Summary: Genetic manipulation of neural precursor cells is an important tool to study mechanisms underlying proliferation, fate specification, and neuron formation. The CRISPR/Cas9 system enables efficient genome editing but requires the clonal expansion of cells containing the desired mutation. Here, we describe a protocol for the effective generation of clonal mouse hippocampal neural precursor lines with CRISPR/Cas9-based gene knockouts. Edited cell lines can be used to investigate gene regulatory networks driving neuronal differentiation and for modeling of diseases that involve hippocampal neurogenesis.For complete details on the use and execution of this protocol, please refer to Pötzsch et al. (2021)
CRISPR/Cas9 system of RNA-guided genome editing is revolutionizing genetics research in a wide spect...
Induced pluripotent stem cells (iPSCs) can self-renew and differentiate into many other cell types. ...
CRISPR/Cas9-based functional genomics have transformed our ability to elucidate mammalian cell biolo...
Recent advances in genome editing have brought new hopes for personalized and precision medicine but...
Mammalian neural stem cell (NSC) lines provide a useful experimental model for basic and applied re...
The recent identification of multiple new genetic causes of neurological disorders highlights the ne...
The dynamic orchestration of gene expression is crucial for the proper differentiation, function, an...
We provide a protocol for generating forebrain structures in vivo from mouse embryonic stem cells (E...
We have applied the CRISPR/Cas9 system in vivo to disrupt gene expression in neural stem cells in th...
Parkinson’s disease (PD) is the second most prevalent neurodegenerative disorder. In order to improv...
The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the sub...
Mutant mice are crucial tools for understanding gene functions in vivo. Recently, generation of mous...
The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the sub...
CRISPR/Cas9 genome editing is at the forefront of becoming a vital tool for the study of genes and t...
Genetically modified mice are extremely valuable tools for studying gene function and human diseases...
CRISPR/Cas9 system of RNA-guided genome editing is revolutionizing genetics research in a wide spect...
Induced pluripotent stem cells (iPSCs) can self-renew and differentiate into many other cell types. ...
CRISPR/Cas9-based functional genomics have transformed our ability to elucidate mammalian cell biolo...
Recent advances in genome editing have brought new hopes for personalized and precision medicine but...
Mammalian neural stem cell (NSC) lines provide a useful experimental model for basic and applied re...
The recent identification of multiple new genetic causes of neurological disorders highlights the ne...
The dynamic orchestration of gene expression is crucial for the proper differentiation, function, an...
We provide a protocol for generating forebrain structures in vivo from mouse embryonic stem cells (E...
We have applied the CRISPR/Cas9 system in vivo to disrupt gene expression in neural stem cells in th...
Parkinson’s disease (PD) is the second most prevalent neurodegenerative disorder. In order to improv...
The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the sub...
Mutant mice are crucial tools for understanding gene functions in vivo. Recently, generation of mous...
The ability to reprogram adult somatic cells into induced pluripotent stem cells (iPSCs) and the sub...
CRISPR/Cas9 genome editing is at the forefront of becoming a vital tool for the study of genes and t...
Genetically modified mice are extremely valuable tools for studying gene function and human diseases...
CRISPR/Cas9 system of RNA-guided genome editing is revolutionizing genetics research in a wide spect...
Induced pluripotent stem cells (iPSCs) can self-renew and differentiate into many other cell types. ...
CRISPR/Cas9-based functional genomics have transformed our ability to elucidate mammalian cell biolo...