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miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression

The Journal of pathology, 2021-02, Vol.253 (2), p.186-197

2021

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The CYSMA web server: An example of integrative tool for in silico analysis of missense variants identified in Mendelian disorders

Human mutation, 2020-02, Vol.41 (2), p.375-386

2020

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Highway to Cell: Selection of the Best Cell-Penetrating Peptide to Internalize the CFTR-Stabilizing iCAL36 Peptide

Pharmaceutics, 2022-04, Vol.14 (4), p.808

2022

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Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis

Genetics in medicine, 2015-10, Vol.17 (10), p.796-806

2015

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Phosphorylated C/EBPβ influences a complex network involving YY1 and USF2 in lung epithelial cells

PloS one, 2013-04, Vol.8 (4), p.e60211-e60211

2013

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Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR gene

Journal of cystic fibrosis, 2019-07, Vol.18 (4), p.468-475

2019

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Splicing mutations in the CFTR gene as therapeutic targets

Gene therapy, 2022-08, Vol.29 (7-8), p.399-406

2022

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Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosis

The European respiratory journal, 2015-01, Vol.45 (1), p.116-128

2015

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Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward

Journal of cystic fibrosis, 2022-05, Vol.21 (3), p.448-455

2022

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Current and future molecular approaches in the diagnosis of cystic fibrosis

Expert review of respiratory medicine, 2018-05, Vol.12 (5), p.415-426

2018

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Exon identity influences splicing induced by exonic variants and in silico prediction efficacy

Journal of cystic fibrosis, 2021-05, Vol.20 (3), p.464-472

2021

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The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis

The international journal of biochemistry & cell biology, 2017-07, Vol.88, p.124-132

2017

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CCSP G38A polymorphism environment interactions regulate CCSP levels differentially in COPD

American journal of physiology. Lung cellular and molecular physiology, 2016-10, Vol.311 (4), p.L696-L703

2016

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Should diffuse bronchiectasis still be considered a CFTR-related disorder?

Journal of cystic fibrosis, 2015-09, Vol.14 (5), p.646-653

2015

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Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosis

The European respiratory journal, 2014-12, Vol.45 (1), p.116-128

2014

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Phosphorylated C/EBP[beta] Influences a Complex Network Involving YY1 and USF2 in Lung Epithelial Cells

PloS one, 2013-04, Vol.8 (4), p.e60211

2013

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The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy

Journal of cystic fibrosis, 2023-05, Vol.22 (3), p.515-524

2023

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miRNA repertoires of cystic fibrosis ex vivo models highlight miR‐181a and miR‐101 that regulate WISP1 expression

The CYSMA web server: An example of integrative tool for in silico analysis of missense variants identified in Mendelian disorders

Highway to Cell: Selection of the Best Cell-Penetrating Peptide to Internalize the CFTR-Stabilizing iCAL36 Peptide

Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis

Phosphorylated C/EBPβ influences a complex network involving YY1 and USF2 in lung epithelial cells

Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR gene

Splicing mutations in the CFTR gene as therapeutic targets

Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosis

Reclassifying inconclusive diagnosis after newborn screening for cystic fibrosis. Moving forward

Current and future molecular approaches in the diagnosis of cystic fibrosis

Exon identity influences splicing induced by exonic variants and in silico prediction efficacy

The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis

Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children

CCSP G38A polymorphism environment interactions regulate CCSP levels differentially in COPD

Should diffuse bronchiectasis still be considered a CFTR-related disorder?

Transcription factors and miRNAs that regulate fetal to adult CFTR expression change are new targets for cystic fibrosis

Phosphorylated C/EBP[beta] Influences a Complex Network Involving YY1 and USF2 in Lung Epithelial Cells

The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy

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