DK2471954T3 - Genetiske modtagelighedsvarianter forbundet med kardiovaskulære sygdomme - Google Patents
Genetiske modtagelighedsvarianter forbundet med kardiovaskulære sygdomme Download PDFInfo
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- DK2471954T3 DK2471954T3 DK11194162.1T DK11194162T DK2471954T3 DK 2471954 T3 DK2471954 T3 DK 2471954T3 DK 11194162 T DK11194162 T DK 11194162T DK 2471954 T3 DK2471954 T3 DK 2471954T3
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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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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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
- C12Q2600/106—Pharmacogenomics, i.e. genetic variability in individual responses to drugs and drug metabolism
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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
- C12Q2600/136—Screening for pharmacological compounds
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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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- 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
- C12Q2600/172—Haplotypes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A90/00—Technologies having an indirect contribution to adaptation to climate change
- Y02A90/10—Information and communication technologies [ICT] supporting adaptation to climate change, e.g. for weather forecasting or climate simulation
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Organic Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
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- Zoology (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
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- Immunology (AREA)
- Biotechnology (AREA)
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- Molecular Biology (AREA)
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- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Claims (8)
1. In v/'tro-fremgangsmåde til bestemmelse af modtageligheden for en arteriel sygdom i et humant individ, hvilken fremgangsmåde omfatter bestemmelse af tilstedeværelse eller fravær af mindst et allel af mindst en polymorf markør i en nukleinsyreprøve, der er opnået fra individet, hvori det mindst ene allel af den mindste ene polymorfe markør er valgt blandt de polymorfe markører rsl0757278 (SEQ ID NO:88) allel G, rsl0116277 (SEQ ID NO:56) allel T, rsl333040 (SEQ ID NO:59) allel T og rs2383207 (SEQ ID NO:82) allel G, and korrelerede markører i sammenkædnings-uligevægt dermed lokaliseret inden for sammenkædnings-uligevægtsblokken på kromosom 9 med sekvensen som angivet i SEQ ID NO:94, hvilke er kendetegnet ved værdier på r2 > 0,2 og er valgt fra gruppen bestående af markørerne angivet i Tabel 3 og Tabel 21, og hvori tilstedeværelsen af det mindste ene allel er indikativ for modtageligheden af arteriel sygdom.
2. Fremgangsmåden ifølge krav 1, hvilken fremgangsmåde yderligere omfatter vurdering af mindst én biomarkør i en prøve fra individet.
3. Fremgangsmåden ifølge krav 2, hvori biomarkøren er en kardiel markør eller en inflammatorisk markør.
4. Fremgangsmåden ifølge krav 2 eller krav 3, hvori den mindst ene markør er valgt blandt creatin-kinase, troponin, glycogen-phosphorylase, C-reactivt protein (CRP), serum amyloid A, fibrinogen, interleukin-6, vævsnekrose-faktor-alfa, opløselige vaskulære celleadhæsionsmolekyler (sVCAM), opløselige intervasculære adhæsionsmolekyler (sICAM), E-selectin, matrix-metalloprotease type-1, matrix-metalloprotease type-2, matrix-metalloprotease type-3, matrix-metalloprotease type-9, serum sCD40L, leukotriener, leukotrien-metabolitter, interleukin-6, vævsnekrose-faktor-alfa, myeloperoxidase (MPO), og N-tyrosin.
5. Fremgangsmåden ifølge krav 4, hvori leukotrienen er valgt blandt LTB4, LTC4, LTD4 og LTE4.
6. Fremgangsmåden ifølge et hvilket som helst af de foregående krav, hvori den arterielle sygdom er valgt fra gruppen bestående af myokardie-infarkt, koronaarteriesygdom, akut koronart syndrome, slagtilfælde, perifer arteriel sygdom, restenose, intrakraniel aneurisme og aorta abdominal aneurisme.
