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What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?

International journal of molecular sciences, 2020-04, Vol.21 (9), p.3133

2020

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Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

Nature genetics, 2013-10, Vol.45 (10), p.1160-1167

2013

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Rescuing mutant CFTR: a multi-task approach to a better outcome in treating cystic fibrosis

Current pharmaceutical design, 2013, Vol.19 (19), p.3497

2013

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CFTR, Cell Junctions and the Cytoskeleton

International journal of molecular sciences, 2022-02, Vol.23 (5), p.2688

2022

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Synergy in Cystic Fibrosis Therapies: Targeting SLC26A9

International journal of molecular sciences, 2021-12, Vol.22 (23), p.13064

2021

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Inhibition of calpain 1 restores plasma membrane stability to pharmacologically rescued Phe508del-CFTR variant

The Journal of biological chemistry, 2019-09, Vol.294 (36), p.13396-13410

2019

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Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies

International journal of molecular sciences, 2021-12, Vol.23 (1), p.24

2021

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Impact of KLF4 on Cell Proliferation and Epithelial Differentiation in the Context of Cystic Fibrosis

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6717

2020

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A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint

Science signaling, 2015-05, Vol.8 (377), p.ra48

2015

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CyFi-MAP: an interactive pathway-based resource for cystic fibrosis

Scientific reports, 2021-11, Vol.11 (1), p.22223-22223, Article 22223

2021

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Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Genomics (San Diego, Calif.), 2015-11, Vol.106 (5), p.268-277

2015

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Most F508del-CFTR Is Targeted to Degradation at an Early Folding Checkpoint and Independently of Calnexin

Molecular and Cellular Biology, 2005-06, Vol.25 (12), p.5242-5252

2005

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Targeting CFTR: how to treat cystic fibrosis by CFTR-repairing therapies

Current drug targets, 2011-05, Vol.12 (5), p.683

Amaral, Margarida D

2011

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Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

International journal of molecular sciences, 2020-06, Vol.21 (12), p.4524

2020

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New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls

Pharmacology & therapeutics (Oxford), 2015-01, Vol.145, p.19-34

2015

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Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis

EBioMedicine, 2015-02, Vol.2 (2), p.147-153

2015

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Integrity and Stability of PTC Bearing CFTR mRNA and Relevance to Future Modulator Therapies in Cystic Fibrosis

Genes, 2021-11, Vol.12 (11), p.1810

2021

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Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis

PloS one, 2012-10, Vol.7 (10), p.e47708-e47708

2012

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Pediatric population with cystic fibrosis in the centre of Portugal: candidates for new therapies

Jornal de pediatria, 2022-03, Vol.98 (2), p.212-217

2022

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KLF4 Acts as a wt-CFTR Suppressor through an AKT-Mediated Pathway

Cells (Basel, Switzerland), 2020-07, Vol.9 (7), p.1607

2020

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Transcription-Dependent Spatial Arrangements of CFTR and Adjacent Genes in Human Cell Nuclei

The Journal of cell biology, 2004-09, Vol.166 (6), p.815-825

2004

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CFTR and chaperones: processing and degradation

Journal of molecular neuroscience, 2004-01, Vol.23 (1-2), p.41-48

Amaral, Margarida D

2004

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The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

PloS one, 2011, Vol.6 (8), p.e24445-e24445

2011

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Antagonistic Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Cell Surface Expression by Protein Kinases WNK4 and Spleen Tyrosine Kinase

Molecular and Cellular Biology, 2011-10, Vol.31 (19), p.4076-4086

2011

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What Role Does CFTR Play in Development, Differentiation, Regeneration and Cancer?

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

Rescuing mutant CFTR: a multi-task approach to a better outcome in treating cystic fibrosis

CFTR, Cell Junctions and the Cytoskeleton

Synergy in Cystic Fibrosis Therapies: Targeting SLC26A9

Inhibition of calpain 1 restores plasma membrane stability to pharmacologically rescued Phe508del-CFTR variant

Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies

Impact of KLF4 on Cell Proliferation and Epithelial Differentiation in the Context of Cystic Fibrosis

A molecular switch in the scaffold NHERF1 enables misfolded CFTR to evade the peripheral quality control checkpoint

CyFi-MAP: an interactive pathway-based resource for cystic fibrosis

Transcriptome meta-analysis reveals common differential and global gene expression profiles in cystic fibrosis and other respiratory disorders and identifies CFTR regulators

Most F508del-CFTR Is Targeted to Degradation at an Early Folding Checkpoint and Independently of Calnexin

Targeting CFTR: how to treat cystic fibrosis by CFTR-repairing therapies

Human Epididymis Protein 4: A Novel Serum Inflammatory Biomarker in Cystic Fibrosis

Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions

New pharmacological approaches for cystic fibrosis: promises, progress, pitfalls

Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis

Integrity and Stability of PTC Bearing CFTR mRNA and Relevance to Future Modulator Therapies in Cystic Fibrosis

Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis

Pediatric population with cystic fibrosis in the centre of Portugal: candidates for new therapies

KLF4 Acts as a wt-CFTR Suppressor through an AKT-Mediated Pathway

Transcription-Dependent Spatial Arrangements of CFTR and Adjacent Genes in Human Cell Nuclei

CFTR and chaperones: processing and degradation

The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients

Antagonistic Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Cell Surface Expression by Protein Kinases WNK4 and Spleen Tyrosine Kinase

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