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Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection

Journal of leukocyte biology, 2012-11, Vol.92 (5), p.1111-1122

2012

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A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis

Diabetologia, 2009-09, Vol.52 (9), p.1858-1865

2009

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Understanding the population structure of North American patients with cystic fibrosis

Clinical genetics, 2011-02, Vol.79 (2), p.136-146

2011

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Genetic Modifiers of Lung Disease in Cystic Fibrosis

The New England journal of medicine, 2005-10, Vol.353 (14), p.1443-1453

2005

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Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping

Science (American Association for the Advancement of Science), 1989-09, Vol.245 (4922), p.1059-1065

1989

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Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter

The Journal of biological chemistry, 1993-02, Vol.268 (5), p.3781-3790

1993

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Modulation of cystic fibrosis lung disease by variants in interleukin-8

Genes and immunity, 2008-09, Vol.9 (6), p.501-508

2008

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Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells

The Journal of clinical investigation, 1998-09, Vol.102 (6), p.1200-1207

1998

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CFTR-mediated chloride permeability is regulated by type III phosphodiesterases in airway epithelial cells

American journal of respiratory cell and molecular biology, 1995-12, Vol.13 (6), p.657-664

1995

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Pitfall in the use of genotype analysis as the sole diagnostic criterion for cystic fibrosis

Pediatrics (Evanston), 1999-04, Vol.103 (4 Pt 1), p.823-826

1999

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The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice

Journal of medical genetics, 2006-06, Vol.43 (6), p.e29-e29

2006

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Modifier genes and variation in cystic fibrosis

Respiratory research, 2001-01, Vol.2 (3), p.125-128, Article 125

Drumm, M L

2001

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Genetic variation and clinical heterogeneity in cystic fibrosis

Annual review of pathology, 2012-01, Vol.7 (1), p.267-282

2012

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Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

Science (American Association for the Advancement of Science), 1989-09, Vol.245 (4922), p.1066-1073

1989

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Rectification of whole cell cystic fibrosis transmembrane conductance regulator chloride current

American Journal of Physiology: Cell Physiology, 1995-03, Vol.268 (3), p.C636-C646

1995

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Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs in Xenopus Oocytes

Science (American Association for the Advancement of Science), 1991-12, Vol.254 (5039), p.1797-1799

1991

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Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4792), p.1046-1049

1987

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In vivo Activation of the Cystic Fibrosis Transmembrane Conductance Regulator Mutant Δ F508 in Murine Nasal Epithelium

Proceedings of the National Academy of Sciences - PNAS, 1997-03, Vol.94 (6), p.2604-2608

1997

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Chromosome Jumping from D4S10 (G8) toward the Huntington Disease Gene

Proceedings of the National Academy of Sciences - PNAS, 1988-09, Vol.85 (17), p.6437-6441

1988

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3849+10 kb C→T mutation and disease severity in cystic fibrosis

The Lancet (British edition), 1995-07, Vol.346 (8970), p.274-276

1995

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Examining basal chloride transport using the nasal potential difference response in a murine model

American journal of physiology. Lung cellular and molecular physiology, 2001-11, Vol.281 (5), p.1173-L1179

2001

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Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Anion Binding as a Probe of the Pore

Biophysical journal, 1998-03, Vol.74 (3), p.1320-1332

1998

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Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8

American journal of human genetics, 1989-05, Vol.44 (5), p.695-703

1989

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A31 MECHANISMS IN CYSTIC FIBROSIS AND OTHER BRONCHIECTATIC DISEASES: Integrative Transcriptomic And Genomic Analysis Reveals Gene Networks Associated With Cystic Fibrosis Lung Disease Severity

American journal of respiratory and critical care medicine, 2017-01, Vol.195

2017

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Nitric oxide-mediated regulation of transepithelial sodium and chloride transport in murine nasal epithelium

American journal of physiology. Lung cellular and molecular physiology, 1999-03, Vol.276 (3), p.466-L473

1999

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Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection

A susceptibility gene for type 2 diabetes confers substantial risk for diabetes complicating cystic fibrosis

Understanding the population structure of North American patients with cystic fibrosis

Genetic Modifiers of Lung Disease in Cystic Fibrosis

Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping

Expression of the cystic fibrosis transmembrane conductance regulator from a novel adeno-associated virus promoter

Modulation of cystic fibrosis lung disease by variants in interleukin-8

Inducible nitric oxide synthase expression is reduced in cystic fibrosis murine and human airway epithelial cells

CFTR-mediated chloride permeability is regulated by type III phosphodiesterases in airway epithelial cells

Pitfall in the use of genotype analysis as the sole diagnostic criterion for cystic fibrosis

The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice

Modifier genes and variation in cystic fibrosis

Genetic variation and clinical heterogeneity in cystic fibrosis

Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

Rectification of whole cell cystic fibrosis transmembrane conductance regulator chloride current

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs in Xenopus Oocytes

Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis

In vivo Activation of the Cystic Fibrosis Transmembrane Conductance Regulator Mutant Δ F508 in Murine Nasal Epithelium

Chromosome Jumping from D4S10 (G8) toward the Huntington Disease Gene

3849+10 kb C→T mutation and disease severity in cystic fibrosis

Examining basal chloride transport using the nasal potential difference response in a murine model

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Anion Binding as a Probe of the Pore

Isolation of additional polymorphic clones from the cystic fibrosis region, using chromosome jumping from D7S8

A31 MECHANISMS IN CYSTIC FIBROSIS AND OTHER BRONCHIECTATIC DISEASES: Integrative Transcriptomic And Genomic Analysis Reveals Gene Networks Associated With Cystic Fibrosis Lung Disease Severity

Nitric oxide-mediated regulation of transepithelial sodium and chloride transport in murine nasal epithelium

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