Genetic modification of primate hemopoietic repopulating stem cells
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Gene delivery vectors for stem cells
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Gene delivery vehicles and use thereof in the preparation of a medicament and/or vaccine
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Modified adenoviral vectors for use in gene therapy
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Methods and means for inhibiting angiogenesis
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Methods and means for enhancing skin transplantation using gene delivery vehicles having tropism for primary fibroblasts, as well as other uses thereof
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Gene therapy to promote angiogenesis.
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Method of administering adenovirus
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Production of vaccines from immortalised mammalian cell lines
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Adenoviral gene delivery vectors provided with a tissue tropism for smooth muscle cells and /or endothelial cells
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Gene therapy of alzheimer's disease by delivery of an encoded apolipoprotein e
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Modified adenoviral vectors for use in gene therapy
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Smooth muscle cell promoter and uses thereof
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Packaging systems for human recombinant adenovirus to be used in gene therapy
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Gene therapy for enhancing and/or inducing angiogenesis
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Infection with chimaeric adenoviruses of cells negative for the adenovirus serotype 5 Coxsacki adenovirus receptor (CAR)
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Chimaeric adenoviruses
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High-throughput screening of gene function using libraries for functional genomics applications
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Targeted delivery through a cationic amino acid transporter
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Display of viral proteins as ligands for cell-surface receptor