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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...
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| Publicado en: | eLife |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
eLife Sciences Publications, Ltd
2020
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| Assuntos: | |
| Acceso en liña: | 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 |
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