Human in vitro disease models to aid pathway and target discovery for neurological disorders
Author:
Muralidharan Bhavana
Reference146 articles.
1. Abrahams, B.S., Arking, D.E., Campbell, D.B. et al. (2013). SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). Molecular Autism, 4, 36. https://doi.org/10.1186/2040-2392-4-36.
2. Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration;Alves;Frontiers in Cellular Neuroscience,2015
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nature Genetics,1999
4. Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations;Amir;American Journal of Medical Genetics,2000
5. Organoids required! A new path to understanding human brain development and disease;Arlotta;Nature Methods,2018