WO2006069592A3 - Method for diagnosing an/or predicting preeclampsia and/or related disorders - Google Patents
Method for diagnosing an/or predicting preeclampsia and/or related disorders Download PDFInfo
- Publication number
- WO2006069592A3 WO2006069592A3 PCT/EP2004/014879 EP2004014879W WO2006069592A3 WO 2006069592 A3 WO2006069592 A3 WO 2006069592A3 EP 2004014879 W EP2004014879 W EP 2004014879W WO 2006069592 A3 WO2006069592 A3 WO 2006069592A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- diagnosing
- related disorders
- predicting
- nucleic acid
- preeclampsia
- Prior art date
Links
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
- C12Q1/6876—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
-
- 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
-
- 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
- C12Q2600/158—Expression markers
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Pathology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
The present invention relates to methods for predicting and/or diagnosing a pregnancy at risk for preeclampsia and/or related disorders, comprising: (a) obtaining at least one marker nucleic acid from a biological sample; (b) providing the diagnosis based on at least one of the quantity, activity and/or sequence of said marker nucleic acid in said sample. The invention further relates to the marker nucleic acid per se for use in predicting, diagnosing, preventing and/or treating preeclampsia and/or related disorders, as well as to kits and primers for use in the methods of the invention.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2004/014879 WO2006069592A2 (en) | 2004-12-31 | 2004-12-31 | Method for diagnosing an/or predicting preeclampsia and/or related disorders |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP2004/014879 WO2006069592A2 (en) | 2004-12-31 | 2004-12-31 | Method for diagnosing an/or predicting preeclampsia and/or related disorders |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006069592A2 WO2006069592A2 (en) | 2006-07-06 |
WO2006069592A3 true WO2006069592A3 (en) | 2008-01-03 |
Family
ID=34960411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2004/014879 WO2006069592A2 (en) | 2004-12-31 | 2004-12-31 | Method for diagnosing an/or predicting preeclampsia and/or related disorders |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2006069592A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100041026A1 (en) * | 2005-06-28 | 2010-02-18 | Majercak John M | Method for Identiflying Modulators of Rufy2 Useful for Treating Alzheimer's Disease |
US20110237649A1 (en) * | 2008-12-04 | 2011-09-29 | Opko Curna, Llc | Treatment of sirtuin 1 (sirt1) related diseases by inhibition of natural antisense transcript to sirtuin 1 |
EP2403946A4 (en) * | 2009-03-04 | 2012-11-14 | Treatment of sirtuin 1 (sirt1) related diseases by inhibition of natural antisense transcript to sirt 1 | |
EP2985348B1 (en) * | 2009-07-24 | 2020-12-30 | CuRNA, Inc. | Treatment of sirtuin 6 (sirt6) related diseases by inhibition of natural antisense transcript to sirt6 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5763168A (en) * | 1992-09-30 | 1998-06-09 | University Of Utah Research Foundation | Method to determine predisposition to hypertension |
WO1999043851A1 (en) * | 1998-02-25 | 1999-09-02 | National University Of Ireland, Cork | Hla linked pre-eclampsia and miscarriage susceptibility gene |
US6177252B1 (en) * | 1999-08-27 | 2001-01-23 | University Of Utah Research Foundation | Method to determine predisposition to hypertension |
WO2001057190A2 (en) * | 2000-02-03 | 2001-08-09 | Hyseq, Inc. | Novel nucleic acids and polypeptides |
WO2002004678A2 (en) * | 2000-07-07 | 2002-01-17 | Genetics Institute, Llc. | Methods and compositions for diagnosing and treating preeclampsia and gestational trophoblast disorders |
US20030219776A1 (en) * | 2001-12-18 | 2003-11-27 | Jean-Marc Lalouel | Molecular variants, haplotypes and linkage disequilibrium within the human angiotensinogen gene |
-
2004
- 2004-12-31 WO PCT/EP2004/014879 patent/WO2006069592A2/en not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5763168A (en) * | 1992-09-30 | 1998-06-09 | University Of Utah Research Foundation | Method to determine predisposition to hypertension |
WO1999043851A1 (en) * | 1998-02-25 | 1999-09-02 | National University Of Ireland, Cork | Hla linked pre-eclampsia and miscarriage susceptibility gene |
US6177252B1 (en) * | 1999-08-27 | 2001-01-23 | University Of Utah Research Foundation | Method to determine predisposition to hypertension |
WO2001057190A2 (en) * | 2000-02-03 | 2001-08-09 | Hyseq, Inc. | Novel nucleic acids and polypeptides |
WO2002004678A2 (en) * | 2000-07-07 | 2002-01-17 | Genetics Institute, Llc. | Methods and compositions for diagnosing and treating preeclampsia and gestational trophoblast disorders |
US20030219776A1 (en) * | 2001-12-18 | 2003-11-27 | Jean-Marc Lalouel | Molecular variants, haplotypes and linkage disequilibrium within the human angiotensinogen gene |
Non-Patent Citations (3)
Title |
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DATABASE BIOSIS [online] BIOSCIENCES INFORMATION SERVICE, PHILADELPHIA, PA, US; 1 August 2004 (2004-08-01), OUDEJANS CEES B M ET AL: "The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas", XP002339275, Database accession no. PREV200400354632 * |
IRIYAMA CHISAKO ET AL: "Cloning and sequencing of a novel human gene which encodes a putative hydroxylase", JOURNAL OF HUMAN GENETICS, vol. 46, no. 5, 2001, pages 289 - 292, XP002339241, ISSN: 1434-5161 * |
MOLECULAR HUMAN REPRODUCTION, vol. 10, no. 8, 1 August 2004 (2004-08-01), pages 589 - 598, ISSN: 1360-9947 * |
Also Published As
Publication number | Publication date |
---|---|
WO2006069592A2 (en) | 2006-07-06 |
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