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Journal of Cell Science|September 19, 2013
Activity-dependent secretion of progranulin from synapsesEugenia Petoukhov, Sarah Fernando, Fergil Mills, et al.Human Molecular Genetics|July 6, 2016
An enhanced Q175 knock-in mouse model of Huntington disease with higher mutant huntingtin levels and accelerated disease phenotypesAmber L Southwell, Amy Smith-Dijak, Chris Kay, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 8, 2014
In vivo evaluation of candidate allele-specific mutant huntingtin gene silencing antisense oligonucleotidesAmber L Southwell, Niels H Skotte, Holly B Kordasiewicz, et al.Plos One|September 11, 2014
Allele-specific suppression of mutant huntingtin using antisense oligonucleotides: providing a therapeutic option for all Huntington disease patientsNiels H Skotte, Amber L Southwell, Michael E Østergaard, et al.Human Molecular Genetics|January 21, 2017
A novel humanized mouse model of Huntington disease for preclinical development of therapeutics targeting mutant huntingtin allelesAmber L Southwell, Niels H Skotte, Erika B Villanueva, et al.Pageof 1