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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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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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Theranostics vs theratyping or theranostics plus theratyping?

Journal of cystic fibrosis, 2024-09

2024

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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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Revertant Mutants G550E and 4RK Rescue Cystic Fibrosis Mutants in the First Nucleotide-Binding domain of CFTR by Different Mechanisms

Proceedings of the National Academy of Sciences - PNAS, 2006-11, Vol.103 (47), p.17891-17896

2006

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Cytoskeleton regulators CAPZA2 and INF2 associate with CFTR to control its plasma membrane levels under EPAC1 activation

Biochemical journal, 2020-07, Vol.477 (13), p.2561-2580

2020

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Prolonged co-treatment with HGF sustains epithelial integrity and improves pharmacological rescue of Phe508del-CFTR

Scientific reports, 2018-08, Vol.8 (1), p.13026-14, Article 13026

2018

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Chimeric Constructs Endow the Human CFTR Cl⁻ Channel with the Gating Behavior of Murine CFTR

Proceedings of the National Academy of Sciences - PNAS, 2007-10, Vol.104 (41), p.16365-16370

2007

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Pharmacological evaluation of hybrid thiazolidin-4-one-1,3,5-triazines for NF-κB, biofilm and CFTR activity

RSC advances, 2015-01, Vol.5 (18), p.8871-88718

2015

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A Mathematical Model of the Phosphoinositide Pathway

Scientific reports, 2018-03, Vol.8 (1), p.3904-12, Article 3904

2018

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Classification of CFTR mutation classes – Authors' reply

The lancet respiratory medicine, 2016-08, Vol.4 (8), p.e39-e39

2016

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Protein Traffic Disorders: an Effective High-Throughput Fluorescence Microscopy Pipeline for Drug Discovery

Scientific reports, 2015-03, Vol.5 (1), p.9038-9038, Article 9038

2015

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Investigating Alternative Transport of Integral Plasma Membrane Proteins from the ER to the Golgi: Lessons from the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

Methods in molecular biology (Clifton, N.J.), 2016, Vol.1459, p.105

2016

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F508del-CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis

Biochimica et biophysica acta, 2011-11, Vol.1812 (11), p.1385

2011

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The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70

Biochemical journal, 2002-09, Vol.366 (Pt 3), p.797-806

2002

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Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts

Journal of cystic fibrosis, 2004-08, Vol.3, p.11-15

2004

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Rationale and design of the HIT-CF organoid study: stratifying cystic fibrosis patients based on intestinal organoid response to different CFTR-modulators

Translational medicine communications, 2020-06, Vol.5 (1), p.1-8, Article 9

2020

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CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy

Journal of cystic fibrosis, 2014-07, Vol.13 (4), p.363-372

2014

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Activating alternative chloride channels to treat CF: Friends or Foes?

Journal of cystic fibrosis, 2020-01, Vol.19 (1), p.11-15

2020

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Hodson and Geddes' Cystic Fibrosis: Fifth Edition

5, 2024

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Detection of cystic fibrosis related DNA targets using AC field focusing of magnetic labels and spin-valve sensors

IEEE transactions on magnetics, 2005-10, Vol.41 (10), p.4140-4142

2005

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Direct access of 4-acyl-1,2,3-triazoles from acetophenones: A synthetic shortcut for novel p.Phe508del-CFTR traffic correctors

Journal of molecular structure, 2025-02, Vol.1321, p.139897, Article 139897

2025

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Microarray analysis in cystic fibrosis

Journal of cystic fibrosis, 2004-08, Vol.3, p.29-33

2004

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Biochemical methods to assess CFTR expression and membrane localization

Journal of cystic fibrosis, 2004-08, Vol.3, p.73-77

2004

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Finding new medicines to fight CF: multiple steps of a success story

Orphanet journal of rare diseases, 2012-01, Vol.7 (Suppl 2), p.A19-A19

Amaral, Margarida D

2012

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

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

Theranostics vs theratyping or theranostics plus theratyping?

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

Revertant Mutants G550E and 4RK Rescue Cystic Fibrosis Mutants in the First Nucleotide-Binding domain of CFTR by Different Mechanisms

Cytoskeleton regulators CAPZA2 and INF2 associate with CFTR to control its plasma membrane levels under EPAC1 activation

Prolonged co-treatment with HGF sustains epithelial integrity and improves pharmacological rescue of Phe508del-CFTR

Chimeric Constructs Endow the Human CFTR Cl⁻ Channel with the Gating Behavior of Murine CFTR

Pharmacological evaluation of hybrid thiazolidin-4-one-1,3,5-triazines for NF-κB, biofilm and CFTR activity

A Mathematical Model of the Phosphoinositide Pathway

Classification of CFTR mutation classes – Authors' reply

Protein Traffic Disorders: an Effective High-Throughput Fluorescence Microscopy Pipeline for Drug Discovery

Investigating Alternative Transport of Integral Plasma Membrane Proteins from the ER to the Golgi: Lessons from the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)

F508del-CFTR increases intracellular Ca(2+) signaling that causes enhanced calcium-dependent Cl(-) conductance in cystic fibrosis

The human DnaJ homologue (Hdj)-1/heat-shock protein (Hsp) 40 co-chaperone is required for the in vivo stabilization of the cystic fibrosis transmembrane conductance regulator by Hsp70

Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts

Rationale and design of the HIT-CF organoid study: stratifying cystic fibrosis patients based on intestinal organoid response to different CFTR-modulators

CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy

Activating alternative chloride channels to treat CF: Friends or Foes?

Hodson and Geddes' Cystic Fibrosis: Fifth Edition

Detection of cystic fibrosis related DNA targets using AC field focusing of magnetic labels and spin-valve sensors

Direct access of 4-acyl-1,2,3-triazoles from acetophenones: A synthetic shortcut for novel p.Phe508del-CFTR traffic correctors

Microarray analysis in cystic fibrosis

Biochemical methods to assess CFTR expression and membrane localization

Finding new medicines to fight CF: multiple steps of a success story

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