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To this end we assessed individual differences in rates of cross-language interference, reflecting language control problems, and thus included both switches to the "wrong" target language as well as failures to switch to the "correct" target language.
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Consequently, the inappropriate triggering of danger signals, or a failure to switch these off once the immune response has been resolved, can have serious consequences for the host.
We suggest that inadvertent language switching as well as failure to switch languages when necessary reflect the speaker's language control abilities.
(E ) Blocking transmission in MBON-α′2 MBON-α′291C resulted in a failure to swithh froMB091Csive to appetitive memoresultedthanol intoxication, confailure toe reswitcheen with MB018B.
This ensured a train of prepotent responses (once contingencies had been learnt), such that only occasional errors were made (failure to switch response sets following a reversal trial).
The mean duration of treatment failure on first line ART and the mean duration from detection of treatment failure to switch to second line ART were longer in our study than the studies in Malawi [ 17] and South Africa [ 19].
However, the majority of patients did require use of an endoscope not used during prior incomplete colonoscopy suggesting that failure to switch to another available endoscope may be an important contributing factor to incomplete colonoscopy.
The initial acquisition deficit arose from a failure to switch from an innately preferred strategy (nonmatching) to a new strategy (matching), as reflected by a specific increase in perseverative errors.
Failure to switch off OCT4 in GC perinatally can lead to development of carcinoma in situ (CIS), the precursor of testicular germ cell cancer (TGCC), for which there is no animal model.
These observations strongly support that the tumorous proliferation in the puf-8; gap-3 double mutant is caused by the failure to switch from proliferative to meiotic fate, rather than by the dedifferentiation of cells that have already entered into meiosis.
That OCT4+ GC disappear rapidly after birth is important, as maturational delay or failure to switch off expression of pluripotency factors in some GC in the human, may predispose such cells to becoming CIS/TGCC (Cools et al., 2005; Rajpert-de Meyts, 2006; Hersmus et al., 2012).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com