451

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010508970A Pending JP2010527603A (ja) 2007-05-25 2008-05-21 乳癌のリスクアセスメント、診断、予後診断および治療における使用のためのマーカーとしてのCHR5p12および10q26上の遺伝的変異

Country Status (12)

Country Link
US (2) US8580501B2 (enExample)
EP (2) EP2535425A1 (enExample)
JP (1) JP2010527603A (enExample)
KR (1) KR20100017865A (enExample)
CN (1) CN101772578A (enExample)
AU (1) AU2008256219B2 (enExample)
CA (1) CA2688312A1 (enExample)
EA (1) EA018444B1 (enExample)
IL (1) IL202292A0 (enExample)
MX (1) MX2009012722A (enExample)
NZ (1) NZ581858A (enExample)
WO (1) WO2008146309A2 (enExample)

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CN102144036B (zh) 2008-07-07 2014-07-16 解码遗传学私营有限责任公司 用于乳腺癌风险评估的遗传变型
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US11261494B2 (en) 2012-06-21 2022-03-01 The Chinese University Of Hong Kong Method of measuring a fractional concentration of tumor DNA
WO2014160876A2 (en) * 2013-03-27 2014-10-02 Memorial Sloan-Kettering Cancer Center Brca2-specific modifier locus related to breast cancer risk
KR101748867B1 (ko) * 2013-04-19 2017-06-20 주식회사 젠큐릭스 조기 유방암 예후 예측 진단용 자동화 시스템
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CN103966310A (zh) * 2014-01-27 2014-08-06 广州市体育科学研究所 乳腺癌易感基因快速检测试剂盒及检测方法
CN104232774A (zh) * 2014-09-17 2014-12-24 湖北维达健基因技术有限公司 用于检测乳腺癌易感基因snp的引物、荧光探针及应用
EP3201360A4 (en) 2014-09-30 2018-05-09 Genetic Technologies Limited Methods for assessing risk of developing breast cancer
CN107250356A (zh) * 2014-12-16 2017-10-13 加文医学研究所 测序对照
ES2908347T3 (es) 2015-02-10 2022-04-28 Univ Hong Kong Chinese Detección de mutaciones para cribado de cáncer y análisis fetal
CN106295241A (zh) * 2015-06-25 2017-01-04 杭州圣庭生物技术有限公司 基于brca1和brca2突变的乳腺癌患病风险评估算法
EP4279612B1 (en) 2015-07-23 2025-07-02 The Chinese University of Hong Kong Analysis of fragmentation patterns of cell-free dna
CN105586427B (zh) * 2016-03-10 2020-06-19 厦门艾德生物医药科技股份有限公司 检测人类brca1和brca2基因突变的引物、试剂盒及方法
CN107723350A (zh) * 2016-08-12 2018-02-23 嘉兴允英医学检验有限公司 一种遗传性乳腺癌突变基因高通量筛查方法
AU2018212272B2 (en) 2017-01-25 2022-04-28 Grail, Inc. Diagnostic applications using nucleic acid fragments
CN111051536A (zh) 2017-07-26 2020-04-21 香港中文大学 利用不含细胞的病毒核酸改善癌症筛选
CN107254545B (zh) * 2017-08-16 2020-09-15 复旦大学附属华山医院北院 一种与乳腺癌化疗毒性相关的snp标志物及其应用
CN107254546B (zh) * 2017-08-16 2020-11-03 复旦大学附属华山医院 一种与乳腺癌新辅助化疗疗效相关的snp标志物及其应用
CN107729241B (zh) * 2017-10-12 2020-11-03 中国矿业大学 一种基于变异体分组的软件变异测试数据进化生成方法
KR101985864B1 (ko) * 2017-12-28 2019-06-05 주식회사 엔젠바이오 유방암 및 난소암 등 암 진단용 조성물 및 이의 용도
CN109913550A (zh) * 2019-03-21 2019-06-21 吉林省银丰生物工程技术有限公司 乳腺癌新辅助化疗效果预测基因试剂盒
RU2702755C1 (ru) * 2019-06-24 2019-10-11 Федеральное государственное бюджетное научное учреждение "Федеральный исследовательский центр фундаментальной и трансляционной медицины" (ФИЦ ФТМ) Способ молекулярно-генетической диагностики наследственных форм рака молочной железы
CN110358834B (zh) * 2019-07-12 2023-05-16 深圳大学 一种lncRNA的应用以及试剂盒和药物
CN112837749B (zh) * 2021-02-01 2021-11-26 北京百奥纳芯生物科技有限公司 一种癌症筛查用基因芯片探针的优选方法

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CN101772578A (zh) * 2007-05-25 2010-07-07 解码遗传学私营有限责任公司 作为标记物用在乳腺癌风险评估、诊断、预后和治疗中的在CHR 5p12和10q26上的遗传变异体

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