Intron retention is a widespread mechanism of tumor-suppressor inactivation
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Intron retention is a widespread mechanism of tumor-suppressor inactivation
Authors
Keywords
-
Journal
NATURE GENETICS
Volume 47, Issue 11, Pages 1242-1248
Publisher
Springer Nature
Online
2015-10-05
DOI
10.1038/ng.3414
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Identification of recurrent regulated alternative splicing events across human solid tumors
- (2015) Miri Danan-Gotthold et al. NUCLEIC ACIDS RESEARCH
- Regularization Paths for Generalized Linear Models via Coordinate Descent
- (2015) Jerome Friedman et al. Journal of Statistical Software
- Synonymous Mutations Frequently Act as Driver Mutations in Human Cancers
- (2014) Fran Supek et al. CELL
- Comprehensive molecular profiling of lung adenocarcinoma
- (2014) Eric A. Collisson et al. NATURE
- Discovery and saturation analysis of cancer genes across 21 tumour types
- (2014) Michael S. Lawrence et al. NATURE
- The human splicing code reveals new insights into the genetic determinants of disease
- (2014) H. Y. Xiong et al. SCIENCE
- Interplay between the Cancer Genome and Epigenome
- (2013) Hui Shen et al. CELL
- Pick one, but be quick: 5' splice sites and the problems of too many choices
- (2013) X. Roca et al. GENES & DEVELOPMENT
- Integrated genomic characterization of endometrial carcinoma
- (2013) Gad Getz et al. NATURE
- Mutational landscape and significance across 12 major cancer types
- (2013) Cyriac Kandoth et al. NATURE
- Transcriptome and genome sequencing uncovers functional variation in humans
- (2013) Tuuli Lappalainen et al. NATURE
- Pan-cancer patterns of somatic copy number alteration
- (2013) Travis I Zack et al. NATURE GENETICS
- Nonsense-mediated mRNA decay: Inter-individual variability and human disease
- (2013) Lam Son Nguyen et al. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
- RefSeq: an update on mammalian reference sequences
- (2013) Kim D. Pruitt et al. NUCLEIC ACIDS RESEARCH
- The UCSC Genome Browser database: 2014 update
- (2013) Donna Karolchik et al. NUCLEIC ACIDS RESEARCH
- Identification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseases
- (2013) Roberta Spinelli et al. Molecular Genetics & Genomic Medicine
- Genomic signatures for predicting survival and adjuvant chemotherapy benefit in patients with non-small-cell lung cancer
- (2012) Ryan K Van Laar BMC Medical Genomics
- SystemicVHLgene functions and the VHL disease
- (2012) Hannah L. Bader et al. FEBS LETTERS
- Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events
- (2012) J. Liu et al. GENOME RESEARCH
- Comprehensive molecular portraits of human breast tumours
- (2012) Daniel C. Koboldt et al. NATURE
- TSGene: a web resource for tumor suppressor genes
- (2012) Min Zhao et al. NUCLEIC ACIDS RESEARCH
- Recurrent Hemizygous Deletions in Cancers May Optimize Proliferative Potential
- (2012) N. L. Solimini et al. SCIENCE
- ARID1A Mutations in Cancer: Another Epigenetic Tumor Suppressor?
- (2012) Jennifer N. Wu et al. Cancer Discovery
- Differential GC Content between Exons and Introns Establishes Distinct Strategies of Splice-Site Recognition
- (2012) Maayan Amit et al. Cell Reports
- Regulation of nonsense-mediated mRNA decay
- (2012) Lulu Huang et al. Wiley Interdisciplinary Reviews-RNA
- pROC: an open-source package for R and S+ to analyze and compare ROC curves
- (2011) Xavier Robin et al. BMC BIOINFORMATICS
- Hallmarks of Cancer: The Next Generation
- (2011) Douglas Hanahan et al. CELL
- A continuum model for tumour suppression
- (2011) Alice H. Berger et al. NATURE
- Integrated genomic analyses of ovarian carcinoma
- (2011) D. Bell et al. NATURE
- Non-coding RNAs in human disease
- (2011) Manel Esteller NATURE REVIEWS GENETICS
- Using positional distribution to identify splicing elements and predict pre-mRNA processing defects in human genes
- (2011) K. H. Lim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- BEDTools: a flexible suite of utilities for comparing genomic features
- (2010) Aaron R. Quinlan et al. BIOINFORMATICS
- Alternative splicing and evolution: diversification, exon definition and function
- (2010) Hadas Keren et al. NATURE REVIEWS GENETICS
- COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
- (2010) S. A. Forbes et al. NUCLEIC ACIDS RESEARCH
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Activation of the hedgehog-signaling pathway in human cancer and the clinical implications
- (2009) L Yang et al. ONCOGENE
- Alternative splicing and disease
- (2008) Jamal Tazi et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Splicing regulation: From a parts list of regulatory elements to an integrated splicing code
- (2008) Z. Wang et al. RNA
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started