Cellular Models and High-Throughput Screening for Genetic Causality of Intellectual Disability
Open Access
- 2 January 2021
- journal article
- review article
- Published by Elsevier BV in Trends in Molecular Medicine
- Vol. 27 (3), 220-230
- https://doi.org/10.1016/j.molmed.2020.12.003
Abstract
No abstract availableKeywords
Funding Information
- Austrian Science Fund
This publication has 88 references indexed in Scilit:
- Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndromeNature Medicine, 2011
- RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemiaNature, 2011
- MicroRNA-mediated conversion of human fibroblasts to neuronsNature, 2011
- Induction of human neuronal cells by defined transcription factorsNature, 2011
- A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem CellsCell, 2010
- Differential Modeling of Fragile X Syndrome by Human Embryonic Stem Cells and Induced Pluripotent Stem CellsCell Stem Cell, 2010
- Direct conversion of fibroblasts to functional neurons by defined factorsNature, 2010
- Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutationsNeurobiology of Disease, 2009
- Non–cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphologyNature Neuroscience, 2009
- Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined FactorsCell, 2007