Cargando…
Coexpression enrichment analysis at the single-cell level reveals convergent defects in neural progenitor cells and their cell-type transitions in neurodevelopmental disorders
A large number of genes have been implicated in neurodevelopmental disorders (NDDs), but their contributions to NDD pathology are difficult to decipher without understanding their diverse roles in different brain cell types. Here, we integrated NDD genetics with single-cell RNA sequencing data to as...
Autores principales: | Pang, Kaifang, Wang, Li, Wang, Wei, Zhou, Jian, Cheng, Chao, Han, Kihoon, Zoghbi, Huda Y., Liu, Zhandong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370880/ https://www.ncbi.nlm.nih.gov/pubmed/32554779 http://dx.doi.org/10.1101/gr.254987.119 |
Ejemplares similares
-
A kinome-wide RNAi screen identifies ERK2 as a druggable regulator of Shank3 stability
por: Wang, Li, et al.
Publicado: (2019) -
Zika infection of neural progenitor cells perturbs transcription in neurodevelopmental pathways
por: Yi, Lynn, et al.
Publicado: (2017) -
An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function
por: Wang, Li, et al.
Publicado: (2019) -
Editorial: Identifying genetics-based mechanisms and treatments for neurodevelopmental and psychiatric disorders through data integration
por: Pang, Kaifang, et al.
Publicado: (2023) -
Defects in translation-dependent quality control pathways lead to convergent molecular and neurodevelopmental pathology
por: Terrey, Markus, et al.
Publicado: (2021)