标题
FUBP1: a new protagonist in splicing regulation of the DMD gene
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 43, Issue 4, Pages 2378-2389
出版商
Oxford University Press (OUP)
发表日期
2015-02-07
DOI
10.1093/nar/gkv086
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- The Splicing Factor FUBP1 Is Required for the Efficient Splicing of OncogeneMDM2Pre-mRNA
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- The splicing activator DAZAP1 integrates splicing control into MEK/Erk-regulated cell proliferation and migration
- (2014) Rajarshi Choudhury et al. Nature Communications
- Dynamic Integration of Splicing within Gene Regulatory Pathways
- (2013) Ulrich Braunschweig et al. CELL
- Therapy for Duchenne muscular dystrophy: renewed optimism from genetic approaches
- (2013) Rebecca J. Fairclough et al. NATURE REVIEWS GENETICS
- Dystrophin rescue by trans -splicing: a strategy for DMD genotypes not eligible for exon skipping approaches
- (2013) Stéphanie Lorain et al. NUCLEIC ACIDS RESEARCH
- DAZAP1 regulates the splicing of Crem, Crisp2 and Pot1a transcripts
- (2013) Hsiang-Ying Chen et al. NUCLEIC ACIDS RESEARCH
- Far upstream element-binding protein 1 and RNA secondary structure both mediate second-step splicing repression
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- Intronic splicing enhancers, cognate splicing factors and context-dependent regulation rules
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- (2012) J Zhang et al. ONCOGENE
- Variants Affecting Exon Skipping Contribute to Complex Traits
- (2012) Younghee Lee et al. PLoS Genetics
- Loss of exon identity is a common mechanism of human inherited disease
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- Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders
- (2011) Kamel Mamchaoui et al. Skeletal Muscle
- Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene
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- RNase-assisted RNA chromatography
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- RNA and Disease
- (2009) Thomas A. Cooper et al. CELL
- Sequence contexts that determine the pathogenicity of base substitutions at position +3 of donor splice-sites
- (2009) Sandie Le Guédard-Méreuze et al. HUMAN MUTATION
- Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase
- (2009) Sylvie Tuffery-Giraud et al. HUMAN MUTATION
- Functional properties and evolutionary splicing constraints on a composite exonic regulatory element of splicing in CFTR exon 12
- (2009) A. Haque et al. NUCLEIC ACIDS RESEARCH
- Dystrophin Nonsense Mutations Can Generate Alternative Rescue Transcripts in Lymphocytes
- (2008) A. Nishiyama et al. ANNALS OF HUMAN GENETICS
- The SR protein family of splicing factors: master regulators of gene expression
- (2008) Jennifer C. Long et al. BIOCHEMICAL JOURNAL
- Structure and function of KH domains
- (2008) Roberto Valverde et al. FEBS Journal
- The pathological splicing mutation c.6792C > G inNF1exon 37 causes a change of tenancy between antagonistic splicing factors
- (2008) Natasa Skoko et al. FEBS LETTERS
- Binding of DAZAP1 and hnRNPA1/A2 to an Exonic Splicing Silencer in a Natural BRCA1 Exon 18 Mutant
- (2008) E. Goina et al. MOLECULAR AND CELLULAR BIOLOGY
- Hierarchical mechanisms build the DNA-binding specificity of FUSE binding protein
- (2008) L. R. Benjamin et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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