Broad-spectrum gRNAs abolish HIV-1 LTR-mediated transcription in cells that receive CRISPR/Cas9 therapy by B. Wigdahl, A. Allen, S. Worell, G. Nwaozo, R. Madrid, W. Dampier, M. Nonnemacher

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Utilizing the binding capacity of CRISPR/Cas9 to target the HIV-1 quasispecies by M. Nonnemacher, W. Dampier, M. Desimone, V. Pirrone, K. Kercher, S. Passic, J. Williams, B. Wigdahl

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PP 1.43 – 00206 Evaluating integrated HIV-1 quasispecies using Near Full Length sequencing in ART-suppressed individuals in the Drexel CARES Cohort by M. Collins, D. De Souza, W. Dampier, C. Spector, V. Pirrone, S. Passic, K. Malone, S. Tillman, B. Wigdahl, M. Nonnemacher

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PP 6.5 – 00205 Utilization of high-throughput assays and deep-learning for selection of CRISPR/Cas9-gRNA pairs used in an HIV-1 cure strategy by R. Berman, W. Dampier, A. Atkins, A. Allen, V. Pirrone, S. Passic, A. Ahmed, Z. Szep, M. Nonnemacher, B. Wigdahl

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