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1. Alternative Splicing of In‐Frame Exon Associated with Premature Termination Codons: Implications for Readthrough Therapies. Issue 2 (8th November 2012)

2. Analysis of nasal potential in murine cystic fibrosis models. (November 2016)

3. Cis variants identified in F508del complex alleles modulate CFTR channel rescue by small molecules. Issue 4 (16th January 2018)

4. Combined Computational–Experimental Analyses of CFTR Exon Strength Uncover Predictability of Exon‐Skipping Level. Issue 6 (28th March 2013)

5. Correlating genotype with phenotype using CFTR‐mediated whole‐cell Cl− currents in human nasal epithelial cells. (8th December 2021)

6. Design of Crotoxin-Based Peptides with Potentiator Activity Targeting the ΔF508NBD1 Cystic Fibrosis Transmembrane Conductance Regulator. Issue 3 (1st February 2023)

7. Factors influencing readthrough therapy for frequent cystic fibrosis premature termination codons. Issue 1 (23rd February 2018)

8. Identification of a Novel 5′ Alternative CFTR mRNA Isoform in a Patient with Nasal Polyposis and CFTR Mutations. Issue 7 (9th April 2014)

10. The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible. Issue 5 (30th March 2017)