Single-Nucleotide Polymorphisms in NAGNAG Acceptors Are Highly Predictive for Variations of Alternative Splicing
- 1 February 2006
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 78 (2), 291-302
- https://doi.org/10.1086/500151
Abstract
No abstract availableKeywords
Funding Information
- Bundesministerium für Bildung und Forschung (01GR0105, 01GS0426, 0312704E)
- Deutsche Forschungsgemeinschaft (SFB604-02)
This publication has 25 references indexed in Scilit:
- Frequent occurrence of protein isoforms with or without a single amino acid residue by subtle alternative splicing: the case of Gln in DRPLA affects subcellular localization of the productsJournal of Human Genetics, 2005
- Are splicing mutations the most frequent cause of hereditary disease?FEBS Letters, 2005
- DNA sequence and comparative analysis of chimpanzee chromosome 22Nature, 2004
- Genomic variants in exons and introns: identifying the splicing spoilersNature Reviews Genetics, 2004
- Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamicsNature Reviews Molecular Cell Biology, 2004
- Insights into the ubiquitin transfer cascade from the structure of the activating enzyme for NEDD8Nature, 2003
- Listening to silence and understanding nonsense: exonic mutations that affect splicingNature Reviews Genetics, 2002
- A CD45 Polymorphism Associated with Multiple Sclerosis Disrupts an Exonic Splicing SilencerJournal of Biological Chemistry, 2001
- An Alternative-Exon Database and Its Statistical AnalysisDNA and Cell Biology, 2000
- Donor splice-site mutations in WT1 are responsible for Frasier syndromeNature Genetics, 1997