WO2008052016A3 - Récepteur associé à la sortiline sorl1 présentant un lien fonctionnel et génétique avec la maladie d'alzheimer - Google Patents
Récepteur associé à la sortiline sorl1 présentant un lien fonctionnel et génétique avec la maladie d'alzheimer Download PDFInfo
- Publication number
- WO2008052016A3 WO2008052016A3 PCT/US2007/082308 US2007082308W WO2008052016A3 WO 2008052016 A3 WO2008052016 A3 WO 2008052016A3 US 2007082308 W US2007082308 W US 2007082308W WO 2008052016 A3 WO2008052016 A3 WO 2008052016A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- disease
- alzheimer
- sortilin
- functionally
- related receptor
- 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.)
- Ceased
Links
Classifications
-
- 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
-
- 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
Landscapes
- 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
La présente invention concerne des procédés permettant de déterminer si un patient présente un risque de développer la maladie d'Alzheimer en analysant l'ADN du patient et en déterminant si des variants nucléotidiques se situent dans la région du gène pour SORL1 au niveau des sites SNP 4 ou 8-12 et 19-26.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85384106P | 2006-10-23 | 2006-10-23 | |
| US60/853,841 | 2006-10-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2008052016A2 WO2008052016A2 (fr) | 2008-05-02 |
| WO2008052016A3 true WO2008052016A3 (fr) | 2008-07-31 |
Family
ID=39325361
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2007/082308 Ceased WO2008052016A2 (fr) | 2006-10-23 | 2007-10-23 | Récepteur associé à la sortiline sorl1 présentant un lien fonctionnel et génétique avec la maladie d'alzheimer |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2008052016A2 (fr) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016164608A1 (fr) | 2015-04-07 | 2016-10-13 | Alector Llc | Procédés de recherche par criblage d'antagonistes de liaison à la sortiline |
| SMT202200065T1 (it) | 2015-04-07 | 2022-03-21 | Alector Llc | Anticorpi anti-sortilina e loro metodi d'impiego |
| MY202133A (en) | 2018-07-13 | 2024-04-05 | Alector Llc | Anti-sortilin antibodies and methods of use thereof |
| WO2023275376A1 (fr) * | 2021-07-02 | 2023-01-05 | Aarhus Universitet | Méthodes de traitement de la maladie d'alzheimer |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050106573A1 (en) * | 2003-11-13 | 2005-05-19 | Council Of Scientific And Industrial Research | Method of detection of predisposition to high altitude pulmonary edema (HAPE) |
| US20050177881A1 (en) * | 2001-12-04 | 2005-08-11 | Andreas Papassotiropoulos | Methods of identifying genetic risk for and evaluating treatment of alzheimer's disease by determining single nucleotide polymorphisms |
| US20060134664A1 (en) * | 2004-11-03 | 2006-06-22 | Scherzer Clemens R | Identification of dysregulated genes in patients with neurological diseases |
-
2007
- 2007-10-23 WO PCT/US2007/082308 patent/WO2008052016A2/fr not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050177881A1 (en) * | 2001-12-04 | 2005-08-11 | Andreas Papassotiropoulos | Methods of identifying genetic risk for and evaluating treatment of alzheimer's disease by determining single nucleotide polymorphisms |
| US20050106573A1 (en) * | 2003-11-13 | 2005-05-19 | Council Of Scientific And Industrial Research | Method of detection of predisposition to high altitude pulmonary edema (HAPE) |
| US20060134664A1 (en) * | 2004-11-03 | 2006-06-22 | Scherzer Clemens R | Identification of dysregulated genes in patients with neurological diseases |
Non-Patent Citations (4)
| Title |
|---|
| DATABASE GENBANK [online] 25 May 2006 (2006-05-25), Database accession no. (rs560573) * |
| DATABASE GENBANK [online] 25 May 2006 (2006-05-25), Database accession no. (rs593769) * |
| DATABASE GENBANK [online] 25 May 2006 (2006-05-25), Database accession no. (rs985421) * |
| ROGAEVA ET AL.: "The Neuronal Sortilin-Related Receptor SORL1 is Genetically Associated with Alzheimer Disease", NATURE GENETICS, vol. 39, no. 2, February 2007 (2007-02-01), pages 168 - 177, XP055050412, DOI: doi:10.1038/ng1943 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008052016A2 (fr) | 2008-05-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| WO2009059318A3 (fr) | Gènes et polymorphismes associés à l'amd | |
| EP2639317A3 (fr) | Polymorphismes génétiques associés au psoriasis, procédés de détection et utilisations associées | |
| WO2009073345A3 (fr) | Dosage pour détecter des anomalies génétiques dans des acides nucléiques génomiques | |
| EP1246114A3 (fr) | Procédés d'analyse génomique | |
| WO2007002904A3 (fr) | Procedes et sequences permettant de supprimer de maniere preferentielle l'expression de la huntingtine mutee | |
| WO2008016356A3 (fr) | Carte génique des gènes humains associés au psoriaris | |
| WO2008067195A8 (fr) | Carte génétique des gènes humains associés à la maladie de crohn | |
| NZ593628A (en) | Genetic variants useful for risk assessment of thyroid cancer using rs944289 | |
| WO2008118258A8 (fr) | Carte génique des gènes humains associés au trouble déficitaire de l'attention avec hyperactivité (adhd) | |
| WO2008112177A8 (fr) | Cartographie des gènes de l'homme associés avec la schizophrénie | |
| WO2007025085A8 (fr) | Carte genetique de genes humains associes a la maladie de crohn | |
| WO2007119179A3 (fr) | Utilisation d'ornithine transcarbamylase (otc), en tant que marqueur de diagnostic de traumatismes cérébraux | |
| WO2008052016A3 (fr) | Récepteur associé à la sortiline sorl1 présentant un lien fonctionnel et génétique avec la maladie d'alzheimer | |
| WO2008033461A3 (fr) | Procédés pour l'identification, l'évaluation et le traitement de patients ayant des troubles à médiation par le récepteur 2 de la chimiokine cc (ccr-2) | |
| WO2009039244A3 (fr) | Carte génique des gènes humains associés à la maladie de crohn | |
| WO2008123901A3 (fr) | Carte génétique des gènes humains associés à l'endométriose | |
| EP2002020A4 (fr) | Détection de polymorphismes de nucléotide simple à partir d'adn génomique non amplifié | |
| WO2005072151A3 (fr) | Marqueurs genetiques apoe associes a l'age de l'apparition de la maladie d'alzheimer | |
| WO2003026488A3 (fr) | Diagnostic et traitement d'une maladie vasculaire | |
| WO2008065544A3 (fr) | Prédicteurs génétiques d'un risque de diabète sucré de type 2 | |
| WO2000058510A3 (fr) | Genes, proteines, et marqueurs bialleliques associes a la schizophrenie | |
| WO2003020120A3 (fr) | Diagnostic et traitement de maladies vasculaires | |
| WO2005049866A3 (fr) | Procede de detection de la maladie de charcot-marie de type 2a | |
| WO2008018789A3 (fr) | Procédés et moyens pour diagnostiquer et traiter l'ostéoarthrite | |
| EP1262565A3 (fr) | Polymorphismes génétiques dans le gène humain du récepteur de la neurokinine 1 et leurs usages dans diagnostic et traitement de maladies |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07863461 Country of ref document: EP Kind code of ref document: A2 |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 07863461 Country of ref document: EP Kind code of ref document: A2 |