Laura P. Ranum
Affiliations: | Molecular, Cellular, Developmental Biology and Genetics | University of Minnesota, Twin Cities, Minneapolis, MN |
Area:
Molecular Biology, Neuroscience BiologyGoogle:
"Laura Ranum"Mean distance: 35622
Children
Sign in to add traineeBrian B. Gibbens | grad student | 2011 | UMN |
Christopher M. Chamberlain | grad student | 2012 | UMN |
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Publications
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Perez BA, Shorrock HK, Banez-Coronel M, et al. (2021) CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity. Embo Molecular Medicine. e14095 |
Ayhan F, Perez BA, Shorrock HK, et al. (2018) SCA8 RAN polySer protein preferentially accumulates in white matter regions and is regulated by eIF3F. The Embo Journal |
Chen G, Carter RE, Cleary JD, et al. (2018) Altered levels of the splicing factor muscleblind modifies cerebral cortical function in mouse models of myotonic dystrophy. Neurobiology of Disease |
Cleary JD, Ranum LP. (2017) New developments in RAN translation: insights from multiple diseases. Current Opinion in Genetics & Development. 44: 125-134 |
Liu Y, Pattamatta A, Zu T, et al. (2016) C9orf72 BAC Mouse Model with Motor Deficits and Neurodegenerative Features of ALS/FTD. Neuron |
Bañez-Coronel M, Ayhan F, Tarabochia AD, et al. (2015) RAN Translation in Huntington Disease. Neuron. 88: 667-77 |
Goodwin M, Mohan A, Batra R, et al. (2015) MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain. Cell Reports |
Xia G, Gao Y, Jin S, et al. (2015) Genome modification leads to phenotype reversal in human myotonic dystrophy type 1 induced pluripotent stem cell-derived neural stem cells. Stem Cells (Dayton, Ohio). 33: 1829-38 |
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 |
Lee KY, Li M, Manchanda M, et al. (2013) Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900 |