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The CIGB-552 in vitro antineoplastic effect has been documented by using human cancer cells of different histological origins [ 5].
Blood flow abnormalities in glaucoma have been documented by using different techniques, such as fluorescein angiography [ 25], colour Doppler imaging [ 26], laser Doppler flowmetry [ 27], and pulsatile ocular blood flow (POBF) measurements [ 28].
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After 6 cycles of mFOLFOX6 plus bevacizumab, a major response of the liver metastases was documented by using CT.
Occurrence of DNA damage in the same cells was documented by using the single cell gel electrophoresis (comet) assay, which showed a remarkable increase in DNA single- and double-strand breaks in CS-exposed mice, as compared with sham-exposed mice.
Morphological changes of cells were documented by using a Zeiss Axiovert 40 inverted microscope (Zeiss, Göttingen, Germany) and Canon PowerShot G6 digital camera.
Cell morphology and esterase stain were documented by using a Zeiss Axiovert 40 inverted microscope (Zeiss, Germany) and Canon PowerShot G6 digital camera.
Each of these concepts is documented by using the RoundUp Ready® soy GTS40-3-2 GTS40-3-2 GTS40-3-2
This was documented by using an insulin clamp at low insulin infusion rates, which incompletely suppressed hepatic glucose production.
The morphology of colonies was documented by using a Zeiss Axiovert 40 inverted microscope (Zeiss, Göttingen, Germany) and Canon PowerShot G6 digital camera.
Disease extension and vasculitis activity were documented by using the Disease Extension Index (DEI) and the Birmingham Vasculitis Activity Score (BVAS) as outlined elsewhere [ 17, 18].
Production of KPC enzyme was documented by using a phenotypic test based on the inhibitory activity of boronic acid compounds as reported by Pournaras et al. [ 1], and carbapenemase producing- Klebsiella pneumoniae (KPC-Kp) was identified.
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