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Journal Abstract Search
155 related items for PubMed ID: 9315877
1. Kinetic properties of saquinavir-resistant mutants of human immunodeficiency virus type 1 protease and their implications in drug resistance in vivo. Ermolieff J, Lin X, Tang J. Biochemistry; 1997 Oct 07; 36(40):12364-70. PubMed ID: 9315877 [Abstract] [Full Text] [Related]
7. Crystal structure of an in vivo HIV-1 protease mutant in complex with saquinavir: insights into the mechanisms of drug resistance. Hong L, Zhang XC, Hartsuck JA, Tang J. Protein Sci; 2000 Oct 07; 9(10):1898-904. PubMed ID: 11106162 [Abstract] [Full Text] [Related]
9. Human immunodeficiency virus type 1 protease cleavage site mutations associated with protease inhibitor cross-resistance selected by indinavir, ritonavir, and/or saquinavir. Côté HC, Brumme ZL, Harrigan PR. J Virol; 2001 Jan 07; 75(2):589-94. PubMed ID: 11134271 [Abstract] [Full Text] [Related]
10. Multidrug resistance to HIV-1 protease inhibition requires cooperative coupling between distal mutations. Ohtaka H, Schön A, Freire E. Biochemistry; 2003 Nov 25; 42(46):13659-66. PubMed ID: 14622012 [Abstract] [Full Text] [Related]
11. Insights into the mechanism of drug resistance: X-ray structure analysis of G48V/C95F tethered HIV-1 protease dimer/saquinavir complex. Prashar V, Bihani SC, Das A, Rao DR, Hosur MV. Biochem Biophys Res Commun; 2010 Jun 11; 396(4):1018-23. PubMed ID: 20471372 [Abstract] [Full Text] [Related]
16. Predictive value of drug levels, HIV genotyping, and the genotypic inhibitory quotient (GIQ) on response to saquinavir/ritonavir in antiretroviral-experienced HIV-infected patients. Valer L, de Mendoza C, Soriano V. J Med Virol; 2005 Dec 11; 77(4):460-4. PubMed ID: 16254964 [Abstract] [Full Text] [Related]