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Infant onset spinocerebellar ataxia type 13 mutation leads to developmental and rapid degenerative phenotypes related to hyperexcitability in Purkinje cells

Autor: Ulrich, Brittany Nicole

Publikováno v: Ulrich, Brittany Nicole. (2017). Infant onset spinocerebellar ataxia type 13 mutation leads to developmental and rapid degenerative phenotypes related to hyperexcitability in Purkinje cells. UCLA: Molec, Cell, & Integ Physiology 0568. Retrieved from: http://www.escholarship.org/uc/item/9n59d9rk

Spinocerebellar ataxia type 13 (SCA13) is an autosomal dominant neurodegenerative disease that leads to cerebellar ataxia and atrophy. It can exist in both adult and infant onset forms, caused by different mutations in voltage-gated K+ channel 3.3 (K

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::96f83b346d84d4e5f3fe456d256251a9
http://www.escholarship.org/uc/item/9n59d9rk

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Amyloid β-Protein C-Terminal Fragments: Formation of Cylindrins and β-Barrels.

Autor: Do, Thanh D., LaPointe, Nichole E., Nelson, Rebecca, Krotee, Pascal, Hayden, Eric Y., Ulrich, Brittany, Quan, Sarah, Feinstein, Stuart C., Teplow, David B., Eisenberg, A. David, Shea, Joan-Emma, Bowers, Michael T.

Publikováno v: Journal of the American Chemical Society; 1/20/2016, Vol. 138 Issue 2, p549-557, 9p