Exact(3)
In the twin boundary, a broader range of interactions is observed, including defect transmission from matrix to twin and decomposition in the interface into discrete defects.
In this paper we present a methodology for generating a realistic volume element with discrete defects that are statistically equivalent random defects in a Sic/SiNC samples.
This mutant is predicted to erroneously and stochastically incorporate valine instead of alanine into growing peptide chains, nonetheless resulting in discrete defects in mediating auxin effects on cell proliferation (Perry et al., 2005).
Similar(56)
The results offer insights into the interaction of propagating cracks in adhesive layers and their interactions with discrete, localized defects, which could lead to improvements in surface preparations and bond integrity or even to joint designs having intentionally placed defects useful in controlled disassembly or for other purposes.
Dcx knockout (KO) mice show no major isocortical abnormalities, but have discrete hippocampal defects.
Hoffman K Yoo H Karagiannis J Synthetically Engineered rpb1 Alleles Altering RNA Pol II Carboxy Terminal Domain Phosphorylation Induce Discrete Morphogenetic Defects in Schizosaccharomyces pombe.
Syndromic obesity arises from discrete genetic defects or chromosomal abnormalities at several genes, and can be autosomal or X-linked.
Moreover, analysis of protein abundance in an Schizosaccharomyces pombe Δelp3 mutant linked codon usage and Elongator-dependent variations in translational efficiency to discrete growth defects (Bauer et al., 2012).
The phenotypes detected in this study vary from discrete specific defects (e.g., decreased platelet cell number in Crlf3 tmutantsa mutonts) to complex phenotypes in which many organ systems are involved (e.g., Spns2 tm1a(KOMP)Wtsi homozygotes show eye, hearing, and immune defects; Nijnik et al., 2012).
In summary, we describe here the first functional consequences associated with discrete hippocampal lamination defects.
Adaptive-optics imaging identified a small, focal hyporeflective lesion at the foveal center in both eyes of the subject with RGS9-associated disease, corresponding to a discrete outer retinal defect also observed on spectral-domain optical coherence tomography; however, the photoreceptor mosaic remained intact at all other observed eccentricities.
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