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pro vyhledávání: '"Steve Wring"'
Autor:
N. Isham, Steve Wring, David Angulo, Katyna Borroto-Esoda, Lisa Long, Stephen Barat, Emily L Larkin, Mahmoud A. Ghannoum
Publikováno v:
Antimicrobial Agents and Chemotherapy. 63
Ibrexafungerp (IBX) (formerly SCY-078) is a novel glucan synthase inhibitor whose oral availability is being evaluated for efficacy against vulvovaginal candidiasis (VVC). Bioavailability and in vitro activity are important efficacy indicators, but a
Autor:
Steve P. Rannard, Andrew Owen, Marco Siccardi, Steve Wring, Rajith K. R. Rajoli, Darren M. Moss, Melynda E. Watkins, Ryan Randolph, Seonghee Park, Paul L. Domanico, James J. Hobson
Publikováno v:
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Tenofovir disoproxil fumarate (TDF), a prodrug of tenofovir, has oral bioavailability (25%) limited by intestinal transport (P-glycoprotein), and intestinal degradation (carboxylesterase). However, the influence of luminal pancreatic enzymes is not f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::960d86ad95272ee9e418e4f9666e4b5b
Autor:
Mauricio Retuerto, Iman Salem, Emily L Larkin, Christopher L. Hager, N. Isham, Pranab K. Mukherjee, David Angulo, Lisa Long, Jyotsna Chandra, Steve Wring, Katyna Borroto-Esoda, Mahmoud A. Ghannoum, Laura L. Kovanda
Publikováno v:
Antimicrobial Agents and Chemotherapy
Candida auris , a new multidrug-resistant Candida spp. which is associated with invasive infection and high rates of mortality, has recently emerged. Here, we determined the virulence factors (germination, adherence, biofilm formation, phospholipase
Publikováno v:
Pharmaceutical Research. 20:757-764
Purpose. The purpose of this study was to investigate whether midazolam exhibits characteristics of a highly permeable P-glycoprotein (P-gp) substrate and to evaluate the potential influence of P-gp inhibition on 1-OH midazolam formation during midaz
Publikováno v:
Pharmaceutical research. 20(5)
The purpose of this study was to investigate whether midazolam exhibits characteristics of a highly permeable P-glycoprotein (P-gp) substrate and to evaluate the potential influence of P-gp inhibition on 1-OH midazolam formation during midazolam tran