7. Fremgangsmåden ifølge krav 6, hvori myokardie-infarktet har tidlig indtræden.
8. Fremgangsmåden ifølge krav 7, hvori den tidlige indtræden er før en alder af 50 for mænd og før en alder af 60 for kvinder.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IS8613 | 2007-02-21 | ||
IS8640 | 2007-04-30 | ||
IS8701 | 2007-12-21 | ||
EP08710293A EP2115172A1 (en) | 2007-02-21 | 2008-02-21 | Genetic susceptibility variants associated with cardiovascular disease |
Publications (1)
Publication Number | Publication Date |
---|---|
DK2471954T3 true DK2471954T3 (da) | 2016-09-12 |
Family
ID=39432938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DK11194162.1T DK2471954T3 (da) | 2007-02-21 | 2008-02-21 | Genetiske modtagelighedsvarianter forbundet med kardiovaskulære sygdomme |
Country Status (16)
Country | Link |
---|---|
US (2) | US9617597B2 (da) |
EP (2) | EP2115172A1 (da) |
JP (1) | JP5646179B2 (da) |
KR (1) | KR101571523B1 (da) |
CN (1) | CN101668865B (da) |
AU (1) | AU2008218542B2 (da) |
BR (1) | BRPI0807927A2 (da) |
CA (1) | CA2679581C (da) |
DK (1) | DK2471954T3 (da) |
EA (1) | EA022610B1 (da) |
HU (1) | HUE030996T2 (da) |
IL (1) | IL200453A (da) |
MX (1) | MX2009008878A (da) |
NZ (1) | NZ579445A (da) |
SG (1) | SG178811A1 (da) |
WO (1) | WO2008102380A1 (da) |
Families Citing this family (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7883851B2 (en) | 2007-05-02 | 2011-02-08 | Board Of Regents, The University Of Texas System | Common allele on chromosome 9 associated with coronary heart disease |
AU2009205956B2 (en) | 2008-01-18 | 2015-07-02 | President And Fellows Of Harvard College | Methods of detecting signatures of disease or conditions in bodily fluids |
US20090221620A1 (en) * | 2008-02-20 | 2009-09-03 | Celera Corporation | Gentic polymorphisms associated with stroke, methods of detection and uses thereof |
ES2344396B1 (es) * | 2009-02-24 | 2011-06-24 | Fina Biotech Slu | Marcadores geneticos del riesgo de sufrir reestenosis. |
WO2010131268A1 (en) * | 2009-05-11 | 2010-11-18 | Decode Genetics Ehf | Genetic variants for basal cell carcinoma, squamous cell carcinoma and cutaneous melanoma |
EP2264183B1 (en) * | 2009-06-09 | 2016-12-07 | Gendiag.exe, S.L. | Risk markers for cardiovascular disease |
CN102803951A (zh) * | 2009-06-15 | 2012-11-28 | 心脏Dx公司 | 冠状动脉疾病风险的测定 |
WO2011159157A1 (en) * | 2010-06-15 | 2011-12-22 | Cellagenics B.V. | Novel intergenic elements for enhancing gene expression |
EP2596349B1 (en) | 2010-07-23 | 2017-12-13 | President and Fellows of Harvard College | Methods of detecting cardiovascular diseases or conditions |
SG10201505724SA (en) | 2010-07-23 | 2015-09-29 | Harvard College | Methods of detecting diseases or conditions using phagocytic cells |
MX361944B (es) | 2010-07-23 | 2018-12-19 | President And Fellows Of Harvard College Star | Metodos para detectar firmas de enfermedad o condiciones en fluidos corporales. |
EP2596353A4 (en) | 2010-07-23 | 2014-01-15 | Harvard College | METHOD FOR DETECTING PRENATAL OR PREGNANT DISEASES OR SUFFERING |
