112255 ⎘
Vectors comprising a targeting moiety; Vectors comprising as targeting moiety peptide derived from defined protein from vertebrates mammalian from growth factors; from growth regulators
CO-EXPRESSION OF CONSTRUCTS AND IMMUNOINHIBITORY COMPOUNDS
#2METHODS OF DELIVERING ANIONIC AGENTS IN VIVO USING NON-VIRAL NANOPARTICLE-BASED DELIVERY SYSTEMS
#3Methods of delivering anionic agents in vivo using non-viral nanoparticle-based delivery systems
#4Identification of mutations in herpes simplex virus envelope glycoproteins that enable or enhance vector retargeting to novel non-HSV receptors
#5Method of making peptide-tagged PEGylated chitosan nanoparticles
#6Targeted gene delivery to non-phagocytic mammalian cells via bacterially derived intact minicells
#7NON-VIRAL NANOPARTICLE-BASED DELIVERY SYSTEM
#8Identification of mutations in herpes simplex virus envelope glycoproteins that enable or enhance vector retargeting to novel non-HSV receptors
#9Method of targeting gene delivery using viral vectors
#10Targeted gene delivery to non-phagocytic mammalian cells via bacterially derived intact minicells
#11Infectivity-enhanced conditionally-replicative adenovirus and uses thereof
#12Viral Vectors with Improved Properties
#13INFECTIVITY-ENHANCED CONDITIONALLY-REPLICATIVE ADENOVIRUS AND USES THEREOF
#14CONSTRUCT COATED WITH VIRUS COAT-CONSTITUTING PROTEIN AND METHOD FOR PRODUCING SAME
#15Method of targeted gene delivery using viral vectors
#16Infectivity-enhanced conditionally-replicative adenovirus and uses thereof
#17Methods of Making Viral Particles Having a Modified Cell Binding Activity and Uses Thereof
#18Humanised Baculovirus
#19Compositions and Methods for Elimination of Unwanted Cells
#20Compositions and Methods for Elimination of Unwanted Cells
#21Compositions and Methods for Elimination of Unwanted Cells
#22Compositions and methods for elimination of unwanted cells
#23DEVICES CONTAINING DNA ENCODING NEUROTROPHIC AGENTS AND RELATED COMPOSITIONS AND METHODS
#24GENE TRANSFER METHODS
#25Targeted gene delivery to non-phagocytic mammalian cells via bacterially derived intact minicells
#26Method of targeted gene delivery using viral vectors
#27Hollow nanoparticles of protein and drug using the same
#28Viral vectors with improved properties
#29Methods of making viral particles having a modified cell binding activity and uses thereof
#30Non-invasive gene targeting to ocular cells
#31Compositions and methods for elimination of unwanted cells
#32Targeted adenovirus vectors for delivery of heterologous genes
#33Altering viral tropism