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Taubner, T., Korobkin, D., Urzhumov, Y., Shvets, G. & Hillenbrand, R. Near-field microscopy through a SiC superlens.
This paper addresses the inferential problems associated with material indentation and atomic force microscopy, through a framework for the changepoint analysis of pre- and post-contact data that is applicable to experiments across a variety of physical scales.
The identification of mycorrhizal root infection is realized by optical microscopy through a technique not vital staining with trypan blue (TB), described by Hayman [9] revealing the set of fungal biomass.
The identification of mycorrhizal root infection is in optical microscopy through a technique not vital staining with trypan blue (TB), described by Hayman [48], revealing the set of fungal biomass.
For events near the cortical surface they used two-photon microscopy through a cranial window.
Sections were observed by conventional light microscopy through a DM600 Leica microscope and photographed.
Similar(49)
The fiber-matrix interface, fiber surface and toughening mechanisms were assessed using field emission scan electron microscopy (FESEM) and atomic force microscopy (AFM) through a period of 56 days.
The fluorescent label Cy3 was imaged using prism-type total internal reflection microscopy, through excitation by a 532 nm (Compass 215M-50, Coherent).
Lymphatic vessels in the brain, for example, were recently identified for the first time using in vivo multiphoton microscopy imaging through a thinned skull preparation2.
Hydration characteristics were assessed using thermogravimetric analysis/differential thermal analysis (TGA/DTA), and fiber-matrix interface and fiber surface characteristics were assessed using scanning electron microscopy (SEM) through a period of 90 days.
Both the segments of active filaments and the intermetallic particles (IMPs) were successfully imaged in a humid air (ca. 85% RH) environment by scanning Kelvin probe force microscopy (SKPFM) through a plasma polymer coating of about 340 nm thickness.
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