WO2019153241A1 - Loci de polymorphisme mononucléotidique associés à des événements cardiovasculaires indésirables majeurs et application de ceux-ci - Google Patents
Loci de polymorphisme mononucléotidique associés à des événements cardiovasculaires indésirables majeurs et application de ceux-ci Download PDFInfo
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- WO2019153241A1 WO2019153241A1 PCT/CN2018/075986 CN2018075986W WO2019153241A1 WO 2019153241 A1 WO2019153241 A1 WO 2019153241A1 CN 2018075986 W CN2018075986 W CN 2018075986W WO 2019153241 A1 WO2019153241 A1 WO 2019153241A1
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- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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Abstract
La présente invention concerne 17 loci de polymorphisme mononucléotidique (SNP) associés à des événements cardiovasculaires indésirables majeurs (MACE) et une application de ceux-ci. Les 17 loci de SNP fournis par la présente invention sont obtenus sur la base de visites de suivi à grande échelle et d'analyse de données sur des patients souffrant d'une coronaropathie, et peuvent être utilisés en tant que marqueurs pour prédire l'apparition d'événements cardiovasculaires indésirables majeurs. De plus, la présente invention concerne en outre un kit pour prédire l'apparition de MACE chez un sujet, qui comprend des paires d'amorces et des paires de sondes utilisées pour amplifier et détecter les 17 loci de SNP décrits, étant capables de prédire le risque de MACE chez des sujets.
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CN201880088474.2A CN111670256B (zh) | 2018-02-09 | 2018-02-09 | 与主要不良心血管事件相关的单核苷酸多态性位点及其应用 |
PCT/CN2018/075986 WO2019153241A1 (fr) | 2018-02-09 | 2018-02-09 | Loci de polymorphisme mononucléotidique associés à des événements cardiovasculaires indésirables majeurs et application de ceux-ci |
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PCT/CN2018/075986 WO2019153241A1 (fr) | 2018-02-09 | 2018-02-09 | Loci de polymorphisme mononucléotidique associés à des événements cardiovasculaires indésirables majeurs et application de ceux-ci |
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WO2019153241A1 true WO2019153241A1 (fr) | 2019-08-15 |
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PCT/CN2018/075986 WO2019153241A1 (fr) | 2018-02-09 | 2018-02-09 | Loci de polymorphisme mononucléotidique associés à des événements cardiovasculaires indésirables majeurs et application de ceux-ci |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN107312851A (zh) * | 2017-07-19 | 2017-11-03 | 北京泱深生物信息技术有限公司 | 心肌梗死生物标志物miR‑1283 |
CN107513576A (zh) * | 2017-10-18 | 2017-12-26 | 北京生命科学研究所 | 一种用于检测遗传性心肌疾病的试剂盒及其应用 |
Family Cites Families (7)
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EP1294934A2 (fr) * | 2000-03-08 | 2003-03-26 | Complexe Hospitalier de la Sagamie | Polymorphismes de recepteurs de lipoproteines tres basse densite et utilisations associees |
US20040018522A1 (en) * | 2002-05-09 | 2004-01-29 | Brigham And Women's Hospital, Inc. | Identification of dysregulated genes in patients with multiple sclerosis |
JP5479663B2 (ja) * | 2002-12-20 | 2014-04-23 | セレラ コーポレーション | 心筋梗塞に関連する遺伝的多型、その検出方法および使用 |
CN101240320A (zh) * | 2007-02-06 | 2008-08-13 | 上海主健生物工程有限公司 | 一种检测心血管疾病发病遗传风险的试剂盒 |
WO2009079762A1 (fr) * | 2007-12-21 | 2009-07-02 | Genesis Group Inc. | Test permettant de diagnostiquer une myocardiopathie |
CN102858985A (zh) * | 2009-07-24 | 2013-01-02 | 西格马-奥尔德里奇有限责任公司 | 基因组编辑方法 |
CN105002286B (zh) * | 2015-07-30 | 2018-04-10 | 中国医学科学院阜外心血管病医院 | 与高血压和/或心血管疾病发病风险相关的多个单核苷酸多态性位点及相关应用 |
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2018
- 2018-02-09 WO PCT/CN2018/075986 patent/WO2019153241A1/fr active Application Filing
- 2018-02-09 CN CN201880088474.2A patent/CN111670256B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN107312851A (zh) * | 2017-07-19 | 2017-11-03 | 北京泱深生物信息技术有限公司 | 心肌梗死生物标志物miR‑1283 |
CN107513576A (zh) * | 2017-10-18 | 2017-12-26 | 北京生命科学研究所 | 一种用于检测遗传性心肌疾病的试剂盒及其应用 |
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CN111670256A (zh) | 2020-09-15 |
CN111670256B (zh) | 2023-10-27 |
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