For each of the 206 Petri dishes, we determined regeneration rate as proportion of fecal pellets with regenerated lichen structures.
We surveyed regeneration plots in the summer of 2008, and re-visited these plots in 2009 and 2010.
We measured regeneration of valuable hardwoods to quantify the relative effects of stand factors and landscape patterns on that regeneration.
To define the role of nerve architecture, we evaluated regeneration through acellular motor and sensory nerve grafts.
We varied regeneration rates at one of five densities (1400, 1005, 670, 335, and 165 seedlings ha-1) in our sensitivity analysis.
We found regeneration of all three target species in the core zone; however, a small number of regeneration individuals of F. hodginsii and A. spectabilis was found in the buffer and restoration zones.
In the next phase of our study, we examined regeneration phenotypes of these genes after two rounds of dsRNA feeding and found that trunk pieces showed severe regeneration defects following each of 23 genes RNAi (Fig. S1B).
We report regeneration of capillaries and resolution of the non-angiogenic phenotype after HDIT/HCT.
We induced regeneration by injecting cardiotoxin directly into the muscle of 8-week-old control and α-KO mice.
We divided regeneration into stages, to obtain a clearer view of the complex temporal and spatial changes occurring during this process.
