Found: 7
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DFI-seq identification of environment-specific gene expression in uropathogenic Escherichia coli.
- Published in:
- BMC Microbiology, 2017, v. 17, p. 1, doi. 10.1186/s12866-017-1008-4
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- Article
RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent introns.
- Published in:
- Nucleic Acids Research, 2017, v. 45, n. 1, p. 395, doi. 10.1093/nar/gkw731
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- Article
Splice-shifting oligonucleotide (SSO) mediated blocking of an exonic splicing enhancer (ESE) created by the prevalent c.903+469T>C MTRR mutation corrects splicing and restores enzyme activity in patient cells.
- Published in:
- Nucleic Acids Research, 2015, v. 43, n. 9, p. 4627, doi. 10.1093/nar/gkv275
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- Article
Absence of an Intron Splicing Silencer in Porcine <i>Smn1</i> Intron 7 Confers Immunity to the Exon Skipping Mutation in Human <i>SMN2</i>.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0098841
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- Article
DeepCLIP: predicting the effect of mutations on protein–RNA binding with deep learning.
- Published in:
- Nucleic Acids Research, 2020, v. 48, n. 13, p. 7099, doi. 10.1093/nar/gkaa530
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- Article
SMN2 exon 7 splicing is inhibited by binding of hnRNP A1 to a common ESS motif that spans the 3′ splice site.
- Published in:
- Human Mutation, 2011, v. 32, n. 2, p. 220, doi. 10.1002/humu.21419
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- Article
The deep intronic c.903+469T>C mutation in the MTRR gene creates an SF2/ASF binding exonic splicing enhancer, which leads to pseudoexon activation and causes the cblE type of homocystinuria.
- Published in:
- Human Mutation, 2010, v. 31, n. 4, p. 437, doi. 10.1002/humu.21206
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- Article