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The new methods allow maintenance of long-term, large-scale cultures of cells that retain the full complement of surface properties and that maintain the cobblestone monolayer morphology and differentiated functional properties.
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The differentiated cells reveal functional properties with respect to voltage‐activated Na+ and ATP‐modulated K+ channels and normalize blood glucose levels in streptozotocin‐treated diabetic mice.
Although how the differentiated functional modules confer phenotypic properties directly or indirectly is still unclear, a series of the above results should be helpful in better understanding of the physiological properties.
Using this new method, we found significant difference in module completion ratio by 8 bacilli in terms of at least 19 pathway and 35 complex modules, although how the differentiated functional modules confer phenotypic properties directly or indirectly is unclear thus far.
At this point, it is still unclear whether such differences affect only culture and differentiation behavior or may extend to functional properties of differentiated derivatives.
DOI: http://dx.doi.org/10.7554/eLife.00966.002 In adults, stem cells reside at the apex of proliferative hierarchies and, either directly, or through a sequence of terminal divisions, give rise to the specialist differentiated cells that provide the functional properties of tissue.
These methylation changes cannot be explained by technical biases since all iPSC‐derived DAn lines were equally generated and characterized in parallel, blind to the researcher, and differentiated DAn had similar morphological and functional properties (Sanchez‐Danes et al, 2012b).
Rats are widely used as hosts to evaluate functional properties of cells which are differentiated in vitro from mouse ES cells [1], [2].
We report the conditions required to generate adult murine dentate gyrus precursor cell cultures and to analyze functional properties of precursor cells and their differentiated granule cell-like progeny in vitro.
In the process of developing iPS-cell-based therapies, the major goal is to determine whether differentiated cells derived from iPS cells, such as cardiomyocytes (CMs), have the same functional properties as their physiological in vivo counterparts.
Although several studies emphasized that cryopreservation does not alter phenotypic or functional properties of DC [ 9, 45, 46], these studies evaluated already differentiated iDC or mDC for IPA-cryopreservation and may not reflect all aspects of cryopreserving cells for DC immunotherapy.
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