Works by Mall, Marcus A.
Results: 183
Intestinal current measurement detects age-dependent differences in CFTR function in rectal epithelium.
- Published in:
- Frontiers in Pharmacology, 2025, p. 1, doi. 10.3389/fphar.2025.1537095
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- Publication type:
- Article
Reply to Martin and Grasemann: Is There a Role for Lumacaftor/Ivacaftor in Young Children with Cystic Fibrosis?
- Published in:
- Annals of the American Thoracic Society, 2025, v. 22, n. 3, p. 469, doi. 10.1513/AnnalsATS.202411-1237LE
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- Publication type:
- Article
BPIFB1 (LPLUNC1) is upregulated in cystic fibrosis lung disease.
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- Histochemistry & Cell Biology, 2012, v. 138, n. 5, p. 749, doi. 10.1007/s00418-012-0990-8
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- Publication type:
- Article
Mesenchymal stromal cells reduce inflammation and improve lung function in a mouse model of cystic fibrosis lung disease.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-81276-3
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- Publication type:
- Article
Role of the SLC26A9 Chloride Channel as Disease Modifier and Potential Therapeutic Target in Cystic Fibrosis.
- Published in:
- Frontiers in Pharmacology, 2018, p. N.PAG, doi. 10.3389/fphar.2018.01112
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- Publication type:
- Article
The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia.
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- PLoS ONE, 2020, v. 15, n. 3, p. 1, doi. 10.1371/journal.pone.0230252
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- Publication type:
- Article
Analysis of Severe Acute Respiratory Syndrome 2 Replication in Explant Cultures of the Human Upper Respiratory Tract Reveals Broad Tissue Tropism of Wild-Type and B.1.1.7 Variant Viruses.
- Published in:
- 2021
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- Publication type:
- journal article
Computerized image analysis of iron-stained macrophages.
- Published in:
- Annals of Hematology, 2013, v. 92, n. 9, p. 1195, doi. 10.1007/s00277-013-1740-2
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- Publication type:
- Article
Control of ion transport in mammalian airways by protease activated receptors type 2 (PAR-2).
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- FASEB Journal, 2005, v. 19, n. 8, p. 969, doi. 10.1096/fj.04-2469fje
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- Publication type:
- Article
Nanoparticle uptake by airway phagocytes after fungal spore challenge in murine allergic asthma and chronic bronchitis.
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- BMC Pulmonary Medicine, 2014, v. 14, n. 1, p. 116, doi. 10.1186/1471-2466-14-116
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- Publication type:
- Article
Nanoparticle uptake by airway phagocytes after fungal spore challenge in murine allergic asthma and chronic bronchitis.
- Published in:
- 2014
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- Publication type:
- journal article
Control of epithelial Na<sup>+</sup> conductance by the cystic fibrosis transmembrane conductance regulator.
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- Pflügers Archiv: European Journal of Physiology, 2000, v. 440, n. 2, p. 193, doi. 10.1007/s004240000255
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- Publication type:
- Article
The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl<sup>-</sup> concentration.
- Published in:
- EMBO Reports, 2001, v. 2, n. 11, p. 1047, doi. 10.1093/embo-reports/kve232
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- Publication type:
- Article
Management of Busulfan-Induced Lung Injury in Pediatric Patients with High-Risk Neuroblastoma.
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- Journal of Clinical Medicine, 2024, v. 13, n. 19, p. 5995, doi. 10.3390/jcm13195995
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- Publication type:
- Article
Longitudinal Magnetic Resonance Imaging of Changes in Lung Morphology and Perfusion in Children with Cystic Fibrosis from Infancy through Adolescence.
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- Annals of the American Thoracic Society, 2025, v. 22, n. 1, p. 93, doi. 10.1513/AnnalsATS.202404-396OC
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- Publication type:
- Article
Long-Term Impact of Lumacaftor/Ivacaftor Treatment on Cystic Fibrosis Disease Progression in Children 2–5 Years of Age Homozygous for F508del-CFTR : A Phase 2, Open-Label Clinical Trial.
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- Annals of the American Thoracic Society, 2024, v. 21, n. 11, p. 1550, doi. 10.1513/AnnalsATS.202402-201OC
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- Publication type:
- Article
Magnetic Resonance Imaging of Pulmonary and Paranasal Sinus Abnormalities in Children with Primary Ciliary Dyskinesia Compared to Children with Cystic Fibrosis.
