نتایج جستجو برای: ul97 protein

تعداد نتایج: 1234792  

Journal: :Journal of virology 1999
D Michel S Kramer S Höhn P Schaarschmidt K Wunderlich T Mertens

Thirteen point mutations targeting predicted domains conserved in homologous protein kinases were introduced into the UL97 coding region of the human cytomegalovirus. All mutagenized proteins were expressed in cells infected with recombinant vaccinia viruses (rVV). Several mutations drastically reduced ganciclovir (GCV) phosphorylation. Mutations at amino acids G340, A442, L446, and F523 result...

Journal: :Antimicrobial agents and chemotherapy 2013
Brian G Gentry Laura E Vollmer Ellie D Hall Katherine Z Borysko Jiri Zemlicka Jeremy P Kamil John C Drach

Human cytomegalovirus (HCMV) is a widespread pathogen in the human population, affecting many immunologically immature and immunocompromised patients, and can result in severe complications, such as interstitial pneumonia and mental retardation. Current chemotherapies for the treatment of HCMV infections include ganciclovir (GCV), foscarnet, and cidofovir. However, the high incidences of advers...

Journal: :Antimicrobial agents and chemotherapy 1997
D J Tenney G Yamanaka S M Voss C W Cianci A V Tuomari A K Sheaffer M Alam R J Colonno

Lobucavir (LBV) is a deoxyguanine nucleoside analog with broad-spectrum antiviral activity. LBV was previously shown to inhibit herpes simplex virus (HSV) DNA polymerase after phosphorylation by the HSV thymidine kinase. Here we determined the mechanism of action of LBV against human cytomegalovirus (HCMV). LBV inhibited HCMV DNA synthesis to a degree comparable to that of ganciclovir (GCV), a ...

Journal: :The Journal of infectious diseases 1998
A Erice N Borrell W Li W J Miller H H Balfour

Ganciclovir susceptibilities and UL97 sequences were analyzed in 20 cytomegalovirus (CMV) isolates recovered from 15 bone marrow transplant recipients with active CMV infection after prophylaxis with acyclovir (group I; 12 isolates) or after acyclovir prophylaxis followed by ganciclovir therapy (group II; 8 isolates). All group I isolates were susceptible to ganciclovir. Five group II isolates ...

2013
Natalia I. Reim Jeremy P. Kamil Depeng Wang Alison Lin Maria Ericsson Jean M. Pesola David E. Golan Donald M. Coen

Inactivation of Retinoblastoma Protein Does Not Overcome 1 the Requirement for Human Cytomegalovirus UL97 2 in Lamina Disruption and Nuclear Egress 3 Natalia I. Reim, Jeremy P. Kamil, Depeng Wang, Alison Lin, Mayuri 4 Sharma, Maria Ericsson, Jean M. Pesola, David E. Golan, and Donald M. Coen 5 Running Title: HPV16 E7 does not replace HCMV UL97 for nuclear egress 6 1 Department of Biological Che...

Journal: :The Journal of general virology 2002
Manfred Marschall Matthias Stein-Gerlach Martina Freitag Regina Kupfer Miriam van den Bogaard Thomas Stamminger

The protein kinase pUL97, encoded by human cytomegalovirus (HCMV), is an important determinant of virus replication. Recently, indolocarbazoles were identified as a class of substances that inhibit the pUL97 kinase activity in vitro. In parallel, it was shown that indolocarbazoles interfere with HCMV replication; however, the causal relationship between inhibition of pUL97 kinase activity and v...

2017
Jessica Rose Vincent C Emery Deepali Kumar Anders Asberg Anders Hartmann Alan G Jardine Angelo A Bignamini Atul Humar Avidan U Neumann

Human cytomegalovirus (CMV) infection is a substantial cause of morbidity and mortality in immunocompromised hosts and globally is one of the most important congenital infections. The nucleoside analogue ganciclovir (GCV), which requires initial phosphorylation by the viral UL97 kinase, is the mainstay for treatment. To date, CMV decay kinetics during GCV therapy have not been extensively inves...

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