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To elucidate the mechanistic basis of the effects induced by Th1-conditioned cell transfer, we analyzed immune cell accumulation in the injured spinal cord.
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To assess rate heterogeneity and possible lateral gene transfers, we analyzed each gene individually prior to concatenation and then applied a variety of phylogenetic inference methods with both DNA and the inferred protein sequences.
By applying transfer theory, we analyzed whether strategic consistency signifying the similarity of strategic direction of acquisitions has positive performance effects on serial acquisitions.
Utilizing the intrinsic fluorescence of single tryptophan residue and fluorescence resonance energy transfer [FRET], we analyzed the accessibility and strength of their binding with an ameloblast cell membrane-mimicking model membrane (ACML) and a negatively charged liposome used as a membrane model.
Using formalism similar to the transfer matrix, we analyze the problem of direct and indirect coupling of cascaded cavities in resonator-waveguide systems based on the temporal coupled-mode theory.
Since shoulder pain is more commonly associated with transfers [ 7], we analyzed the maximum superior and posterior shoulder forces and extension, abduction, and internal rotation shoulder moments.
To investigate the underlying basis for these observed detrimental effects of the passively transferred human IgA we analyzed serum cytokines responses in all the animals using the cytometric bead array mouse Th1/Th2 10plex kit (Bender Medsystems) on day 10 post-challenge when all mice were killed.
At 18 days after transfer (28 total days), we analyzed their phenotypes.
Thus, the events of horizontal gene transfer for the genomes we analyzed could not have significantly affected the identification of functional classes dramatically undergoing gene loss.
We analyzed heat transfer entropy generation rate and viscous dissipation of coupled heat and momentum transport phenomena in Rayleigh-Bénard convection, and proposed a hypothesis that the velocity and temperature distributions can be governed by the balance between the maximization of entropy generation and the minimization of viscous dissipation.
We analyzed the transfer of energy occurring in the absence of any phagocytic challenges since confocal analysis had shown that, while colocalized at rest, ABCA1 and MEGF10 distributed differentially during phagocytosis (Figure 4A).
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