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For the quantification of proteins, the relative amounts of IFNAR2 in the tumors were expressed as a ratio of the optical density of the bands from the tumor specimen to those from the corresponding normal tissue; the latter was set at 1.0 by densitometric analysis as described previously [ 8, 14].
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To this end, various laboratory tests, including Hamburg wheel tracking test, Overlay test, indirect tensile strength test, resilient modulus test, and dynamic modulus test were performed to compare the engineering properties of PMLC specimens to those of plant-mixed and field compacted (PMFC) field core specimens at different aging stages.
The other material examined had no differences from the L. terrestris specimens other than measurements (Figs 3A C., which include additional specimens to those examined in detail).
We compared recently sampled hybrid zone specimens to those collected 10 20 years earlier, to test directly the long-standing hypothesis of hybrid zone movement between these species.
We further compared human specimens to those obtained from the Tg2576 mouse model of AD.
The holotype of the last of these species was collected from a gravel pit; following Tidwell et al. [ 110], we consider the age of this specimen to be likely concordant with those of other Mesozoic permineralized fern stems from eastern Tasmania, which have recently been dated as Early Jurassic [ 111].
PCR and qPCR based testing with universal primers is to be used as the first screen of clinical specimens to identify those samples containing bacterial DNA, regardless of species, to alert the clinician that infection is highly probable in those patients testing positive.
Within the age group <50 years, the risk or axillary recurrence was 82% lower (95% CI: 45 94%) for patients with more than six lymph nodes found in the axillary specimen compared to those with six or less than six lymph nodes.
The larger quantities of C-S-H and much smaller total cumulative pore volume were obtained for the steam-cured specimens, compared to those for the ambient-cured specimens.
Although collection of NP specimens with a flocked swab is one of the best methods for obtaining specimens to detect influenza, those specimens might have been improperly collected by the nurses.
Yet, increased CB1R levels were demonstrated in human PCa specimens compared to those of the benign samples [10].
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