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A distinct response to endogenous DNA damage in the development of Nbs1-deficient cortical neurons
Microcephaly is a clinical characteristic for human nijmegen breakage syndrome (NBS, mutated in NBS1 gene), a chromosomal instability syndrome. However, the underlying molecular pathogenesis remains elusive. In the present study, we demonstrate that neuronal disruption of NBS (Nbn in mice) causes mi...
Autores principales: | Li, Rui, Yang, Yun-Gui, Gao, Yunzhou, Wang, Zhao-Qi, Tong, Wei-Min |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343649/ https://www.ncbi.nlm.nih.gov/pubmed/22212482 http://dx.doi.org/10.1038/cr.2012.3 |
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