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HGG Advances|July 26, 2023
Erratum: Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencingLi Fang, Alex Mas Monteys, Alexandra Dürr, et al.
Nucleic Acids Research|September 4, 2012
siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouseRyan L Boudreau, Ryan M Spengler, Ray H Hylock, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 19, 2008
Restoring Acid-sensing ion channel-1a in the amygdala of knock-out mice rescues fear memory but not unconditioned fear responsesMatthew W Coryell, Amanda M Wunsch, Jill M Haenfler, et al.
Plos One|April 25, 2014
RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degenerationPavitra S Ramachandran, Sajag Bhattarai, Pratibha Singh, et al.
HGG Advances|October 20, 2022
Haplotyping SNPs for allele-specific gene editing of the expanded huntingtin allele using long-read sequencingLi Fang, Alex Mas Monteys, Alexandra Dürr, et al.
Trends in Molecular Medicine|February 18, 2025
Gene therapies for neurogenetic disordersOrrin Devinsky, Jeff Coller, Rebecca Ahrens-Nicklas, et al.
Nature|July 29, 2021
Regulated control of gene therapies by drug-induced splicingAlex Mas Monteys, Amiel A Hundley, Paul T Ranum, et al.
Nucleic Acids Research|July 16, 2016
Elucidation of transcriptome-wide microRNA binding sites in human cardiac tissues by Ago2 HITS-CLIPRyan M Spengler, Xiaoming Zhang, Congsheng Cheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 2, 2011
Widespread establishment and regulatory impact of Alu exons in human genesShihao Shen, Lan Lin, James J Cai, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 26, 2008
Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosisMichael Chang, Jonathan D Cooper, David E Sleat, et al.
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