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Electrospinning has been used to produce nanofibrous scaffolds consisting of high surface area to volume ratios and various pore sizes that mimic the tissue ECM morphology and support cell attachment, proliferation, and differentiation [ 7– 9].
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This is consistent with previous results showing that the laser photonic densities (≤1 W) used in this study do not result in polymer degradation and/or changes in PLGA particle morphology and supports the conclusion that release requires strong absorbance of NIR light by water.
The model has been shown to correlate well with real transgranular stress-corrosion cracks grown in a boiling MgCl2 environment, offering explanations for observed morphologies and support for proposed crack growth models of this system.
These important findings support the primary importance of mtDNA mutations in the changes observed in cardiac morphology, and may support more intensive cardiac evaluation of patients with higher mutation loads and/or NMDAS scores.
A study combining morphology and genetics supported two species complexes of amphi-Atlantic cold-seep mussels [52]: a first including Bathymodiolus boomerang Cosel & Olu, 1998 from Barbados, B. heckerae from the Gulf of Mexico, and Bathymodiolus aff.
Ins2Akita-WT and Ins2Akita-HET microglia exhibit a similar morphology and distribution supporting the rationale that WT and HET microglia function is readily comparable and can be attributed an undistinguishable phenotype in retinal tissues.
Parallel improvements in inorganic synthetic protocols offer finer control over preparative methods to direct the nanostructure (composition, morphology, size, valence and support architecture) of palladium catalysts [59, 60, 61] and thereby enhance activity, selectivity and lifetime in an informed manner.
Surface morphology and spectroscopy data support the formation of a homogenous polymer blend at the synthesis ratio of 1: 4.13 × 10−3.
Although the evidence is not completely clear cut, analysis of data from molecular markers, cytogenetics, morphology and geographical distributions support that A. duranensis and A. ipaënsis are the direct ancestors of cultivated peanut [ 8, 30].
The two soils showed certain similarity in the morphology and properties, thus supporting the hypothesis of their common pedogenetic origin.
Morphology and microstructure of supported Pt electrodes have been studied using scanning electron microscopy, high-resolution transmission electron microscopy and X-ray diffraction.
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