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Accordingly, the increased percentage of FOXP3+ cells could only have been derived from cells that were FOXP3- at t = 0.
Most of this information on HGF/SF and TGF-β signal transduction has been derived from cells in culture, however, and has not been extrapolated to, or confirmed in the mammary gland in vivo.
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The secretory cells of the ultimobranchial glands are derived from cells that migrated from the embryonic nervous system.
There are also several glands that are derived from cells that originate in multiple regions of the embryo.
Other endocrine glands, such as the parathyroid glands and the adrenal medulla, are derived from cells that arise in the embryonic nervous system.
Some endocrine glands, such as the thyroid gland and the islets of Langerhans in the pancreas, are derived from cells that arise in the embryonic digestive system.
It is possible that these organs could be derived from cells, which could be modified from the individual herself, thereby overcoming all rejection phenomena.
Some of the ectomesoderm in annelids, echiurans and molluscs is derived from cells 3a and 3b, while the ectomesoderm of polyclad flatworms is derived from the 2b cell and acoel flatworms produce no ectomesoderm.
TAF cells are derived from cells of two different origins, most likely a combination of both.
Extracts were derived from cells that were serum starved, stimulated with 10% serum, or stimulated with both 10% serum and 50 ng/ml IGF-1 for 15 minutes.
It is well known that CD1d-restricted Vα14 invariant natural killer T (NKT) cells are derived from cells in the CD4+CD8+ double-positive (DP) population in the thymus.
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