Final Program - American Society of Gene & Cell Therapy
Final Program - American Society of Gene & Cell Therapy
Final Program - American Society of Gene & Cell Therapy
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<strong>Program</strong> Schedule, Saturday, May 18, 2013<br />
ASGCT Business Meeting<br />
7:30 am - 8:00 am<br />
ROOM: 150 ABC<br />
Plenary Session 400<br />
8:00 am - 10:00 am<br />
ROOM: BALLROOM E-J<br />
Outstanding New Investigator Symposium<br />
CHAIR<br />
SPEAKERS<br />
Katherine P. Ponder, MD<br />
Aravind Asokan, PhD<br />
A Sweet Side to AAV Biology<br />
Adeno-associated viruses (AAV) exploit a spectrum <strong>of</strong> glycans for cell surface attachment and transduction. Understanding the<br />
structural basis and functional implications <strong>of</strong> such virus-host interactions can guide development <strong>of</strong> recombinant AAV vectors<br />
for clinical gene therapy applications. This talk will highlight our contributions towards discovery <strong>of</strong> AAV receptors, structural<br />
determinants <strong>of</strong> AAV tissue tropism and new strategies to re-engineer AAV-glycan interactions.<br />
Paloma H. Giangrande, PhD<br />
Targeted-Image Guided RNA (TIGR) Therapies<br />
The successful application <strong>of</strong> RNAi therapeutics to humans awaits the development <strong>of</strong> robust delivery technologies. <strong>Cell</strong> conjugation<br />
<strong>of</strong> siRNAs to cell-speciic ligands provides a viable solution to this problem. Synthetic RNA ligands (aptamers) represent an<br />
emerging class <strong>of</strong> pharmaceuticals with great potential for targeted therapeutic/diagnostic applications. Here, we describe<br />
advancements in aptamer technology for enabling the development <strong>of</strong> effective image-guided RNA therapies.<br />
Saturday, May 18, 2013<br />
<strong>Final</strong> <strong>Program</strong> SALT LAKE CITY, UTAH May 15–18, 2013<br />
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