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In this paper, we introduce direct and dynamic formation of variants of light sheet illumination behind scattering layers.
In a number of studies, associations have been reported between genomic regions enriched with CNVs and segmental duplications [4], [5], [11], which have been suggested to mediate the formation of variants by non-allelic homologous recombination (NAHR).
Independent evolution of viral variants in the MGT may induce the formation of variants that harbour the ability to escape the effects of immune system and drugs, vary tropism and pathogenicity.
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We have mentioned the possibility of these being reservoirs for formation of variant or new proteins.
The presence of multiple copies of these T4SS components, which probably all are coexpressed, indicates that the primary function of the Bartonella Trw system may be the formation of variant pilus forms.
Furthermore, the formation of six variants in a given packet and the preferential arrangement into blocks of low-misorientation variant pairs demonstrate a universality of morphology and crystallography of lath martensite.
(i) Our calculations correctly predict the formation of different variants of β′ phases for Mg RE systems across the RE series.
The complicated crystallographic orientation relationship between austenite and martensite grains strongly restricts the formation of some variants of deformation-induced martensites.
The oriented lamellar structure satisfied the crystallographic relationship of (0001 C40//(110)C11b, <1̄21̄0]C40//[11̄0]C11b and <101̄0]C40//[001]C11b, resulting in formation of three variants of the C11b phase and two kinds of boundary: a type of C11b/C11b grain boundary and a type of C11b/C40 phase boundary.
In light of the texture-dependent tension compression asymmetry in Nitinol, this reduction in fatigue life and preferential crack initiation in pre-strained wires is thought to be attributed to compressive pre-strain-induced plasticity and tensile residual stresses as well as the formation of martensite variants.
This active turnover of genetic elements in the vicinity of CNVs could be associated with the formation of structural variants (26, 27).
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