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- Annals of the American Thoracic Society, 2024, v. 21, n. 3, p. 438, doi. 10.1513/AnnalsATS.202305-453OC
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- Publication type:
- Article
Elexacaftor/Tezacaftor/Ivacaftor Improves Bronchial Artery Dilatation Detected by Magnetic Resonance Imaging in Patients with Cystic Fibrosis.
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- Annals of the American Thoracic Society, 2023, v. 20, n. 11, p. 1595, doi. 10.1513/AnnalsATS.202302-168OC
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- Publication type:
- Article
Effects of Lumacaftor/Ivacaftor on Cystic Fibrosis Disease Progression in Children 2 through 5 Years of Age Homozygous for F508del-CFTR: A Phase 2 Placebo-controlled Clinical Trial.
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- Annals of the American Thoracic Society, 2023, v. 20, n. 8, p. 1144, doi. 10.1513/AnnalsATS.202208-684OC
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- Publication type:
- Article
Longitudinal Magnetic Resonance Imaging Detects Onset and Progression of Chronic Rhinosinusitis from Infancy to School Age in Cystic Fibrosis.
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- Annals of the American Thoracic Society, 2023, v. 20, n. 5, p. 687, doi. 10.1513/AnnalsATS.202209-763OC
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- Publication type:
- Article
Effects of Lumacaftor-Ivacaftor on Lung Clearance Index, Magnetic Resonance Imaging, and Airway Microbiome in Phe508del Homozygous Patients with Cystic Fibrosis.
- Published in:
- 2021
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- Publication type:
- journal article
Magnetic Resonance Imaging Detects Chronic Rhinosinusitis in Infants and Preschool Children with Cystic Fibrosis.
- Published in:
- 2020
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- Publication type:
- journal article
Emerging Concepts and Therapies for Mucoobstructive Lung Disease.
- Published in:
- 2018
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- Publication type:
- journal article
Unplugging Mucus in Cystic Fibrosis and Chronic Obstructive Pulmonary Disease.
- Published in:
- 2016
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- Publication type:
- journal article
Cellular distribution and function of ion channels involved in transport processes in rat tracheal epithelium.
- Published in:
- Physiological Reports, 2017, v. 5, n. 12, p. n/a, doi. 10.14814/phy2.13290
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- Publication type:
- Article
Potential of Intestinal Current Measurement for Personalized Treatment of Patients with Cystic Fibrosis.
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- Journal of Personalized Medicine, 2021, v. 11, n. 5, p. 384, doi. 10.3390/jpm11050384
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- Publication type:
- Article
Changes in Microbiome Dominance Are Associated With Declining Lung Function and Fluctuating Inflammation in People With Cystic Fibrosis.
- Published in:
- Frontiers in Microbiology, 2022, v. 13, p. 1, doi. 10.3389/fmicb.2022.885822
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- Publication type:
- Article
FRET-based and other fluorescent proteinase probes.
- Published in:
- Biotechnology Journal, 2014, v. 9, n. 2, p. 266, doi. 10.1002/biot.201300201
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- Publication type:
- Article
Spatially Resolved Monitoring of Neutrophil Elastase Activity with Ratiometric Fluorescent Reporters.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 25, p. 6258, doi. 10.1002/anie.201109226
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- Publication type:
- Article
Airway Mucus Obstruction Triggers Macrophage Activation and Matrix Metalloproteinase 12-Dependent Emphysema.
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- American Journal of Respiratory Cell & Molecular Biology, 2014, v. 51, n. 5, p. 709, doi. 10.1165/rcmb.2013-0407OC
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- Publication type:
- Article
Hypertonic Saline Is Effective in the Prevention and Treatment of Mucus Obstruction, but Not Airway Inflammation, in Mice with Chronic Obstructive Lung Disease.
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- American Journal of Respiratory Cell & Molecular Biology, 2013, v. 49, n. 3, p. 410, doi. 10.1165/rcmb.2013-0050OC
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- Publication type:
- Article
mCLCA3 Does Not Contribute to Calcium-Activated Chloride Conductance in Murine Airways.
