JP2010507388A5 - - Google Patents

Download PDF

Info

Publication number
JP2010507388A5
JP2010507388A5 JP2009534057A JP2009534057A JP2010507388A5 JP 2010507388 A5 JP2010507388 A5 JP 2010507388A5 JP 2009534057 A JP2009534057 A JP 2009534057A JP 2009534057 A JP2009534057 A JP 2009534057A JP 2010507388 A5 JP2010507388 A5 JP 2010507388A5
Authority
JP
Japan
Prior art keywords
prostate cancer
marker
allele
diagnosed
polymorphic
Prior art date
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.)
Granted
Application number
JP2009534057A
Other languages
English (en)
Japanese (ja)
Other versions
JP5631000B2 (ja
JP2010507388A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/IS2007/000019 external-priority patent/WO2008050356A1/en
Publication of JP2010507388A publication Critical patent/JP2010507388A/ja
Publication of JP2010507388A5 publication Critical patent/JP2010507388A5/ja
Application granted granted Critical
Publication of JP5631000B2 publication Critical patent/JP5631000B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2009534057A 2006-10-27 2007-10-26 Chr8q24.21上の癌感受性変異体 Expired - Fee Related JP5631000B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IS8560 2006-10-27
IS8560 2006-10-27
PCT/IS2007/000019 WO2008050356A1 (en) 2006-10-27 2007-10-26 Cancer susceptibility variants on chr8q24.21

Publications (3)

Publication Number Publication Date
JP2010507388A JP2010507388A (ja) 2010-03-11
JP2010507388A5 true JP2010507388A5 (https=) 2011-01-27
JP5631000B2 JP5631000B2 (ja) 2014-11-26

Family

ID=39060300

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009534057A Expired - Fee Related JP5631000B2 (ja) 2006-10-27 2007-10-26 Chr8q24.21上の癌感受性変異体

Country Status (13)

Country Link
US (1) US20100129799A1 (https=)
EP (1) EP2089548A1 (https=)
JP (1) JP5631000B2 (https=)
CN (1) CN101641451A (https=)
AU (1) AU2007310412B2 (https=)
BR (1) BRPI0718322A2 (https=)
CA (1) CA2667737A1 (https=)
IL (1) IL198305A0 (https=)
MX (1) MX2009004522A (https=)
NZ (1) NZ576591A (https=)
SG (1) SG175680A1 (https=)
WO (1) WO2008050356A1 (https=)
ZA (1) ZA200903173B (https=)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12366585B2 (en) 2006-05-18 2025-07-22 Caris Mpi, Inc. Molecular profiling of tumors
AU2008212117B2 (en) * 2007-02-07 2014-09-11 Decode Genetics Ehf. Genetic variants contributing to risk of prostate cancer
KR20100016525A (ko) 2007-04-17 2010-02-12 산뗀세이야구가부시기가이샤 녹내장 진행 리스크의 판정 방법
US8697360B2 (en) 2007-11-30 2014-04-15 Decode Genetics Ehf. Genetic variants on CHR 11Q and 6Q as markers for prostate and colorectal cancer predisposition
WO2009085196A1 (en) * 2007-12-21 2009-07-09 Wake Forest University Health Sciences Methods and compositions for correlating genetic markers with prostate cancer risk
US8951735B2 (en) * 2008-07-07 2015-02-10 Decode Genetics Ehf. Genetic variants for breast cancer risk assessment
WO2010028288A2 (en) 2008-09-05 2010-03-11 Aueon, Inc. Methods for stratifying and annotating cancer drug treatment options
WO2010045318A2 (en) * 2008-10-14 2010-04-22 Caris Mpi, Inc. Gene and gene expressed protein targets depicting biomarker patterns and signature sets by tumor type
EP2451975A4 (en) * 2009-05-08 2013-08-14 Decode Genetics Ehf GENETIC VARIANTS CONTRIBUTING TO A RISK OF PROSTATE CANCER
WO2011004404A1 (en) * 2009-07-10 2011-01-13 Decode Genetics Ehf Genetic variants for predicting risk of glaucoma
US20120316218A1 (en) * 2009-07-17 2012-12-13 Glinsky Gennadi V SMALL NON-CODING REGULARTORY RNA's and METHODS FOR THEIR USE
WO2011009089A1 (en) * 2009-07-17 2011-01-20 Ordway Research Institute, Inc. SMALL NON-CODING REGULATORY RNAs AND METHODS FOR THEIR USE
KR101918004B1 (ko) 2009-10-26 2018-11-13 애보트 모레큘러 인크. 비-소세포 폐암의 예후를 측정하기 위한 진단 방법
TW201120449A (en) 2009-10-26 2011-06-16 Abbott Lab Diagnostic methods for determining prognosis of non-small-cell lung cancer
WO2012029080A1 (en) * 2010-08-30 2012-03-08 Decode Genetics Ehf Sequence variants associated with prostate specific antigen levels
US9732389B2 (en) 2010-09-03 2017-08-15 Wake Forest University Health Sciences Methods and compositions for correlating genetic markers with prostate cancer risk
EP2619329B1 (en) 2010-09-24 2019-05-22 The Board of Trustees of The Leland Stanford Junior University Direct capture, amplification and sequencing of target dna using immobilized primers
US9534256B2 (en) 2011-01-06 2017-01-03 Wake Forest University Health Sciences Methods and compositions for correlating genetic markers with risk of aggressive prostate cancer
AU2012214312A1 (en) * 2011-02-09 2013-08-22 Bio-Rad Laboratories, Inc. Analysis of nucleic acids
CN102304567B (zh) * 2011-04-29 2013-03-27 广州益善生物技术有限公司 一种染色体8q24区段多态性检测特异性引物和液相芯片
US10233502B2 (en) 2011-06-22 2019-03-19 Indiana University Research And Technology Corporation Compositions for and methods of detecting, diagnosing, and prognosing thymic cancer
WO2013065072A1 (en) * 2011-10-30 2013-05-10 Decode Genetics Ehf Risk variants of prostate cancer
CN105555972B (zh) 2013-07-25 2020-07-31 伯乐生命医学产品有限公司 遗传测定
CN108292326B (zh) * 2015-08-27 2022-04-01 皇家飞利浦有限公司 用于识别功能性患者特异性体细胞畸变的整合方法和系统
WO2017164699A1 (ko) * 2016-03-24 2017-09-28 서울대학교병원 (분사무소) 전립선암과 관련된 단일염기다형성 및 이를 이용한 유전 위험도 점수의 개발
KR101944927B1 (ko) 2016-03-24 2019-02-07 서울대학교산학협력단 전립선암과 관련된 단일염기다형성 및 이를 이용한 유전 위험도 점수의 개발
CN106480211A (zh) * 2016-11-24 2017-03-08 深圳市核子基因科技有限公司 一种用于检测睾丸癌易感性的试剂盒及其snp标志物
JP7138112B2 (ja) * 2017-02-01 2022-09-15 ファディア・アクチボラゲット 特定の特徴を有する個体において前立腺癌の存在または不存在を示すための方法
JPWO2020111169A1 (ja) * 2018-11-28 2021-11-04 国立大学法人千葉大学 多因子遺伝疾患の遺伝子検査法、及び検査キット
EP3963092A1 (en) * 2019-05-02 2022-03-09 Predictive Technology Group, Inc. Somatic cancer driver mutations in endometriosis lesions contribute to secondary cancer risk
US20230119558A1 (en) * 2020-03-06 2023-04-20 The Henry M. Jackson Foundation For The Advancement Of Military Medicine, Inc. Dna damage repair genes in cancer
KR102177222B1 (ko) * 2020-04-24 2020-11-10 유니젠바이오 주식회사 머신러닝 기반 암진단 예측 시스템
KR102177218B1 (ko) * 2020-04-24 2020-11-10 유니젠바이오 주식회사 머신러닝 기반 암진단 예측 장치
KR20250074712A (ko) 2023-11-15 2025-05-28 주식회사 바스젠바이오 전립선암 발병의 위험도를 예측하기 위한 조성물 및 이를 이용한 방법

