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Some IL-17Apos T cells coproduced IL-22, consistent with what has been described for mouse as well as human Th17 cells.
If hiPSC are to be considered for future applications in transfusion medicine, it is important to demonstrate that hiPSC-derived erythropoiesis is capable of producing RBCs that express adult globins, as has been described for mouse ES cells (Wiles & Keller, 1991).
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Similar findings have been described for mice infected with H. felis [32], [35].
It has been previously hypothesized that detailed analysis of paw trajectories would capture the gait abnormalities of ataxic mice like pcd, but detailed 3D paw kinematics have not been described for mice.
Length and sequence heterogeneity in the non-coding and coding regions of rDNA allows for the possibility of functional rRNA variants (v-rRNAs) as have been described for mice and humans.
Consistent with these findings, schizophrenia-like deficits and impaired maturation of glutamatergic synapses have also been described for mice deficient in Nrg1, ErbB4 and BACE1, a protease that initiates Nrg1 processing by cleaving its extracellular domain (Chen et al., 2008; Barros et al., 2009; Del Pino et al., 2013).
The gene for Ifnphi1, which belongs to the type I interferon group (Hamming et al., 2011), was dependent on MyD88 for its induction during S. typhimurium infection, as was described for mouse IFN1 when macrophages lacking MYD88 were stimulated with LPS (Hirotani et al., 2005).
a Acc No, EMBL/DDBJ/GenBank Accession Number b AT, annealing temperature c this position is equivalent to 1 20 in AJ619019 d GAPDH, glyceraldehyde-3-phosphate dehydrogenase An alternatively spliced exon between the first two exons of the TβRII gene was described for mouse and human [ 28- 30] (Fig. 2A C).
Asymmetric cell division in ISCs is remarkably similar to what has been described for the mouse epidermis.
To this end we made use of the fact that XY body formation is followed by a replacement of histone variants H3.1 and H3.2 by H3.3, as has been described for the mouse [ 58], allowing a distinction between early and mid-to-late pachytene spermatocytes.
In addition, we found no MV-bound IgG in 8- to 10-week-old MRL/lpr mice, using a labeled anti-mouse IgG antibody (data not shown), which has been described for MRL/lpr mice >14 weeks old [ 23].
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