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J7-21 celineine generated in our lab by stable transduction of GFP-Ipr1 in J774A.1 cells.
The Cdc42loxP/loxP Fgfr3-iCre-ERT2 Cdc42loxP/loxP Fgfr3-iCre-ERT2 Cdc42loxP/loxP Fgfr3-iCre-ERT2nowledge the first in vivo mouse modelineth impaired scar formation followingeneratedto the organ of Cortin
The in vitro protease assays with recombinant PfHslV and the transgenic parasite line generated in the present study may be exploited in the screening of novel inhibitors to evaluate their anti-malarial activity.
The yellow line is the line detected by the image processing; the purple one is the line filtered in time in the perception layer and the white one the reference line generated in the planning layer.
For that purpose we used a Cx57-deficient mouse line, generated in a C57BL/6 background, and compared it to wild-type C57BL/6 mice, in which horizontal cell coupling was unperturbed (Fig. 1).
The following T cells were used: DRB1*0101-restricted, HA306-318-specific mouse hybridoma line EvHA/X5 [12] and human CD4+ T cell line PD2 [33]; the ABL 908-922-specific T cell hybridoma SaABL/G2 was generated after fusing a CD4+ T cell line generated in HLA-DR1 tg mice [34] with BW cells (Hopner et al., unpublished).
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Line H20961 is a male human iPSC line generated in-house used as reference.
We also examined REX1 expression levels in 73 human iPSC lines generated in-house from Caucasian individuals using the Illumina HT12v4 array.
Next, we analysed whole-transcriptome data of 17 TSCC and 6 TSCC cell lines (generated in-house at ACTREC, unpublished data) using the HPVDetector.
We analysed whole-exome data from 23 paired and one orphan tongue squamous cell carcinoma (TSCC) sample and 7 HNSCC cell lines (generated in-house at ACTREC, unpublished data).
This line generates, in vitro, cells with characteristics of 0-2A progenitor cells, oligodendrocytes and astrocytes.
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