Results 21 to 30 of about 6,641 (226)

Application of microphysiological systems to unravel the mechanisms of schistosomiasis egg extravasation. [PDF]

open access: yesFront Cell Infect Microbiol
Alfred MO   +7 more
europepmc   +2 more sources

A Microphysiological System for Studying Nonalcoholic Steatohepatitis [PDF]

open access: yesHepatology Communications, 2019
Nonalcoholic steatohepatitis (NASH) is the most severe form of nonalcoholic fatty liver disease (NAFLD), which to date has no approved drug treatments. There is an urgent need for better understanding of the genetic and molecular pathways that underlie NAFLD/NASH, and currently available preclinical models, be they
Kostrzewski, T   +7 more
openaire   +4 more sources

Modeling inflammation and oxidative stress in gastrointestinal disease development using novel organotypic culture systems. [PDF]

open access: yes, 2013
Gastroesophageal reflux disease (GERD), Barrett's esophagus (BE), graft-versus-host disease (GVHD), and inflammatory bowel diseases such as ulcerative colitis and Crohn's disease are common human gastrointestinal diseases that share inflammation as a key
Bortner, James D   +6 more
core   +2 more sources

Interconnected Microphysiological Systems for Quantitative Biology and Pharmacology Studies [PDF]

open access: yes, 2018
Microphysiological systems (MPSs) are in vitro models that capture facets of in vivo organ function through use of specialized culture microenvironments, including 3D matrices and microperfusion.
Brij M. Bhushan   +37 more
core   +2 more sources

Integrated Gut and Liver Microphysiological Systems for Quantitative In Vitro Pharmacokinetic Studies [PDF]

open access: yes, 2017
Investigation of the pharmacokinetics (PK) of a compound is of significant importance during the early stages of drug development, and therefore several in vitro systems are routinely employed for this purpose.
Chen, Wen Li   +5 more
core   +2 more sources

Integration of systems biology with organs-on-chips to humanize therapeutic development [PDF]

open access: yes, 2017
"Mice are not little people" - a refrain becoming louder as the gaps between animal models and human disease become more apparent. At the same time, three emerging approaches are headed toward integration: powerful systems biology analysis of cell-cell ...
Chen, Wen Li   +6 more
core   +1 more source

Microphysiological Systems to Assess Nonclinical Toxicity [PDF]

open access: yesCurrent Protocols in Toxicology, 2017
AbstractThe liver and the kidney are key toxicity target organs during drug development campaigns, as they typically carry the burden of drug transport and metabolism. Primary hepatocytes and proximal tubule epithelial cells grown in traditional in vitro 2‐D culture systems do not maintain transporter and metabolic functions, thus limiting their ...
Kirk P, Van Ness   +5 more
openaire   +2 more sources

Physiome-on-a-Chip: The Challenge of “Scaling” in Design, Operation, and Translation of Microphysiological Systems [PDF]

open access: yes, 2015
Scaling of a microphysiological system (MPS) or physiome-on-a-chip is arguably two interrelated, modeling-based activities: on-platform scaling and in vitro-in vivo translation.
Cirit, Murat   +2 more
core   +1 more source

Real-time monitoring of liver fibrosis through embedded sensors in a microphysiological system

open access: yesNano Convergence, 2021
Hepatic fibrosis is a foreshadowing of future adverse events like liver cirrhosis, liver failure, and cancer. Hepatic stellate cell activation is the main event of liver fibrosis, which results in excessive extracellular matrix deposition and hepatic ...
Hafiz Muhammad Umer Farooqi   +7 more
doaj   +1 more source

Chip-based human liver-intestine and liver-skin co-culture : A first step toward systemic repeated dose substance testing in vitro [PDF]

open access: yes, 2015
Systemic repeated dose safety assessment and systemic efficacy evaluation of substances are currently carried out on laboratory animals and in humans due to the lack of predictive alternatives.
Ayehunie, Seyoum   +12 more
core   +1 more source

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