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1 TWEAK inhibited proliferation of neural progenitor cells through its membrane receptor Fn14.
2 In this study, we generated neural progenitor cell-specific Pen-2 conditional KO mice.
3 Endogenous neural progenitor cell migration in vivo can be monitored using MRI-based cell tracking.
4 During the conversion process, the cells did not pass through a proliferative neural progenitor cell intermediate.
5 This suggests a role for Geminin in the formation and maintenance of the neural progenitor cells.
6 Damage to dynamic neural progenitor cell populations in the brain are emerging as important etiologic factors.
7 Recent research shows that eCBs stimulate neural progenitor proliferation and inhibit hippocampal neurogenesis in normal adult brain.
8 Development of brain circuitry requires precise regulation and timing of proliferation and differentiation of neural progenitor cells.
9 Here we evaluate the safety of IA neural progenitor cell (NPC) delivery to the brain.
10 MPIOs are endocytosed and incorporated into the neural progenitor cell population, making them visible by gradient echo MRI.
11 TWEAK regulates proliferation and differentiation of progenitor cells but its effect on adult neural progenitor cells is still unknown.
12 By using a reporter assay we found that TWEAK activated the transcription factor NF-kB in adult neural progenitor cells.
13 Likewise, in adult CB1-deficient mice, neural progenitor proliferation is decreased but is increased in fatty acid amide hydrolase-deficient mice.
14 Many studies have shown that transplanted or endogenous neural progenitor cells will migrate toward damaged areas of the brain.
15 However, some neural progenitor cells are resistant to Kras(V12) and can retain their ability to differentiate into neurons.
16 The aim of this study was to evaluate whether chromaffin cells can provide a supportive microenvironment for neural progenitor cells.
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This collocation consists of: Neural progenitor across language varieties