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Furthermore, cheek/chin skin SKP cells were shown to express markers for undifferentiated stem cells, including a high expression level of the Sox9 gene.
In conventional adherent petri-dish cultures, Lig-8 cells divide exponentially, express markers for definitive endoderm HNF3β and hepatocyte lineage, including CK8 and α-fetoprotein, but lack expression of mature hepatocyte markers.
In addition END2 cells also express markers for the PE.
Thus, PYS2 and XEN cells express markers for both the extra-embryonic VE and the embryonic VE, whereas END2 cells only expressed panVE markers such as Ttr.
These hNSCs did not express the pluripotency markers Oct4 or Nanog, nor did they express markers for the mesoderm or endoderm lineages.
Conversely END2 cells, which were previously characterized as VE-like, fail to express many markers that are widely expressed in the VE, but instead express markers for only a subset of the VE, the anterior visceral endoderm.
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In contrast, cells on the control gels expressed markers for adipogenesis.
The hNSCs were self-renewable, multipotent, and expressed markers for neural stem cells.
HEI-OC1, an inner ear cell line derived from the immortomouse, expresses markers for auditory sensory cells and, therefore, is a potential tool to study the ototoxic mechanisms of drugs like aminoglycoside antibiotics and CDDP.
No human nuclear antigen-positive cells expressed markers for oligodendrocytes.
Both PYS2 and XEN cells represent mixed populations expressing markers for several ExEn lineages.
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