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Furthermore, Muse cells express classic pluripotency markers and differentiate into cells from the three embryonic germ layers both spontaneously and under media-specific induction.
All of them express myogenic markers and differentiate to muscle fibers in vitro.
Moreover, PGCCs were able to express certain normal and cancer stem cell markers and differentiate into the adipose tissue, cartilage, and bone.
We isolated these cells from growth plates of Col10CreYFP+ long bones and show that they express stem cell and osteoblast markers and differentiate into osteoblasts in vitro.
Our results show that ball mutant NBs proliferate at a reduced speed and progressively lose stem cell markers and differentiate untimely during development.
ASCs represent heterogeneous populations of cells able to respond to variable stimuli by expressing different lineage-specific markers and differentiate, at least under in vitro conditions, towards adipocytes, chondrocytes and osteoblasts [24].
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They were positive for normal and cancer stem cell markers, and differentiated into adipose, cartilage, and bone.
They expressed undifferentiated pluripotent cell markers, and could differentiate into all three germ layers via embryoid body and teratoma formation.
In addition, the resulting sequence information can be used to assess pathogenicity, mutations, virulence markers, and to differentiate detected agents from closely related species.
These EST-SSR primers were named as DPGxxxx, where DPG was referred to date palm gene-based markers and to differentiate from those SSR markers developed from genomic sequences in date palm, such as those developed by [ 27- 29].
Investigation of EAEC-STEC O104:H4 strains from sporadic cases of human infection could reveal these markers and help differentiate between strains that were introduced from other areas and strains that were newly generated by phage transduction.
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