Ryan L. Boudreau, Ph.D.
Affiliations: | 2008 | University of Iowa, Iowa City, IA |
Area:
http://www.biomedexperts.com/Profile.bme/292624/Beverly_L_DavidsonGoogle:
"Ryan Boudreau"Mean distance: 17811
Parents
Sign in to add mentorBeverly L. Davidson | grad student | 2008 | University of Iowa | |
(Comparative analyses of hairpin-based RNA interference vectors for neurodegenerative disease therapy.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Saad NY, Al-Kharsan M, Garwick-Coppens SE, et al. (2021) Human miRNA miR-675 inhibits DUX4 expression and may be exploited as a potential treatment for Facioscapulohumeral muscular dystrophy. Nature Communications. 12: 7128 |
Zhang X, Yoon JY, Morley M, et al. (2018) A common variant alters SCN5A-miR-24 interaction and associates with heart failure mortality. The Journal of Clinical Investigation |
Kim YC, Miller A, Lins LC, et al. (2017) RNA Interference of Human α-Synuclein in Mouse. Frontiers in Neurology. 8: 13 |
Spengler RM, Zhang X, Cheng C, et al. (2016) Elucidation of transcriptome-wide microRNA binding sites in human cardiac tissues by Ago2 HITS-CLIP. Nucleic Acids Research |
Piedrahita D, Castro-Alvarez JF, Boudreau RL, et al. (2015) β-Secretase 1's Targeting Reduces Hyperphosphorilated Tau, Implying Autophagy Actors in 3xTg-AD Mice. Frontiers in Cellular Neuroscience. 9: 498 |
Madhavan L, Daley BF, Davidson BL, et al. (2015) Sonic Hedgehog Controls the Phenotypic Fate and Therapeutic Efficacy of Grafted Neural Precursor Cells in a Model of Nigrostriatal Neurodegeneration. Plos One. 10: e0137136 |
Monteys AM, Wilson MJ, Boudreau RL, et al. (2015) Artificial miRNAs Targeting Mutant Huntingtin Show Preferential Silencing In Vitro and In Vivo. Molecular Therapy. Nucleic Acids. 4: e234 |
Lee JH, Sowada MJ, Boudreau RL, et al. (2014) Rhes suppression enhances disease phenotypes in Huntington's disease mice. Journal of Huntington's Disease. 3: 65-71 |
Ramachandran PS, Boudreau RL, Schaefer KA, et al. (2014) Nonallele specific silencing of ataxin-7 improves disease phenotypes in a mouse model of SCA7. Molecular Therapy : the Journal of the American Society of Gene Therapy. 22: 1635-42 |
Ramachandran PS, Bhattarai S, Singh P, et al. (2014) RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration. Plos One. 9: e95362 |