Found: 15
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Full-length transcript alterations in human bronchial epithelial cells with U2AF1 S34F mutations.
- Published in:
- Life Science Alliance, 2023, v. 6, n. 10, p. 1, doi. 10.26508/lsa.202000641
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- Article
The developmental transcriptome of Drosophila melanogaster.
- Published in:
- Nature, 2011, v. 471, n. 7339, p. 473, doi. 10.1038/nature09715
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- Article
Inflammation drives alternative first exon usage to regulate immune genes including a novel iron- regulated isoform of Aim2.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.69431
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- Article
A Pan-Cancer Analysis of Transcriptome Changes Associated with Somatic Mutations in <i>U2AF1</i> Reveals Commonly Altered Splicing Events.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0087361
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- Article
Detecting haplotype-specific transcript variation in long reads with FLAIR2.
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- Genome Biology, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s13059-024-03301-y
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- Article
SOX2 and p63 colocalize at genetic loci in squamous cell carcinomas.
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- Journal of Clinical Investigation, 2014, v. 124, n. 4, p. 1636, doi. 10.1172/JCI71545
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- Article
The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs.
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- Nucleic Acids Research, 2005, v. 33, n. suppl 2, p. w686, doi. 10.1093/nar/gki366
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- Article
Proteasome inhibitor-induced modulation reveals the spliceosome as a specific therapeutic vulnerability in multiple myeloma.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15521-4
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- Publication type:
- Article
Full-length transcript characterization of SF3B1 mutation in chronic lymphocytic leukemia reveals downregulation of retained introns.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15171-6
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- Publication type:
- Article
High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-13885-w
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- Article
Author Correction: Butler enables rapid cloud-based analysis of thousands of human genomes.
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- 2023
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- Correction Notice
Publisher Correction: Butler enables rapid cloud-based analysis of thousands of human genomes.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Visualizing and interpreting cancer genomics data via the Xena platform.
- Published in:
- 2020
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- Publication type:
- Letter
Butler enables rapid cloud-based analysis of thousands of human genomes.
- Published in:
- Nature Biotechnology, 2020, v. 38, n. 3, p. 288, doi. 10.1038/s41587-019-0360-3
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- Publication type:
- Article
eVIP2: Expression-based variant impact phenotyping to predict the function of gene variants.
- Published in:
- PLoS Computational Biology, 2021, v. 17, n. 7, p. 1, doi. 10.1371/journal.pcbi.1009132
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- Article