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5384261A (en) * 1991-11-22 1995-01-24 Affymax Technologies N.V. Very large scale immobilized polymer synthesis using mechanically directed flow paths
AU785425B2 (en) * 2001-03-30 2007-05-17 Genetic Technologies Limited Methods of genomic analysis
WO2003014143A2 (en) * 2001-08-04 2003-02-20 Whitehead Institute For Biomedical Research Haplotype map of the human genome and uses therefor
US20040023237A1 (en) * 2001-11-26 2004-02-05 Perelegen Sciences Inc. Methods for genomic analysis
US20040146870A1 (en) * 2003-01-27 2004-07-29 Guochun Liao Systems and methods for predicting specific genetic loci that affect phenotypic traits

Similar Documents

Publication Publication Date Title
JP2010507388A5 (https=)
JP2011530306A5 (https=)
JP2010527603A5 (https=)
JP2010520745A5 (https=)
Zhang et al. Comprehensive one-step molecular analyses of mitochondrial genome by massively parallel sequencing
Coulombe-Huntington et al. Fine-scale variation and genetic determinants of alternative splicing across individuals
JP2010533477A5 (https=)
JP2010522555A5 (https=)
JP2010518848A5 (https=)
JP2008546403A5 (https=)
CA2511042A1 (en) Association of single nucleotide polymorphisms in ppar.gamma. with osteoporosis
JP2011520433A5 (https=)
EP3332031B1 (en) Snp rs12603226 as a predictive marker for nafld
JP2010510804A5 (https=)
JP2013544536A5 (https=)
TW202438680A (zh) 可實施2種以上檢測的遺傳學分析方法
JP5807894B2 (ja) 一塩基多型に基づく前立腺癌の検査方法
KR101536213B1 (ko) 복부비만 예측용 snp 마커 및 이의 용도
JP5721150B2 (ja) 加齢黄斑変性症の発症リスクの予測方法
KR101532308B1 (ko) 복부비만 예측용 snp 마커 및 이의 용도
CN109182490B (zh) Lrsam1基因snp突变位点分型引物及其在冠心病预测中的应用
US20160053333A1 (en) Novel Haplotype Tagging Single Nucleotide Polymorphisms and Use of Same to Predict Childhood Lymphoblastic Leukemia
KR102346185B1 (ko) 피부 색소 침착 위험도 예측용 바이오마커 및 이의 용도
JP2008505060A5 (https=)
KR102883401B1 (ko) 우울증 진단용 단일염기다형성 및 이의 용도