Related references
Note: Only part of the references are listed.Genetic variants of small airways and interstitial pulmonary disease in children
Mohammed T. Alsamri et al.
SCIENTIFIC REPORTS (2021)
Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
Gregory Costain et al.
JAMA NETWORK OPEN (2020)
Muco-Obstructive Lung Diseases
Richard C. Boucher
NEW ENGLAND JOURNAL OF MEDICINE (2019)
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis
Brian D. Hobbs et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2019)
Airway Mucus Hyperconcentration in Non-Cystic Fibrosis Bronchiectasis
Kathryn A Ramsey et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2019)
Localization of Secretory Mucins MUC5AC and MUC5B in Normal/Healthy Human Airways
Kenichi Okuda et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2019)
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
Anath C. Lionel et al.
GENETICS IN MEDICINE (2018)
E-Cigarette Use Causes a Unique Innate Immune Response in the Lung, Involving Increased Neutrophilic Activation and Altered Mucin Secretion
Boris Reidel et al.
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2018)
MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease
P. -A. Juge et al.
NEW ENGLAND JOURNAL OF MEDICINE (2018)
Airway Mucin Concentration as a Marker of Chronic Bronchitis
Mehmet Kesimer et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
Reduced mucociliary clearance in old mice is associated with a decrease in Muc5b mucin
Barbara R. Grubb et al.
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek et al.
NATURE (2016)
Duration of action of hypertonic saline on mucociliary clearance in the normal lung
W. D. Bennett et al.
JOURNAL OF APPLIED PHYSIOLOGY (2015)
Salivary Mucins Protect Surfaces from Colonization by Cariogenic Bacteria
Erica Shapiro Frenkel et al.
APPLIED AND ENVIRONMENTAL MICROBIOLOGY (2015)
Impact of Different Etiologies of Bronchiectasis on the Pulmonary Function Tests
Agnaldo Jose Lopes et al.
CLINICAL MEDICINE & RESEARCH (2015)
Muc5b is required for airway defence
Michelle G. Roy et al.
NATURE (2014)
MUC5B Promoter Polymorphism and Interstitial Lung Abnormalities
Gary M. Hunninghake et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
A Common MUC5B Promoter Polymorphism and Pulmonary Fibrosis
Max A. Seibold et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
MEDICAL PROGRESS Airway Mucus Function and Dysfunction
John V. Fahy et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
A physical linkage between cystic fibrosis airway surface dehydration and Pseudomonas aeruginosa biofilms
Hirotoshi Matsui et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Mucus clearance and lung function in cystic fibrosis with hypertonic saline
SH Donaldson et al.
NEW ENGLAND JOURNAL OF MEDICINE (2006)
Mucus properties in children with primary ciliary dyskinesia - Comparison with cystic fibrosis
A Bush et al.
CHEST (2006)
Share Paper
