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Ablation of RIP3 protects from dopaminergic neurodegeneration in experimental Parkinson's disease

Cell death & disease, 2019-11, Vol.10 (11), p.840-14, Article 840

2019

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Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids

Cells (Basel, Switzerland), 2022-07, Vol.11 (15), p.2295

2022

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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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Activating alternative chloride channels to treat CF: Friends or Foes?: Report on the Meeting of the Basic Science Working Group in Dubrovnik, Croatia

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

2020

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Additive Potentiation of R334W-CFTR Function by Novel Small Molecules

Journal of personalized medicine, 2023-01, Vol.13 (1), p.102

2023

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Adherence and Self-Management in Cystic Fibrosis Care

Hodson and Geddes' Cystic Fibrosis, 2024, p.438-443

5, 2024

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Adolescent Health and Transition in Cystic Fibrosis

Hodson and Geddes' Cystic Fibrosis, 2024, p.648-657

5, 2024

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Alternative respiratory system and formamide hydro-lyase activity as the key components of the cyanide-resistance mechanism in Fusarium oxysporum

Canadian journal of microbiology, 1997-10, Vol.43 (10), p.929-936

1997

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AMPK controls epithelial Na+ channels through Nedd4-2 and causes an epithelial phenotype when mutated

Pflügers Archiv, 2009-08, Vol.458 (4), p.713-721

2009

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Analysis of CFTR folding and degradation in transiently transfected cells

Methods in molecular biology (Clifton, N.J.), 2011, Vol.741, p.219

2011

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Analysis of CFTR interactome in the macromolecular complexes

Methods in molecular biology (Clifton, N.J.), 2011, Vol.741, p.255

2011

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Analysis of genomic CFTR DNA

Journal of cystic fibrosis, 2004-08, Vol.3, p.7-10

2004

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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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Antibodies for CFTR studies

Journal of cystic fibrosis, 2004-08, Vol.3, p.69-72

2004

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Applicability of Different Antibodies for the Immunohistochemical Localization of CFTR In Respiratory and Intestinal Tissues of Human and Murine Origin

The journal of histochemistry and cytochemistry, 2003-09, Vol.51 (9), p.1191-1199

2003

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Application of high-resolution single-channel recording to functional studies of cystic fibrosis mutants

Methods in molecular biology (Clifton, N.J.), 2011, Vol.741, p.419

2011

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Application of mass spectrometry to study proteomics and interactomics in cystic fibrosis

Methods in molecular biology (Clifton, N.J.), 2011, Vol.742, p.227

2011

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Approaches to study CFTR pre-mRNA splicing defects

Methods in molecular biology (Clifton, N.J.), 2011, Vol.741, p.155

2011

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Approaches to study differentiation and repair of human airway epithelial cells

Methods in molecular biology (Clifton, N.J.), 2011, Vol.742, p.173

2011

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Assessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.784-791

2014

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Assessment of CFTR function in native epithelia for the diagnosis of cystic fibrosis

Pediatric pulmonology, 2004-01, Vol.37 (S26), p.243-243

2004

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Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing

Journal of cystic fibrosis, 2004-08, Vol.3, p.43-48

2004

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Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis

Frontiers in physiology, 2020-12, Vol.11, p.604580-604580

2020

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BAG-1 Stabilizes Mutant F508del-CFTR in a Ubiquitin-Like-Domain-Dependent Manner

Cellular physiology and biochemistry, 2012-01, Vol.30 (5), p.1120-1133

2012

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Biochemical and biophysical approaches to probe CFTR structure

Methods in molecular biology (Clifton, N.J.), 2011, Vol.741, p.365

2011

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Ablation of RIP3 protects from dopaminergic neurodegeneration in experimental Parkinson's disease

Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids

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

Activating alternative chloride channels to treat CF: Friends or Foes?: Report on the Meeting of the Basic Science Working Group in Dubrovnik, Croatia

Additive Potentiation of R334W-CFTR Function by Novel Small Molecules

Adherence and Self-Management in Cystic Fibrosis Care

Adolescent Health and Transition in Cystic Fibrosis

Alternative respiratory system and formamide hydro-lyase activity as the key components of the cyanide-resistance mechanism in Fusarium oxysporum

AMPK controls epithelial Na+ channels through Nedd4-2 and causes an epithelial phenotype when mutated

Analysis of CFTR folding and degradation in transiently transfected cells

Analysis of CFTR interactome in the macromolecular complexes

Analysis of genomic CFTR DNA

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

Antibodies for CFTR studies

Applicability of Different Antibodies for the Immunohistochemical Localization of CFTR In Respiratory and Intestinal Tissues of Human and Murine Origin

Application of high-resolution single-channel recording to functional studies of cystic fibrosis mutants

Application of mass spectrometry to study proteomics and interactomics in cystic fibrosis

Approaches to study CFTR pre-mRNA splicing defects

Approaches to study differentiation and repair of human airway epithelial cells

Assessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis

Assessment of CFTR function in native epithelia for the diagnosis of cystic fibrosis

Assessment of CFTR localisation in native airway epithelial cells obtained by nasal brushing

Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis

BAG-1 Stabilizes Mutant F508del-CFTR in a Ubiquitin-Like-Domain-Dependent Manner

Biochemical and biophysical approaches to probe CFTR structure

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