Heffernan et al., 2012 |
Australia |
glial cells |
Human |
new therapeutic strategy for the treatment of as MS(101)
|
Payne et al., 2012 |
Australia |
46C-NS cells |
Mouse |
Improving the efficiency at which NSCs home to inflammatory sites may enhance their therapeutic potential in MS(102)
|
Song et al., 2012 |
Australia |
induced pluripotent stem (iPS) cells |
Human |
A novel approach for the study of MS pathophysiology and potential drug discovery(103)
|
Rasmussen et al., 2011 |
USA |
Sub-ventricular zone cells |
Mouse |
treatments targeting chronic microglial activation have the potential for enhancing repair in MS(104)
|
Huang et al., 2011 |
UK |
oligodendrocyte precursor cells (OPCs) |
Human |
might be useful pharmacological targets to overcoming remyelination failure in MS(105)
|
Giannakopoulou et al., 2011 |
Greece |
neural precursor cell (NPC) |
Mouse |
NPC intraventricular transplantation should be accountable for their therapeutic effect in MS(106)
|
Carbajal et al., 2011 |
USA |
oligodendrocyteprogentior cells (OPCs) |
Mouse |
highlight the importance of the CXCL12:CXCR4 pathway in regulating homing of engrafted stem cells to sites of tissue damage in the MS(107)
|
Yip et al., 2003 |
USA |
oligodendrocyteprogentior cells (OPCs) |
Human |
Emerging knowledge of the molecules that may be involved in such responses may help in the design of future stem cell-based treatment of demyelinating diseases such as multiple sclerosis(108)
|