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                The
                  National Human Neural Stem Cell Resource provides neural
                  stem cells harvested from the post-natal, post-mortem,
                  human and animal brain to the research community for stem cell research.
                  Several brain areas as well as cultures from normal and
                  genetically mutant specimens are represented in the Resource. Cells
                  derived from other organ systems are also available.
                
               
              
                Stem
                  cell research will increase our understanding of the nervous
                  system and may allow us to develop treatments for currently
                  incurable brain diseases and injuries.
               
              
                The
                  Resource encourages stem cell research for the study of
                  these neural stem cells as potential transplantable tissue
                  for the repair of injury such as that sustained during
                  traumatic brain injury or stroke, for the repair of pathological
                  processes such as those seen in the neurogenetic diseases
                  Hurler's disease or Leigh's disease, or for repair
                  of neurodegenerative processes such as those seen in Parkinson's
                  or Alzheimer Diseases.  
                   
                   
                  In addition, the stem cells should be used for stem cell
                  research aimed at the detailed study of mechanisms of neural
                  differentiation and transdifferentiation and the genetic
                  and environmental signals that direct the specialization
                  of the cells into particular cell types. 
                   
                  Philip H. Schwartz, Ph.D., Director 
                  [email protected] 
               
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                 A)
                  A primary culture of proliferating cells showed a high proportion
                  of nestin (red) to GFAP (blue) staining in monolayer culture;
                  co-staining was relatively frequent (10x).  
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                B) Budding neurosphere showed nestin cells (red) at the
                  circumference with a much higher proportion of GFAP (blue)
                  to nestin in the interior of the sphere (10x).  
                C) Nestin (green) and Sox2 (red) staining in proliferating
                  hNPCs (40x). Arrows show occasional nestin-negative/Sox2-positive
                  cells.  
                D) Doublecortin (DCX) staining of hNPCs revealed a subpopulation
                  of small, 5 - 10 um diameter, DCX-positive (green) cells
                  against a phase-contrast background (40x).  
               
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