AU2011280997A1 (en) | 2010-07-23 | 2013-02-28 | President And Fellows Of Harvard College | Methods of detecting autoimmune or immune-related diseases or conditions |
EP2640857A4 (en) * | 2010-11-18 | 2014-04-30 | Decode Genetics Ehf | GENETIC RISK FACTORS OF SINUS NODE SYNDROME |
WO2012135657A2 (en) * | 2011-03-31 | 2012-10-04 | Yale University | Compositions and methods for diagnosis, preventing and treating intracranial aneurysms |
DK2554679T3 (da) * | 2011-08-05 | 2016-04-04 | Gendiag Exe Sl | Genetiske markører til risikovurdering for hjertekarsygdom |
WO2013032883A2 (en) * | 2011-08-26 | 2013-03-07 | Ottawa Heart Institute Research Corporation | Methods of detecting and treating cardiovascular diseases |
AU2013274002A1 (en) | 2012-06-15 | 2015-02-05 | Harry Stylli | Methods of detecting diseases or conditions |
KR20150035818A (ko) | 2012-06-15 | 2015-04-07 | 해리 스타일리 | 순환 병든 세포를 사용하여 질환 또는 병태를 검출하는 방법 |
MD707Z (ro) * | 2013-01-18 | 2014-07-31 | Институт Зоологии Академии Наук Молдовы | Metodă de identificare a secvenţelor polimorfe 4a/4b ale genei sintetazei endoteliale a oxidului nitric |
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US10494675B2 (en) | 2013-03-09 | 2019-12-03 | Cell Mdx, Llc | Methods of detecting cancer |
WO2014175287A1 (ja) * | 2013-04-26 | 2014-10-30 | 国立大学法人 京都大学 | 脳動脈瘤の形成および/または増大の抑制若しくは縮小用医薬組成物 |
KR101602688B1 (ko) | 2013-12-30 | 2016-03-11 | 가톨릭관동대학교산학협력단 | microRNA-365 활성화제를 포함하는 혈관평활근세포 증식 또는 이동 억제용 약학적 조성물 |
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WO2016123163A2 (en) | 2015-01-27 | 2016-08-04 | Kardiatonos, Inc. | Biomarkers of vascular disease |
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RU2693997C2 (ru) * | 2017-12-04 | 2019-07-08 | Федеральное Государственное Бюджетное Научное Учреждение "Федеральный Научно-Клинический Центр Реаниматологии И Реабилитологии" (Фнкц Рр) | Способ определения степени предрасположенности к сердечно-сосудистым заболеваниям |
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US10468141B1 (en) | 2018-11-28 | 2019-11-05 | Asia Genomics Pte. Ltd. | Ancestry-specific genetic risk scores |
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KR102366097B1 (ko) * | 2021-05-03 | 2022-02-23 | 주식회사 바이오에이지 | 임상 및 유전변이 정보를 통합한 한국인 뇌혈관 질환 예측 방법 및 관련 검사추천방법 |
KR102344173B1 (ko) * | 2021-05-03 | 2021-12-29 | 주식회사 바이오에이지 | 임상 및 유전변이 정보를 통합한 한국인 관상동맥 질환 예측 방법 및 관련 검사추천방법 |
CN113484453B (zh) * | 2021-07-07 | 2022-08-09 | 天津中医药大学 | 一种缺血性脑卒中预警方法 |
CN114672548B (zh) * | 2022-03-10 | 2024-04-19 | 华捷生物科技(青岛)有限公司 | 一种人类静脉血栓风险基因pai-1,thbd和proc基因多态性检测试剂盒及其制备方法和应用 |
WO2023205243A1 (en) * | 2022-04-19 | 2023-10-26 | The Regents Of The University Of Michigan | Determining risk of fibromuscular dysplasia and systems and methods of use thereof |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4376110A (en) | 1980-08-04 | 1983-03-08 | Hybritech, Incorporated | Immunometric assays using monoclonal antibodies |
ATE167524T1 (de) | 1983-01-10 | 1998-07-15 | Gen Probe Inc | Verfahren zum nachweis, identifizieren und quantifizieren von organismen und viren |
US5288611A (en) | 1983-01-10 | 1994-02-22 | Gen-Probe Incorporated | Method for detecting, identifying, and quantitating organisms and viruses |
