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miR-200b downregulates CFTR during hypoxia in human lung epithelial cells

Cellular & molecular biology letters, 2017-11, Vol.22 (1), p.23-14, Article 23

2017

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Somatic mosaicism for copy number variation in differentiated human tissues

Human mutation, 2008-09, Vol.29 (9), p.1118-1124

2008

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ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartments

PloS one, 2015-04, Vol.10 (4), p.e0123131-e0123131

2015

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Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulator

Biochemical journal, 2012-01, Vol.441 (2), p.633-643

2012

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Efficient Intracellular Processing of the Endogenous Cystic Fibrosis Transmembrane Conductance Regulator in Epithelial Cell Lines

The Journal of biological chemistry, 2004-05, Vol.279 (21), p.22578-22584

2004

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Targets for cystic fibrosis therapy: proteomic analysis and correction of mutant cystic fibrosis transmembrane conductance regulator

Expert review of proteomics, 2010-08, Vol.7 (4), p.495-506

2010

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Evidence that Systemic Gentamicin Suppresses Premature Stop Mutations in Patients with Cystic Fibrosis

American journal of respiratory and critical care medicine, 2001-06, Vol.163 (7), p.1683-1692

2001

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Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line

Nature medicine, 1997-11, Vol.3 (11), p.1280-1284

1997

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Extracellular Zinc and ATP Restore Chloride Secretion across Cystic Fibrosis Airway Epithelia by Triggering Calcium Entry

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.10720-10729

2004

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Activation of the Unfolded Protein Response by ΔF508 CFTR

American journal of respiratory cell and molecular biology, 2008-10, Vol.39 (4), p.448-457

2008

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Mutations in the Amino Terminus of the Cystic Fibrosis Transmembrane Conductance Regulator Enhance Endocytosis

The Journal of biological chemistry, 2006-02, Vol.281 (6), p.3329-3334

2006

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Endoplasmic reticulum stress and the unfolded protein response regulate genomic cystic fibrosis transmembrane conductance regulator expression

American Journal of Physiology: Cell Physiology, 2007-02, Vol.292 (2), p.C756-C766

2007

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A Synonymous Single Nucleotide Polymorphism in ΔF508 CFTR Alters the Secondary Structure of the mRNA and the Expression of the Mutant Protein

The Journal of biological chemistry, 2010-09, Vol.285 (37), p.28741-28748

2010

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The CFTR and ENaC debate: how important is ENaC in CF lung disease?

American journal of physiology. Lung cellular and molecular physiology, 2012-06, Vol.302 (11), p.L1141-L1146

2012

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Pkhd1cyli/cyli mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver disease

Journal of molecular medicine (Berlin, Germany), 2023-09, Vol.101 (9), p.1141-1151

2023

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The Unfolded Protein Response (UPR)-activated Transcription Factor X-box-binding Protein 1 (XBP1) Induces MicroRNA-346 Expression That Targets the Human Antigen Peptide Transporter 1 (TAP1) mRNA and Governs Immune Regulatory Genes

The Journal of biological chemistry, 2011-12, Vol.286 (48), p.41862-41870

2011

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The Mechanism of Cystic Fibrosis Transmembrane Conductance Regulator Transcriptional Repression during the Unfolded Protein Response

The Journal of biological chemistry, 2008-05, Vol.283 (18), p.12154-12165

2008

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Ablation of Internalization Signals in the Carboxyl-terminal Tail of the Cystic Fibrosis Transmembrane Conductance Regulator Enhances Cell Surface Expression

The Journal of biological chemistry, 2002-12, Vol.277 (51), p.49952-49957

2002

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F508 CFTR Surface Stability Is Regulated by DAB2 and CHIP-Mediated Ubiquitination in Post-Endocytic Compartments

PloS one, 2015-04, Vol.10 (4)

2015

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Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

The New England journal of medicine, 2003-10, Vol.349 (15), p.1433-1441

2003

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Regulation of angiogenesis by hypoxia: the role of microRNA

Cellular & molecular biology letters, 2013-03, Vol.18 (1), p.47-57

2013

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CFTR Expression Regulation by the Unfolded Protein Response

Methods in Enzymology, 2011, Vol.491, p.3-24

2011

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Suppression of CFTR premature termination codons and rescue of CFTR protein and function by the synthetic aminoglycoside NB54

Journal of molecular medicine (Berlin, Germany), 2011-11, Vol.89 (11), p.1149-1161

2011

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Failure of cAMP agonists to activate rescued ΔF508 CFTR in CFBE41o– airway epithelial monolayers

The Journal of physiology, 2005-12, Vol.569 (2), p.601-615

2005

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Functional stability of rescued delta F508 cystic fibrosis transmembrane conductance regulator in airway epithelial cells

American journal of respiratory cell and molecular biology, 2010-03, Vol.42 (3), p.363-372

2010

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miR-200b downregulates CFTR during hypoxia in human lung epithelial cells

Somatic mosaicism for copy number variation in differentiated human tissues

ΔF508 CFTR surface stability is regulated by DAB2 and CHIP-mediated ubiquitination in post-endocytic compartments

Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulator

Efficient Intracellular Processing of the Endogenous Cystic Fibrosis Transmembrane Conductance Regulator in Epithelial Cell Lines

Targets for cystic fibrosis therapy: proteomic analysis and correction of mutant cystic fibrosis transmembrane conductance regulator

Evidence that Systemic Gentamicin Suppresses Premature Stop Mutations in Patients with Cystic Fibrosis

Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line

Extracellular Zinc and ATP Restore Chloride Secretion across Cystic Fibrosis Airway Epithelia by Triggering Calcium Entry

Activation of the Unfolded Protein Response by ΔF508 CFTR

Mutations in the Amino Terminus of the Cystic Fibrosis Transmembrane Conductance Regulator Enhance Endocytosis

Endoplasmic reticulum stress and the unfolded protein response regulate genomic cystic fibrosis transmembrane conductance regulator expression

A Synonymous Single Nucleotide Polymorphism in ΔF508 CFTR Alters the Secondary Structure of the mRNA and the Expression of the Mutant Protein

The CFTR and ENaC debate: how important is ENaC in CF lung disease?

Pkhd1cyli/cyli mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver disease

The Unfolded Protein Response (UPR)-activated Transcription Factor X-box-binding Protein 1 (XBP1) Induces MicroRNA-346 Expression That Targets the Human Antigen Peptide Transporter 1 (TAP1) mRNA and Governs Immune Regulatory Genes

The Mechanism of Cystic Fibrosis Transmembrane Conductance Regulator Transcriptional Repression during the Unfolded Protein Response

Ablation of Internalization Signals in the Carboxyl-terminal Tail of the Cystic Fibrosis Transmembrane Conductance Regulator Enhances Cell Surface Expression

F508 CFTR Surface Stability Is Regulated by DAB2 and CHIP-Mediated Ubiquitination in Post-Endocytic Compartments

Gentamicin-Induced Correction of CFTR Function in Patients with Cystic Fibrosis and CFTR Stop Mutations

Regulation of angiogenesis by hypoxia: the role of microRNA

CFTR Expression Regulation by the Unfolded Protein Response

Suppression of CFTR premature termination codons and rescue of CFTR protein and function by the synthetic aminoglycoside NB54

Failure of cAMP agonists to activate rescued ΔF508 CFTR in CFBE41o– airway epithelial monolayers

Functional stability of rescued delta F508 cystic fibrosis transmembrane conductance regulator in airway epithelial cells

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