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While we present here only the use of our new Hprt targeting constructs for analysis of enhancers in cardiac and haematopoietic lineages, it is not limited to these.
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While the evidence we present here is consistent with this conclusion, there are some caveats that should be noted regarding their findings.
While not presented here, we have tested the efficacy of tenofovir in the presence of semen and have found no reduction of activity against HIV-1 [46].
While the approaches presented here were developed independently, we have chosen to present our results together in order to support the notion that generating structure based predictions of peptide:MHC binding without using binding data is unlikely to give satisfactory results.
While studies presented here clearly demonstrate the importance of TG2 in promoting the EMT in mammry epithelial cells, we are still working on the molecular intricacies through which TG2 modulates these functions.
While not presented here, multicolor phantoms have been developed where the spectral signatures are more distinct, making estimation of the abundance fraction (somewhat) easier[ 11, 5, 6].
While outcomes were not presented here, we know from other work that the consequence of a missed compartment syndrome or a lengthy delay in treatment can be devastating to the patient.
While our results presented here accurately reflect the burden of ALRI ED presentations in metropolitan-born children in WA, we cannot extrapolate these findings to rural and remote WA.
While the data presented here can say nothing about initial refusal, at subsequent waves we found no association between depression and anxiety scores at previous waves and refusal.
While the data presented here suggest 3DL0 to be the ancestral KIR gene in primates, we cannot rule out the possibility of selection to have caused the observed divergence.
While the results presented here are expected to offer some clues to further study the viral infection mechanisms, we see a new trigger to induce cell death in the measles virus nucleoprotein which is amenable to re-engineering as a targeted molecule.
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