AAAAAA

   
Results: 1-20 |
Results: 20
THE INTERRELATIONSHIP BETWEEN TUBULAR AND PAPILLARY SECTORS OF TUBULO-VILLOUS COLORECTAL ADENOMAS - COMPARATIVE MORPHOMETRIC ANALYSIS AND EVALUATION OF CELL-PROLIFERATION
Authors: REISSENWEBER N GUALCO G ARDAO G VELAZQUEZ S KLICHE I FOSMAN E ALMEIDA E
Citation: N. Reissenweber et al., THE INTERRELATIONSHIP BETWEEN TUBULAR AND PAPILLARY SECTORS OF TUBULO-VILLOUS COLORECTAL ADENOMAS - COMPARATIVE MORPHOMETRIC ANALYSIS AND EVALUATION OF CELL-PROLIFERATION, Human pathology, 29(5), 1998, pp. 431-437
ABASIC ANALOGS OF TSAO-T AS THE FIRST SUGAR-DERIVATIVES THAT SPECIFICALLY INHIBIT HIV-1 REVERSE-TRANSCRIPTASE
Authors: VELAZQUEZ S CHAMORRO C PEREZPEREZ MJ ALVAREZ R JIMENO ML MARTINDOMENECH A PEREZ C GAGO F DECLERCQ E BALZARINI J SANFELIX A CAMARASA MJ
Citation: S. Velazquez et al., ABASIC ANALOGS OF TSAO-T AS THE FIRST SUGAR-DERIVATIVES THAT SPECIFICALLY INHIBIT HIV-1 REVERSE-TRANSCRIPTASE, Journal of medicinal chemistry, 41(23), 1998, pp. 4636-4647
SYNTHESIS AND EVALUATION OF 5-HALO 2',3'-DIDEHYDRO-2',3'-DIDEOXYNUCLEOSIDES AND THEIR BLOCKED PHOSPHORAMIDATES AS POTENTIAL ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENTS - AN EXAMPLE OF KINASE BYPASS
Authors: MCGUIGAN C VELAZQUEZ S DECLERCQ E BALZARINI J
Citation: C. Mcguigan et al., SYNTHESIS AND EVALUATION OF 5-HALO 2',3'-DIDEHYDRO-2',3'-DIDEOXYNUCLEOSIDES AND THEIR BLOCKED PHOSPHORAMIDATES AS POTENTIAL ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS AGENTS - AN EXAMPLE OF KINASE BYPASS, Antiviral chemistry & chemotherapy, 8(6), 1997, pp. 519-527
EFFECT OF HIGH IONIC-STRENGTH AND INHIBITORS OF H,K-ATPASE ON THE OUABAIN-SENSITIVE K-P-NITROPHENYLPHOSPHATASE ACTIVITY IN THE SEA-ANEMONE STICHODACTYLA-HELIANTHUS
Authors: SPECHT SC RODRIGUEZ C QUINONES L VELAZQUEZ S
Citation: Sc. Specht et al., EFFECT OF HIGH IONIC-STRENGTH AND INHIBITORS OF H,K-ATPASE ON THE OUABAIN-SENSITIVE K-P-NITROPHENYLPHOSPHATASE ACTIVITY IN THE SEA-ANEMONE STICHODACTYLA-HELIANTHUS, Comparative biochemistry and physiology. B. Comparative biochemistry, 117(2), 1997, pp. 217-224
PHOSPHORAMIDATE DERIVATIVES OF D4T AS INHIBITORS OF HIV - THE EFFECT OF AMINO-ACID VARIATION
Authors: MCGUIGAN C TSANG HW CAHARD D TURNER K VELAZQUEZ S SALGADO A BIDOIS L NAESENS L DECLERCQ E BALZARINI J
Citation: C. Mcguigan et al., PHOSPHORAMIDATE DERIVATIVES OF D4T AS INHIBITORS OF HIV - THE EFFECT OF AMINO-ACID VARIATION, Antiviral research, 35(3), 1997, pp. 195-204
TSAO DERIVATIVES - HIGHLY SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) REPLICATION
Authors: CAMARASA MJ PEREZPEREZ MJ VELAZQUEZ S SANFELIX A ALVAREZ R INGATE S JIMENO ML KARLSSON A DECLERCQ E BALZARINI J
Citation: Mj. Camarasa et al., TSAO DERIVATIVES - HIGHLY SPECIFIC INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) REPLICATION, Nucleosides & nucleotides, 14(3-5), 1995, pp. 585-594
SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF 4-SUBSTITUTED AND 5-SUBSTITUTED 1,2,3-TRIAZOLE-TSAO DERIVATIVES
Authors: SANFELIX A ALVAREZ R VELAZQUEZ S DECLERCQ E BALZARINI J CAMARASA MJ
Citation: A. Sanfelix et al., SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF 4-SUBSTITUTED AND 5-SUBSTITUTED 1,2,3-TRIAZOLE-TSAO DERIVATIVES, Nucleosides & nucleotides, 14(3-5), 1995, pp. 595-598
EVIDENCE FOR THE INVOLVEMENT OF THE SMALL-SUBUNIT OF HIV-1 REVERSE-TRANSCRIPTASE (RT) IN THE TSAO-RESISTANCE
