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In particular, prospective math majors (including engineers considering mathematics as a second major) should not take the engineering sequence MATH 216 followed by MATH 353; they should instead take MATH 221 followed by MATH 356 for a first course in differential equations.
This group [ 40, 41] has recently developed an approach for engineering sequence pools that links RNA sequence space regions with corresponding structural distributions via a "mixing matrix" approach combined with a graph theory analysis.
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Recently developments have been made in engineering sequence-specific zinc finger DNA-binding proteins.
Despite its ubiquity in science and engineering, sequence-dependent effects of displacement kinetics have not been extensively characterized.
Pumilio and FBF homology (PUF) proteins represent highly promising candidates for engineering sequence-specific RNA recognition, but were only known to recognize G, A, and U, significantly limiting applications.
Provides technical support for the teaching labs in all of the introductory physics courses, including: the undergraduate engineering sequences P1112, 2213 and 2214, their counterparts for majors P1116, 2217, 2218, and introductory courses offered to non-majors P1101-1102, 2207-2208.
Although degradation of lignocellulose has been shown to be possible with minicellulosomes containing only three enzymes [ 31], should we wish to increase the complexity of our minicellulosomes in the future, we may have to examine ways of increasing the stability, for example, by examining the effects of different 5′ mRNA leader sequences, or by engineering the sequence to reduce homology.
The defining characteristic of the engineering mathematics sequence, MATH 1910-1920-2930-2940, is its randd and utilitarian coverage of a wide variety of mathematical topics important in engineering and the physical sciences.
Here we review recent studies that examine the engineering of sequence specificity of PUF proteins and its applications as well as studies that increase our understanding of the natural diversity of RNA recognition by this family of proteins.
In addition, by engineering the sequence elements of the Hepatitis delta virus ribozyme and the nopaline synthase 3′ untranslated region immediately downstream of the last nucleotide of LCV RNAs 1 and 2 in the binary vector constructs, the in planta produced LCV transcripts were expected to bear authentic 3′ termini.
Briand et al. [8] have proposed an approach for reverse engineering UML sequence diagrams using dynamic analysis.
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