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Chris Meier

Showing results (31-40 of 131) with videos related to

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The Journal of Organic Chemistry|December 16, 2006
Synthesis and properties of oligonucleotides containing C8-deoxyguanosine arylamine adducts of borderline carcinogensNicolas Böge, Sonja Gräsl, Chris Meier
Chemmedchem|September 12, 2014
Nucleoside mono- and diphosphate prodrugs of 2',3'-dideoxyuridine and 2',3'-dideoxy-2',3'-didehydrouridineFlorian Pertenbreiter, Jan Balzarini, Chris Meier
Journal of Medicinal Chemistry|October 16, 2010
Diastereoselective synthesis of aryloxy phosphoramidate prodrugs of 3'-deoxy-2',3'-didehydrothymidine monophosphateCristina Arbelo Roman, Jan Balzarini, Chris Meier
Nucleosides, Nucleotides & Nucleic Acids|December 11, 2007
New developments of the "lock-in" modified cycloSal-d4TMPsDalibor Vukadinović-Tenter, Jan Balzarini, Chris Meier
Journal of Medicinal Chemistry|October 2, 2008
Intracellular trapping of cycloSal-pronucleotides: modification of prodrugs with amino acid estersHenning J Jessen, Jan Balzarini, Chris Meier
Chembiochem : a European Journal of Chemical Biology|June 26, 2015
Tagging Glycoproteins with Fluorescently Labeled GDP-Fucoses by Using α1,3-FucosyltransferasesKatrin Seelhorst, Katharina Pahnke, Chris Meier, et al.
Journal of Medicinal Chemistry|September 13, 2022
Triphosphate Prodrugs of the Anti-HIV-Active Compound 3'-Deoxy-3'-fluorothymidine (FLT)Simon Weising, Stefan Weber, Dominique Schols, et al.
Antiviral Chemistry & Chemotherapy|March 18, 2006
Inhibitory efficacy of cyclosal-nucleoside monophosphates of aciclovir and brivudin on DNA synthesis of orthopoxvi rusesAndreas Sauerbrei, Chris Meier, Astrid Meerbach, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|June 5, 2025
Development of a HILIC-MS/MS method for simultaneous quantification of lipophilic antitumor TriPPPro-prodrugs and their polar metabolites in HT29 cell extractsMichelle Vogts, Julian Witt, Maria Riedner, et al.
Journal of Medicinal Chemistry|November 1, 2002
CycloSal-BVDUMP pronucleotides: how to convert an antiviral-inactive nucleoside analogue into a bioactive compound against EBVChris Meier, Andreas Lomp, Astrid Meerbach, et al.
Pageof 14

Showing results (31-40 of 131) with videos related to

Sort By:
Pageof 14
The Journal of Organic Chemistry|December 16, 2006
Synthesis and properties of oligonucleotides containing C8-deoxyguanosine arylamine adducts of borderline carcinogensNicolas Böge, Sonja Gräsl, Chris Meier
Chemmedchem|September 12, 2014
Nucleoside mono- and diphosphate prodrugs of 2',3'-dideoxyuridine and 2',3'-dideoxy-2',3'-didehydrouridineFlorian Pertenbreiter, Jan Balzarini, Chris Meier
Journal of Medicinal Chemistry|October 16, 2010
Diastereoselective synthesis of aryloxy phosphoramidate prodrugs of 3'-deoxy-2',3'-didehydrothymidine monophosphateCristina Arbelo Roman, Jan Balzarini, Chris Meier
Nucleosides, Nucleotides & Nucleic Acids|December 11, 2007
New developments of the "lock-in" modified cycloSal-d4TMPsDalibor Vukadinović-Tenter, Jan Balzarini, Chris Meier
Journal of Medicinal Chemistry|October 2, 2008
Intracellular trapping of cycloSal-pronucleotides: modification of prodrugs with amino acid estersHenning J Jessen, Jan Balzarini, Chris Meier
Chembiochem : a European Journal of Chemical Biology|June 26, 2015
Tagging Glycoproteins with Fluorescently Labeled GDP-Fucoses by Using α1,3-FucosyltransferasesKatrin Seelhorst, Katharina Pahnke, Chris Meier, et al.
Journal of Medicinal Chemistry|September 13, 2022
Triphosphate Prodrugs of the Anti-HIV-Active Compound 3'-Deoxy-3'-fluorothymidine (FLT)Simon Weising, Stefan Weber, Dominique Schols, et al.
Antiviral Chemistry & Chemotherapy|March 18, 2006
Inhibitory efficacy of cyclosal-nucleoside monophosphates of aciclovir and brivudin on DNA synthesis of orthopoxvi rusesAndreas Sauerbrei, Chris Meier, Astrid Meerbach, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|June 5, 2025
Development of a HILIC-MS/MS method for simultaneous quantification of lipophilic antitumor TriPPPro-prodrugs and their polar metabolites in HT29 cell extractsMichelle Vogts, Julian Witt, Maria Riedner, et al.
Journal of Medicinal Chemistry|November 1, 2002
CycloSal-BVDUMP pronucleotides: how to convert an antiviral-inactive nucleoside analogue into a bioactive compound against EBVChris Meier, Andreas Lomp, Astrid Meerbach, et al.
Pageof 14