The trophic effects of MSCs include the inhibition of apoptosis, support of regeneration and stimulation, maintenance, proliferation and differentiation of tissue-specific progenitors [ 19].
The three-dimensional (3D) architecture of bone marrow (BM) supports the renewal, maintenance, proliferation and differentiation of haematopoietic stem cells (HSCs).
Foxe3 continues to be expressed in the mouse lens epithelium until adulthood, being indispensable for a complete closure of the lens vesicle and for the maintenance, proliferation and survival of the lens epithelial cells [ 37].
The three-dimensional (3-D) architecture of the bone marrow (BM) supports the renewal, maintenance, proliferation and differentiation of haematopoietic stem cells (HSCs).
These results suggest that the Wnt/β-catenin and Hh pathways play a causal role in the initiation, maintenance, proliferation and survival of CSE-transformed epithelial cells.
Wnt/β-catenin signalling controls maintenance, proliferation and differentiation of embryonic cardiovascular progenitors in a multi-phasic fashion.
The voluminous capsular layer is involved in adhesion, maintenance, proliferation and development of infections by this pathogen [ 25].
These factors are directly involved in the survival, maintenance, proliferation, and self-renewal of GSCs.
ECM represents an essential player in stem cell niche, since it can directly or indirectly modulate the maintenance, proliferation, self-renewal and differentiation of stem cells.
Downregulation of human NAP1L3 in umbilical cord blood (UCB) HSCs impairs the maintenance and proliferation of HSCs both in vitro and in vivo.
CXCR4 is a G-protein coupled receptor with crucial roles in homing, maintenance, and proliferation of a wide range of haematological cancers.
