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Because the transcriptional pattern of several intracellular pathogens exhibit host-cell specific features [34], we may hypothesize that the second candidate is differentially regulated by the host cell.
In our report, we hypothesize that the second gastrointestinal bleed, occurring when platelet count was back to normal, could have possibly been triggered by a degree of prolonged uremic platelet dysfunction and by low-dose unfractionated heparin.
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We hypothesize that the second-stage vaporization is sustained by low-temperature, soot-free, "cool-flame" chemical heat release.
We hypothesize that the first event is due to the uplift and denudation of regional, permanent topography generated after the breakup of Brazil and Africa.
The investigators hypothesize that the third molars that developed in a deep impaction pattern according to Pell and Gregory and Winter classifications can be associated with local changes and pathologies.
One can hypothesize that the first phase, similar for HMA6 and HMA8, corresponds to the fast 'E-P' to 'E' dephosphorylation (Supplementary Figure S1, step 4).
We thus hypothesize that the first HyPRP gene may have been a LTP derivative that acquired a sequence encoding proline-rich N-terminal domain either by means of gene fusion or by introduction of an in-frame repetitive element.
We hypothesize that the first CSL gene might have been created from a Rel-type transcription factor gene by the insertion of a beta-trefoil domain-encoding DNA sequence in between the amino- and carboxy-terminal Rel domains.
To account for this, we may hypothesize that the first step to Clonopsis parthenogenetic strains might be a diploid hybrid, showing two complete series of chromosomes of two different species.
Specifically, using the model as a guide, we hypothesize that the first step in the generation of a new nuclear pore is recruitment of elements of the outer ring of the NPC to bend the inner nuclear membrane outwards, similar to the process generating extracellular protrusions in the original proto-eukaryote.
We thus hypothesized that the second member of the pair would also be expressed in E. granulosus and attempted to isolate the corresponding full-coding cDNA with a set of oligonucleotide primers designed on the basis of the E. multilocularis sequence.
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