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We have characterized a newly developed chicken 44K whole genome oligonucleotide microarray using four major tissues.
In summary, the results above demonstrated that this newly developed chicken 44K whole genome array is a powerful genomic tool to investigate different biological processes in chickens.
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Also, the expression pattern of Prdm1 in developing chicken limbs needs to be studied throughout development to determine if Prdm1 becomes limited to posterior limb bud regions as found in the mouse embryo and suggested by the previous in situ hybridization study in chicken embryos [35].
As a negative control, enrichment of predicted targets of the transcription factor PAX6 was examined, given its known role in retinal development [77], [78] and absence of expression in the developing chicken inner ear [79].
The properties of biofunctionalized nDPs were investigated on cultivated human mesenchymal stem cells and on the developing chicken embryo chorio-allantoic membrane.
By manipulating the genes' proteins, they have seemingly turned back the evolutionary clock, producing snouts in developing chicken embryos that resemble those of alligators today.
For another example, we show that developing chicken and duck beaks contain differently configured localized growth zones (LoGZs) and can modulate chicken beaks to phenocopy diverse avian beaks in nature by altering the position, number, size, and duration of LoGZs.
When ARIA isolated from chick embryo brain was applied to chicken myotubes, which are developing chicken muscle fibers, it was shown to increase the rate of insertion of acetylcholine receptors into chicken myotube membranes.
We used our previous nomenclature for myogenic cells in the developing chicken [31].
Myogenesis in the developing chicken embryo proceeds through distinct stages in which multiple types of myoblasts and myofibers appear [16] [20].
The authors showed that swip1 was regulated by sonic hedgehog in somites and limb buds in the developing chicken.
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