Sadhna Joshi
Affiliations: | University of Toronto, Toronto, ON, Canada |
Area:
Microbiology Biology, Molecular Biology, Mental HealthGoogle:
"Sadhna Joshi"Children
Sign in to add trainee| Maria F. Medina | grad student | 2000 | University of Toronto |
| Ali Ramezani | grad student | 2002 | University of Toronto |
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Publications
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| Falkenhagen A, Joshi S. (2018) Genetic Strategies for HIV Treatment and Prevention. Molecular Therapy. Nucleic Acids. 13: 514-533 |
| Falkenhagen A, Joshi S. (2018) HIV Entry and Its Inhibition by Bifunctional Antiviral Proteins. Molecular Therapy. Nucleic Acids. 13: 347-364 |
| Falkenhagen A, Singh J, Asad S, et al. (2017) Control of HIV Infection In Vivo Using Gene Therapy with a Secreted Entry Inhibitor. Molecular Therapy. Nucleic Acids. 9: 132-144 |
| Falkenhagen A, Joshi S. (2017) Further Characterization of the Bifunctional HIV Entry Inhibitor sCD4-FIT45. Molecular Therapy. Nucleic Acids. 7: 387-395 |
| Falkenhagen A, Asad S, Read SE, et al. (2016) Lentiviral expression system for the purification of secreted proteins from human cell cultures. Bmc Biotechnology. 16: 66 |
| Landry I, Zhu L, Abutarif M, et al. (2016) Model-based Phase 3 dose selection for HIV-1 attachment inhibitor prodrug BMS-663068 in HIV-1-infected patients: population pharmacokinetics/pharmacodynamics of the active moiety, BMS-626529. Antimicrobial Agents and Chemotherapy |
| Falkenhagen A, Ameli M, Asad S, et al. (2014) A novel gene therapy strategy using secreted multifunctional anti-HIV proteins to confer protection to gene-modified and unmodified target cells. Gene Therapy. 21: 175-87 |
| Falkenhagen A, Ameli M, Asad S, et al. (2013) Gene therapy using a secreted single chain variable fragment targeting CCR5 to inhibit HIV infection Journal of Antivirals and Antiretrovirals. 5: 85-91 |
| LEE-RUFF E, OSTROWSKI M, LADHA A, et al. (2010) ChemInform Abstract: Synthesis and HIV Inhibition Activity of 2′,3′-Dideoxy-3′-C-hydroxymethyl Nucleosides. Cheminform. 28: no-no |
| Nazari R, Joshi S. (2009) HIV-1 gene therapy at pre-integration and provirus DNA levels. Current Gene Therapy. 9: 20-5 |