Authors: JONCKHEERE H TAYMANS JM BALZARINI J VELAZQUEZ S CAMARASA MJ DESMYTER J DECLERCQ E ANNE J
Citation: H. Jonckheere et al., EVIDENCE FOR THE INVOLVEMENT OF THE SMALL-SUBUNIT OF HIV-1 REVERSE-TRANSCRIPTASE (RT) IN THE TSAO-RESISTANCE, Nucleosides & nucleotides, 14(3-5), 1995, pp. 599-602
HOLISTIC RISK ASSESSMENT - AN EMERGING PROCESS FOR ENVIRONMENTAL DECISIONS
Authors: HARVEY T MAHAFFEY KR VELAZQUEZ S DOURSON M
Citation: T. Harvey et al., HOLISTIC RISK ASSESSMENT - AN EMERGING PROCESS FOR ENVIRONMENTAL DECISIONS, Regulatory toxicology and pharmacology, 22(2), 1995, pp. 110-117
MONOMER CHAIN CROSS-TRANSFER CONSTANTS AND CROSS TERMINATION FACTOR EVALUATIONS ON STYRENE-ACRYLONITRILE COPOLYMERIZATION
Authors: MENDIZABAL E VELAZQUEZ S GONZALEZ V JASSO CF
Citation: E. Mendizabal et al., MONOMER CHAIN CROSS-TRANSFER CONSTANTS AND CROSS TERMINATION FACTOR EVALUATIONS ON STYRENE-ACRYLONITRILE COPOLYMERIZATION, Polymer engineering and science, 35(2), 1995, pp. 195-201
SUPPRESSION OF THE BREAKTHROUGH OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) IN CELL-CULTURE BY THIOCARBOXANILIDE DERIVATIVES WHEN USED INDIVIDUALLY OR IN COMBINATION WITH OTHER HIV-1 SPECIFIC INHIBITORS (IE, TSAO DERIVATIVES)
Authors: BALZARINI J PEREZPEREZ MJ VELAZQUEZ S SANFELIX A CAMARASA MJ DECLERCQ E KARLSSON A
Citation: J. Balzarini et al., SUPPRESSION OF THE BREAKTHROUGH OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) IN CELL-CULTURE BY THIOCARBOXANILIDE DERIVATIVES WHEN USED INDIVIDUALLY OR IN COMBINATION WITH OTHER HIV-1 SPECIFIC INHIBITORS (IE, TSAO DERIVATIVES), Proceedings of the National Academy of Sciences of the United Statesof America, 92(12), 1995, pp. 5470-5474
SYNTHESIS AND ANTI-HIV ACTIVITY OF [AZT]-[TSAO-T] AND [AZT]-[HEPT] DIMERS AS POTENTIAL MULTIFUNCTIONAL INHIBITORS OF HIV-1 REVERSE-TRANSCRIPTASE
Authors: VELAZQUEZ S ALVAREZ R SANFELIX A JIMENO ML DECLERCQ E BALZARINI J CAMARASA MJ
Citation: S. Velazquez et al., SYNTHESIS AND ANTI-HIV ACTIVITY OF [AZT]-[TSAO-T] AND [AZT]-[HEPT] DIMERS AS POTENTIAL MULTIFUNCTIONAL INHIBITORS OF HIV-1 REVERSE-TRANSCRIPTASE, Journal of medicinal chemistry, 38(10), 1995, pp. 1641-1649
RADICAL CYCLIZATIONS ON SUGAR TEMPLATES - STEREOSELECTIVE SYNTHESIS OF FUSED GAMMA-BUTYROLACTONES OF CARBOHYDRATES
Authors: VELAZQUEZ S CAMARASA MJ
Citation: S. Velazquez et Mj. Camarasa, RADICAL CYCLIZATIONS ON SUGAR TEMPLATES - STEREOSELECTIVE SYNTHESIS OF FUSED GAMMA-BUTYROLACTONES OF CARBOHYDRATES, Tetrahedron : asymmetry, 5(11), 1994, pp. 2141-2154
SYNTHESIS OF ,5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-ARABINO AND -5''-(4''-AMINO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE) - ANALOGS OF THE HIGHLY SPECIFIC ANTI-HIV-1 AGENT TSAO-T
Authors: VELAZQUEZ S JIMENO ML CAMARASA MJ BALZARINI J
Citation: S. Velazquez et al., SYNTHESIS OF ,5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-ARABINO AND -5''-(4''-AMINO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE) - ANALOGS OF THE HIGHLY SPECIFIC ANTI-HIV-1 AGENT TSAO-T, Tetrahedron, 50(37), 1994, pp. 11013-11022
STEREOSPECIFIC SYNTHESIS AND MMR CONFORMATIONAL STUDIES OF GAMMA-BUTYROLACTONES OF NUCLEOSIDES AS CHIRAL SYNTHONS FOR THE PREPARATION OF 2'-C-BRANCHED-CHAIN AND 3'-C-BRANCHED-CHAIN NUCLEOSIDES
