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Brain Research|October 3, 2015
iPSC-based drug screening for Huntington's diseaseNingzhe Zhang, Barbara J Bailus, Karen L Ring, et al.
Frontiers in Neuroscience|February 21, 2018
Altered Expression of Matrix Metalloproteinases and Their Endogenous Inhibitors in a Human Isogenic Stem Cell Model of Huntington's DiseaseSwati Naphade, Alexander Embusch, Kuruwitage Lakshika Madushani, et al.
Cell Stem Cell|June 12, 2012
Direct reprogramming of mouse and human fibroblasts into multipotent neural stem cells with a single factorKaren L Ring, Leslie M Tong, Maureen E Balestra, et al.
The Journal of Biological Chemistry|May 31, 2015
Integration-independent Transgenic Huntington Disease Fragment Mouse Models Reveal Distinct Phenotypes and Life Span in VivoRobert O'Brien, Francesco DeGiacomo, Jennifer Holcomb, et al.
Stem Cell Reports|December 10, 2013
Genetic correction of tauopathy phenotypes in neurons derived from human induced pluripotent stem cellsHelen Fong, Chengzhong Wang, Johanna Knoferle, et al.
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