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Results: 1-8 |
Results: 8
ENHANCED BIOLOGICAL-ACTIVITY OF ANTISENSE OLIGONUCLEOTIDES CONTAINING5-(1-HEXYNYL)-SUBSTITUTED PYRIMIDINE NUCLEOTIDES
Authors: UHLMANN E HORNUNG L HEIN S AUGUSTIN S PEYMAN A WILL DW HELSBERG M SAGI J OTVOS L OJWANG JO MUSTAIN S RANDO RF
Citation: E. Uhlmann et al., ENHANCED BIOLOGICAL-ACTIVITY OF ANTISENSE OLIGONUCLEOTIDES CONTAINING5-(1-HEXYNYL)-SUBSTITUTED PYRIMIDINE NUCLEOTIDES, Nucleosides & nucleotides, 16(7-9), 1997, pp. 1717-1720
NUCLEASE STABILITY AS DOMINANT FACTOR IN THE ANTIVIRAL ACTIVITY OF OLIGONUCLEOTIDES DIRECTED AGAINST HSV-1 IE110
Authors: PEYMAN A HELSBERG M KRETZSCHMAR G MAG M RYTE A UHLMANN E
Citation: A. Peyman et al., NUCLEASE STABILITY AS DOMINANT FACTOR IN THE ANTIVIRAL ACTIVITY OF OLIGONUCLEOTIDES DIRECTED AGAINST HSV-1 IE110, Antiviral research, 33(2), 1997, pp. 135-139
ENHANCED CELLULAR UPTAKE OF G-RICH OLIGONUCLEOTIDES
Authors: PEYMAN A RYTE A HELSBERG M KRETZSCHMAR G MAG M UHLMANN E
Citation: A. Peyman et al., ENHANCED CELLULAR UPTAKE OF G-RICH OLIGONUCLEOTIDES, Nucleosides & nucleotides, 14(3-5), 1995, pp. 1077-1081
INHIBITION OF VIRAL GROWTH BY ANTISENSE OLIGONUCLEOTIDES DIRECTED AGAINST THE IE110 AND THE UL30 MESSENGER-RNA OF HERPES-SIMPLEX VIRUS TYPE-1
Authors: PEYMAN A HELSBERG M KRETZSCHMAR G MAG M GRABLEY S UHLMANN E
Citation: A. Peyman et al., INHIBITION OF VIRAL GROWTH BY ANTISENSE OLIGONUCLEOTIDES DIRECTED AGAINST THE IE110 AND THE UL30 MESSENGER-RNA OF HERPES-SIMPLEX VIRUS TYPE-1, Biological chemistry Hoppe-Seyler, 376(3), 1995, pp. 195-198
EVALUATION OF RETINAL TOXICITY AND EFFICACY OF THE ANTICYTOMEGALOVIRUS COMPOUND 2-AMINO-7-[(1,3-DIHYDROXY-2-PROPOXY)METHYL]PURINE
Authors: BESEN G CHAVEZDELAPAZ E TATEBAYASHI M FLORESAGUILAR M GANGAN PA MUNGUIA D WILEY CA JAHNE G WINKLER I HELSBERG M BERGERONLYNN G FREEMAN WR
Citation: G. Besen et al., EVALUATION OF RETINAL TOXICITY AND EFFICACY OF THE ANTICYTOMEGALOVIRUS COMPOUND 2-AMINO-7-[(1,3-DIHYDROXY-2-PROPOXY)METHYL]PURINE, Antimicrobial agents and chemotherapy, 39(7), 1995, pp. 1485-1488
REGIOSELECTIVE SYNTHESIS AND ANTIVIRAL ACTIVITY OF PURINE NUCLEOSIDE ANALOGS WITH ACYCLIC SUBSTITUENTS AT N7
Authors: JAHNE G KROHA H MULLER A HELSBERG M WINKLER I GROSS G SCHOLL T
Citation: G. Jahne et al., REGIOSELECTIVE SYNTHESIS AND ANTIVIRAL ACTIVITY OF PURINE NUCLEOSIDE ANALOGS WITH ACYCLIC SUBSTITUENTS AT N7, Angewandte Chemie, International Edition in English, 33(5), 1994, pp. 562-563
EVALUATION OF RETINAL TOXICITY AND EFFICACY OF THE ANTI-CMV COMPOUND 2-AMINO-7-[(1,3-DIHIDROXY-2-PROPOXY) METHYL] PURINE (COMPOUND-I)
Authors: BESEN G JAHNE G WINKLER I HELSBERG M FLORESAGUILAR M TATEBAYASHI M GANGAN P DELAPAZ EC MUNGUIA D CHANDLER B BERGERONLYNN G FREEMAN WR
Citation: G. Besen et al., EVALUATION OF RETINAL TOXICITY AND EFFICACY OF THE ANTI-CMV COMPOUND 2-AMINO-7-[(1,3-DIHIDROXY-2-PROPOXY) METHYL] PURINE (COMPOUND-I), Investigative ophthalmology & visual science, 35(4), 1994, pp. 2102-2102
THE N-7-SUBSTITUTED ACYCLIC NUCLEOSIDE ANALOG 2-AMINO-7-[(1,3-DIHYDROXY-2-PROPOXY)METHYL]PURINE IS A POTENT AND SELECTIVE INHIBITOR OF HERPESVIRUS REPLICATION
Authors: NEYTS J ANDREI G SNOECK R JAHNE G WINKLER I HELSBERG M BALZARINI J DECLERCQ E
Citation: J. Neyts et al., THE N-7-SUBSTITUTED ACYCLIC NUCLEOSIDE ANALOG 2-AMINO-7-[(1,3-DIHYDROXY-2-PROPOXY)METHYL]PURINE IS A POTENT AND SELECTIVE INHIBITOR OF HERPESVIRUS REPLICATION, Antimicrobial agents and chemotherapy, 38(12), 1994, pp. 2710-2716
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