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FINAL PROGRAM - American Society of Gene & Cell Therapy

FINAL PROGRAM - American Society of Gene & Cell Therapy

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94<strong>American</strong> <strong>Society</strong> <strong>of</strong> <strong>Gene</strong> & <strong>Cell</strong> <strong>Therapy</strong>Abstract DirectoryThursday, May 20 thThursday, May 20, 2010Poster Session I — continued6:15 PM - 8:15 PMRoom: Exhibit Hall C & B-South<strong>Gene</strong>tic and Metabolic Diseases <strong>Gene</strong> & <strong>Cell</strong> <strong>Therapy</strong> I136Efficacious <strong>Gene</strong> <strong>Therapy</strong> in Pompe Disease Requires Mannose-6-Phosphate Receptor ExpressionBaodong Sun, Deeksha Bali, Y.-T. Chen, Dwight D. Koeberl.137Development <strong>of</strong> a Safe Hematopoietic Stem <strong>Cell</strong> (HSC) MobilizationStrategy for <strong>Gene</strong> <strong>Therapy</strong> <strong>of</strong> ThalassemiaEvangelia Yannaki, Thalia Papayannopoulou, Erica Jonlin, Ioannis Batsis, Pamela Becker,Fani Zervou, Angeliki Xagorari, Garyfalia Karponi, Varnavas Constantinou, AchillesAnagnostopoulos, Athanasios Fassas, George Stamatoyannopoulos.138Long Term Expression in Liver from scAAV Seems Derived fromIntegrated Vector GenomesPaula S. M. Miranda, Maude Flageul, Christine Kaeppel, Lysbeth ten Bloemendaal,Dominique Aubert, Nowrouzi Ali, Manfred Schmidt, Nicolas Ferry, Piter J. Bosma.139Human Amnion Epithelial (AE) Stem <strong>Cell</strong> Transplant Improves DiseasePhenotype and Survival in Mouse Models <strong>of</strong> Intermediate MapleSyrup Urine Disease (MSUD)K. J. Skvorak, K. Dorko, M. Hansel, F. Marongiu, V. Tahan, K. M. Gibson, Q. Sun, T.Bottiglieri, E. Arning, J. Davila, S. Strom.140<strong>Gene</strong> <strong>Therapy</strong> Approaches Combining the ImmunomodulatoryProperties <strong>of</strong> Liver and IGF-I To Prevent Type I DiabetesSabrina Tafuro, Xavier M. Anguela, Judith Agudo, Alba Casellas, David Callejas, MercèObach, Carles Roca, Albert Ruzo, Fàtima Bosch.141Hepatocyte Engineering and <strong>Gene</strong>tic Modification Approaches <strong>of</strong>Hemophilia Hepatocytes within a Living MouseKazuo Ohashi, Kohei Tatsumi, Chise Tateno, Hiroyuki Nakai, Anja Ehrhardt, Rie Utoh,Katsutoshi Yoshizato, Teruo Okano.142Serotype Optimization <strong>of</strong> an AAV Vector for <strong>Gene</strong> <strong>Therapy</strong> in Canineand Murine Glycogen Storage Disease Type Ia (GSD-Ia)Xiaoyan Luo, Amanda K. Demaster, Songtao Li, Kyha Williams, Talmage T. Brown, DanielM. Kozink, Andrew Bird, Dwight D. Koeberl.143Systemic Delivery <strong>of</strong> Bioactive Glucagon-Like Peptide 1 FollowingAdenoviral Vector-Mediated <strong>Gene</strong> Transfer to Murine SubmandibularGlandsAntonis Voutetakis, Anne M. Rowzee, Ana P. Cotrim, Changyu Zheng, Trushar Rathod,Tulin Yanik, Y. P. Loh, Bruce J. Baum, Niamh X. Cawley.144A Non-Viral, GNE-Lipoplex Treatment to Correct Sialylation Defectsin Gne-Mutant (M712T) MiceTal Yardeni, Carla Ciccone, Shelley Hoogstraten-Miller, Daniel Darvish, Yair Anikster, PhilMaples, Chris Jay, William A. Gahl, John Nemunaitis, Marjan Huizing.145Lentivirally Induced Over-Expression in the Mouse Hypothalamus;a Study <strong>of</strong> the Effects <strong>of</strong> Melanin Stimulating Hormones (MSH) inObesity and DiabetesKim Eerola, Siru Virtanen, Eriika Savontaus, Mikko Savontaus.146Alternative Methods for Ex Vivo <strong>Gene</strong> Transfer to Primary Murine B<strong>Cell</strong>Babak Moghimi, Ou Cao.147A Full Characterization <strong>of</strong> the CAG 140 Huntington’s Disease MouseModelAaron C. Rising, Eileen Denovan-Wright, Ron Mandel.Musculo-skeletal <strong>Gene</strong> & <strong>Cell</strong> <strong>Therapy</strong> I148Assessment <strong>of</strong> Pre-Clinical Safety <strong>of</strong> GMP Grade GNE-Lipoplexesafter Repeat Intravenous Injections in Balb/c MiceAnagha P. Phadke, Chris M. Jay, Phillip B. Maples, Neil Senzer, John Nemunaitis, AlexW. Tong.149Pre-Existing Antibodies to AAV8 Attenuates Micro-DystrophinExpression Following Targeted Vascular DeliveryLouise R. Rodino-Klapac, Chrystal Montgomery, William Bremer, Nancy Davis, KimberlyShontz, Vinod Malik, Katherine Campbell, Thomas J. Preston, Zarife Sahenk, K. ReedClark, Brian D. Coley, Christopher M. Walker, Jerry R. Mendell, Louis G. Chicoine.150AAV Microgene Transfer Reveals the <strong>Cell</strong>ular Motif for Dystrophin-Mediated Sarcolemmal Neuronal Nitric Oxide Synthase (nNOS)LocalizationYi Lai, Yongping Yue, Dongsheng Duan.151<strong>Cell</strong> Therapeutic Approach to Duchenne Muscular Dystrophy UsingMyogenic Differentiation <strong>of</strong> Multipotent Mesenchymal Stromal <strong>Cell</strong>sYuko N. Kasahara, Hiromi H. Kinoh, Hironori Okada, Jin-Hong Shin, Akiyo Nishiyama,Sachiko O. Hosoyama, Michiko W. Maeda, Akinori Nakamura, Takashi Okada, Shin’ichiTakeda.EXHIBITOR PROSPECTUSfinal program

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