Erin B. Clabough, Ph.D. - Publications
Affiliations: | 2006 | University of Virginia, Charlottesville, VA |
Area:
Neuroscience BiologyYear | Citation | Score | |||
---|---|---|---|---|---|
2018 | Ingersoll J, Moody M, Holland R, Kuegler W, Murrah C, Winslow J, Reynolds N, Lloyd N, Dugan B, Hammock M, Houlé K, Clabough E. Analyzing Spatial Learning and Prosocial Behavior in Mice Using the Barnes Maze and Damsel-in-Distress Paradigms. Journal of Visualized Experiments : Jove. PMID 30507926 DOI: 10.3791/58008 | 0.316 | |||
2013 | Clabough EB. Huntington's disease: the past, present, and future search for disease modifiers. The Yale Journal of Biology and Medicine. 86: 217-33. PMID 23766742 | 0.42 | |||
2012 | Neveklovska M, Clabough EB, Steffan JS, Zeitlin SO. Deletion of the huntingtin proline-rich region does not significantly affect normal huntingtin function in mice. Journal of Huntington's Disease. 1: 71-87. PMID 22956985 DOI: 10.3233/JHD-2012-120016 | 0.569 | |||
2012 | Zeitlin SO, Neveklovksa M, Williams MK, Goodman E, Clabough EB. Generation of knockin mouse models expressing 7Q- or 140Q-htt with precise deletions of their proline-rich regions F1000research. 3. DOI: 10.7490/F1000Research.1090515.1 | 0.371 | |||
2010 | Zheng S, Clabough EB, Sarkar S, Futter M, Rubinsztein DC, Zeitlin SO. Deletion of the huntingtin polyglutamine stretch enhances neuronal autophagy and longevity in mice. Plos Genetics. 6: e1000838. PMID 20140187 DOI: 10.1371/journal.pgen.1000838 | 0.571 | |||
2006 | Clabough EB, Zeitlin SO. Deletion of the triplet repeat encoding polyglutamine within the mouse Huntington's disease gene results in subtle behavioral/motor phenotypes in vivo and elevated levels of ATP with cellular senescence in vitro. Human Molecular Genetics. 15: 607-23. PMID 16403806 DOI: 10.1093/hmg/ddi477 | 0.587 | |||
Show low-probability matches. |