| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7fd38ff393036b78f4fa402ddeeae2d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_61b8921781f8b544d6f3d2fe6b0c8f63 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-2828
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2400-40 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6896 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68 |
| filingDate |
2004-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdca3d95dfb0fc45631d9ceaeb5eb862 |
| publicationDate |
2005-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2005026740-A1 |
| titleOfInvention |
Methods and kits for the detection of prion diseases |
| abstract |
A method and kit for the diagnosis of a prion-associated neurodegenerative disorder in a mammalian subject comprising: (a) providing a body fluid sample of the subject; (b) qualitatively and/or quantitatively detecting glycosaminoglycans (GAGs) in the sample by suitable means. The presence of GAGs in the sample indicates that the subject carries a prion-associated neurodegenerative disorder, which may be a spongiform encephalopathy such as Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker Syndrome (GSS), Kuru, scrapie and bovine spongiform encephalopathy (BSE). |
| isCitedBy |
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2005080590-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2764114-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9631237-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8158441-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7566530-B2 |
| priorityDate |
2003-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |