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Under acidic pretreatment conditions, the predominant reactions associated with lignin are fragmentation by acidolysis of aryl ether linkages and acid-catalyzed recondensation, while linkages like resinol and phenylcoumaran sub-units are fairly stable.
While linkages between increased ROS levels and phosphatase activity of DUSP6 have been shown in non-T cells [ 63, 64] whether such a link exists in aging NCD4 T cells is not yet clear.
Under acidic pretreatment conditions, the predominant reactions in lignin are fragmentation by acidolysis of aryl ether linkages (primarily β-O-4 linkages) and acid catalyzed recondensation [ 31- 33], while linkages such as resinol and phenylcoumaran subunits (see Figure 1) are fairly stable [ 24, 34].
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While linkage studies in F2 or recombinant inbred (RI) lines are thought to have reasonable statistical power, the limited number of recombination events in such crosses produces large QTL intervals that make the selection of candidate genes difficult.
It should be stressed that while linkage disequilibrium is detected in the population as a whole and in some subpopulations, the values of the index of association are all close to zero (ISA = 0.074 0.095), indicating a limited level of disequilibrium.
While linkage still influences these estimates, correlations of QTL effects on traits displayed similar trends to those on line values.
While linkage analysis shows that this effect undoubtedly occurs, it seems unlikely that this is the purpose of the protein.
Thus while linkage to PAR1 has been ruled out some questions regarding this region (class 1 above) remain.
While linkage is systematic but not powerful, association is powerful but, until the advent of microarrays, association was not systematic.
Linkage group 9 containing 1,565 markers was the biggest group, while Linkage group 10 was the smallest group with 565 markers.
While linkage information was accounted for during reconstruction of haplotypes based on available relationships, linkage disequilibrium is considered in the estimation of LocIBD.
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