Student/Fellow Presentations

Annual Gene Therapy Symposium for
Heart, Lung, and Blood Diseases

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	2nd Annual Gene Therapy Symposium for Heart, Lung, and Blood Diseases Focus Topic: Fetus and Infant November 19-21, 2003 - Sonoma, California Student/Fellow Presentations
	Thursday, November 20

	Colette C. Chambers, BS, UC Davis Overexpression of Lefty A reduces extracellular matrix production in hepatic stellate cells	Shuo Gu, BS, UC Davis Creation of novel lentiviral vector with potent anti-HIV activity

	Benjamin Hendrickson, BS, Childrens Hospital Los Angeles Development of lentiviral vectors for expression specifically in lung epithelia	Chistoph A. Kahl, PhD, Indiana University School of Medicine Lentiviral vectors pseudotyped with envelope glycoproteins from Ross River Virus: Marked variability in transduction related to cell type

	Mi-Young Lee, BS, UC Davis Comparison of gene expression following DNA delivery to dermis and muscle	Mingjie Li, PhD, City of Hope Beckman Research Institute Development of lentiviral vectors expressing PolIII promoted therapeutic RNAs for human gene therapy

	Aaron C. Logan, BS, Childrens Hospital Los Angeles Self-inactivating lentiviral vectors produce genomic-length transcripts competent for encapsidation and integration	Patrick L. Sinn, PhD, University of Iowa Pseudotyping FIV-based lentiviral vectors: Three glycoprotieins that confer apical entry to airway epithelia
	Friday, November 21

	Yuyou Duan, PhD, UC Davis SV-40 mediated gene therapy for bi-functional treatment of human alpha 1-antitrypsis deficiency in an animal model	Suzan Imren, MD, Terry Fox Laboratory Preferred intragenic integration with high-level erythroid expression of a lentiviral vector bearing an anti-sickling Β-globin transgene in NOD/SCID mouse repopulating human cord blood cells

	Daniel F. Jimenez, PhD, UC Davis Fetal progenitor cells in the maternal circulation and long-term microchimerism in rhesus macaques (Macaca mulatta)	Kiarash Khosrotehrani, MD, Tufts-New England Medical Center Fetal microchimeric cells are transferred into maternal circulation during all murine pregnancies and specifically home to the damaged liver

	Christina A. Pacak, BS, University of Florida rAAV-mediated gene therapy to treat limb girdle muscular dystrophy type 2D (LGMD-2D)	Ryan Rodriguez, BS, UC San Francisco Suppression of a stably expressed transgene in human embryonic stem cells by RNA interference

	Rosa H. Won, MD, UC Davis Maternal immune response to fetal gene therapy in rhesus monkeys (Macaca mulatta) Not pictured: Jacqueline Fischer-Lougheed, PhD, USC Keck School of Medicine Induction of chimerism using lentiviral vectors expressing porcine alpha 1,3 galactosyltransferase Naoki Yamamoto, MD, UC Davis Differentiation of human embryonic stem cells along a hepatocyte lineage