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In class I modifications, the saddle was designed as 10 mm mesiodistally, 2.5 mm buccally, and 2.5 mm lingually from the center of the implant (Fig. 2).
This may be due to the difficulty in preparation of form II samples whose quality is high enough for PL studies; actual form II samples usually contain significant fractions of form I modifications as well as amorphous backbones.
Fig. 1 The basic design for the analysis of FEA models Fig. 2 Class I modifications Fig. 3 Class II modifications Fig. 4 Class III modifications Fig. 5 Class IV modifications Table 1 Mechanical properties of the materials used in the study Material Young's modulus Poisson ratio Cortical bone 14.8 0.30 Cancellousus bone 1.85 0.30 Titanium 110 0.32 Cobalt-chromium alloy 220 0.30 .
In the analysis of the top 50 (Table S7) sequences of the mature miR-122 and miR-21, A→I modifications, U→C, G→A, U→A, and C→U modifications were observed, as evidenced by the presence of a single peak (Figure 3B).
No quantitative or qualitative topoisomerase I modifications were observed.
Applying Phase I modifications on this substructure generates an arene oxide PCB3 (PCBI1) and 3-hydroxy-PCB3 (Fig. 6 PCBI4).
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With such sample, the transitional mechanism from form II to form I modification is further investigated by in situ WAXD combined with FTIR spectroscopy.
Surface engineering was carried out on oxide ceramics (Al2O3 ZrO2, ZrO2) using two different laser-assisted processes: (i) modification of the edge layer of the ceramic by laser induced remelting and alloying and/or (ii) surface microtexturing by laser ablation.
Under ambient conditions, there are two possible ways of such influence: (i) modification of nanocrystal surface leading to the increase of luminescence intensity and (ii) photooxidation of nanocrystals resulting in degradation of the luminescence spectra.
This increased intensity indicates increased collagen I modification around the invasive lesion [ 15].
Nevertheless, the HsdS proteins can combine with the HsdM proteins to form a functional type I modification enzyme.
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