Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage
Published 2016 View Full Article
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Title
Cancer-associated SF3B1 mutations affect alternative splicing by promoting alternative branchpoint usage
Authors
Keywords
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Journal
Nature Communications
Volume 7, Issue -, Pages 10615
Publisher
Springer Nature
Online
2016-02-04
DOI
10.1038/ncomms10615
References
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Related references
Note: Only part of the references are listed.- Genome-wide discovery of human splicing branchpoints
- (2015) Tim R. Mercer et al. GENOME RESEARCH
- Cancer-Associated SF3B1 Hotspot Mutations Induce Cryptic 3′ Splice Site Selection through Use of a Different Branch Point
- (2015) Rachel B. Darman et al. Cell Reports
- Transcriptome Sequencing Reveals Potential Mechanism of Cryptic 3’ Splice Site Selection in SF3B1-mutated Cancers
- (2015) Christopher DeBoever et al. PLoS Computational Biology
- SF3B1mutations constitute a novel therapeutic target in breast cancer
- (2014) Sarah L Maguire et al. JOURNAL OF PATHOLOGY
- A common alternative splicing signature is associated with SF3B1 mutations in malignancies from different cell lineages
- (2014) D Gentien et al. LEUKEMIA
- Rare SF3B1 R625 mutations in cutaneous melanoma
- (2014) Yong Kong et al. MELANOMA RESEARCH
- Establishment of novel cell lines recapitulating the genetic landscape of uveal melanoma and preclinical validation of mTOR as a therapeutic target
- (2014) Nabil Amirouchene-Angelozzi et al. Molecular Oncology
- Mechanisms for U2AF to define 3′ splice sites and regulate alternative splicing in the human genome
- (2014) Changwei Shao et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
- (2013) Marcel Martin et al. NATURE GENETICS
- Recurrent mutations at codon 625 of the splicing factor SF3B1 in uveal melanoma
- (2013) J William Harbour et al. NATURE GENETICS
- SF3B1 Mutations Are Associated with Alternative Splicing in Uveal Melanoma
- (2013) S. J. Furney et al. Cancer Discovery
- Misregulation of Pre-mRNA Alternative Splicing in Cancer
- (2013) J. Zhang et al. Cancer Discovery
- TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
- (2013) Daehwan Kim et al. GENOME BIOLOGY
- The spliceosome as a target of novel antitumour drugs
- (2012) Sophie Bonnal et al. NATURE REVIEWS DRUG DISCOVERY
- Reduced fidelity of branch point recognition and alternative splicing induced by the anti-tumor drug spliceostatin A
- (2011) A. Corrionero et al. GENES & DEVELOPMENT
- Perturbation of U2AF65/NXF1-mediated RNA nuclear export enhances RNA toxicity in polyQ diseases
- (2011) Ho Tsoi et al. HUMAN MOLECULAR GENETICS
- Frequent pathway mutations of splicing machinery in myelodysplasia
- (2011) Kenichi Yoshida et al. NATURE
- Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
- (2011) Víctor Quesada et al. NATURE GENETICS
- SF3B1and Other Novel Cancer Genes in Chronic Lymphocytic Leukemia
- (2011) Lili Wang et al. NEW ENGLAND JOURNAL OF MEDICINE
- Genome-Wide Association between Branch Point Properties and Alternative Splicing
- (2010) André Corvelo et al. PLoS Computational Biology
- The Spliceosome: Design Principles of a Dynamic RNP Machine
- (2009) Markus C. Wahl et al. CELL
- Human Splicing Finder: an online bioinformatics tool to predict splicing signals
- (2009) François-Olivier Desmet et al. NUCLEIC ACIDS RESEARCH
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