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Species boundaries were explored using changes in branching rates following Pons et al [ 56].
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These commonalities were explored using Fourier analysis.
Information is presented regarding the surface topography of the terraces and of the grain boundary regions, which have mainly been explored using AFM.
This hypothesis was explored using homology modelling.
Neither of these boundaries has been explored.
Secondly, the politics and practice of boundary crossing is explored.
Interactions between crack growth and tilt boundary mobility are explored.
Intron boundaries were displayed using WebLogo [ 72].
Initially, repeat boundaries were determined using RepeatMasker.
The significance of these markers at boundary cells remains to be explored.
Two different types of boundary constraints generally used in MM simulation are explored in detail and few interesting findings are brought out.
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