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To assess sperm morphology, we evaluated 200 sperm using the Tygerberg Strict Criteria (Kruger et al. 1988).
To explore further the impact of altered p32 levels on mitochondrial morphology, we evaluated the consequences of the converse situation of increased expression of p32 through transient transfection of the full-length p32(1 282)–Myc construct for 18 or 24 h.
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Combining a finite element model of the spinal cord and compartmentalized models of both simple and complex neuron morphologies, we evaluated the use of the "ground surface" configuration, which consists in the integration of a conductive layer on the front side of electrode shanks, for the return of the stimulation current.
We evaluated morphology, adhesion, expression of PDGF, Factor VIII, CD41α and CD43 and apoptosis (Fig. 4).
To understand the consequences of ischemia in the context of apoptotic versus necrotic types of neuronal death, we evaluated morphology of apoptosis and necrosis in the spinal cord.
To evaluate mitochondrial distribution and morphology, we used TOM20 staining and determined indices of mitochondrial interconnectivity and mitochondrial elongation.
On hematoxylin and eosin stained sections we evaluated the morphology of liver, kidney, heart and spleen and we selected slides for VEGF immunostaining.
Following a two month acclimation period of culturing under identical conditions, we evaluated the morphology (Figure 1) and growth kinetics (Figure 2) of each Huh7 line.
To investigate a potential role for CXCR5 in cardiac remodeling and development of HF, we evaluated cardiac morphology and function in WT and CXCR5−/− mice.
Hence, we evaluated the morphology of spheroids growing in simulated microgravity.
We evaluated the morphology of the meibomian glands using our originally developed quantitative image analysis software.
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