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Publications by Philip H. Karp
Loss of Anion Transport Without Increased Sodium Absorption Characterizes Newborn Porcine Cystic Fibrosis Airway Epithelia
Cell
Biochemistry
Genetics
Molecular Biology
Chemosensory Functions for Pulmonary Neuroendocrine Cells
American Journal of Respiratory Cell and Molecular Biology
Respiratory Medicine
Pulmonary
Clinical Biochemistry
Cell Biology
Molecular Biology
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In Vivo Analysis of Fluid Transport in Cystic Fibrosis Airway Epithelia of Bronchial Xenografts
American Journal of Physiology - Cell Physiology
Physiology
Cell Biology
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Thymosin Α-1 Does Not Correct F508del-CFTR in Cystic Fibrosis Airway Epithelia
JCI insight
Medicine
Cystic Fibrosis Airway Secretions Exhibit Mucin Hyperconcentration and Increased Osmotic Pressure
Journal of Clinical Investigation
Medicine
Bypassing CFTR Dysfunction in Cystic Fibrosis With Alternative Pathways for Anion Transport
Current Opinion in Pharmacology
Drug Discovery
Pharmacology
Chlorzoxazone or 1-Ebio Increases Na+absorption Across Cystic Fibrosis Airway Epithelial Cells
American Journal of Physiology - Lung Cellular and Molecular Physiology
Pulmonary
Respiratory Medicine
Physiology
Cell Biology
Cystic Fibrosis Screening in the Newborn.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Characteristics of Cystic Fibrosis Patients Diagnosed After False Negative Cystic Fibrosis Newborn Screening Results
Turkish Thoracic Journal
Pulmonary
Respiratory Medicine
Exercise Reduces Airway Sodium Ion Reabsorption in Cystic Fibrosis but Not in Exercise Asthma
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine