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These lesions were present in three of the nine multiple sclerosis brains examined.
Collectively, these data support the SVZ as one source of new neurons in multiple sclerosis brains.
Similar discrepancies exist regarding immunocytochemical detection of EBV antigens in multiple sclerosis brains and lesions.
These results support neurogenesis in a subpopulation of demyelinated subcortical white matter lesions in multiple sclerosis brains.
Detection of increased DARC immunostaining in brain microvessels in acute lesions of multiple sclerosis brains further corroborates the contribution of DARC to autoimmune neuroinflammation.
Expression levels of PGRN, whose release is facilitated by anti-inflammatory stimuli in microglia, are elevated in multiple sclerosis brains [ 28, 29].
Similar(44)
Hametner, S. et al. Iron and neurodegeneration in the multiple sclerosis brain.
Baranzini, S. E. et al. B cell repertoire diversity and clonal expansion in multiple sclerosis brain lesions.
Stern, J. N. et al. B cells populating the multiple sclerosis brain mature in the draining cervical lymph nodes.
Stern, J. N. H. et al. B cells populating the multiple sclerosis brain mature in the draining cervical lymph nodes.
The chapter outlines the human neurological diseases studied by microarray technology, such as multiple sclerosis, brain tumors, neuromuscular disorders, and alzheimer's disease.
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