US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
US5223409A (en) | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
JP3771253B2 (ja) | 1988-09-02 | 2006-04-26 | ダイアックス コープ. | 新規な結合タンパク質の生成と選択 |
US5424186A (en) | 1989-06-07 | 1995-06-13 | Affymax Technologies N.V. | Very large scale immobilized polymer synthesis |
US5143854A (en) | 1989-06-07 | 1992-09-01 | Affymax Technologies N.V. | Large scale photolithographic solid phase synthesis of polypeptides and receptor binding screening thereof |
US5288644A (en) | 1990-04-04 | 1994-02-22 | The Rockefeller University | Instrument and method for the sequencing of genome |
US5427908A (en) | 1990-05-01 | 1995-06-27 | Affymax Technologies N.V. | Recombinant library screening methods |
EP0585287B1 (en) | 1990-07-10 | 1999-10-13 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
GB9015198D0 (en) | 1990-07-10 | 1990-08-29 | Brien Caroline J O | Binding substance |
DK0564531T3 (da) | 1990-12-03 | 1998-09-28 | Genentech Inc | Berigelsesfremgangsmåde for variantproteiner med ændrede bindingsegenskaber |
EP0562025B1 (en) | 1990-12-06 | 2001-02-07 | Affymetrix, Inc. (a Delaware Corporation) | Compounds and their use in a binary synthesis strategy |
CA2105300C (en) | 1991-03-01 | 2008-12-23 | Robert C. Ladner | Process for the development of binding mini-proteins |
PT100379B (pt) | 1991-04-10 | 1999-01-29 | Scripps Research Inst | Bibliotecas de receptores heterodimericos usando fagomideos |
DE4122599C2 (de) | 1991-07-08 | 1993-11-11 | Deutsches Krebsforsch | Phagemid zum Screenen von Antikörpern |
US5384261A (en) | 1991-11-22 | 1995-01-24 | Affymax Technologies N.V. | Very large scale immobilized polymer synthesis using mechanically directed flow paths |
US5858659A (en) | 1995-11-29 | 1999-01-12 | Affymetrix, Inc. | Polymorphism detection |
US5837832A (en) | 1993-06-25 | 1998-11-17 | Affymetrix, Inc. | Arrays of nucleic acid probes on biological chips |
CN1141398C (zh) * | 2000-03-28 | 2004-03-10 | 陈高明 | 一种多基因扩增芯片及其制备方法 |
USH2191H1 (en) * | 2000-10-24 | 2007-06-05 | Snp Consortium | Identification and mapping of single nucleotide polymorphisms in the human genome |
USH2220H1 (en) * | 2001-08-10 | 2008-07-01 | Snp Consortium | Identification and mapping of single nucleotide polymorphisms in the human genome |
US20040267458A1 (en) * | 2001-12-21 | 2004-12-30 | Judson Richard S. | Methods for obtaining and using haplotype data |
WO2004035746A2 (en) * | 2002-10-17 | 2004-04-29 | Decode Genetics Ehf. | Susceptibility gene for myocardial infarction |
EP1613774A2 (en) * | 2003-03-10 | 2006-01-11 | Applera Corporation | Genetic polymorphisms associated with stenosis, methods of detection and uses thereof |
CA2832293C (en) * | 2003-11-26 | 2015-08-04 | Celera Corporation | Single nucleotide polymorphisms associated with cardiovascular disorders and statin response, methods of detection and uses thereof |
US20050191678A1 (en) * | 2004-02-12 | 2005-09-01 | Geneob Usa Inc. | Genetic predictability for acquiring a disease or condition |
