Comparative activities of lipid esters of cidofovir and cyclic cidofovir against replication of herpesviruses in vitro.
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CMX001 (1-O-hexadecyloxypropyl-cidofovir) inhibits polyomavirus JC replication in human brain progenitor-derived astrocytesEfficacy of CMX001 against herpes simplex virus infections in mice and correlations with drug distribution studiesManagement of Epstein-Barr Virus infections and post-transplant lymphoproliferative disorders in patients after allogeneic hematopoietic stem cell transplantation: Sixth European Conference on Infections in Leukemia (ECIL-6) guidelinesCytomegalovirus antivirals and development of improved animal modelsProdrugs of phosphonates and phosphates: crossing the membrane barrierCurrent and potential treatments for ubiquitous but neglected herpesvirus infectionsSeco-pregnane steroids target the subgenomic RNA of alphavirus-like RNA virusesVirucidal activity of polysaccharide extracts from four algal species against herpes simplex virusHuman cytomegalovirus induces TGF-β1 activation in renal tubular epithelial cells after epithelial-to-mesenchymal transition.Identification of a varicella-zoster virus replication inhibitor that blocks capsid assembly by interacting with the floor domain of the major capsid protein.Development of CMX001 for the Treatment of Poxvirus Infections.Alkoxyalkyl esters of (S)-9-[3-hydroxy-2-(phosphonomethoxy)propyl]adenine are potent inhibitors of the replication of wild-type and drug-resistant human immunodeficiency virus type 1 in vitro.Synthesis and early development of hexadecyloxypropylcidofovir: an oral antipoxvirus nucleoside phosphonate.Cyclopropavir inhibits the normal function of the human cytomegalovirus UL97 kinase.CMX001 potentiates the efficacy of acyclovir in herpes simplex virus infectionsUpdate on emerging antivirals for the management of herpes simplex virus infections: a patenting perspective.Progress in the development of new therapies for herpesvirus infectionsAntiviral activities of novel 5-phosphono-pent-2-en-1-yl nucleosides and their alkoxyalkyl phosphonoestersOral 1-O-octadecyl-2-O-benzyl-sn-glycero-3-cidofovir targets the lung and is effective against a lethal respiratory challenge with ectromelia virus in micePreclinical evaluation of a genetically engineered herpes simplex virus expressing interleukin-12Update on new antivirals under development for the treatment of double-stranded DNA virus infectionsBrincidofovir Use after Foscarnet Crystal Nephropathy in a Kidney Transplant Recipient with Multiresistant Cytomegalovirus Infection.Synthesis and antiviral activity of certain second generation methylenecyclopropane nucleosidesHuman cytomegalovirus UL97 kinase alters the accumulation of CDK1.Recent advances in the understanding of infectious mononucleosis: are prospects improved for treatment or control?Amphipathic DNA polymers exhibit antiherpetic activity in vitro and in vivo.Treatment of herpes simplex virus infections in pediatric patients: current status and future needs.Selection and recombinant phenotyping of a novel CMX001 and cidofovir resistance mutation in human cytomegalovirus.The genetic basis of human cytomegalovirus resistance and current trends in antiviral resistance analysis.How we treat cytomegalovirus in hematopoietic cell transplant recipients.Human herpesvirus 6 U69 kinase phosphorylates the methylenecyclopropane nucleosides cyclopropavir, MBX 2168, and MBX 1616 to their monophosphates.Alkoxyalkyl prodrugs of acyclic nucleoside phosphonates enhance oral antiviral activity and reduce toxicity: current state of the art.Inhibition of herpesvirus replication by 5-substituted 4'-thiopyrimidine nucleosides.How I treat adenovirus in hematopoietic stem cell transplant recipientsThe search for new therapies for human cytomegalovirus infections.Current and emerging antivirals for the treatment of cytomegalovirus (CMV) retinitis: an update on recent patents.Prodrug strategies in ocular drug delivery.Anti-herpesvirus agents: a patent and literature review (2003 to present).The development of new therapies for human herpesvirus 6.Helicase-primase as a target of new therapies for herpes simplex virus infections.
P2860
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P2860
Comparative activities of lipid esters of cidofovir and cyclic cidofovir against replication of herpesviruses in vitro.
description
2005 nî lūn-bûn
@nan
2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@ast
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@en
type
label
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@ast
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@en
prefLabel
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@ast
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@en
P2093
P2860
P1476
Comparative activities of lipi ...... ion of herpesviruses in vitro.
@en
P2093
Caroll B Hartline
Earl R Kern
Emma A Harden
James R Beadle
Karl Y Hostetler
Mark N Prichard
Nicole L Kushner
Shannon L Daily
Stephanie L Williams-Aziz
W Brad Wan
P2860
P304
P356
10.1128/AAC.49.9.3724-3733.2005
P407
P577
2005-09-01T00:00:00Z