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CAR-Independent Gene Transfer to Accomplish Efficient and Specific Genetic
Modification of Target Cells Via Adenoviral Vectors p6
David T. Curiel, M.D., Director
doi:10.1038/70113
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(72K)
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Lentiviral Vectors p7
Inder Verma, Ph.D., Professor
doi:10.1038/70115
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(72K)
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Challenges of Genetic Disease: Gene Addition or Gene Repair p8
R. Michael Blaese, M.D., Chief Scientific Officer
doi:10.1038/70117
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(69K)
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Non-Viral Gene Transfer p9
Jon Wolff, M.D., Director
doi:10.1038/70119
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(78K)
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Self-Assembly and Soft Lithography: An Overview p10
George Whitesides, Ph.D., Mallinckrodt Professor
of Chemistry
doi:10.1038/70121
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(74K)
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DNA Nanotechnology p11
Nadrian Seeman, Ph.D., Professor
doi:10.1038/70123
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(70K)
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Self Assembled Structures of Lipid-DNA Nonviral Gene Delivery Systems
p12
Cyrus Safinya, Ph.D., Professor
doi:10.1038/70125
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(77K)
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Constitutive and Regulated Expression in the Systemic Delivery of Erythropoietin
Following Skeletal Muscle Transduction with DNA Viral Vectors p13
James M. Wilson, M.D., Ph.D., Director
doi:10.1038/70127
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(74K)
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Uptake of Cationic Liposomes by Normal and Angiogenic Endothelial Cells
In Vivo p14
Donald M. McDonald, M.D., Ph.D., Professor
doi:10.1038/70129
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(68K)
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Polymer Based Systems for Tumor-Targeted Gene Delivery p15
Ernst Wagner, Ph.D., Director
doi:10.1038/70131
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(74K)
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Generation of a Mouse Model for Studying AAV Targeted Integration p16
Richard Jude Samulski, Ph.D., Director
doi:10.1038/70133
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(43K)
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The Role of Microtubule-Dependent Motility During Intracellular Trafficking
of Vector Genome to the Nucleus p17
Philip L. Leopold, Ph.D., Assistant Professor
of Biochemistry
doi:10.1038/70134
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(70K)
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LPD Nanoparticles for Gene Delivery p18
Leaf Huang, Ph.D., Professor
doi:10.1038/70136
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(71K)
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In Vivo Gene Transfer with Retrovirus Vectors p19
Theodore Friedmann, M.D., Director
doi:10.1038/70138
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(72K)
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Regulating the Regulators p20
Helen M. Blau, Ph.D., Director
doi:10.1038/70140
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(72K)
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Large Chimeric Circular MACs for Gene Therapy and Animal Transgenesis
p21
Jean-Michel H. Vos, D.Sc., Associate Professor
doi:10.1038/70142
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(77K)
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Evaluation of AAV Vectors for the Treatment of Hemophilia A and B p22
Alan McClelland, Ph.D., Vice President, R&D
doi:10.1038/70144
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(67K)
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Barrie Carter, Ph.D. p23
Barrie Carter, Ph.D., Executive Vice President,
Director of R&D
doi:10.1038/70146
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(41K)
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Systemic Delivery of Tumor-Targeted p53 Gene Therapy Results in Chemo/Radiosensitization
p24
Esther H. Chang, Ph.D., Professor
doi:10.1038/70147
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(73K)
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Fas Ligand (CD95L) and Cancer Gene Therapy p25
Gary J. Nabel, M.D., Ph.D., Director
doi:10.1038/70149
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(69K)
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Pharmaceutical Gene Medicines for Local and Systemic Therapy p26
Alain Rolland, Pharm. D., Ph.D., Vice President,
R&D
doi:10.1038/70151
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(72K)
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The Novartis Approach to Gene Therapy p27
J. Tyler Martin, M.D., Executive Director
doi:10.1038/70153
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(61K)