JP2009521905A (ja) * | 2004-03-05 | 2009-06-11 | アプレラ コーポレイション | 冠動脈心疾患に関連する遺伝的多型、その検出方法および使用 |
CA2566257A1 (en) * | 2004-05-07 | 2005-11-24 | Applera Corporation | Genetic polymorphisms associated with vascular diseases, methods of detection and uses thereof |
US20060004526A1 (en) * | 2004-07-01 | 2006-01-05 | Ambion, Inc. | System and method for processing results of a complex genetic test |
US20080131887A1 (en) * | 2006-11-30 | 2008-06-05 | Stephan Dietrich A | Genetic Analysis Systems and Methods |
US7883851B2 (en) | 2007-05-02 | 2011-02-08 | Board Of Regents, The University Of Texas System | Common allele on chromosome 9 associated with coronary heart disease |
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2008
- 2008-02-21 CA CA2679581A patent/CA2679581C/en active Active
- 2008-02-21 EP EP08710293A patent/EP2115172A1/en not_active Withdrawn
- 2008-02-21 EA EA200970781A patent/EA022610B1/ru not_active IP Right Cessation
- 2008-02-21 CN CN200880011908.5A patent/CN101668865B/zh not_active Expired - Fee Related
- 2008-02-21 WO PCT/IS2008/000007 patent/WO2008102380A1/en active Application Filing
- 2008-02-21 EP EP11194162.1A patent/EP2471954B1/en active Active
- 2008-02-21 HU HUE11194162A patent/HUE030996T2/en unknown
- 2008-02-21 AU AU2008218542A patent/AU2008218542B2/en not_active Ceased
- 2008-02-21 JP JP2009550777A patent/JP5646179B2/ja not_active Expired - Fee Related
- 2008-02-21 SG SG2012012233A patent/SG178811A1/en unknown
- 2008-02-21 MX MX2009008878A patent/MX2009008878A/es active IP Right Grant
- 2008-02-21 US US12/302,538 patent/US9617597B2/en active Active
- 2008-02-21 NZ NZ579445A patent/NZ579445A/en not_active IP Right Cessation
- 2008-02-21 BR BRPI0807927-7A2A patent/BRPI0807927A2/pt not_active Application Discontinuation
- 2008-02-21 DK DK11194162.1T patent/DK2471954T3/da active
- 2008-02-21 KR KR1020097019455A patent/KR101571523B1/ko active IP Right Grant
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2009
- 2009-08-18 IL IL200453A patent/IL200453A/en active IP Right Grant
-
2012
- 2012-04-19 US US13/451,210 patent/US20120208709A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
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US20100068705A1 (en) | 2010-03-18 |
MX2009008878A (es) | 2009-08-28 |
IL200453A0 (en) | 2010-04-29 |
KR20090117896A (ko) | 2009-11-13 |
EA200970781A1 (ru) | 2010-04-30 |
EP2471954A1 (en) | 2012-07-04 |
CN101668865A (zh) | 2010-03-10 |
IL200453A (en) | 2014-12-31 |
BRPI0807927A2 (pt) | 2014-06-24 |
CA2679581A1 (en) | 2008-08-28 |
SG178811A1 (en) | 2012-03-29 |
CN101668865B (zh) | 2015-05-06 |
EP2471954B1 (en) | 2016-08-24 |
US9617597B2 (en) | 2017-04-11 |
KR101571523B1 (ko) | 2015-11-24 |
CA2679581C (en) | 2020-12-22 |
JP2010518848A (ja) | 2010-06-03 |
EP2115172A1 (en) | 2009-11-11 |
EA022610B1 (ru) | 2016-02-29 |
NZ579445A (en) | 2012-02-24 |
JP5646179B2 (ja) | 2014-12-24 |
US20120208709A1 (en) | 2012-08-16 |
AU2008218542B2 (en) | 2014-06-26 |
AU2008218542A1 (en) | 2008-08-28 |
HUE030996T2 (en) | 2017-06-28 |
WO2008102380A1 (en) | 2008-08-28 |
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