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By both RT-PCR and immunohistochemistry, we mapped the localization of CXCL12γ both in mouse and human tissues, where it showed discrete differential expression.
This shows that the wholemount adult can be stained without any manipulation and that this stain penetrates well as we have mapped the localization pattern with respect to the internal anatomy.
We have mapped the localization and characterized histologically the cellular composition of the microlesions induced by T. gondii infection within the murine brain.
We mapped the localization of transcription regulators in presumptive eyespot centers onto the species tree, and performed ancestral character reconstructions using both parsimony and maximum likelihood (ML) methods.
In addition, super-resolution analysis of human centrosomes has mapped the localization of γ-tubulin towards the N-terminus of PCNT (Lawo et al., 2012; Mennella et al., 2012; Sonnen et al., 2012).
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We map the localization along the intestinal tract of all murine mucins for which antibodies are available: Muc1, Muc2, Muc4, Muc5AC, Muc13 and Muc3 (orthologue of human MUC17, therefore hereafter referred to as Muc17. There is currently no Muc3 orthologue annotated in the mouse genome.
Because the spatial distribution of PHB within the sugarcane leaf is crucial to achieving high yields, a robust tool for quantifiably mapping the localization of PHB within the leaf would be of great value.
We therefore mapped the chromosomal localization of orphan PCGs in N. crassa to evaluate the link between the generation of new genes and subtelomeric regions.
They then constructed the phylogeny for 45 yeast families, mapped the subcellular localizations of these onto the phylogenies and finally used a parsimony-based analysis to deduce the ancestral and derived states (function).
Here, we map the genomic localization of all somatic replication-dependent H1 subtypes in human lung fibroblasts using an integrative DNA adenine methyltransferase identification (DamID) analysis.
We have previously used an early version of this methodology for mapping the chromatin localization of RXRα and RARγ nuclear receptors [ 24], as well as for profiling RNA polymerase II [ 16].
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