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)...
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| Gepubliceerd in: | EMBO J |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group
2002
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| Onderwerpen: | |
| Online toegang: | 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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