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For tiny organisms, this is advantageous for conservation of tissue: there is no reason to evolve or to maintain a tissue that is not functionally important.
For example, by applying tools and concepts used in the analysis of human populations to cell populations, it may be possible to derive quantitative estimates regarding the cell dynamics and the number of stem cells which maintain a tissue.
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Cells maintain a tissue-specific balance of activities of SR proteins and antagonizing hnRNP proteins that can vary during development and mitogenic stress, and these proteins require a specific level of phosphorylation for their activity [74], [75].
Giusti's organization maintains a tissue bank of more than fourteen hundred bone-marrow samples and nearly twelve hundred blood samples from patients with myeloma, which researchers use to test novel compounds, and it helps finance clinical trials of experimental myeloma drugs.
The foundation runs three major studies of the life span and health of the 280,000 survivors and their children, plus it maintains a tissue bank and other records.
This model postulates that long-lived multicellular organisms have evolved stem cell populations with high fitness, not only as a means of efficiently maintaining a tissue, but also because high fitness in a cell population will oppose somatic cell evolution.
These aspects are also of highest relevance for establishing and maintaining a tissue-like situation in vitro.
It is therefore important to maintain a constant tissue temperature during the measurements.
The minimal protein requirement can be defined as the amount required to maintain a neutral tissue protein balance, at least in physiological conditions [ 58].
Throughout life, the tight equilibrium between cell death and the prompt clearance of dead corpses is required to maintain a proper tissue homeostasis and prevent inflammation.
Although mutations can occur at every level of this cell hierarchy, the relatively short lifetime of more mature cell stages means that, in effect, the real risk of long-lasting oncogenic mutations is restricted to the small population of stem cells and early progenitor cells that maintain a given tissue.
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