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There is some information available on the electron microscopy characteristics of platelet and fibrin networks in humans [ 13] and other animal species [ 14].
However, to our knowledge, there have been few studies on the electron microscopy characteristics of platelet and fibrin networks in clots of PC (in a platelet gel form) from dogs and cats encountered in experimental and clinical settings.
This study describes the electron microscopy characteristics of canine and feline PC activated with a non-proteic activating substance (calcium gluconate, CG) or the combination of a proteic activating substance (batroxobin) with calcium gluconate (CGB).
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The instrument we describe combines the potential for near-field microscopy with the characteristics of a conventional far-field light microscope.
Detailed analysis of CNS infiltrates by flow cytometry and fluorescence microscopy revealed unanticipated characteristics of myeloid cell populations in the CNS.
Observations with electron microscopy of ultrastructural characteristics of hepatoblastoma cells have demonstrated prominent glycogen granules in the cytoplasm [ 22, 23].
For completeness, transmission electron microscopy and mechanical characteristics of the material are presented.
Based on morphological changes identified by inverse microscopy, typical morphological characteristics of apoptosis and the reduction of the cells were observed.
After the deposition process, the surface morphology of prepared specimens was examined by scanning electron microscopy and transmission electron microscopy, and the electrochemical characteristics of the specimens were also investigated by cyclic voltammetry in nitrogen saturated sulfuric acid aqueous solutions and in mixed sulfuric acid and methanol aqueous solutions.
Neither tumour growth (assessed by wet weight), vascular density (assessed by light microscopy), nor any ultrastructural characteristics of the tumour or its vasculature (assessed by electron microscopy) were affected by copper deficiency.
In this study, we used hyperspectral two-photon microscopy to explore the characteristics of both normal and diseased gastrointestinal (GI) tissues, relying only on their endogenous fluorescence and second harmonic generation to provide contrast.
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