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It is not known whether the cells can colonize all the tissues of a human embryo, but it is presumed from their other properties that they are indeed pluripotent cells, and they therefore are regarded as a possible source of differentiated cells for cell therapy the replacement of a patient's defective cell type with healthy cells.
These BE cells may be a novel source of differentiated cell types for liver engineering.
Stem cells constitute the source of differentiated cells for the generation of tissues during development and for regeneration of tissues that are diseased or injured postnatally.
These cells represent a potentially unlimited source of differentiated cells or tissue for transplantation for common diseases such as type 1 diabetes mellitus.
Furthermore, we exploited these undifferentiated photoprotein mES cells to produce a transgenic mouse, which may be useful for ex vivo imaging studies and as a source of differentiated primary cells expressing a Ca2+ reporter gene.
Although human embryonic stem cells (hESCs) hold great promise as a source of differentiated cells to treat several human diseases, many obstacles still need to be surmounted before this can become a reality.
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Stem cells are an ongoing source of the differentiated cells that make up the tissues and organs of animals and plants.
The aim is to employ stem cells as a source of appropriately differentiated cells to replace those lost through physical, chemical or ischaemic injury, or as a result of degenerative disease.
In higher plants post-embryonic growth is maintained by the activities of meristems, which comprise stem cells and their derivatives, serving as the source of all differentiated cell types.
Adult stem cells hold great promise as a source of diverse terminally differentiated cell types for tissue engineering applications.
This suggests that the foci of neuroendocrine-like cells that express SV40-Tag and synaptophysin, but lack AR, arise independent of androgen-deprivation and represent the source of the poorly differentiated tumors that are the lethal phenotype in the TRAMP model.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com