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Antimicrobial Activity of Murine Lung Cells against Staphylococcus aureus Is Increased In Vitro and In Vivo after Elafin Gene Transfer

Infection and Immunity, 2005-06, Vol.73 (6), p.3609-3617

2005

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Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Gene therapy, 1997-03, Vol.4 (3), p.210-218

1997

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Evidence for stem-cell niches in the tracheal epithelium

American journal of respiratory cell and molecular biology, 2001-06, Vol.24 (6), p.662-670

2001

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Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

Nature genetics, 1993-10, Vol.5 (2), p.135-142

1993

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A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction

Gene therapy, 1996-09, Vol.3 (9), p.797

1996

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

American Journal of Physiology: Cell Physiology, 1997-03, Vol.272 (3), p.C853-C859

1997

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Rapid sequence divergence in mammalian β-defensins by adaptive evolution

Molecular immunology, 2003-11, Vol.40 (7), p.413-421

2003

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Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis

The European respiratory journal, 1997-09, Vol.10 (9), p.2018-2022

1997

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CFTR and calcium-activated chloride currents in pancreatic duct cells of a transgenic CF mouse

American Journal of Physiology: Cell Physiology, 1994-01, Vol.266 (1), p.C213-C221

1994

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Expression pattern of two related cystic fibrosis-associated calcium-binding proteins in normal and abnormal tissues

Journal of cell science, 1988-10, Vol.91 (2), p.221-230

1988

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Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAP

Gene therapy, 1996-12, Vol.3 (12), p.1113

1996

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Development of mouse models for cystic fibrosis

Journal of inherited metabolic disease, 1995-07, Vol.18 (4), p.495-500

Dorin, J. R.

1995

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Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens

Nature genetics, 1995-04, Vol.9 (4), p.351-357

1995

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Cystic fibrosis in the mouse by targeted insertional mutagenesis

Nature (London), 1992-09, Vol.359 (6392), p.211-215

1992

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Importance of -defensins in sperm function

Molecular human reproduction, 2014-09, Vol.20 (9), p.821-826

2014

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Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humans

American Journal of Physiology: Cell Physiology, 1995-02, Vol.268 (2), p.C297-C307

1995

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Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype‐phenotype correlations

The EMBO journal, 1996-03, Vol.15 (5), p.955-963

1996

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A mouse model of intestinal stem cell function and regeneration

Journal of cell science, 1999-09, Vol.112 Pt 18 (18), p.3029-3038

1999

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Evaluation in vitro and in vivo of cationic liposome-expression construct complexes for cystic fibrosis gene therapy

Gene therapy, 1995-11, Vol.2 (9), p.614

1995

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A clue to the basic defect in cystic fibrosis from cloning the CF antigen gene

Nature (London), 1987-04, Vol.326 (6113), p.614-617

1987

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The changing of the guard: Molecular diversity and rapid evolution of beta-defensins

Molecular diversity, 2006-11, Vol.10 (4), p.575-584

2006

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Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Nature medicine, 1995-01, Vol.1 (1), p.39-46

1995

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Selection for Precise Chromosomal Targeting of a Dominant Marker by Homologous Recombination

Science (American Association for the Advancement of Science), 1989-03, Vol.243 (4896), p.1357-1360

1989

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Signal sequence conservation and mature peptide divergence within subgroups of the murine beta-defensin gene family

Molecular biology and evolution, 2003-03, Vol.20 (3), p.460-470

2003

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Gene therapy for cystic fibrosis in humans by liposome-mediated DNA transfer: the production of resources and the regulatory process

Gene therapy, 1994-03, Vol.1 (2), p.139

1994

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Antimicrobial Activity of Murine Lung Cells against Staphylococcus aureus Is Increased In Vitro and In Vivo after Elafin Gene Transfer

Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Evidence for stem-cell niches in the tracheal epithelium

Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction

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

Rapid sequence divergence in mammalian β-defensins by adaptive evolution

Correlation between nasal potential difference measurements, genotype and clinical condition in patients with cystic fibrosis

CFTR and calcium-activated chloride currents in pancreatic duct cells of a transgenic CF mouse

Expression pattern of two related cystic fibrosis-associated calcium-binding proteins in normal and abnormal tissues

Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAP

Development of mouse models for cystic fibrosis

Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens

Cystic fibrosis in the mouse by targeted insertional mutagenesis

Importance of -defensins in sperm function

Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humans

Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype‐phenotype correlations

A mouse model of intestinal stem cell function and regeneration

Evaluation in vitro and in vivo of cationic liposome-expression construct complexes for cystic fibrosis gene therapy

A clue to the basic defect in cystic fibrosis from cloning the CF antigen gene

The changing of the guard: Molecular diversity and rapid evolution of beta-defensins

Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

Selection for Precise Chromosomal Targeting of a Dominant Marker by Homologous Recombination

Signal sequence conservation and mature peptide divergence within subgroups of the murine beta-defensin gene family

Gene therapy for cystic fibrosis in humans by liposome-mediated DNA transfer: the production of resources and the regulatory process

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