检索结果 - S. Passic

Utilizing the binding capacity of CRISPR/Cas9 to target the HIV-1 quasispecies 由 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 由 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 由 R. Berman, W. Dampier, A. Atkins, A. Allen, V. Pirrone, S. Passic, A. Ahmed, Z. Szep, M. Nonnemacher, B. Wigdahl

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Genetic variation continues to occur in well-controlled HIV-1-infected patients 由 W. Dampier, M.R. Nonnemacher, J. Chang Mell, J. Earl, V. Pirrone, B. Aiamkitsumrit, W. Zhong, K. Kercher, S. Passic, J.W. Williams, J.M. Jacobson, B. Wigdahl

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Designing broad-spectrum gRNAs to target the HIV-1 LTR with CRISPR/cas9-based therapeutic strategies 由 A. Allen, N.T. Sullivan, W. Dampier, C.H. Chung, A. Atkins, G. Homan, V. Pirrone, S. Passic, J. Williams, Z. Szep, J.M. Jacobson, M.R. Nonnemacher, B. Wigdahl

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SNPs within the HIV-1 LTR associate with increased virus persistence 由 N.T. Sullivan, M.R. Nonnemacher, V. Pirrone, R. Feng, B. Moldover, W. Dampier, S. Passic, J. Williams, B. Aiamkitsumrit, W. Zhong, B. Blakey, S. Shah, J.M. Jacobson, B. Wigdahl

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Examining functional alterations of HIV-1 Tat variants associated with neurocognitively impaired patients in the Drexel Medicine CARES Cohort 由 M.R. Nonnemacher, A.R. Mele, K.M. King, G. Antell, W. Dampier, R. Tata, V. Pirrone, J. Williams, G. Homan, S. Passic, K. Kercher, W. Zhong, Z. Szep, J. Jacobson, B. Wigdahl, S. Kortagere

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