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In the murine infection model, the phenotype of the mutant was indistinguishable from that of the parent strain.
The bacterial burden as measured by colony forming units (cfu) (Figure 2a) and histopathology (data not shown) of the mutant was indistinguishable from the parent strain H37Rv.
In contrast, the sexual development of the dmtA+/tmdA− (DLAN3) mutant was indistinguishable from that of the wild type (Figures 5C and 5F).
Instead, the association of Cbl with the 1045/1068/1086+ mutant was indistinguishable from EGFR-WT.
The edr2-6 mutant was indistinguishable from wild type in growth and development up to ~3 weeks of age (Fig. 1A,1B).
Also, the egg production of the mek-1/ g6pdouble) double mutant was indistinguishable to that of Gi C. elegans (P=0.471, n=60).
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(D ) shd ; sbr mutant is indistinguishable from shd. (E ) nacre (nac ) mutant, which lacks melanophores.
(D ) Localization of GFP EFA-6N150 GFP EFA-6N150ptrn-1(0) double mutant in indistac-1 lfable tac-1 lfd typtrn-1 0
However, root hair growth in the AtrabD2b/2c double mutant is indistinguishable from that of wild-type plants.
Furthermore, a hy5 cry1 double mutant is indistinguishable from either single mutant in blue light, suggesting that both cry1 and HY5 operate in the same pathway.
However, the AtrabD2b/2c double mutant is indistinguishable from wild-type plants, except for shorter siliques due to the pollen and pollen tube defects.
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CEO of Professional Science Editing for Scientists @ prosciediting.com