Laura P. Ranum

Affiliations: 
Molecular, Cellular, Developmental Biology and Genetics University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Molecular Biology, Neuroscience Biology
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"Laura Ranum"
Mean distance: 35622
 
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Publications

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Bañez-Coronel M, Ayhan F, Tarabochia AD, et al. (2015) RAN Translation in Huntington Disease. Neuron. 88: 667-77
Armbrust KR, Wang X, Hathorn TJ, et al. (2014) 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
Cleary JD, Ranum LP. (2014) Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders. Current Opinion in Genetics & Development. 26: 6-15
Pletnikova O, Sloane KL, Renton AE, et al. (2014) Hippocampal sclerosis dementia with the C9ORF72 hexanucleotide repeat expansion. Neurobiology of Aging. 35: 2419.e17-21
Lee KY, Li M, Manchanda M, et al. (2013) Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900
Zu T, Liu Y, Bañez-Coronel M, et al. (2013) RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia. Proceedings of the National Academy of Sciences of the United States of America. 110: E4968-77
Cleary JD, Ranum LP. (2013) Repeat-associated non-ATG (RAN) translation in neurological disease. Human Molecular Genetics. 22: R45-51
Chamberlain CM, Ranum LP. (2012) Mouse model of muscleblind-like 1 overexpression: skeletal muscle effects and therapeutic promise. Human Molecular Genetics. 21: 4645-54
Ishiura H, Takahashi Y, Mitsui J, et al. (2012) C9ORF72 repeat expansion in amyotrophic lateral sclerosis in the Kii peninsula of Japan. Archives of Neurology. 69: 1154-8
Martins S, Soong BW, Wong VCN, et al. (2012) Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and Yirrkala Archives of Neurology. 69: 746-751
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