Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Rosie K. Bunton-Stasyshyn"'
Autor:
Sherylanne Newton, Carlos Aguilar, Rosie K. Bunton-Stasyshyn, Marisa Flook, Michelle Stewart, Walter Marcotti, Steve Brown, Michael R. Bowl
Publikováno v:
iScience, Vol 26, Iss 10, Pp 108056- (2023)
Summary: Mouse studies continue to help elaborate upon the genetic landscape of mammalian disease and the underlying molecular mechanisms. Here, we have investigated an Embigintm1b allele maintained on a standard C57BL/6N background and on a co-isoge
Externí odkaz:
https://doaj.org/article/2819d577fd2b45fe87edb7949f255790
Autor:
Julie M. Jones, Louise Dionne, James Dell'Orco, Rachel Parent, Jamie N. Krueger, Xiaoyang Cheng, Sulayman D. Dib-Hajj, Rosie K. Bunton-Stasyshyn, Lisa M. Sharkey, James J. Dowling, Geoffrey G. Murphy, Vikram G. Shakkottai, Peter Shrager, Miriam H. Meisler
Publikováno v:
Neurobiology of Disease, Vol 89, Iss , Pp 36-45 (2016)
Mutations of the neuronal sodium channel gene SCN8A are associated with lethal movement disorders in the mouse and with human epileptic encephalopathy. We describe a spontaneous mouse mutation, Scn8a9J, that is associated with a chronic movement diso
Externí odkaz:
https://doaj.org/article/9eb1c33b64e947e4a2caa9a6ffc5dba2
Autor:
Matthew Mackenzie, Alex Fower, Alasdair J. Allan, Gemma F. Codner, Rosie K. Bunton-Stasyshyn, Lydia Teboul
Publikováno v:
Methods in Molecular Biology ISBN: 9781071629895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afbfcf2311037e778782e70023dbafb4
https://doi.org/10.1007/978-1-0716-2990-1_4
https://doi.org/10.1007/978-1-0716-2990-1_4