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203 related items for PubMed ID: 23357451
1. Mechanism of resistance to S138A substituted enfuvirtide and its application to peptide design. Izumi K, Kawaji K, Miyamoto F, Shimane K, Shimura K, Sakagami Y, Hattori T, Watanabe K, Oishi S, Fujii N, Matsuoka M, Kaku M, Sarafianos SG, Kodama EN. Int J Biochem Cell Biol; 2013 Apr; 45(4):908-15. PubMed ID: 23357451 [Abstract] [Full Text] [Related]
2. Design of peptide-based inhibitors for human immunodeficiency virus type 1 strains resistant to T-20. Izumi K, Kodama E, Shimura K, Sakagami Y, Watanabe K, Ito S, Watabe T, Terakawa Y, Nishikawa H, Sarafianos SG, Kitaura K, Oishi S, Fujii N, Matsuoka M. J Biol Chem; 2009 Feb 20; 284(8):4914-20. PubMed ID: 19073606 [Abstract] [Full Text] [Related]
3. Increasing hydrophobicity of residues in an anti-HIV-1 Env peptide synergistically improves potency. Leung MY, Cohen FS. Biophys J; 2011 Apr 20; 100(8):1960-8. PubMed ID: 21504732 [Abstract] [Full Text] [Related]
5. Resistance and replicative capacity of HIV-1 strains selected in vivo by long-term enfuvirtide treatment. Menzo S, Castagna A, Monachetti A, Hasson H, Danise A, Carini E, Bagnarelli P, Lazzarin A, Clementi M. New Microbiol; 2004 Apr 20; 27(2 Suppl 1):51-61. PubMed ID: 15646065 [Abstract] [Full Text] [Related]
6. Emergence and evolution of enfuvirtide resistance following long-term therapy involves heptad repeat 2 mutations within gp41. Xu L, Pozniak A, Wildfire A, Stanfield-Oakley SA, Mosier SM, Ratcliffe D, Workman J, Joall A, Myers R, Smit E, Cane PA, Greenberg ML, Pillay D. Antimicrob Agents Chemother; 2005 Mar 20; 49(3):1113-9. PubMed ID: 15728911 [Abstract] [Full Text] [Related]
10. Vicriviroc resistance decay and relative replicative fitness in HIV-1 clinical isolates under sequential drug selection pressures. Tsibris AM, Hu Z, Paredes R, Leopold KE, Putcharoen O, Schure AL, Mazur N, Coakley E, Su Z, Gulick RM, Kuritzkes DR. J Virol; 2012 Jun 20; 86(12):6416-26. PubMed ID: 22491471 [Abstract] [Full Text] [Related]
11. Impact of human immunodeficiency virus type 1 gp41 amino acid substitutions selected during enfuvirtide treatment on gp41 binding and antiviral potency of enfuvirtide in vitro. Mink M, Mosier SM, Janumpalli S, Davison D, Jin L, Melby T, Sista P, Erickson J, Lambert D, Stanfield-Oakley SA, Salgo M, Cammack N, Matthews T, Greenberg ML. J Virol; 2005 Oct 20; 79(19):12447-54. PubMed ID: 16160172 [Abstract] [Full Text] [Related]
13. HIV-1 variants with a single-point mutation in the gp41 pocket region exhibiting different susceptibility to HIV fusion inhibitors with pocket- or membrane-binding domain. Lu L, Tong P, Yu X, Pan C, Zou P, Chen YH, Jiang S. Biochim Biophys Acta; 2012 Dec 20; 1818(12):2950-7. PubMed ID: 22867851 [Abstract] [Full Text] [Related]
18. Characterization of Gp41 polymorphisms in the fusion peptide domain and T-20 (Enfuvirtide) resistance-associated regions in Korean HIV-1 isolates. Jang DH, Yoon CH, Choi BS, Chung YS, Kim HY, Chi SG, Kim SS. J Korean Med Sci; 2014 Mar 20; 29(3):456-9. PubMed ID: 24616600 [Abstract] [Full Text] [Related]