Matricellular protein knockout mice are often viable, but typically exhibit abnormal responses to mechanical stress, wound healing, inflammation and tumor metastasis.
Mutants affecting these genes are often viable, but show growth and developmental defects, suggesting incomplete functional redundancy within the families.
Mutants of C. elegans with widespread nervous system defects are often viable, which means that mutations in a large number of neuronal genes can be tested for altered behaviors in genetic screens.
Knockout mouse models of these specific matricellular proteins are often viable but characteristically display impaired responses to mechanical stress and wound healing (Bradshaw et al, 2003; Rios et al, 2005; Vetrone et al, 2009; Okamura et al, 2010).
So it is often a viable option to have multiple design patents based on a single UX/UI.
The fungus Banksiamyces toomansis, of the order Helotiales, infects older cones and seed, and hence seed older than about five years is often not viable.
Given the massive volume of administrative data, such an audit is often not viable.
Due to the relatively large size of fluorescent proteins and potential complications of protein folding, sorting, and function sometimes observed when adding a large protein tag to a target, genetic addition of fluorescent proteins is often not viable for studying protein biology in cells.
Its findings suggest that the recovery and reuse of key components is an economically viable reverse logistics strategy in a high-modularity case; in contrast, scrapping or recycling of materials is often the most viable strategy for integrated architectures.
For these patients, organ transplantation is often the only viable solution.
