19 results on '"Varilh, Jessica"'
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2. Exon identity influences splicing induced by exonic variants and in silico prediction efficacy
3. The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthrough
4. Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis
5. RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiology
6. Highway to Cell: Selection of the Best Cell-Penetrating Peptide to Internalize the CFTR-Stabilizing iCAL36 Peptide
7. Role of Non-coding RNAs in Cystic Fibrosis
8. miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR ‐101 that regulate WISP1 expression
9. miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression.
10. Large phenotypic spectrum associated with two new deep intronic variants on the CFTR gene
11. Additional file 3: Table S2. of DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis
12. Additional file 2: Figure S2. of DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis
13. Additional file 5: Table S1. of DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis
14. Erratum: Targeted RNA-Seq profiling of splicing pattern in the DMD gene: exons are mostly constitutively spliced in human skeletal muscle
15. DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis
16. Targeted RNA-Seq profiling of splicing pattern in the DMD gene: exons are mostly constitutively spliced in human skeletal muscle
17. CCSP G38A polymorphism environment interactions regulate CCSP levels differentially in COPD
18. Cellular mechanisms underlying CCSP SNP association with chronic airway diseases
19. The RNA Binding Protein Tristetraprolin Contributes to CFTR mRNA Stability in Cystic Fibrosis.
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