Wade Gibson
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Cell Biology, Molecular Biology, Microbiology BiologyGoogle:
"Wade Gibson"Children
Sign in to add traineeBarry J Margulies | grad student | Johns Hopkins (Neurotree) | |
Michael K. Baxter | grad student | 2000 | Johns Hopkins |
Edward J. Brignole | grad student | 2005 | Johns Hopkins |
Rebecca J. Casaday | grad student | 2005 | Johns Hopkins |
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Publications
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Tullman JA, Harmon ME, Delannoy M, et al. (2014) Recovery of an HMWP/hmwBP (pUL48/pUL47) complex from virions of human cytomegalovirus: subunit interactions, oligomer composition, and deubiquitylase activity. Journal of Virology. 88: 8256-67 |
Fernandes SM, Brignole EJ, Taori K, et al. (2011) Cytomegalovirus capsid protease: biological substrates are cleaved more efficiently by full-length enzyme (pUL80a) than by the catalytic domain (assemblin). Journal of Virology. 85: 3526-34 |
Kim ET, Oh SE, Lee YO, et al. (2009) Cleavage specificity of the UL48 deubiquitinating protease activity of human cytomegalovirus and the growth of an active-site mutant virus in cultured cells. Journal of Virology. 83: 12046-56 |
Nguyen NL, Loveland AN, Gibson W. (2008) Nuclear localization sequences in cytomegalovirus capsid assembly proteins (UL80 proteins) are required for virus production: inactivating NLS1, NLS2, or both affects replication to strikingly different extents. Journal of Virology. 82: 5381-9 |
Brignole EJ, Gibson W. (2007) Enzymatic activities of human cytomegalovirus maturational protease assemblin and its precursor (pPR, pUL80a) are comparable: [corrected] maximal activity of pPR requires self-interaction through its scaffolding domain. Journal of Virology. 81: 4091-103 |
Loveland AN, Nguyen NL, Brignole EJ, et al. (2007) The amino-conserved domain of human cytomegalovirus UL80a proteins is required for key interactions during early stages of capsid formation and virus production. Journal of Virology. 81: 620-8 |
Margulies BJ, Gibson W. (2007) The chemokine receptor homologue encoded by US27 of human cytomegalovirus is heavily glycosylated and is present in infected human foreskin fibroblasts and enveloped virus particles. Virus Research. 123: 57-71 |
Brignole EJ, Gibson W. (2007) Erratum: Enzymatic activities of human cytomegalovirus maturational protease assemblin and its precursor (pPR, pUL80a) are comparable: Maximal activity of pPR requires self-interaction through its scaffolding domain (Journal of Virology (2007) 81, 8 (4091-4103)) Journal of Virology. 81 |
Wang J, Loveland AN, Kattenhorn LM, et al. (2006) High-molecular-weight protein (pUL48) of human cytomegalovirus is a competent deubiquitinating protease: mutant viruses altered in its active-site cysteine or histidine are viable. Journal of Virology. 80: 6003-12 |
Loveland AN, Chan CK, Brignole EJ, et al. (2005) Cleavage of human cytomegalovirus protease pUL80a at internal and cryptic sites is not essential but enhances infectivity. Journal of Virology. 79: 12961-8 |