J. Hinnrasky

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Growth and characterization of isolated bovine tracheal gland cells in culture. Influence of a reconstituted basement membrane matrix

E. Puchelle, C. Fuchey, J. Jacquot, 1989, Biology of the cell.

Fibronectin and its alpha 5 beta 1-integrin receptor are involved in the wound-repair process of airway epithelium.

J. Zahm, H. Kaplan, D. Sheppard, 1996, The American journal of physiology.

CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.

B. Tümmler, S. Brézillon, F. Dupuit, 1995, The Journal of clinical investigation.

Reconstituted Skin from Murine Embryonic Stem Cells

C. Dani, J. Ortonne, C. Hilmi, 2003, Current Biology.

Production of lipocortin‐like proteins by cultured human tracheal submucosal gland cells

F. Antonicelli, B. Haye, J. Jacquot, 1990, FEBS letters.

Culture and characterization of human tracheal gland cells.

J. Tournier, M. Merten, C. Fuchey, 1990, The American review of respiratory disease.

Differentiated and functional human airway epithelium regeneration in tracheal xenografts.

E. Mongodin, S. de Bentzmann, D. Gaillard, 2000, American journal of physiology. Lung cellular and molecular physiology.

Airway epithelial integrity is protected by a long-acting beta2-adrenergic receptor agonist.

P. Devillier, J. Zahm, M. Polette, 2004, American journal of respiratory cell and molecular biology.

Dynamic interaction between airway epithelial cells and Staphylococcus aureus.

M. de Assis, M. Plotkowski, J. Zahm, 2004, American journal of physiology. Lung cellular and molecular physiology.

regeneration in tracheal xenografts Differentiated and functional human airway epithelium

E. Mongodin, D. Gaillard, F. Dupuit, 2016 .

Dysregulation of IL‐2 and IL‐8 production in circulating T lymphocytes from young cystic fibrosis patients

M. Guenounou, C. Hubeau, M. Guenounou, 2004, Clinical and experimental immunology.

Differentiation of human surface upper airway epithelial cells in primary culture on a floating collagen gel.

J. Klossek, J. Zahm, M. Chevillard, 1993, Epithelial cell biology.

Inflammation and infection in naive human cystic fibrosis airway grafts.

S. de Bentzmann, C. Hubeau, R. Tirouvanziam, 2000, American journal of respiratory cell and molecular biology.

Stimulation of β2-Adrenergic Receptor Increases Cystic Fibrosis Transmembrane Conductance Regulator Expression in Human Airway Epithelial Cells through a cAMP/Protein Kinase A-independent Pathway*

J. Klossek, P. Corlieu, K. Taouil, 2003, The Journal of Biological Chemistry.

Distribution of Integrins During Human Fetal Lung Development

D. Gaillard, C. Coraux, B. Péault, 1998, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Early alterations in airway mucociliary clearance and inflammation of the lamina propria in CF mice.

D. Porteous, J. Zahm, J. Dorin, 1997, The American journal of physiology.

Characterization of ion and fluid transport in human bronchioles.

E. Naline, T. Chinet, Sabine Blouquit, 2002, American journal of respiratory cell and molecular biology.

Evaluation of the 99mtechnetium labelling effect on Pseudomonas aeruginosa surface properties.

M. Bernardo Filho, G. Beck, J. Hinnrasky, 1987, Annales de l'Institut Pasteur. Microbiology.

Early expression of β- and γ-subunits of epithelial sodium channel during human airway development

P. Barbry, M. Matthay, S. Coscoy, 2000 .

Aquaporin‐3 Expression in Human Fetal Airway Epithelial Progenitor Cells

B. Péault, J. Hinnrasky, I. Casal, 2005, Stem cells.

Epithelial barrier integrity during in vitro wound repair of the airway epithelium.

J. Zahm, D. Pierrot, C. Fuchey, 1996, American journal of respiratory cell and molecular biology.

Pseudomonas Aeruginosa Virulence Factors Delay Airway Epithelial Wound Repair by Altering the Actin Cytoskeleton and Inducing Overactivation of Epithelial Matrix Metalloproteinase–2

J. Klossek, J. Zahm, M. Polette, 2000, Laboratory Investigation.

Proliferation, differentiation and ciliary beating of human respiratory ciliated cells in primary culture

M. Plotkowski, J. Zahm, M. Chevillard, 1991, Cell and Tissue Research.

Polarized Expression of Cystic Fibrosis Transmembrane Conductance Regulator and Associated Epithelial Proteins during the Regeneration of Human Airway Surface Epithelium in Three-Dimensional Culture

Edith Puchelle, Bruno Péault, J. Klossek, 2002, Laboratory Investigation.

Tubule formation and functional differentiation by human epithelial respiratory cells cultured in a three-dimensional collagen matrix.

