http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2203808-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e3830f35387a1c32061dea3ee310851
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N7-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N7-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K48-00
filingDate 1995-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31b70a7e6659180c9e67fa056fe05624
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0331adfe9e9031835ede7c6062b55fe0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09fc4ac0c4e08cf51f4d4e410ec498d2
publicationDate 2000-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2203808-C
titleOfInvention Hybrid adenovirus-aav virus and method of use thereof
abstract The present invention provides a hybrid vector construct which comprises a portion of an adenovirus, 5' and 3' ITR sequences from an AAV, and a selected transgene. Also provided is a hybrid virus linked via a polycation conjugate to an AAV rep gene to form a single particle. These trans-infection particles are characterized by high titer transgene delivery to a host cell and the ability to stably integrate the transgene into the host cell chromosome. Also disclosed is the use of the hybrid vectors and viruses to produce large quantities of recombinant AAV.
priorityDate 1994-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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