Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Carrie L Tatar"'
Autor:
Carrie L Tatar, Sunita Appikatla, Denise A Bessert, Ajaib S Paintlia, Inderjit Singh, Robert P Skoff
Publikováno v:
ASN Neuro, Vol 2 (2010)
PMD (Pelizaeus-Merzbacher disease) is a rare neurodegenerative disorder that impairs motor and cognitive functions and is associated with a shortened lifespan. The cause of PMD is mutations of the PLP1 [proteolipid protein 1 gene (human)] gene. Trans
Externí odkaz:
https://doaj.org/article/bf7872d795bf4914aad48bc15cffe042
Publikováno v:
Glia. 61:192-209
Multiple sclerosis is a sexually dimorphic (SD) disease that causes oligodendrocyte death, but SD of glial cells is poorly studied. Here, we analyze SD of neural progenitors in 6–8 weeks and 6–8 months normal C57BL/6, SJL/J, and BALB/c mice in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea4fd2b1ea4081a582d6eb60ad538cc1
https://doi.org/10.1002/glia.22426
https://doi.org/10.1002/glia.22426
Autor:
Sunita Appikatla, Ajaib S. Paintlia, Carrie L Tatar, Denise Bessert, Inderjit Singh, Robert P. Skoff
Publikováno v:
ASN NEURO
PMD (Pelizaeus-Merzbacher disease) is a rare neurodegenerative disorder that impairs motor and cognitive functions and is associated with a shortened lifespan. The cause of PMD is mutations of the PLP1 [proteolipid protein 1 gene (human)] gene. Trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0551f435b30e52869025b9ef0ef05fd5
https://pubmed.ncbi.nlm.nih.gov/20885931
https://pubmed.ncbi.nlm.nih.gov/20885931