J. Klossek, J. Zahm, M. Chevillard, 1992, Chest.

Ultrastructural localization of bronchial inhibitor in human airways using protein A‐gold technique

J. Tournier, J. Adnet, J. Hinnrasky, 1985, Biology of the cell.

Quantitation of in vitro ciliated cell growth through image analysis

J. Zahm, M. Chevillard, D. Pierrot, 1990, In Vitro Cellular & Developmental Biology.

Selective up-regulation of chemokine IL-8 expression in cystic fibrosis bronchial gland cells in vivo and in vitro.

J. Zahm, M. Guenounou, M. Guenounou, 1998, The American journal of pathology.

Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium.

A. Pavirani, M. Boutterin, D. Gaillard, 1992, American journal of respiratory cell and molecular biology.

Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands.

A. Pavirani, D. Dreyer, C. Fuchey, 1993, The European respiratory journal.

Immunocytochemical analysis reveals differences between the subcellular localization of normal and delta Phe508 recombinant cystic fibrosis transmembrane conductance regulator.

A. Pavirani, P. Slos, W. Dalemans, 1992, Experimental cell research.

Early expression of beta- and gamma-subunits of epithelial sodium channel during human airway development.

P. Barbry, M. Matthay, S. Coscoy, 2000, American journal of physiology. Lung cellular and molecular physiology.

A change in gating mode leading to increased intrinsic Cl‐ channel activity compensates for defective processing in a cystic fibrosis mutant corresponding to a mild form of the disease.

V. Gribkoff, M. Lazdunski, P. Barbry, 1995, The EMBO journal.

Tubule formation by human surface respiratory epithelial cells cultured in a three-dimensional collagen lattice.

J. Klossek, J. Zahm, J. Tournier, 1993, The American journal of physiology.

Decreased expression of the CFTR protein in remodeled human nasal epithelium from non-cystic fibrosis patients.

B. Tümmler, S. Brézillon, F. Dupuit, 1995, Laboratory investigation; a journal of technical methods and pathology.

ATP Depletion Induces a Loss of Respiratory Epithelium Functional Integrity and Down-regulates CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) Expression*

J. Klossek, J. Zahm, B. Tümmler, 1997, The Journal of Biological Chemistry.

Expression of gelatinase A, a mediator of extracellular matrix remodeling, by tracheal gland serous cells in culture and in vivo.

Z. Werb, M. Polette, J. Tournier, 1994, The Journal of biological chemistry.

Immunocytochemical demonstration of quantitative differences in the distribution of lysozyme in human airway secretory granule phenotypes

M. Chevillard, J. Hinnrasky, É. Puchelle, 1990, Biology of the cell.

Embryonic stem cells generate airway epithelial tissue.

C. Dani, B. Nawrocki-Raby, D. Gaillard, 2005, American journal of respiratory cell and molecular biology.

Semi-automatic quantitation of dense markers in cytochemistry

S. Lebonvallet, N. Bonnet, J. Hinnrasky, 2004, Histochemistry.

Immunohistochemistry of CFTR in native tissues and primary epithelial cell cultures.

C. Férec, M. Amaral, D. Penque, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Immunohistochemical Localization of Cystic Fibrosis Transmembrane Conductance Regulator in Human Fetal Airway and Digestive Mucosa

D. Gaillard, W. Dalemans, J. Hinnrasky, 1994, Pediatric Research.

Cell Wall-associated Protein A as a Tool for Immunolocalization of Staphylococcus aureus in Infected Human Airway Epithelium

E. Mongodin, S. de Bentzmann, O. Bajolet, 2000, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Decreased expression of the cystic fibrosis transmembrane conductance regulator protein in remodeled airway epithelium from lung transplanted patients.

B. Tümmler, T. Wagner, S. Brézillon, 1997, Human pathology.

CFTR is involved in membrane endocytosis but not in fluid-phase and receptor-mediated endocytosis in human respiratory epithelial cells.

J. Zahm, J. Kuhry, J. Jacquot, 1996, Biochemical and biophysical research communications.

Fibronectin and its α5β1-integrin receptor are involved in the wound-repair process of airway epithelium

J. Zahm, H. Kaplan, D. Sheppard, 1996 .

Quantitative X‐ray microanalysis of P, Ca, and S in the mucus secretory granules of the cryofixed frog palate epithelium

G. Balossier, D. Wagner, J. Hinnrasky, 1994, Microscopy research and technique.

Induction of a cAMP-stimulated chloride secretion in regenerating poorly differentiated airway epithelial cells by adenovirus-mediated CFTR gene transfer.

J. Zahm, H. Kaplan, F. Dupuit, 1997, Human gene therapy.

CFTRandDifferentiation Markers Expression inNon-CFandAF 508 Homozygous CFNasalEpithelium

B. Tümmler, S. Brézillon, F. Dupuit, 1995 .

Stimulation of β2-Adrenergic Receptor Increases Cystic Fibrosis Transmembrane Conductance Regulator Expression in Human Airway Epithelial Cells through a cAMP/Protein Kinase A-independent Pathway*

J. Klossek, P. Corlieu, K. Taouil, 2003, The Journal of Biological Chemistry.

Functional activity of ciliated outgrowths from cultured human nasal and tracheal epithelia.

J. Zahm, M. Chevillard, D. Pierrot, 1990, Biorheology.