Sentence examples for models for disease from inspiring English sources

Human cell models for disease based on induced pluripotent stem (iPS) cells have proven to be powerful new assets for investigating disease mechanisms.

This novel, chaperon-mediated approach has benefited from insights into the molecular understanding of β-glucocerebrosidase structure, drug design and development in cellular models for disease.

Improvements in large-scale genomic analyses, including transcriptional profiling and next-generation sequencing, in combination with a growing number of genetically engineered mouse models for disease, have resulted in dramatic improvement in our understanding of alterations that drive tumors of the central nervous system (CNS).

As with most models for disease transmission and control, our model is based on the simple susceptible-infected-recovered (SIR) model [22].

It is also important for clinical and translational scientists to consider how to translate the individual therapy into public health models for disease prevention or treatment in a low-resource setting.

Stephen I. Hsu (one of global leading scientists in translational medicine) emphasized that the topic of a "social mission" should be also important for clinical translational scientists, to think ahead about how to translate in a manner that will enable public health models for disease prevention or treatment in low-resource settings to be realistically and successfully implemented.

Multivariate Cox proportional hazard models for disease-free and overall survival were performed.

The base models for the two hospitalization outcomes had lower c-statistics and higher Brier scores than the base models for disease-specific outcomes.

The same six factors were identified as significant for both the measures of survival, and were entered into multivariate analyses, with individual models for disease-free and OS (Table 4).

Paradoxically, analysis of consent models for disease-specific and population-based research reveals such a high degree of similarity that bridging consent could be possible if additional information regarding bridging was incorporated into consent forms.

Univariate and multivariate Cox regression models for disease-free and overall survival were performed, comprising FIGO tumour stage (FIGO I vs FIGO II vs FIGO III and IV), histological grade (G1 vs G2 vs G3), histological subtype (endometrioid adenocarcinoma vs non-endometrioid carcinoma, such as serous and clear cell carcinoma), and pre-treatment plasma fibrinogen levels.