WSTF–ISWI chromatin remodeling complex targets heterochromatic replication foci
The Williams Syndrome Transcription Factor (WSTF), the product of the WBSCR9 gene, is invariably deleted in the haploinsufficiency Williams–Beuren Syndrome. Along with the nucleosome-dependent ATPase ISWI, WSTF forms a novel chromatin remodeling complex, WICH (WSTF–ISWI chromatin remodeling complex)...
Kaydedildi:
| Yayımlandı: | EMBO J |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Nature Publishing Group
2002
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC125993/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11980720/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/emboj/21.9.2231 |
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