Expanded CAG repeats in the murine Huntington's disease gene increases neuronal differentiation of embryonic and neural stem cells
- 19 June 2008
- journal article
- Published by Elsevier in Molecular and Cellular Neuroscience
- Vol. 40 (1) , 1-13
- https://doi.org/10.1016/j.mcn.2008.06.004
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Induction of neostriatal neurogenesis slows disease progression in a transgenic murine model of Huntington diseaseJournal of Clinical Investigation, 2007
- A Progressive and Cell Non-Autonomous Increase in Striatal Neural Stem Cells in the Huntington's Disease R6/2 MouseJournal of Neuroscience, 2006
- Abnormalities of Neurogenesis in the R6/2 Mouse Model of Huntington's Disease Are Attributable to theIn VivoMicroenvironmentJournal of Neuroscience, 2005
- Reduced hippocampal neurogenesis in R6/2 transgenic Huntington's disease miceNeurobiology of Disease, 2005
- Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genesNature Genetics, 2003
- Conversion of embryonic stem cells into neuroectodermal precursors in adherent monocultureNature Biotechnology, 2003
- Parsing the prosencephalonNature Reviews Neuroscience, 2002
- Pallial and subpallial derivatives in the embryonic chick and mouse telencephalon, traced by the expression of the genes Dlx-2, Emx-1, Nkx-2.1, Pax-6, and Tbr-1Journal of Comparative Neurology, 2000
- Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic MiceCell, 1996
- LOCALIZATION OF MYELIN-ASSOCIATED GLYCOPROTEINJournal of Neurochemistry, 1984