421
TITLE: A primate T-lymphotropic virus, PTLV-L, different from human T-lymphotropic viruses types I and II, in a wild-caught baboon (Papio hamadryas).
AUTHORS: Goubau, P; Van Brussel, M; Vandamme, AM; Liu, HF; Desmyter, J;
PUBLISHED: 1994, SOURCE: Proceedings of the National Academy of Sciences, VOLUME: 91, ISSUE: 7
INDEXED IN: CrossRef
IN MY: ORCID
422
TITLE: HTLV-II SEROPREVALENCE IN PYGMIES ACROSS AFRICA SINCE 1970
AUTHORS: GOUBAU, P; LIU, HF; DELANGE, GG; VANDAMME, AM; DESMYTER, J;
PUBLISHED: 1993, SOURCE: AIDS RESEARCH AND HUMAN RETROVIRUSES, VOLUME: 9, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef
423
TITLE: HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) STRAINS SELECTED FOR RESISTANCE AGAINST THE HIV-1-SPECIFIC [2',5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-3'-SPIRO-5''-(4''-AMINO-1'',2''-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;
PUBLISHED: 1993, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 90, ISSUE: 15
INDEXED IN: Scopus WOS
424
TITLE: HIV-1-SPECIFIC REVERSE-TRANSCRIPTASE INHIBITORS SHOW DIFFERENTIAL ACTIVITY AGAINST HIV-1 MUTANT STRAINS CONTAINING DIFFERENT AMINO-ACID SUBSTITUTIONS IN THE REVERSE-TRANSCRIPTASE  Full Text
AUTHORS: BALZARINI, J; KARLSSON, A; PEREZPEREZ, MJ; VRANG, L; WALBERS, J; ZHANG, H; OBERG, B; VANDAMME, AM; CAMARASA, MJ; DECLERCQ, E;
PUBLISHED: 1993, SOURCE: VIROLOGY, VOLUME: 192, ISSUE: 1
INDEXED IN: Scopus WOS
425
TITLE: POTENT AND HIGHLY SELECTIVE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 (HIV-1) INHIBITION BY A SERIES OF ALPHA-ANILINOPHENYLACETAMIDE DERIVATIVES TARGETED AT HIV-1 REVERSE-TRANSCRIPTASE
AUTHORS: PAUWELS, R; ANDRIES, K; DEBYSER, Z; VAN DAELE, P; SCHOLS, D; STOFFELS, P; DEVREESE, K; WOESTENBORGHS, R; VANDAMME, AM; JANSSEN, CGM; ANNE, J; CAUWENBERGH, G; DESMYTER, J; HEYKANTS, J; JANSSEN, MAC; DE CLERCQ, E; JANSSEN, PAJ;
PUBLISHED: 1993, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 90, ISSUE: 5
INDEXED IN: Scopus WOS
426
TITLE: Human immunodeficiency virus type 1 (HIV-1) strains selected for resistance against the HIV-1-specific [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro- 5''-(4''-amino-1'',2''-oxathiole-2'',2''-dioxide)]-beta-D-pentofurano syl (TSAO) nucleoside analogues retain sensitivity to HIV-1-specific nonnucleoside inhibitors.
AUTHORS: Balzarini, J; Karlsson, A; Vandamme, AM; Perez-Perez, MJ; Zhang, H; Vrang, L; Oberg, B; Backbro, K; Unge, T; San-Felix, A;
PUBLISHED: 1993, SOURCE: Proceedings of the National Academy of Sciences, VOLUME: 90, ISSUE: 15
INDEXED IN: CrossRef
IN MY: ORCID
427
TITLE: Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of alpha-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase.
AUTHORS: Pauwels, R; Andries, K; Debyser, Z; Van Daele, P; Schols, D; Stoffels, P; De Vreese, K; Woestenborghs, R; Vandamme, AM; Janssen, CG;
PUBLISHED: 1993, SOURCE: Proceedings of the National Academy of Sciences, VOLUME: 90, ISSUE: 5
INDEXED IN: CrossRef
IN MY: ORCID
428
TITLE: CELL TYPE-SPECIFIC ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 ACTIVITY OF THE TRANSACTIVATION INHIBITOR-RO5-3335
AUTHORS: WITVROUW, M; PAUWELS, R; VANDAMME, AM; SCHOLS, D; REYMEN, D; YAMAMOTO, N; DESMYTER, J; DECLERCQ, E;
PUBLISHED: 1992, SOURCE: ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, VOLUME: 36, ISSUE: 12
INDEXED IN: Scopus WOS
429
TITLE: CHARACTERIZATION OF A RECOMBINANT CHIMERIC PLASMINOGEN-ACTIVATOR COMPOSED OF A FIBRIN FRAGMENT-D-DIMER-SPECIFIC HUMANIZED MONOCLONAL-ANTIBODY AND A TRUNCATED SINGLE-CHAIN UROKINASE
AUTHORS: VANDAMME, AM; DEWERCHIN, M; LIJNEN, HR; BERNAR, H; BULENS, F; NELLES, L; COLLEN, D;
PUBLISHED: 1992, SOURCE: EUROPEAN JOURNAL OF BIOCHEMISTRY, VOLUME: 205, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
430
TITLE: 2',5'-BIS-O-(TERT-BUTYLDIMETHYLSILYL)-3'-SPIRO-5''-(4''-AMINO-1',2''-OXATHIOLE-2'',2''-DIOXIDE)PYRIMIDINE (TSAO) NUCLEOSIDE ANALOGS - HIGHLY SELECTIVE INHIBITORS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 THAT ARE TARGETED AT THE VIRAL REVERSE-TRANSCRIPTASE
AUTHORS: BALZARINI, J; PEREZPEREZ, MJ; SANFELIX, A; SCHOLS, D; PERNO, CF; VANDAMME, AM; CAMARASA, MJ; DECLERCQ, E;
PUBLISHED: 1992, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 89, ISSUE: 10
INDEXED IN: Scopus WOS
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