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- American Journal of Respiratory Cell & Molecular Biology, 2012, v. 47, n. 1, p. 87, doi. 10.1165/rcmb.2010-0508OC
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- Publication type:
- Article
Use of a New-Generation Reverse Tetracycline Transactivator System for Quantitative Control of Conditional Gene Expression in the Murine Lung.
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- American Journal of Respiratory Cell & Molecular Biology, 2011, v. 44, n. 2, p. 244, doi. 10.1165/rcmb.2009-0115OC
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- Publication type:
- Article
Use of a new generation reverse tetracycline transactivator system for quantitative control of conditional gene expression in the murine lung.
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- American Journal of Respiratory Cell & Molecular Biology, 2011, v. 44, n. 2, p. 1, doi. 10.1165/rcmb.2009-0115oc
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- Publication type:
- Article
Modelling Dysregulated Na<sup>+</sup> Absorption in Airway Epithelial Cells with Mucosal Nystatin Treatment.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2008, v. 38, n. 4, p. 423, doi. 10.1165/rcmb.2007-0177OC
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- Publication type:
- Article
Inhibition of Amiloride-Sensitive Epithelial Na<sup>+</sup> Absorption by Extracellular Nucleotides in Human Normal and Cystic Fibrosis Airways.
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- American Journal of Respiratory Cell & Molecular Biology, 2000, v. 23, n. 6, p. 755, doi. 10.1165/ajrcmb.23.6.4207
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- Publication type:
- Article
Role of K<sub>V</sub>LQT1 in Cyclic Adenosine Monophosphate-Mediated Cl<sup>-</sup> Secretion in Human Airway Epithelia.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2000, v. 23, n. 3, p. 283, doi. 10.1165/ajrcmb.23.3.4060
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- Publication type:
- Article
Lentiviral Gene Therapy for Cystic Fibrosis: A Promising Approach and First-in-Human Trial.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2024, v. 210, n. 12, p. 1398, doi. 10.1164/rccm.202402-0389CI
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- Publication type:
- Article
Depression Symptoms in Patients with Cystic Fibrosis Fluctuate at Baseline and Improve with Elexacaftor/Tezacaftor/Ivacaftor Therapy.
- Published in:
- 2024
- By:
- Publication type:
- Letter to the Editor
Pharmacological Improvement of Cystic Fibrosis Transmembrane Conductance Regulator Function Rescues Airway Epithelial Homeostasis and Host Defense in Children with Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2024, v. 209, n. 11, p. 1338, doi. 10.1164/rccm.202310-1836OC
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- Publication type:
- Article
Elexacaftor/Tezacaftor/Ivacaftor Treatment and Depression-related Events.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2024, v. 209, n. 3, p. 299, doi. 10.1164/rccm.202308-1525OC
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- Publication type:
- Article
Phase 3 Open-Label Clinical Trial of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged 2–5 Years with Cystic Fibrosis and at Least One F508del Allele.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2023, v. 208, n. 1, p. 59, doi. 10.1164/rccm.202301-0084OC
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- Publication type:
- Article
Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for and a Minimal Function Mutation: A Phase 3b, Randomized, Placebo-controlled Study.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 206, n. 11, p. 1361, doi. 10.1164/rccm.202202-0392OC
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- Publication type:
- Article
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two Alleles.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 205, n. 5, p. E1, doi. 10.1164/rccm.202110-2249oc
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- Publication type:
- Article
Reply to Dournes .: Contrast-enhanced Magnetic Resonance Imaging Does Not Detect a Progression in Lung Morphological Score in Preschool Children with Cystic Fibrosis.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Magnetic Resonance Imaging Detects Progression of Lung Disease and Impact of Newborn Screening in Preschool Children with Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2021, v. 204, n. 8, p. E1, doi. 10.1164/rccm.202102-0278oc
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- Publication type:
- Article
Magnetic Resonance Imaging Detects Progression of Lung Disease and Impact of Newborn Screening in Preschool Children with Cystic Fibrosis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One Allele.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor for 24 Weeks or Longer in People with Cystic Fibrosis and One or More Alleles: Interim Results of an Open-Label Phase 3 Clinical Trial.
- Published in:
- 2021
- By:
- Publication type:
- clinical trial