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Time-lapse visualization of growing dendrites in live preparations has shown that establishment of a dendritic tree is governed by a combination of local branch dynamics, including elongation, branching and retraction (Dailey and Smith, 1996; Portera-Cailliau et al., 2003; Wu and Cline, 2003; Emoto et al., 2004; Williams and Truman, 2004; Mumm et al., 2006).
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Studies on the presence of protozoa in native rumen content preparations have shown significant differences between the results obtained for the treated and control groups at all three tested periods.
Early studies in animal preparations have shown that stimulus-evoked short-range synchrony between neurons in the primary visual area subserves perceptual binding of sensory information [1], [2].
However, the aforementioned confirmatory experiments with full-length viral RNA genomic preparations have shown that this novel strategy is a suitable alternative for sensitivity validation purposes.
However, BoNT/A preparations have shown efficacy for the treatment of this muscle.
Oxidative enzymes (e.g. GH61) present in new commercial enzyme preparations have shown to increase cellulose conversion yields.
In addition, a number of electrophysiological studies from hypothalamic slice preparations have shown that the VMH contains neurons that respond directly to low glucose (8), as do dissociated VMH neurons (9).
Phase III trials of all the interferon beta preparations have shown beneficial effects in reducing the annualized relapse rate (ARR) by about 30%34%%, reducing the progression of disability in RRMS as well as magnetic resonance imaging (MRI) disease activity 6– 9.
In studies with several other mammals, testicular microsomal preparations have shown very low or no CYP1A activity (Machala et al. 1998; Revel et al. 2001; Roman et al. 1998).
Furthermore, electrophysiological studies using hippocampal slice preparations have shown that somatic action potentials can trigger gene transcription without the involvement of synaptic activation and in the presence of NMDAR antagonists.
An attempt to isolate the translocation chromosomes by Fluorescence Activated Chromosome Sorting had not allowed complete purification of these chromosomes but PCR of sequence tagged sites (STS), on sorted preparations, had shown that sequences in the first 7 Mb of CFA 27 and the last 20 Mb of CFA11 were present in the LE tumour genome, but missing when t(27 11) was excluded.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com