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SHG signals emitted from the Achilles tendon proper region in normal tendon vs tendinosis lesions were next characterized by spectral analysis.
The apoptotic signalling cascade upon treatment with PAP-1, Psora-4 and clofazimine was next characterized by assaying hallmark apoptotic events in CTLL-2/Kv1.3 and CTLL-2/pJK cells.
The expression of netrin-1 was next characterized by Western blotting of cell lysates and supernatants in order to investigate whether different isoforms of netrin-1, with distinct cellular distributions, were synthesized by HUVECs, as has previously been reported for tumour cells (Delloye-Bourgeois et al., 2012).
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The ultrastructure of these intranuclear vesicle clusters was next characterized in 3D by CEMOVIS, resulting in visualization of vesicles with a grainy inner NEC coat and a mean inner diameter of 107 ± 33 nm SD (n = 79).
Given the success of nanoprecipitation for SN-38 prodrugs (6, 7, 8, 12, and 13), we next characterized their morphology by transmission electron microscopy (TEM) and dynamic light scattering (DLS) analysis.
We next characterized the genes disrupted by IS 6110 insertions by assigning them to functional categories based on the NCBI Clusters of Orthologous Groups (COGs) (http://www.ncbi.nlm.nih.gov/sutils/coxik.cgi gi=135) and the Tuberculist database (http://tuberculist.epfl.ch/index.html).html
We next characterized the molecular mechanisms by which H2O2 increased β-cell development.
We next characterized the differentiation profile by real time (RT -PCR analysis of the expRT -PCR of c-kit, the manalysisr differentiating spermatofonia, and Sthe8, thexpressionof pre-meiotic germ cells in the whole testes.
As these clusters had been identified using an interaction contrast, we next characterized the nature of the interaction by extracting individual estimates of the average signal change associated with fearful versus neutral stimuli separately for trials in which attention was directed toward or away from the face.
To specifically know the molecular target of CAFG, we next characterized the cellular signaling events being activated by CAFG.
We next characterized the cellular heterogeneity of PE cells by both immunofluorescence and fluorescence activated cell sorting (FACS) of cell surface proteins.
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CEO of Professional Science Editing for Scientists @ prosciediting.com