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The longitudinal taper and rectangular cross-section provide unequaled primary stability, which promotes consistent secondary osseointegration to the grit-blasted titanium surface, even in osteoporotic bone.
Whereas expansion segments were generally found to be absent in the malacasporeans and the clade of primary marine myxozoan species, they occur in all taxa of the clade containing freshwater species, where they showed a consistent secondary structure throughout.
The results indicated that, in spite of the consistent secondary dendrite arm spacing for all specimens, a wide range of microstructural and defect features were responsible for the fatigue behavior.
No consensus was detected in surrounding sequences of viral RNA that underwent G-to-A editing and there were no consistent secondary structures evident in these regions (Bourara et al, 2000).
A consistent secondary structure represented by θ should satisfy the following constraints: (i) ∑ i < j θ ij +∑ j < i θ ji ≤1 for any j (each position in a sequence is allowed to form a base pair with one other base at most), and (ii) θ ij +θ kl ≤1 for any i < k < j < l (the formation of any two base pairs which results in a pseudo-knot is not allowed).
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Individuals with skin or bony lesions consistent with secondary yaws and dual-positive serology were considered to have secondary yaws.
Skin lesions consistent with secondary yaws were found in 19 (1.3%, 0.6 2.9%), bone lesions consistent with secondary yaws were found in 10 (0.7%, 95% CI 0.3 1.5%) children.
Both hypotheses are consistent with secondary ion mass spectrometry measurements showing a strong increase of the impurity content at the interface and an oxygen concentration of around 1019 cm−3 in the epitaxial layer.
In addition, this population has a clear enhancement of parallel flux extending up to ~100 eV, with a conic signature extending even higher in energy, possibly consistent with secondary electrons and/or photoelectrons accelerated upward from the surface (Halekas et al., 2008c).
The features of the ChI Abs alone are consistent with secondary rearrangement model, in both using distal VH genes and having long CDR-H3s for the same Ab population.
In addition, upon re-challenge with LM-OVA, OVA-specific CD8+ T cells showed rapid and highly transient caspase-3 activation, consistent with secondary expansion of a memory population (data not shown).
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