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The DSC and HD for rabbit, ferret, and mouse are reported in Table 3.
All other tissues in both rat and mouse are reported to be collected from 10-week old animals.
Several mammalian TLRs in mouse are reported to be involved in the testicular innate immune response especially in Sertoli cells [ 44].
The effects of sodium pentobarbitone anaesthesia, the presence of a tumour, and local hyperthermia to a tumour-bearing leg, on the pharmacokinetics of MISO in the mouse are reported.
In a very distinct manner, many 3' UTRs in mouse are reported to be expressed separately from their mRNAs in a developmentally regulated manner [ 20], and some reported regulatory mutations in 3' UTRs do not appear to act in cis to regulate the expression of the associated mRNA.
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This was surprising, since this mouse was reported to be null for the Cav1.4 channel protein [22].
The normal physiological range of plasma E2 concentration in the mouse was reported to be between 5 and 50 pg/ml [35].
More recently, a hypomorphic mutation in the mouse was reported to show neural tube closure defects, while a null mutant exhibited early lethality [10].
Recently, a catalytically inactive IRAK1 D359A mutant mouse was reported (Pauls et al, 2013).
PKCδ deficient mouse is reported to suppress apoptosis in response to chemotherapeutic drug [ 6].
Recently, a kinase-dead IKKα knockin mouse was reported to develop lung SCCs (Xiao et al., 2013).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com