Publications by authors named "Anita Golec"

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Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis children.
Annalisa Orenti, Iwona Pranke, Caroline Faucon, Jessica Varilh, Aurelie Hatton, Anita Golec

J Cyst Fibros· November 2023

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Theratyping cystic fibrosis patients to guide elexacaftor/tezacaftor/ivacaftor out-of-label prescription.
Elise Dreano, Pierre Régis Burgel, Aurelie Hatton, Naim Bouazza, Benoit Chevalier, Anita Golec

Eur Respir J· October 2023

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Keratin 8 is a scaffolding and regulatory protein of ERAD complexes.
Iwona Maria Pranke, Benoit Chevalier, Aiswarya Premchandar, Nesrine Baatallah, Kamil F Tomaszewski, Anita Golec

Cell Mol Life Sci· September 2022

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Differential CFTR-Interactome Proximity Labeling Procedures Identify Enrichment in Multiple SLC Transporters.
Benoît Chevalier, Nesrine Baatallah, Matthieu Najm, Solène Castanier, Vincent Jung, Anita Golec

Int J Mol Sci· August 2022

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Isolation, cultivation, and application of primary respiratory epithelial cells obtained by nasal brushing, polyp samples, or lung explants.
Anita Golec, Iwona Pranke, Paolo Scudieri, Kate Hayes, Elise Dreano

STAR Protoc· June 2022

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Primary Human Nasal Epithelial Cells: Biobanking in the Context of Precision Medicine.
Mairead Kelly, Elise Dreano, Aurelie Hatton, Agathe Lepissier, Anita Golec

J Vis Exp· April 2022

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Correlating genotype with phenotype using CFTR-mediated whole-cell Cl currents in human nasal epithelial cells.
Sabrina Noel, Nathalie Servel, Aurélie Hatton, Anita Golec, Mayuree Rodrat

J Physiol· March 2022

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Antisense oligonucleotide-based drug development for Cystic Fibrosis patients carrying the 3849+10 kb C-to-T splicing mutation.
Yifat S Oren, Michal Irony-Tur Sinai, Anita Golec, Ofra Barchad-Avitzur, Venkateshwar Mutyam

J Cyst Fibros· September 2021

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Modulators of CFTR. Updates on clinical development and future directions.
Emmanuelle Bardin, Alexandra Pastor, Michaela Semeraro, Anita Golec, Kate Hayes

Eur J Med Chem· March 2021

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Author Correction: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Juliette Simonin, Emmanuelle Bille, Gilles Crambert, Sabrina Noel, Elise Dreano, Anita Golec

Sci Rep· November 2019

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Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
Juliette Simonin, Emmanuelle Bille, Gilles Crambert, Sabrina Noel, Elise Dreano, Anita Golec

Sci Rep· April 2019

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Emerging Therapeutic Approaches for Cystic Fibrosis. From Gene Editing to Personalized Medicine.
Iwona Pranke, Anita Golec, Alexandre Hinzpeter, Aleksander Edelman, Isabelle Sermet-Gaudelus

Front Pharmacol· February 2019

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The H2S-generating enzymes cystathionine β-synthase and cystathionine γ-lyase play a role in vascular development during normal lung alveolarization.
Alicia Madurga, Anita Golec, Agnieszka Pozarska, Isao Ishii, Ivana Mižíková

Am J Physiol Lung Cell Mol Physiol· October 2015

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Phenotypical and ultrastructural features of Oct4-positive cells in the adult mouse lung.
Celimene Galiger, Sawa Kostin, Anita Golec, Katrin Ahlbrecht, Sven Becker

J Cell Mol Med· July 2014

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