Results 21 to 30 of about 267,706 (322)

Incorporating Placebo Response in Quantitative Systems Pharmacology Models [PDF]

open access: yesCPT: Pharmacometrics & Systems Pharmacology, 2019
Evan B. Wang   +3 more
doaj   +3 more sources

A Framework for Simplification of Quantitative Systems Pharmacology Models in Clinical Pharmacology [PDF]

open access: yesBritish Journal of Clinical Pharmacology, 2020
Quantitative systems pharmacology (QSP) is a relatively new discipline within modelling and simulation that has gained wide attention over the past few years. The application of QSP models spans drug‐target identification and validation, through all drug development phases as well as clinical applications.
Abdallah Derbalah   +4 more
openaire   +2 more sources

Homeostasis, injury, and recovery dynamics at multiple scales in a self-organizing mouse intestinal crypt

open access: yeseLife, 2023
The maintenance of the functional integrity of the intestinal epithelium requires a tight coordination between cell production, migration, and shedding along the crypt–villus axis.
Louis Gall   +8 more
doaj   +1 more source

A Quantitative Systems Pharmacology Perspective on the Importance of Parameter Identifiability [PDF]

open access: yesBulletin of Mathematical Biology, 2022
AbstractThere is an inherent tension in Quantitative Systems Pharmacology (QSP) between the need to incorporate mathematical descriptions of complex physiology and drug targets with the necessity of developing robust, predictive and well-constrained models.
Sher, A   +8 more
openaire   +4 more sources

Broadening our understanding of genetic risk for scleroderma/systemic sclerosis by querying the chromatin architecture surrounding the risk haplotypes

open access: yesBMC Medical Genomics, 2021
Background Genetic variants in the human leukocyte antigen (HLA) locus contribute to the risk for developing scleroderma/systemic sclerosis (SSc). However, there are other replicated loci that also contribute to genetic risk for SSc, and it is unknown ...
Kerry E. Poppenberg   +3 more
doaj   +1 more source

In vitro to clinical translational pharmacokinetic/pharmacodynamic modeling of doxorubicin (DOX) and dexrazoxane (DEX) interactions: Safety assessment and optimization

open access: yesScientific Reports, 2023
Despite high anticancer activity, doxorubicin (DOX)-induced cardiotoxicity (DIC) limits the extensive utility of DOX in a clinical setting. Amongst various strategies explored, dexrazoxane (DEX) remains the only cardioprotective agent to be approved for ...
Hardik Mody   +2 more
doaj   +1 more source

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