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The PAP copolymers exhibit excellent electroactivity similar to the AP and polyaniline, which may stimulate cell proliferation and differentiation.
The posterior hyaloid of the vitreous and perihole tissue is enzymatically manipulated to create an atraumatic posterior vitreous separation and may stimulate cell proliferation to close macular holes.
Activation of the 5-HT2B receptors may stimulate cell proliferation and angiogenesis and therefore alter the vascular system of the dura mater, which may result in a higher susceptibility for migraine.
It means that low concentration of NCS may stimulate cell differentiation in root tips.
DDX3X is important for translation of Cyclin E1 mRNA and thereby may stimulate cell cycle progression [ 20].
For example, inflammatory responses may stimulate cell division, increasing the likelihood for ionizing radiation to cause DNA strand breaks.
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Alternatively, the release of 'death' signals into the extracellular fluid may stimulate cells not in direct contact to undergo apoptosis.
PDGF can markedly potentiate tissue repair in vivo and also may stimulate cells to express growth factors such as TGFβ [ 36, 37].
Instead, relaxin may directly stimulate cell differentiation in vivo.
Overexpression of PDGF isoforms may then stimulate cell growth and survival in autocrine and paracrine manners.
This also indicates that normal mechanical stress may not stimulate cell replication as demonstrated in previous studies [ 34].
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