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Publications by Lauren N. Meiss

Hyper-Osmolarity and Calcium Chelation: Effects on Cystic Fibrosis Mucus

European Journal of Pharmacology

English

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Is Cystic Fibrosis Mucus Abnormal?

Pediatric Research

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Development of an Airway Mucus Defect in the Cystic Fibrosis Rat

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Cystic Fibrosis Mice Lacking Muc1 Have Reduced Amounts of Intestinal Mucus.

Journal of Clinical Investigation

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Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators Have Differential Effects on Cystic Fibrosis Macrophage Function

Scientific Reports

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Mucus Accumulation in the Lungs Precedes Structural Changes and Infection in Children With Cystic Fibrosis

Science Translational Medicine

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Cystic Fibrosis and Myocardial Fibrosis.

Archives of Disease in Childhood

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Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction in Chronic Bronchitis and Other Diseases of Mucus Clearance

Clinics in Chest Medicine

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Synergistic Effects of cAMP- And Calcium-Mediated Amylase Secretion in Isolated Pancreatic Acini From Cystic Fibrosis Mice

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Cystic Fibrosis. 7. Management of Cystic Fibrosis in Different Countries. Cystic Fibrosis in Melbourne.

Respiratory Medicine

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