Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Abigail Lukowicz"'
Autor:
Wenhui Qu, Andrea Johnson, Joo Hyun Kim, Abigail Lukowicz, Daniel Svedberg, Marija Cvetanovic
Publikováno v:
Journal of Neuroinflammation, Vol 14, Iss 1, Pp 1-11 (2017)
Abstract Background Polyglutamine (polyQ) expansion in the protein Ataxin-1 (ATXN1) causes spinocerebellar ataxia type 1 (SCA1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and
Externí odkaz:
https://doaj.org/article/e6e0d051f5c24c6db0fbb361a15e5c6e
Autor:
Austin Ferro, Wenhui Qu, Abigail Lukowicz, Daniel Svedberg, Andrea Johnson, Marija Cvetanovic
Publikováno v:
PLoS ONE, Vol 13, Iss 7, p e0200013 (2018)
Spinocerebellar Ataxia type 1 (SCA1) is a fatal neurodegenerative genetic disease that is characterized by pronounced neuronal loss and gliosis in the cerebellum. We have previously demonstrated microglial activation, measured as an increase in micro
Externí odkaz:
https://doaj.org/article/397ce78738144359a69f400714dec88d
Publikováno v:
Glia
Spinocerebellar ataxia type 1 (SCA1) is a fatal, dominantly inherited neurodegenerative disease caused by the expansion of CAG repeats in the Ataxin-1 (ATXN1) gene. SCA1 is characterized by balance and coordination deficits due to the predominant los
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7d237888160aad4624516dd60150d3
https://europepmc.org/articles/PMC8049102/
https://europepmc.org/articles/PMC8049102/
Autor:
Andrea Johnson, Marija Cvetanovic, Abigail Lukowicz, Wenhui Qu, Austin Ferro, Daniel Svedberg
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 7, p e0200013 (2018)
PLoS ONE, Vol 13, Iss 7, p e0200013 (2018)
Spinocerebellar Ataxia type 1 (SCA1) is a fatal neurodegenerative genetic disease that is characterized by pronounced neuronal loss and gliosis in the cerebellum. We have previously demonstrated microglial activation, measured as an increase in micro
Autor:
Daniel Svedberg, Andrea Johnson, Joo Hyun Kim, Marija Cvetanovic, Abigail Lukowicz, Wenhui Qu
Publikováno v:
Journal of Neuroinflammation
Journal of Neuroinflammation, Vol 14, Iss 1, Pp 1-11 (2017)
Journal of Neuroinflammation, Vol 14, Iss 1, Pp 1-11 (2017)
Background Polyglutamine (polyQ) expansion in the protein Ataxin-1 (ATXN1) causes spinocerebellar ataxia type 1 (SCA1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and gliosis.