Karen R. Armbrust, Ph.D. - Publications
Affiliations: | 2009 | Molecular, Cellular, Developmental Biology and Genetics | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Genetics, Molecular Biology, Neuroscience BiologyYear | Citation | Score | |||
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2014 | Armbrust KR, Wang X, Hathorn TJ, Cramer SW, Chen G, Zu T, Kangas T, Zink AN, Öz G, Ebner TJ, Ranum LP. Mutant β-III spectrin causes mGluR1α mislocalization and functional deficits in a mouse model of spinocerebellar ataxia type 5. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 9891-904. PMID 25057192 DOI: 10.1523/Jneurosci.0876-14.2014 | 0.418 | |||
2010 | Lorenzo DN, Li MG, Mische SE, Armbrust KR, Ranum LP, Hays TS. Spectrin mutations that cause spinocerebellar ataxia type 5 impair axonal transport and induce neurodegeneration in Drosophila. The Journal of Cell Biology. 189: 143-58. PMID 20368622 DOI: 10.1083/Jcb.200905158 | 0.349 | |||
2006 | Ikeda Y, Dick KA, Weatherspoon MR, Gincel D, Armbrust KR, Dalton JC, Stevanin G, Dürr A, Zühlke C, Bürk K, Clark HB, Brice A, Rothstein JD, Schut LJ, Day JW, et al. Spectrin mutations cause spinocerebellar ataxia type 5. Nature Genetics. 38: 184-90. PMID 16429157 DOI: 10.1038/Ng1728 | 0.461 | |||
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