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pro vyhledávání: '"Scott E. Ugras"'
Publikováno v:
Neurobiology of Disease, Vol 88, Iss , Pp 66-74 (2016)
α-Synuclein is a conserved, abundantly expressed protein that is partially localized in pre-synaptic terminals in the central nervous system. The precise biological function(s) and structure of α-synuclein are under investigation. Recently, the nat
Externí odkaz:
https://doaj.org/article/9a5928b5cdae4427a2bf0c48508ec6f6
Autor:
Scott E. Ugras, James Shorter
Publikováno v:
Neurology Research International, Vol 2012 (2012)
Amyotrophic Lateral Sclerosis (ALS) is an adult onset neurodegenerative disease, which is universally fatal. While the causes of this devastating disease are poorly understood, recent advances have implicated RNA-binding proteins (RBPs) that contain
Externí odkaz:
https://doaj.org/article/875a39e7bdca48c892bdc9200d69fafa
Autor:
Daniel Martinez, Malcolm J. Daniels, Harry Ischiropoulos, Perry Evans, Hua Ding, Steven H. Seeholzer, Hossein Fazelinia, Scott E. Ugras, Kelvin C. Luk, Daniel P. Brown, John E. Duda, Esteban Luna, Neal S. Gould, Anastasia K. Yocum, Chris McKennan
Publikováno v:
EBioMedicine, Vol 31, Iss, Pp 307-319 (2018)
EBioMedicine
EBioMedicine
Accumulation of aggregated α-synuclein into Lewy bodies is thought to contribute to the onset and progression of dopaminergic neuron degeneration in Parkinson's disease (PD) and related disorders. Although protein aggregation is associated with pert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e85f997560715e85a4ca349b9c721b3
http://www.sciencedirect.com/science/article/pii/S2352396418301622
http://www.sciencedirect.com/science/article/pii/S2352396418301622
Publikováno v:
Neurobiology of Disease, Vol 88, Iss, Pp 66-74 (2016)
α-Synuclein is a conserved, abundantly expressed protein that is partially localized in pre-synaptic terminals in the central nervous system. The precise biological function(s) and structure of α-synuclein are under investigation. Recently, the nat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af607d8b9f70b5782b844290fab4bf82
Autor:
James Shorter, Scott E. Ugras
Publikováno v:
Neurology Research International, Vol 2012 (2012)
Neurology Research International
Neurology Research International
Amyotrophic Lateral Sclerosis (ALS) is an adult onset neurodegenerative disease, which is universally fatal. While the causes of this devastating disease are poorly understood, recent advances have implicated RNA-binding proteins (RBPs) that contain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fff14b02d44f50cee7004ee63373a012
https://doaj.org/article/875a39e7bdca48c892bdc9200d69fafa
https://doaj.org/article/875a39e7bdca48c892bdc9200d69fafa