"Mucin-5B" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A gel-forming mucin that is predominantly expressed by submucosal glands of airway tissues and the SUBLINGUAL GLAND. It is one of the principal components of high molecular weight salivary mucin.
| Descriptor ID |
D055257
|
| MeSH Number(s) |
D12.644.848.750 D12.776.395.560.631.207 D12.776.850.850
|
| Concept/Terms |
Mucin-5B- Mucin-5B
- Mucin 5B
- Mucin-5 Subtype B, Tracheobronchial
- Mucin 5 Subtype B, Tracheobronchial
- High Molecular Weight Salivary Mucin MG1
|
Below are MeSH descriptors whose meaning is more general than "Mucin-5B".
Below are MeSH descriptors whose meaning is more specific than "Mucin-5B".
This graph shows the total number of publications written about "Mucin-5B" by people in this website by year, and whether "Mucin-5B" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 1 | 2 |
| 2016 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 4 | 1 | 5 |
| 2022 | 0 | 1 | 1 |
| 2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucin-5B" by people in Profiles.
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Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine. Am J Respir Crit Care Med. 2024 Aug 15; 210(4):401-423.
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MUC5B, telomere length and longitudinal quantitative interstitial lung changes: the MESA Lung Study. Thorax. 2023 06; 78(6):566-573.
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MUC5B promoter variant: genomic fingerprint for early identification of undiagnosed pulmonary fibrosis. Thorax. 2019 12; 74(12):1111-1112.
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MUC5B variant is associated with visually and quantitatively detected preclinical pulmonary fibrosis. Thorax. 2019 12; 74(12):1131-1139.
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Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2019 07 15; 200(2):199-208.
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Telomere length and genetic variant associations with interstitial lung disease progression and survival. Eur Respir J. 2019 04; 53(4).
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Integrating Genomics Into Management of Fibrotic Interstitial Lung Disease. Chest. 2019 05; 155(5):1026-1040.
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Inflammatory signature in lung tissues in patients with combined pulmonary fibrosis and emphysema. Biomarkers. 2019 May; 24(3):232-239.
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CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism. Chest. 2016 05; 149(5):1215-22.
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TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2015 Dec 15; 192(12):1475-82.