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Sequence-Specific Gene Targeting Using Triplex Strategies p28
Claude Helene, Ph.D., Professor and Chair of Biophysics
doi:10.1038/70155
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(71K)
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Nonviral Vectors for the Treatment of Disease p29
Nancy Smyth Templeton, Ph.D., Assistant Professor
doi:10.1038/70157
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(71K)
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PNA-Dependent Gene Chemistry to Control Plasmid Delivery and Expression
p30
Philip Felgner, Ph.D., Chief Scientific Officer
doi:10.1038/70159
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(72K)
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Targeting Adenovirus Vectors p31
Thomas J. Wickham, Ph.D., Director, Vector Targeting
and Selectivity
doi:10.1038/70161
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(69K)
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| Roundtable | Top |
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Roundtable p32
J. Tyler Martin, M.D., Executive Director, Clinical
Research
doi:10.1038/70163
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(61K)
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Roundtable p33
Kenneth A. Sorensen, Ph.D., Portfolio Manager
doi:10.1038/70165
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(58K)
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Roundtable p34
Kenneth Chahine, J.D., Ph.D., Vice President of
Business Development and Chief Patent Counsel
doi:10.1038/70167
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(70K)
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| Poster Abstracts | Top |
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| Anwer, Khursheed |
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Cationic Lipid-Based Systemic Plasmid Delivery for the Treatment of Angiogenesis-Dependent
Tumors p36
Khursheed Anwer, Clare Meaney, Grace Kao, Nasir Hussain, Robert Shelvin, Rosa M. Earls, Pat Leonard, Alain P. Rolland
& Sean M. Sullivan
doi:10.1038/70169
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(41K)
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| Deng, Xiaoming |
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Gene Therapy Accelerates Chronic Duodenal Ulcer Healing in Rats Using
VEGF and PDGF Naked DNA or Adenoviral Plasmids pp36 - 37
X. M. Deng, S. Szabo, M.R. Jadus, T. Khomenko, M. Yoshida, M. Herlyn, M. Nesbit
& W. Florsheim
doi:10.1038/70170
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(46K)
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| Hwang, Ms. Sue |
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A New Class of Polymers for the Delivery of Macromolecular Therapeutics
p37
Sue Hwang
doi:10.1038/70171
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(39K)
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| Kingsman, Susan |
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Preclinical Evaluation of Human Cytochrome P450 2b6 (Cyp2b6) as a Therapeutic
Gene Delivered by a Retroviral Vehicle for Gene-Directed Enzyme Prodrug Therapy
(GDEPT) of Cancer p37
S.M. Kingsman, O. Kan, L. Griffiths, S. Iqball, D. Baban, M. Uden, H. Spearman, A. Slade, A.J. Kingsman
& S. Naylor
doi:10.1038/70172
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(39K)
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The Macrophage-Exploiting Hypoxia With Cell Based Delivery of GDEPT p38
S.M. Kingsman, L. Griffiths, K. Binley, S. Iqball, O. Kan, P. Maxwell, C. Lewis, A. Harris
& S. Naylor
doi:10.1038/70173
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A Physiologically Regulated Adenoviral Vector for the Treatment of Ischaemic
Disease p38
S.M. Kingsman, K. Binley, L. Griffiths, S. Iqball, H. Spearman, A.J. Kingsman
& S. Naylor
doi:10.1038/70174
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(44K)
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| Ma, Haiching |
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Nonclassical Nuclear Localization Signal Provides for High Efficiency,
Nonviral Gene Transfer to Nondividing Endothelium p39
M. Subramanian, S.L. Diamond
& H. Ma
doi:10.1038/70175
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(47K)
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| Nakamura, Shin |
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Assessment of Gene Transfer Using a Non-Viral Liposome Vector in a Monkey
Model p39
Shin Nakamura, Satoko Mitsunaga, Keiko Shimizu, Makoto Hirano, Toshitaka Imamura, Akihiro Abe
& Norihiko Emi
doi:10.1038/70176
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(47K)
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| Normand, Nadia |
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VP22-Mediated Delivery of Oligonucleotides Into Cells p40
Nadia Normand, Hans van Leeuwen, Jeff Drew, Anne Phelan, Neil Brewis
& Peter O'Hare
doi:10.1038/70177
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(48K)
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