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Although there have been extensive studies into the development of various CAD systems for automatic screening diseases, the experts are still unable to use all of them in their decision-making process due to the lack of easily used online methods.
Whilst this simplistic approach was useful for screening diseases, it will not suffice in monitoring or forecasting incidence.
Because this study was retrospective and screening was incomplete for some patients, certain diseases may be underestimated, or if testing was based on symptoms rather than true screening, diseases may be overestimated.
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Thus the length of survival does not necessarily reflect better medical care but rather a better system for screening disease.
Along with the continuous development of the technique of QD nano-carriers for drugs, new development opportunities for drug screening, disease screening, and gene sequencing, plurality of biomedical research will come.
In this chapter, we will overview these advances and their potential application in drug screening, disease modeling, cellular therapy, and bioengineering.
Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) grown in engineered heart tissue (EHT) can be used for drug screening, disease modeling, and heart repair.
The field has progressed extensively in the past decade, and we envision its applications in the areas of drug screening, disease modeling, and precision medicine.
Importantly, these systems have the potential to dramatically impact biomedical applications in the areas of drug development, drug and toxicology screening, disease modeling, and the emerging area of personalized precision medicine.
Thus, hESC and hiPSC differentiation offers a unique opportunity for therapy development, drug screening, disease modeling, and tissue replacement.
hPSCs therefore show potential for application to drug screening, disease modelling and cellular therapies.
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