Wird geladen...

SMC5/6 is required for replication fork stability and faithful chromosome segregation during neurogenesis

Mutations of SMC5/6 components cause developmental defects, including primary microcephaly. To model neurodevelopmental defects, we engineered a mouse wherein Smc5 is conditionally knocked out (cKO) in the developing neocortex. Smc5 cKO mice exhibited neurodevelopmental defects due to neural progeni...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:eLife
Hauptverfasser: Atkins, Alisa, Xu, Michelle J, Li, Maggie, Rogers, Nathaniel P, Pryzhkova, Marina V, Jordan, Philip W
Format: Artigo
Sprache:Inglês
Veröffentlicht: eLife Sciences Publications, Ltd 2020
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7723410/
https://ncbi.nlm.nih.gov/pubmed/33200984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.61171
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!