Mark A. Muesing
Affiliations: | Rockefeller University, New York, NY, United States |
Area:
Molecular Biology, ImmunologyGoogle:
"Mark Muesing"
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Publications
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Luo Y, Jacobs EY, Greco TM, et al. (2016) HIV-host interactome revealed directly from infected cells. Nature Microbiology. 1: 16068 |
Luo Y, Jacobs EY, Greco TM, et al. (2016) HIV-host interactome revealed directly from infected cells. Nature Microbiology. 1 |
Luo Y, Muesing MA. (2014) Mass spectrometry-based proteomic approaches for discovery of HIV-host interactions. Future Virology. 9: 979-992 |
Trinité B, Chan CN, Lee CS, et al. (2014) Suppression of Foxo1 activity and down-modulation of CD62L (L-selectin) in HIV-1 infected resting CD4 T cells. Plos One. 9: e110719 |
Sargeant D, Deverasetty S, Luo Y, et al. (2011) HIVToolbox, an integrated web application for investigating HIV. Plos One. 6: e20122 |
Mohammed KD, Topper MB, Muesing MA. (2011) Sequential deletion of the integrase (Gag-Pol) carboxyl terminus reveals distinct phenotypic classes of defective HIV-1. Journal of Virology. 85: 4654-66 |
Luo Y, Muesing MA. (2010) Prospective strategies for targeting HIV-1 integrase function. Future Medicinal Chemistry. 2: 1055-60 |
Low A, Prada N, Topper M, et al. (2009) Natural polymorphisms of human immunodeficiency virus type 1 integrase and inherent susceptibilities to a panel of integrase inhibitors. Antimicrobial Agents and Chemotherapy. 53: 4275-82 |
Berthoux L, Sebastian S, Muesing MA, et al. (2007) The role of lysine 186 in HIV-1 integrase multimerization. Virology. 364: 227-36 |
Topper M, Luo Y, Zhadina M, et al. (2007) Posttranslational acetylation of the human immunodeficiency virus type 1 integrase carboxyl-terminal domain is dispensable for viral replication. Journal of Virology. 81: 3012-7 |