Results 21 to 30 of about 95,693 (243)

NIH Support for the Emergence of Quantitative and Systems Pharmacology [PDF]

open access: yesCPT: Pharmacometrics & Systems Pharmacology, 2013
The National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health (NIH) sponsored two workshops and the development of a white paper on the emergence of quantitative and systems pharmacology (QSP) as a discipline. In subsequent efforts to encourage this area, NIGMS modified existing research and training offerings.
Rogers, M, Lyster, P, Okita, R
openaire   +2 more sources

Computational methods and applications for quantitative systems pharmacology [PDF]

open access: yesQuantitative Biology, 2019
BackgroundQuantitative systems pharmacology (QSP) is an emerging discipline that integrates diverse data to quantitatively explore the interactions between d rugs and multi‐scale systems including small compounds, nucleic acids, proteins, pathways, cells, organs and disease processes.ResultsVarious computational methods such as ADME/T evaluation ...
Fuda Xie, Jiangyong Gu
openaire   +1 more source

A quantitative systems pharmacology model for acute viral hepatitis B

open access: yesComputational and Structural Biotechnology Journal, 2021
Hepatitis B liver infection is caused by hepatitis B virus (HBV) and represents a major global disease problem when it becomes chronic, as is the case for 80–90% of vertical or early life infections.
Eduardo Asín-Prieto   +7 more
doaj   +1 more source

Quantitative Systems Pharmacology: A Framework for Context [PDF]

open access: yesCurrent Pharmacology Reports, 2016
Quantitative Systems Pharmacology (QSP) is receiving increased attention. As the momentum builds and the expectations grow it is important to (re)assess and formalize the basic concepts and approaches. In this short review, I argue that QSP, in addition to enabling the rational integration of data and development of complex models, maybe more ...
openaire   +2 more sources

Sources of inter-individual variability leading to significant changes in anti-PD-1 and anti-PD-L1 efficacy identified in mouse tumor models using a QSP framework

open access: yesFrontiers in Pharmacology, 2022
While anti-PD-1 and anti-PD-L1 [anti-PD-(L)1] monotherapies are effective treatments for many types of cancer, high variability in patient responses is observed in clinical trials.
Jessica C. Leete   +6 more
doaj   +1 more source

Review of quantitative systems pharmacological modeling in thrombosis

open access: yesCommunications in Information and Systems, 2019
Hemostasis and thrombosis are often thought as two sides of the same clotting mechanism whereas hemostasis is a natural protective mechanism to prevent bleeding and thrombosis is a blood clot abnormally formulated inside a blood vessel, blocking the normal blood flow. The evidence to date suggests that at least arterial thrombosis results from the same
Limei Cheng   +2 more
openaire   +4 more sources

Virtual Populations for Quantitative Systems Pharmacology Models

open access: yes, 2021
AbstractQuantitative systems pharmacology (QSP) places an emphasis on dynamic systems modeling, incorporating considerations from systems biology modeling and pharmacodynamics. The goal of QSP is often to quantitatively predict the effects of clinical therapeutics, their combinations, and their doses on clinical biomarkers and endpoints.
Yougan Cheng   +5 more
openaire   +3 more sources

Pharmacodynamic Modeling to Evaluate the Impact of Cimetidine, an OCT2 Inhibitor, on the Anticancer Effects of Cisplatin

open access: yesCells, 2022
Despite potent anticancer activity, the clinical utilization of cisplatin is limited due to nephrotoxicity. As Organic Cation Transporter 2 (OCT2) has been shown to be one of the key transporters involved in the uptake of cisplatin into renal proximal ...
Hardik Mody   +3 more
doaj   +1 more source

Prediction of Clinical Transporter‐Mediated Drug–Drug Interactions via Comeasurement of Pitavastatin and Eltrombopag in Human Hepatocyte Models

open access: yesCPT: Pharmacometrics & Systems Pharmacology, 2020
A structurally identifiable micro‐rate constant mechanistic model was used to describe the interaction between pitavastatin and eltrombopag, with improved goodness‐of‐fit values through comeasurement of pitavastatin and eltrombopag.
Simon J. Carter   +3 more
doaj   +1 more source

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