Sensitivity of human immunodeficiency virus to bicyclam derivatives is influenced by the three-dimensional structure of gp120.

Por De Vreese, K, Van Nerum, I, Vermeire, K, Anné, J, De Clercq, E
Publicado em 1997

The molecular target of bicyclams, potent inhibitors of human immunodeficiency virus replication.

Por de Vreese, K, Kofler-Mongold, V, Leutgeb, C, Weber, V, Vermeire, K, Schacht, S, Anné, J, de Clercq, E, Datema, R, Werner, G
Publicado em 1996

Highly potent and selective inhibition of human immunodeficiency virus by the bicyclam derivative JM3100.

Por De Clercq, E, Yamamoto, N, Pauwels, R, Balzarini, J, Witvrouw, M, De Vreese, K, Debyser, Z, Rosenwirth, B, Peichl, P, Datema, R
Publicado em 1994

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.

Por Pauwels, R, Andries, K, Debyser, Z, Van Daele, P, Schols, D, Stoffels, P, De Vreese, K, Woestenborghs, R, Vandamme, A M, Janssen, C G
Publicado em 1993

T30177, an oligonucleotide stabilized by an intramolecular guanosine octet, is a potent inhibitor of laboratory strains and clinical isolates of human immunodeficiency virus type 1...

Por Ojwang, J O, Buckheit, R W, Pommier, Y, Mazumder, A, De Vreese, K, Esté, J A, Reymen, D, Pallansch, L A, Lackman-Smith, C, Wallace, T L
Publicado em 1995

Value of allohaemagglutinins in the diagnosis of a polysaccharide antibody deficiency

Por Schaballie, H, Vermeulen, F, Verbinnen, B, Frans, G, Vermeulen, E, Proesmans, M, De Vreese, K, Emonds, MP, De Boeck, K, Moens, L, Picard, C, Bossuyt, X, Meyts, I
Publicado no Clin Exp Immunol (2015)