Transgenic rescue of phenotypic deficits in a mouse model of alternating hemiplegia of childhood.

Kirshenbaum, Greer S; Dachtler, James; Roder, John C; Clapcote, Steven J

Kirshenbaum, Greer S; Dachtler, James; Roder, John C; Clapcote, Steven J.

Affiliation

Kirshenbaum GS; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University Avenue, Toronto, ON, M5G 1X5, Canada.
Dachtler J; Institute of Medical Science, University of Toronto, Toronto, ON, M5S 1A8, Canada.
Roder JC; School of Biomedical Sciences, Garstang Building, University of Leeds, Leeds, LS2 9JT, UK.
Clapcote SJ; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, University Avenue, Toronto, ON, M5G 1X5, Canada.

Neurogenetics ; 17(1): 57-63, 2016 Jan.

Article in En | MEDLINE | ID: mdl-26463346

Subject(s)

Disease Models, Animal; Genetic Therapy; Hemiplegia/genetics; Hemiplegia/therapy; Mice, Transgenic; Sodium-Potassium-Exchanging ATPase/genetics; Animals; Child; Female; Hemiplegia/pathology; Humans; Male; Mice; Mice, Inbred C57BL; Phenotype; Treatment Outcome

Key words

Alternating hemiplegia; Atp1a3; Mice; Na+,K+-ATPase α3; Transgenic rescue

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mice, Transgenic / Genetic Therapy / Sodium-Potassium-Exchanging ATPase / Disease Models, Animal / Hemiplegia Limits: Animals / Child / Female / Humans / Male Language: En Journal: Neurogenetics Journal subject: GENETICA / NEUROLOGIA Year: 2016 Type: Article Affiliation country: Canada

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