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Such a phenomenon is likely to be part of the explanation for the sharp reduction of longevity accompanying male tarantula maturity.
Consistent with the essential role of peroxisomal FFA oxidation as a longevity assurance process only under CR, the pex5 Δ mutation substantially shortened the CLS of CR yeast but caused a significantly lower reduction of longevity in non-CR yeast, especially in yeast grown on 2% glucose.
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We attribute the reduction of the longevity effect seen in D4b2b [7] compared to D4a when moving from centenarians to semi-supercentenarians to the presence of 14979C (Cytb: Ile78Thr) in D4a.
Reduction of maximal longevity was detected only in females.
[ 34] also observed the reduction of leaf longevity; however leaf length was either increased (adult leaves) or reduced (intermediate leaves).
However, the turnover is faster, resulting in a reduction of leaf longevity and an increase on the number of leaves produced per year.
However, the leaf turn-over is faster, resulting in a reduction of leaf longevity and an increase in the number of leaves produced per year.
Thus, stabilized forms of the auxin/indole acetic acid (Aux/IAA) protein HaIAA27 [ 14] or dominant-negative forms of HaHSFA9, but not inactive forms of HaHSFA9 [ 10], both caused reduction of seed longevity and loss of function of the HaHSFA9 program in tobacco seeds.
A staged treatment approach that employs microbial reductive dechlorination after aggressive mass removal may thus provide a cost-effective option for reduction of both source longevity and risk.
As reduction in SIN3 levels has previously been linked to oxidative stress [ 9] and the adult Sin3A knockdown flies are sensitive to paraquat (Fig. 3, Supplemental Fig. 1), we investigated whether reduction of SIN3 affected longevity.
In flies expressing NSP Arctic Aβ42, the pattern of longevity reduction was remarkably similar to control flies, which is consistent with cytoplasmic Aβ not interacting with dPSA.
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