Examples of 'hescs' in a sentence
Meaning of "hescs"
hESCs (noun): Human embryonic stem cells (hESCs) are pluripotent cells derived from the inner cell mass of a blastocyst. They have the potential to differentiate into various cell types and have significant implications in regenerative medicine and research
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- plural of hESC
How to use "hescs" in a sentence
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hescs
The stem cells are also described to be hESCs.
Plates containing hESCs are stained for alkaline phosphatase.
The first of these concerns the development of alternatives to hESCs.
Differentiation of hESCs was induced by culturing them as free floating clusters.
A decrease in proliferation has previously been reported upon exposure of hESCs to nicotinamide.
Adherent and suspension hESCs were differentiated using parallel conditions.
This protocol mainly focuses on the neural retina cell differentiation of hESCs.
Targeting the mutation in hESCs confirmed the causality of a specific genetic defect.
Our laboratory has developed a drug discovery scheme based upon using hESCs to screen drug candidates.
Pluripotent cells do not include hESCs obtained vÃa the destruction of a human embryo.
HESCs may be derived from fertilized embryos.
This is an important fact since the hESCs were often grown on mouse feeder layers.
NK cytotoxicity experiments were also conducted on hEEPs differentiated from hESCs.
In cultures of undifferentiated hESCs there is always some level of background extraembryonic differentiation.
Even more preferably, the stem cells are hESCs.
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Cortical neuroepithelium induced from hESCs were subjected to culture under the following conditions.
HESCs are derived from fertilized embryos.
Differentiated RPE cells derived from hESCs may be used for intraocular transplantation.
In some experiments, this vector can be transfected into hESCs.
Undifferentiated hESCs split to single cells can also grow and proliferate substantially as described.
Even more preferably, the stem cells are described to be hESCs.
Engineering PST genes into hESCs to increase PSA on DA neurons.
Achieving efficient, directed differentiation is of great importance for therapeutic application of hESCs.
Proliferation of pluripotent hESCs clearly demonstrated the bioreactor 's potential.
In comparison, the genetic stability of hiPSCs compared to hESCs was intensively studied.
Furthermore, hESCs were more efficient in producing cardiomyocytes than hiPSCs.
Together, these results uncover a new role of species-specific transposable elements in hESCs.
Methods of maintaining pluripotent hESCs under feeder-free conditions have been described.
However, hESCs are prone to genomic instability, which could limit their clinical utility.
In some processes for producing definitive endoderm cells, hESCs are maintained on a feeder layer.
After trypsin, hESCs were resuspended in the chemically-defined media containing the desired compounds.
We describe a seven-stage protocol that efficiently converts hESCs into insulin-producing cells.
In addition, hESCs may also experience other genetic changes that traditional methods fail to detect.
This selection vector was linearized, and then introduced into hESCs using standard lipofection methods.
Under these conditions hESCs coalesced into small spheres of morphologically viable cells within 24 hours.
This selection vector is linearized, and then introduced into hESCs using standard lipofection methods.
Both reference hESCs and iPSCs were cultured on the Matrigel-coated plates in mTesR1 medium.
We then examined E-cadherin expression in hESCs after trypsin dissociation.
TUNEL assay The hESCs under different treatments were dissociated by trypsin and fixed by 4 % paraformaldehyde.
Thus, BMPs play a role in inducing differentiation of hESCs to RPE cells.
In some embodiments described herein, hESCs in culture begin differentiating at a reference time point.
These results demonstrate that activin A mediates a rapid transition of hESCs to FGF8 expressing cells.
Results confirmed that undifferentiated hESCs can suppress the aggregation of the aggregating p53 mutant.
This is because activation of p53 leads to rapid differentiation of hESCs.
Specifically, two parallel hESCs were cultured for four days in RPMI medium.
The culture of claim 7, wherein the pluripotent mammalian cells are hESCs.
As in the previous Example, hESCs were cultured with or without activins for four days.
The method of claim 1, wherein the pluripotent stem cells are hESCs.
In all cases shown here, RPE cells were derived from hESCs without presence of Activin-A.
Cloning efficiency of hESCs under various culture conditions Culturing conditions Cloning efficiency %.
