JP2007525998A - 脆弱x症候群などのstrpの検出 - Google Patents
脆弱x症候群などのstrpの検出 Download PDFInfo
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Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- 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
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6827—Hybridisation assays for detection of mutation or polymorphism
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- 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
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/791,209 US20050191636A1 (en) | 2004-03-01 | 2004-03-01 | Detection of STRP, such as fragile X syndrome |
| PCT/US2005/007049 WO2005085476A1 (en) | 2004-03-01 | 2005-02-28 | Detection of strp, such as fragile x syndrome |
Publications (2)
| Publication Number | Publication Date |
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| JP2007525998A true JP2007525998A (ja) | 2007-09-13 |
| JP2007525998A5 JP2007525998A5 (enExample) | 2008-04-03 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2007502004A Withdrawn JP2007525998A (ja) | 2004-03-01 | 2005-02-28 | 脆弱x症候群などのstrpの検出 |
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| US (1) | US20050191636A1 (enExample) |
| EP (1) | EP1723261A1 (enExample) |
| JP (1) | JP2007525998A (enExample) |
| KR (1) | KR20070011354A (enExample) |
| CN (1) | CN1926247A (enExample) |
| WO (1) | WO2005085476A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007535928A (ja) * | 2004-05-05 | 2007-12-13 | バイオセプト インコーポレイテッド | 染色体異常の検出 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6913697B2 (en) | 2001-02-14 | 2005-07-05 | Science & Technology Corporation @ Unm | Nanostructured separation and analysis devices for biological membranes |
| JP2006501449A (ja) | 2002-09-27 | 2006-01-12 | ザ ジェネラル ホスピタル コーポレーション | 細胞分離のためのマイクロ流体デバイスおよびその使用 |
| US20070196820A1 (en) | 2005-04-05 | 2007-08-23 | Ravi Kapur | Devices and methods for enrichment and alteration of cells and other particles |
| US8921102B2 (en) | 2005-07-29 | 2014-12-30 | Gpb Scientific, Llc | Devices and methods for enrichment and alteration of circulating tumor cells and other particles |
| EP1857548A1 (en) | 2006-05-19 | 2007-11-21 | Academisch Ziekenhuis Leiden | Means and method for inducing exon-skipping |
| US20080050739A1 (en) | 2006-06-14 | 2008-02-28 | Roland Stoughton | Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats |
| EP2589668A1 (en) | 2006-06-14 | 2013-05-08 | Verinata Health, Inc | Rare cell analysis using sample splitting and DNA tags |
| US8137912B2 (en) | 2006-06-14 | 2012-03-20 | The General Hospital Corporation | Methods for the diagnosis of fetal abnormalities |
| WO2007147074A2 (en) | 2006-06-14 | 2007-12-21 | Living Microsystems, Inc. | Use of highly parallel snp genotyping for fetal diagnosis |
| DK2049664T3 (da) | 2006-08-11 | 2012-01-02 | Prosensa Technologies Bv | Enkeltstrengede oligonukleotider, som er komplementære til repetitive elementer, til behandling af med DNA-repetitiv-ustabilitet associerede lidelser |
| AU2008273094B2 (en) | 2007-07-12 | 2013-05-09 | Prosensa Technologies B.V. | Molecules for targeting compounds to various selected organs, tissues or tumor cells |
| AU2008273096B2 (en) | 2007-07-12 | 2013-05-02 | Academisch Ziekenhuis Leiden | Molecules for targeting compounds to various selected organs or tissues |
| WO2009045467A1 (en) * | 2007-10-02 | 2009-04-09 | Fred Hutchinson Cancer Research Center | Methods and compositions for identifying increased risk of developing fragile x-associated disorders |
| CN101896186A (zh) | 2007-10-26 | 2010-11-24 | 莱顿教学医院 | 对抗肌肉病症的方式和方法 |
| USRE48468E1 (en) | 2007-10-26 | 2021-03-16 | Biomarin Technologies B.V. | Means and methods for counteracting muscle disorders |
| US8008019B2 (en) * | 2007-11-28 | 2011-08-30 | Luminex Molecular Diagnostics | Use of dual-tags for the evaluation of genomic variable repeat regions |
| JP2011510678A (ja) | 2008-02-08 | 2011-04-07 | プロセンサ ホールディング ビーブイ | Dna反復不安定性関連遺伝性障害を治療するための方法及び手段 |
| EP2119783A1 (en) | 2008-05-14 | 2009-11-18 | Prosensa Technologies B.V. | Method for efficient exon (44) skipping in Duchenne Muscular Dystrophy and associated means |
| US20090298709A1 (en) * | 2008-05-28 | 2009-12-03 | Affymetrix, Inc. | Assays for determining telomere length and repeated sequence copy number |
| CA2737643C (en) | 2008-09-20 | 2020-10-06 | Hei-Mun Fan | Noninvasive diagnosis of fetal aneuploidy by sequencing |
