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Both AT-MSC (ASC) and UC-MSC have been successfully differentiated into adipocytes [ 7, 63].
Human BM-MSCs have been successfully differentiated into insulin producing β-cells in vitro and transplanted to streptozotocin-induced diabetic mice which corrected the hyperglycaemic condition [ 106, 107].
MSCs derived from human adipose tissue have been successfully differentiated into functional adult white or brown fat cells as well as neural, muscle, tendon, bone, or cartilage cells [ 10, 24, 25].
J. Li and G. Lepski reviewed different sources of stem cells which can be used for spinal cord injury treatment in the future, including mesenchymal stem cells from human umbilical cord which have already been successfully differentiated into Schwann-like cells in vitro and grafted into the lesion sites of spinal cord injury rats; a partial recovery of motor function was reported.
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Although, this strategy for repair carries risks such as tumorigenic potential [37, 38], MSCs were successfully differentiated into various types of cells including cardiomyocytes, myocytes, and epidermal and endothelial cells [54, 95 97].
The AFCs expressed a degree of plasticity and were successfully differentiated into other types of cells which are otherwise not present in the ovary.
Both lines (a) AD-iPS5 and (b) AD-iPS26B could be successfully differentiated into all three embryonic germ layers in-vitro through an embryoid body (EB) based differentiation approach.
Moreover, Eguizabal et al. [ 7] have recently reported that hESCs and hiPSCs were successfully differentiated into OLCs and then successfully passed through the process of meiosis, were haploid, and expressed several genes related to early and late germ cells as well as the process of meiosis (Table 4).
PDLSCs derived from donors of different ages were successfully differentiated under an osteogenic and adipogenic microenvironment.
They are successfully differentiated by their characteristic CID spectral profiles.
The chromosome 5 amplification was successfully differentiated between the progeny, consistent with the CNV breakpoints predicted by CGH.
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CEO of Professional Science Editing for Scientists @ prosciediting.com