Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Focher

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
Nucleosides, Nucleotides & Nucleic Acids|September 21, 2001
Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivativesR Salvetti, M Pregnolato, A Verri, et al.
Biochimie|January 1, 1995
Lack of stereospecificity of some cellular and viral enzymes involved in the synthesis of deoxyribonucleotides and DNA: molecular basis for the antiviral activity of unnatural L-beta-nucleosidesS Spadari, G Maga, A Verri, et al.
In Vivo (Athens, Greece)|November 1, 1994
Aphidicolin inhibits in vitro the activity of pseudorabies virus (PRV) DNA polymerase and in vivo the viral proliferationA Verri, G Maga, S Spadari, et al.
Journal of Medicinal Chemistry|August 1, 1988
N2-phenyldeoxyguanosine: a novel selective inhibitor of herpes simplex thymidine kinaseF Focher, C Hildebrand, S Freese, et al.
Journal of Medicinal Chemistry|July 8, 1999
Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylaseH Sun, C Zhi, G E Wright, et al.
Biochemical Pharmacology|May 1, 1988
N2-substituted guanine derivatives act as selective non substrate inhibitors of HSV I thymidine kinaseF Focher, S Sangalli, G Ciarrocchi, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
A novel pharmacological approach to herpes virus infectionsF Focher, D Sandoli, G Wright, et al.
Anticancer Research|July 1, 1992
DNA synthesis enzymes and proliferating cell nuclear antigen in normal and neoplastic nerve cellsA Verri, S Verzeletti, P Mazzarello, et al.
The Biochemical Journal|September 1, 1993
Lack of stereospecificity of suid pseudorabies virus thymidine kinaseG Maga, A Verri, L Bonizzi, et al.
Nucleic Acids Research|August 11, 1991
HP 0.35, a cephalosporin degradation product is a specific inhibitor of lentiviral RNAses HP Hafkemeyer, K Neftel, R Hobi, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
Nucleosides, Nucleotides & Nucleic Acids|September 21, 2001
Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivativesR Salvetti, M Pregnolato, A Verri, et al.
Biochimie|January 1, 1995
Lack of stereospecificity of some cellular and viral enzymes involved in the synthesis of deoxyribonucleotides and DNA: molecular basis for the antiviral activity of unnatural L-beta-nucleosidesS Spadari, G Maga, A Verri, et al.
In Vivo (Athens, Greece)|November 1, 1994
Aphidicolin inhibits in vitro the activity of pseudorabies virus (PRV) DNA polymerase and in vivo the viral proliferationA Verri, G Maga, S Spadari, et al.
Journal of Medicinal Chemistry|August 1, 1988
N2-phenyldeoxyguanosine: a novel selective inhibitor of herpes simplex thymidine kinaseF Focher, C Hildebrand, S Freese, et al.
Journal of Medicinal Chemistry|July 8, 1999
Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylaseH Sun, C Zhi, G E Wright, et al.
Biochemical Pharmacology|May 1, 1988
N2-substituted guanine derivatives act as selective non substrate inhibitors of HSV I thymidine kinaseF Focher, S Sangalli, G Ciarrocchi, et al.
Journal of Chemotherapy (Florence, Italy)|July 1, 1989
A novel pharmacological approach to herpes virus infectionsF Focher, D Sandoli, G Wright, et al.
Anticancer Research|July 1, 1992
DNA synthesis enzymes and proliferating cell nuclear antigen in normal and neoplastic nerve cellsA Verri, S Verzeletti, P Mazzarello, et al.
The Biochemical Journal|September 1, 1993
Lack of stereospecificity of suid pseudorabies virus thymidine kinaseG Maga, A Verri, L Bonizzi, et al.
Nucleic Acids Research|August 11, 1991
HP 0.35, a cephalosporin degradation product is a specific inhibitor of lentiviral RNAses HP Hafkemeyer, K Neftel, R Hobi, et al.
Pageof 7