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Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Cornelia de Lange Syndrome (CdLS) is a human developmental disorder caused by mutations that compromise the function of cohesin, a major regulator of 3D genome organization. Cognitive impairment is a universal and as yet unexplained feature of CdLS. We characterize the transcriptional profile of cor...
में बचाया:
| में प्रकाशित: | Nat Commun |
|---|---|
| मुख्य लेखकों: | , , , , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Nature Publishing Group UK
2021
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8131595/ https://ncbi.nlm.nih.gov/pubmed/34006846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-021-23141-9 |
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