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Interestingly, the N-terminal region of Vif protein binds selectively HIV-1 genomic RNA [ 1] and sites in this region have DNA/RNA binding properties and also interact with A3G/F [ 35, 36].
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We also characterized REST binding properties and embryonic phenotypes in a conventional brain-specific Rest KO line (Gao et al., 2011), targeting Rest exon 2, which we show still expresses a C-terminal REST peptide, for comparison with our Rest GT mice.
Results from this study would also be helpful in designing novel neuroregenerative drugs with improved binding properties and low toxicity.
Road surfacing may be necessary, factors to consider are compaction, drainage, subsurface binding properties and gradient.
Previous characterizations of TRF1 and TRF2 binding properties have also revealed that whereas TRF2 binds to telomeric dsDNA as a large oligomeric structure, TRF1 does not oligomerize to the same degree.
Several cochaperones, including p23, Cdc37, Aha1, and Sgt-1 [ 16, 17], and substrate binding properties have also been related to Hsp90-N [ 12, 18, 19].
An investigation of rhesus relaxin-3 bioactivity and RXFP1 binding properties was also performed.
The various structural modifications that HSA can undergo during its in vivo lifetime or during the processes employed to isolate therapeutic HSA from plasma, modify not only its conformation and hence its binding properties but also its redox state [16, 50, 51].
The various structural modifications that HSA can undergo during its in vivo lifetime or during the processes employed to isolate therapeutic HSA from plasma, modify not only its conformation and hence its binding properties but also its redox state [ 16, 50, 51].
Pigment binding properties were also analyzed by HPLC after two hours of light treatment: as shown in figure 6C, after this short light treatment we observed an increase in the zeaxanthin and antheraxanthin content with a corresponding decrease in violaxanthin, implying the presence of an active xanthophyll cycle in this moss.
The goal of this study is to evaluate whether MT-2A, via its zinc- and copper- binding properties, also represents an endogenous protective mechanism against Aβ aggregation and toxicity.
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