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In other words, the MMN cannot be explained by changes in post-synaptic sensitivity or intrinsic connections, only; nor can it be explained by exclusive changes in extrinsic connections.
The early years of the HYMS course involves not only problem-based learning sessions but also a structured weekly programme of lectures, laboratory-based practical classes and tutored clinical experience, so the importance of group functioning to the examination outcomes cannot be explained by exclusive reliance on problem-based group learning.
For instance, the karyotypic heterogeneity observed in DLD1+7 cells, with chromosome numbers ranging between 42 and 53, cannot be explained by exclusive mis-segregation of chromosome 7, because this would produce a narrower chromosome number distribution around the modal number of 47.
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The high level of selectivity can be explained by the exclusive formation of a pentacoordinate transition state, as described by Thornton and Pridgen.
The reason why a large fraction of amino acid states are irreversible may be explained by two nonmutually exclusive mechanisms.
The observed biphasic behavior of TR polymorphism incidence could be explained by two nonmutually exclusive mechanisms involving the probability of slippage events as a function of repeat number.
The lack of a role for RecQ in hyper-TLD by probable death-by-recombination in RuvABC− UvrD+ cells, despite the requirement for RecQ in death-by-recombination in cells lacking UvrD (Magner et al. 2007; Fonville et al. 2010b), including the ∆ uvrD hyper-TLD studied here, can be explained by two nonmutually exclusive hypotheses.
These intriguing observations can be explained by several non-exclusive mechanisms.
The high level of cytochrome P450 enzymes in non-hygienic bees can be explained by two non-exclusive hypotheses.
The "energy production" KEGG class decreases from D1 to D6, which might be explained by two non-exclusive hypothesizes: the oxidative phosphorylation and citrate cycle are more active in D1 in relation to the high energy demand for developmental processes paralleling symbiont multiplication; the host energy production at D6 decreases as a result of the high energy income from symbiont digestion.
The lack of evidence for local adaptation in our experiment may be explained by several non-mutually exclusive causes.
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