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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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
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