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TAZ-deficient mice develop significant renal cyst as early as embryonic day 15.5.
These mice develop significant vacuolization (scored 3 out of 5) in the hippocampus, thalamus, hypothalamus, and anterior and posterior cerebral cortex (also called the secondary visual cortex).
In summary, HeN mice develop significant RN following kidney infection.
LDLR-/-ApoB100/100 mice develop significant coronary atherosclerosis, severe left ventricular dysfunction with preserved but diminished cardiac reserve and signs of chronic myocardial hibernation.
Male Lmna H222P/H222P mice develop significant left ventricular dilatation and decreased ejection fraction by 16 weeks of age (Arimura et al., 2005).
Here we show that BACE1−/− mice develop significant retinal pathology including retinal thinning, apoptosis, reduced retinal vascular density and an increase in the age pigment, lipofuscin.
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Results show that both WT and nNOS KO mice developed significant CPA.
At the end of the study, the wild-type mice developed significant cardiac hypertrophy (23.6+/-2 23.6+/-2e in heart-to-body weight ratio).
Only WT mice developed significant cortical bone loss after OVX.
We found that Myd88−/− mice developed significant hyperglycemia relative to WT controls upon glucose challenge (Figure 4A D).
KitW-sh/KitW-sh mice reconstituted with HDC−/− bone marrow exhibited attenuated pelvic pain responses such that HDC−/−-reconstituted mice did not develop significant pain until PID3 (P<0.05), whereas +/+-reconstituted mice developed significant pain by PID2 (compare Figs. 4A and 1C).
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mice develop early-onset
mice develop myasthenic
mice develop high
mice develop local
mice develop glaucoma-like
mice show significant
mice develop severe
mice develop spontaneous
mice develop progressive
mice develop renal
mice have significant
mice display significant
mice develop mild
mice maintain significant
mice develop lethal
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