Authors: VELAZQUEZ S JIMENO ML HUSS S BALZARINI J CAMARASA MJ
Citation: S. Velazquez et al., STEREOSPECIFIC SYNTHESIS AND MMR CONFORMATIONAL STUDIES OF GAMMA-BUTYROLACTONES OF NUCLEOSIDES AS CHIRAL SYNTHONS FOR THE PREPARATION OF 2'-C-BRANCHED-CHAIN AND 3'-C-BRANCHED-CHAIN NUCLEOSIDES, Journal of organic chemistry, 59(25), 1994, pp. 7661-7670
NOVEL SERIES OF TSAO-T DERIVATIVES - SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF 4-SUBSTITUTED, 5-SUBSTITUTED, AND 6-SUBSTITUTED PYRIMIDINE ANALOGS
Authors: SANFELIX A VELAZQUEZ S PEREZPEREZ MJ BALZARINI J DECLERCQ E CAMARASA MJ
Citation: A. Sanfelix et al., NOVEL SERIES OF TSAO-T DERIVATIVES - SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF 4-SUBSTITUTED, 5-SUBSTITUTED, AND 6-SUBSTITUTED PYRIMIDINE ANALOGS, Journal of medicinal chemistry, 37(4), 1994, pp. 453-460
URANOSYL]-3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOL 2'',2''-DIOXIDE) (TSAO) ANALOGS - SYNTHESIS AND ANTI-HIV-1 ACTIVITY
Authors: ALVAREZ R VELAZQUEZ S SANFELIX A AQUARO S DECLERCQ E PERNO CF KARLSSON A BALZARINI J CAMARASA MJ
Citation: R. Alvarez et al., URANOSYL]-3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOL 2'',2''-DIOXIDE) (TSAO) ANALOGS - SYNTHESIS AND ANTI-HIV-1 ACTIVITY, Journal of medicinal chemistry, 37(24), 1994, pp. 4185-4194
RESISTANCE OF HIV-1 REVERSE-TRANSCRIPTASE AGAINST 5''-(4''-AMINO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)] (TSAO) DERIVATIVES IS DETERMINED BY THE MUTATION GLU(138)-]LYS ON THE P51 SUBUNIT
Authors: JONCKHEERE H TAYMANS JM BALZARINI J VELAZQUEZ S CAMARASA MJ DESMYTER J DECLERCQ E ANNE J
Citation: H. Jonckheere et al., RESISTANCE OF HIV-1 REVERSE-TRANSCRIPTASE AGAINST 5''-(4''-AMINO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)] (TSAO) DERIVATIVES IS DETERMINED BY THE MUTATION GLU(138)-]LYS ON THE P51 SUBUNIT, The Journal of biological chemistry, 269(41), 1994, pp. 25255-25258
HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) STRAINS SELECTED FOR RESISTANCE AGAINST THE HIV-1-SPECIFIC -OXATHIOLE-2'',2''-DIOXIDE)!-BETA-D-PENTOFURANOSYL (TSAO) NUCLEOSIDE ANALOGS RETAIN SENSITIVITY TO HIV-1-SPECIFIC NONNUCLEOSIDE INHIBITORS
Authors: BALZARINI J KARLSSON A VANDAMME AM PEREZPEREZ MJ ZHANG H VRANG L OBERG B BACKBRO K UNGE T SANFELIX A VELAZQUEZ S CAMARASA MJ DECLERCQ E
Citation: J. Balzarini et al., HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) STRAINS SELECTED FOR RESISTANCE AGAINST THE HIV-1-SPECIFIC -OXATHIOLE-2'',2''-DIOXIDE)!-BETA-D-PENTOFURANOSYL (TSAO) NUCLEOSIDE ANALOGS RETAIN SENSITIVITY TO HIV-1-SPECIFIC NONNUCLEOSIDE INHIBITORS, Proceedings of the National Academy of Sciences of the United Statesof America, 90(15), 1993, pp. 6952-6956
TSAO ANALOGS .3. SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF S-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL 3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOLE 2'',2''-DIOXIDE) PURINE AND PURINE-MODIFIED NUCLEOSIDES
Authors: VELAZQUEZ S SANFELIX A PEREZPEREZ MJ BALZARINI J DECLERCQ E CAMARASA MJ
Citation: S. Velazquez et al., TSAO ANALOGS .3. SYNTHESIS AND ANTI-HIV-1 ACTIVITY OF S-O-(TERT-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL 3'-SPIRO-5''-(4''-AMINO-1'',2''-OXATHIOLE 2'',2''-DIOXIDE) PURINE AND PURINE-MODIFIED NUCLEOSIDES, Journal of medicinal chemistry, 36(22), 1993, pp. 3230-3239
Risultati: 1-20 |