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The subjective categorisation practices demonstrated that the GPs perceived the patients' presentations of MUS to be of a more complex nature than reflected by the defining criteria of 'multiple symptoms', and hence this seems to demonstrate a discrepancy between the defining criteria of 'multiple symptoms' and the clinical experience.
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In Figs. 3A and B one can compare the levels of LDH and XTT in the control and in cells treated with 90 μM MP-MUS to be alerted to the fact that large-scale metabolic changes occur in response to MP-MUS.
However, the study points to a need for addressing GPs' conceptual understandings of MUS and diagnosis if classification of mild-to-moderate conditions of MUS is to be applied in daily clinical practice.
The study demonstrates a need for addressing these issues if sub-threshold categories for MUS are to be applied in routine care.
Biological investigations are enabled by the use of animal models, with the laboratory mouse, Mus musculus, proving to be one of the most important species for investigating human disease (3).
The position of African subgenus Nannomys within Mus is variously proposed to be polytomous with the other three subgenera of Mus [ 19, 45], basal within Mus ([ 20], this study), or as sister to the subgenus Mus [ 21].
For invertebrate and vertebrate species where sex determination is well-understood, including C. elegans, Drosophila melanogaster, and Mus musculus, there appears to be little conservation in many of the molecular and genetic mechanisms involved [ 126].
Alternative splicing of exons in the 5' untranslated (UTS) region of Syt1 in mammals (see Additional File 1 and accession numbers aj617615-aj617619 for alternative splicing in Homo, Mus and Rattus) seems to be particularly complex and is the likely explanation for the described variations [ 32].
This compound is N,N-bis 2-chloroethyl -2- 1-methyl-1,2,3,6-tetrahydropyridin-4-yl propanamide (MP-MUS), which was showN,N-bis 2-chloroethyl -2- 1-methyl-1,2,3,6-tetrahydropyridin-4-yl propanamideward MAOA.
African pygmy mice are therefore the first group of African rodents that host two very different lineages of arenaviruses; one of them seems to be Mus-specific (in Africa now reported from two species in the minutoides group), but the second forms the sister lineage of the highly pathogenic Lassa virus (hosted by species from the setulosus and the baoulei groups).
More detailed genetic studies showed that it was a house mouse carrying a big chunk of DNA from Algerian mice (Mus spretus)—a species known to be naturally resistant to warfarin on chromosome 7.
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Justyna Jupowicz-Kozak
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