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Profiling of 3D Genome Organization in Nasopharyngeal Cancer Needle Biopsy Patient Samples by a Modified Hi-C Approach.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.673530
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- Article
Super-Enhancers, Phase-Separated Condensates, and 3D Genome Organization in Cancer.
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- Cancers, 2022, v. 14, n. 12, p. 2866, doi. 10.3390/cancers14122866
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- Article
Chromatin loop anchors predict transcript and exon usage.
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- Briefings in Bioinformatics, 2021, v. 22, n. 6, p. 1, doi. 10.1093/bib/bbab254
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- Article
DeepCPP: a deep neural network based on nucleotide bias information and minimum distribution similarity feature selection for RNA coding potential prediction.
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- Briefings in Bioinformatics, 2021, v. 22, n. 2, p. 2073, doi. 10.1093/bib/bbaa039
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- Article
Long-Distance Repression by Human Silencers: Chromatin Interactions and Phase Separation in Silencers.
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- Cells (2073-4409), 2022, v. 11, n. 9, p. N.PAG, doi. 10.3390/cells11091560
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- Article
Identification of mechanism of cancer-cell-specific reactivation of hTERT offers therapeutic opportunities for blocking telomerase specifically in human colorectal cancer.
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- Nucleic Acids Research, 2023, v. 51, n. 1, p. 1, doi. 10.1093/nar/gkac479
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- Article
SETDB1 acts as a topological accessory to Cohesin via an H3K9me3-independent, genomic shunt for regulating cell fates.
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- Nucleic Acids Research, 2022, v. 50, n. 13, p. 7326, doi. 10.1093/nar/gkac531
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- Article
Super enhancer acquisition drives expression of oncogenic PPP1R15B that regulates protein homeostasis in multiple myeloma.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50910-z
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- Article
H3K27me3-rich genomic regions can function as silencers to repress gene expression via chromatin interactions.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-20940-y
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- Article
ZNF143 mediates CTCF-bound promoter–enhancer loops required for murine hematopoietic stem and progenitor cell function.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20282-1
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- Article