Conventional genetically engineered mouse models enable the study of tumor growth in vivo, but they are neither readily scalable nor sufficiently quantitative to unravel the magnitude and mode of action of many tumor-suppressor genes.
Specifically, mouse models enable study of how a manipulation changes the manifestation or severity of AD related disease measures such as pathology, biochemistry, cognition/behavior, synaptic/network plasticity, or survival.
Because mouse models enable targeted deletion of specific gene(s) in a defined genetic background it is possible to assess the specific function of this gene within an organism.
This project revealed how little we know about mammalian gene function, and the only way to go from there was up… Since its inception, our internationally recognized program has created hundreds of new mouse models, enabling discoveries of gene function in diverse areas such as reproduction, neurobiology, obesity, metabolism, and blood, heart and bone development.
The shared genetic drivers in the KPC mouse model enabled the collection and analysis of sufficient numbers of single CTCs across different animals, yet we note significant animal-specific clustering in RNA-seq data.
In contrast, the use of the TgS100a8a9 hep mouse model enabled for the first time a detailed analysis of physiological and pathophysiological alterations in settings of low and locally restricted S100a8/a9 induction in vivo.
A mouse model enables investigation of the value of this new test during the acute phase and chronic phase of infection and during standardized, well-controlled therapy.
This mouse model enables us to follow NCCs as they migrate through the pharyngeal arch arteries, form the aorticopulmonary septum and differentiate into smooth muscle in the cardiac OFT.
The development of genetically engineered mouse models has enabled detailed study of the regulation of fetal mineral homeostasis.
The development of genetically engineered mouse models has enabled detailed study of the regulation of maternal mineral homeostasis during pregnancy and lactation.
