In vivo selection reveals combinatorial controls that define a critical exon in the spinal muscular atrophy genes
Open Access
- 22 July 2004
- journal article
- Published by Cold Spring Harbor Laboratory in RNA
- Vol. 10 (8) , 1291-1305
- https://doi.org/10.1261/rna.7580704
Abstract
A monthly journal publishing high-quality, peer-reviewed research on all topics related to RNA and its metabolism in all organismsKeywords
This publication has 66 references indexed in Scilit:
- An extended inhibitory context causes skipping of exon 7 of SMN2 in spinal muscular atrophyBiochemical and Biophysical Research Communications, 2004
- Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1Human Genetics, 2003
- New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12Human Molecular Genetics, 2003
- Binding of a Group II Intron-encoded Reverse Transcriptase/Maturase to Its High Affinity Intron RNA Binding Site Involves Sequence-specific Recognition and Autoregulates TranslationJournal of Molecular Biology, 2002
- An extensive network of coupling among gene expression machinesNature, 2002
- Listening to silence and understanding nonsense: exonic mutations that affect splicingNature Reviews Genetics, 2002
- Molecular Cloning and Characterization of a Novel Caspase-3 Variant That Attenuates Apoptosis Induced by Proteasome InhibitionBiochemical and Biophysical Research Communications, 2001
- A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definitionJournal of Molecular Biology, 2001
- The mathematics of SELEX against complex targetsJournal of Molecular Biology, 1998
- Analysis of the CYT-18 Protein Binding Site at the Junction of Stacked Helices in a Group I Intron RNA by Quantitative Binding Assays andin vitroSelectionJournal of Molecular Biology, 1996