Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Helena, Geys"'
Autor:
Mohamed Kreir, Dea Putri, Fetene Tekle, Francesca Pibiri, Constantin d’Ydewalle, Karel Van Ammel, Helena Geys, Ard Teisman, David J. Gallacher, Hua Rong Lu
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
We investigated drug-induced acute neuronal electrophysiological changes using Micro-Electrode arrays (MEA) to rat primary neuronal cell cultures. Data based on 6-key MEA parameters were analyzed for plate-to-plate vehicle variability, effects of pos
Externí odkaz:
https://doaj.org/article/6519f93f4908451c87b4f64f1cc25244
Autor:
Stan Altan, Dhammika Amaratunga, Javier Cabrera, Jeonifer Garren, Helena Geys, John Kolassa, David LeBlond, Dingzhou Li, Jason Liao, Jia Liu, Mariusz Lubomirski, Guillermo Miro-Quesada, Steven Novick, Martin Otava, John Peterson, Katharina Reckermann, Tim Schofield, Charles Tan, Kanaka Tatikola, Fetene Tekle, Jennifer Thomas, Kim Vukovinsky
Publikováno v:
Statistics in Biopharmaceutical Research. 15:343-358
Autor:
Yajie Duan, Chun‐Pang Lin, Davit Sargsyan, Javier Cabrera, Christine Livingston, Robert Vogel, Jocelyn Sendecki, Willem Talloen, Helena Geys, Surya Mohanty
Publikováno v:
Naval Research Logistics (NRL).
Publikováno v:
Journal of Biopharmaceutical Statistics. 31:25-36
Bayesian sequential integration is an appealing approach in drug development, as it allows to recursively update posterior distributions as soon as new data become available, thus considerably reducing the computation time. However, preclinical trial
Autor:
Gary Tresadern, Kanaka Tatikola, Javier Cabrera, Lingle Wang, Robert Abel, Herman van Vlijmen, Helena Geys
Publikováno v:
Journal of chemical information and modeling. 62(3)
The accurate prediction of binding affinity between protein and small molecules with free energy methods, particularly the difference in binding affinities via relative binding free energy calculations, has undergone a dramatic increase in use and im
Pharmacokinetic (PK) studies are conducted to learn about the absorption, distribution, metabolism, and excretion processes of an externally administered compound by measuring its concentration in bodily tissue at a number of time points after admini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc6c8f7b94abe88e71ca358df632ad1a
Publikováno v:
Pharmaceutical Statistics
Coadministration of 2 or more compounds can alter both the pharmacokinetics and pharmacodynamics of individual compounds. While experiments on pharmacodynamic drug-drug interactions are usually performed in an in vitro setting, this experiment focuse
Publikováno v:
Wiley StatsRef: Statistics Reference Online. :1-7
Publikováno v:
Statistics in Medicine. 36:4301-4315
Pharmacokinetic studies aim to study how a compound is absorbed, distributed, metabolised, and excreted. The concentration of the compound in the blood or plasma is measured at different time points after administration and pharmacokinetic parameters
Autor:
Kathleen De Vlieger, Ann Schuermans, Bas-jan van der Leede, Helena Geys, Marjolein van Heerden, Sandra De Jonghe, Terry Van Doninck, Fetene Tekle, Jacky Van Gompel, Sandy Weiner
Publikováno v:
Environmental and Molecular Mutagenesis
Acetaminophen, a nonmutagenic compound as previously concluded from bacteria, in vitro mammalian cell, and in vivo transgenic rat assays, presented a good profile as a nonmutagenic reference compound for use in the international multilaboratory Pig