| CA2759899A1 (en) | 2009-04-24 | 2010-10-28 | Prosensa Technologies B.V. | Oligonucleotide comprising an inosine for treating dmd |
| CA2767521A1 (en) * | 2009-07-10 | 2011-01-13 | Perkinelmer Health Sciences, Inc. | Detecting multinucleotide repeats |
| EP3460074B1 (en) | 2010-02-05 | 2020-10-07 | Quest Diagnostics Investments Incorporated | Method to detect repeat sequence motifs in nucleic acid |
| GB201116131D0 (en) * | 2011-09-19 | 2011-11-02 | Epistem Ltd | Probe |
| US20130183666A1 (en) * | 2012-01-18 | 2013-07-18 | Marc N. Feiglin | Partial genotyping by differential hybridization |
| BR112014018427B1 (pt) | 2012-01-27 | 2021-11-03 | Biomarin Technologies B.V. | Oligonucleotídeos moduladores de rna com características melhoradas para o tratamento da distrofia muscular de duchenne e becker |
| CN102703595B (zh) * | 2012-06-13 | 2014-02-12 | 东南大学 | 一种碱基选择性可控延伸的str序列高通量检测方法及其检测试剂 |
| CN102952794B (zh) * | 2012-09-05 | 2015-02-25 | 张家港蓝苏生物工程有限公司 | 靶向基因dna分子探针的制备方法 |
| CN104531851A (zh) * | 2014-12-10 | 2015-04-22 | 东南大学 | 一种基于磁珠与多糖水解分离发光标记物的核酸检测方法 |
| CN104498600A (zh) * | 2014-12-10 | 2015-04-08 | 东南大学 | 一种基于磁珠与核酸水解分离发光标记物的核酸检测方法 |
| CN108300776A (zh) * | 2017-01-13 | 2018-07-20 | 金赟懿 | 脆性x综合征快速筛查试剂盒 |
| US10459666B2 (en) | 2017-03-03 | 2019-10-29 | Commvault Systems, Inc. | Using storage managers in respective data storage management systems for license distribution, compliance, and updates |
| EA202091646A1 (ru) * | 2018-01-05 | 2020-11-17 | Квошент Сюисс Са | Платформа на основе самособирающегося диагностического массива |
| GB201803019D0 (en) * | 2018-02-26 | 2018-04-11 | Univ Newcastle | Methods for detecting target polynucleotides |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0724646B1 (en) * | 1991-01-04 | 2001-06-27 | Washington University | Dna sequences related to isolated fragile x syndrome |
| US6180337B1 (en) * | 1991-05-24 | 2001-01-30 | Baylor College Of Medicine | Diagnosis of the fragile X syndrome |
| US6200747B1 (en) * | 1992-01-28 | 2001-03-13 | North Shore University Hospital Research Corp. | Method and kits for detection of fragile X specific, GC-rich DNA sequences |
| WO1994003638A1 (en) * | 1992-07-30 | 1994-02-17 | Applied Biosystems, Inc. | Method of detecting aneuploidy by amplified short tandem repeats |
| JP2807612B2 (ja) * | 1993-03-12 | 1998-10-08 | ノボ ノルディスク アクティーゼルスカブ | 新規キシラナーゼ、その製造法、該キシラナーゼによるパルプ処理方法及びキシロオリゴ糖の製造法 |
| US6120992A (en) * | 1993-11-04 | 2000-09-19 | Valigene Corporation | Use of immobilized mismatch binding protein for detection of mutations and polymorphisms, and allele identification in a diseased human |
| US5753439A (en) * | 1995-05-19 | 1998-05-19 | Trustees Of Boston University | Nucleic acid detection methods |
| US5888740A (en) * | 1997-09-19 | 1999-03-30 | Genaco Biomedical Products, Inc. | Detection of aneuploidy and gene deletion by PCR-based gene- dose co-amplification of chromosome specific sequences with synthetic sequences with synthetic internal controls |
| US6143504A (en) * | 1998-10-27 | 2000-11-07 | Arch Development Corporation | Methods and compositions for the diagnosis of fragile X syndrome |
| US6268147B1 (en) * | 1998-11-02 | 2001-07-31 | Kenneth Loren Beattie | Nucleic acid analysis using sequence-targeted tandem hybridization |
| US6225061B1 (en) * | 1999-03-10 | 2001-05-01 | Sequenom, Inc. | Systems and methods for performing reactions in an unsealed environment |
| US6638719B1 (en) * | 1999-07-14 | 2003-10-28 | Affymetrix, Inc. | Genotyping biallelic markers |
| US20040265883A1 (en) * | 2003-06-27 | 2004-12-30 | Biocept, Inc. | mRNA expression analysis |
-
2004
- 2004-03-01 US US10/791,209 patent/US20050191636A1/en not_active Abandoned
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2005
- 2005-02-28 EP EP05724566A patent/EP1723261A1/en not_active Withdrawn
- 2005-02-28 CN CNA2005800064661A patent/CN1926247A/zh active Pending
- 2005-02-28 WO PCT/US2005/007049 patent/WO2005085476A1/en not_active Ceased
- 2005-02-28 JP JP2007502004A patent/JP2007525998A/ja not_active Withdrawn
- 2005-02-28 KR KR1020067020635A patent/KR20070011354A/ko not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007535928A (ja) * | 2004-05-05 | 2007-12-13 | バイオセプト インコーポレイテッド | 染色体異常の検出 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1723261A1 (en) | 2006-11-22 |
| KR20070011354A (ko) | 2007-01-24 |
| CN1926247A (zh) | 2007-03-07 |
| WO2005085476A1 (en) | 2005-09-15 |
| US20050191636A1 (en) | 2005-09-01 |
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