http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002168753-A1

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filingDate 2001-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebcb2ef600b9d9c0f5594ba16231523c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a9c9627d563ed56655a54905e13837e
publicationDate 2002-11-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002168753-A1
titleOfInvention In vitro formation of congophilic maltese-cross amyloid plaques to identify anti-plaque therapeutics for the treatment of Alzheimer's and Prion diseases
abstract Co-incubation of an amyloid protein with sulfated macromolecules as a method for the formation of amyloid plaques. The amyloid protein may be the beta-amyloid protein or the prion protein or the like. Amyoid plaque formation in one embodiment proceeds in vitro and desireably produces amyloid plaques that stain with Congo red and demonstrate a maltese-cross pattern when viewed under polarized light. The method also produces amyloid plaques that demonstrate an “amyloid star” appearance when viewed by transmission electron microscopy. n Sulfated macromolecules include a sulfated proteoglycan selected from the group consisting of perlecan, ˜220 kilodalton heparan sulfate proteoglyean, glypican, cerebroglycan, aggrecan, synaptoglycan (SV2PG), syndecan, N-syndecan (also known as syndecan-3), syndecan-1, syndecan-4, neurocan, phosphacan, decorin, biglycan, versican, amphiglycan, lumican, PG-M, PG-M (3), agrin, betaglycan, claustrin, brevican, appican, epican, neuroglycan-C, and fragments thereof. Thw sulfated macromolecule may be a sulfated glycosaminoglycan selected from the group consisting of heparin, heparan sulfate, dermatan sulfate, chondroitin sulfate, keratan sulfate, and fragments thereof. n An in vivo assay is also presented for selecting a candidate therapeutic agent for inhibiting or disrupting amyloid plaque deposition or persistence. The assay includes a) pre-forming congophilic maltese-cross amyloid plaques in vitro following incubation of an amyloid protein and a selected sulfated macromolecule, b) using a first cannula and osmotic pump to continuously infuse for a selected duration the pre-formed congophilic maltese-cross amyloid plaques into a tissue or organ, c) changing the first cannulae and osmotic pump with a second cannulae and osmotic pump to administer the candidate therapeutic, and d) detecting the candidate therapeutic's ability to disrupt, reduce, or eliminate congophilic maltese-cross amyloid plaque deposition/persistence in the tissue or organ.
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priorityDate 1998-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53736515
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451670180
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID792467
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129051336
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410445424
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556338
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID134410112
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID280733
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID136228930
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID228052670
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID446715
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226472669
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID503792
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ05700
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87714490
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231579572
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21832658
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53788743
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID125409
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231579573
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419580344
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419485087
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128439639
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP86810
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID25592
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11313
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID160375365
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP86348
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57160051
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70469
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231754527
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP02701
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128592451
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23107015

Total number of triples: 651.