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Although a high proportion of the motion selective cells in primate motion area, MT, are disparity-selective, there is no convincing evidence for cells in this area specific to stereomotion-in-depth and the neural basis of stereomotion processing remains obscure.
The microscopic fossils show convincing evidence for cells and bacteria living in an oxygen-free world over 3.4 billion years ago.
Motivated by physiological evidence for cells that are selective for border-ownership information [37] some models were proposed where cues signaled by T-junctions are used to generate consistent representations of layered surfaces [30], [38].
In this work, we present more evidence for cells' internal optimization for efficient complex production.
There is evidence for cells with NK properties in the tunicate Botryllus schlosseri, and the Ciona intestinalis genome includes homologs of some NK cell receptors [ 5, 8].
In chelicerates and myriapods there is no evidence for cells similar to the neural stem cells that arise out of proneural clusters and repress their neighbours through Notch signalling and the E spl -C in Drosophila [ 83– 87].
Similar(53)
Scanning electron microscopy provided evidence for cell surface damage by the reported di-alkylated paromomycins.
Independent evidence for cell-cell interactions in vivo has also been obtained in a V. cholerae animal model through Tn-seq mutational analysis12.
Hagan, I. & Yanagida, M. Evidence for cell-cycle-specific, spindle pole body-mediated, nuclear positioning in the fission yeast Schizosaccharomyces pombe.
Pontin interacts directly with both TERT and dyskerin, and the amount of TERT bound to pontin and reptin peaks in S phase, evidence for cell-cycle-dependent regulation of TERT.
Evidence for cell-specific expression and a multi-gene family., The Journal of Biological Chemistry, vol. 262 no.
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