Cystic Fibrosis
"Cystic Fibrosis" 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.
An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
Descriptor ID |
D003550
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MeSH Number(s) |
C06.689.202 C08.381.187 C16.320.190 C16.614.213
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Concept/Terms |
Pancreatic Cystic Fibrosis- Pancreatic Cystic Fibrosis
- Cystic Fibrosis, Pancreatic
- Fibrocystic Disease of Pancreas
- Pancreas Fibrocystic Disease
- Pancreas Fibrocystic Diseases
- Cystic Fibrosis of Pancreas
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Below are MeSH descriptors whose meaning is more general than "Cystic Fibrosis".
Below are MeSH descriptors whose meaning is more specific than "Cystic Fibrosis".
This graph shows the total number of publications written about "Cystic Fibrosis" by people in this website by year, and whether "Cystic Fibrosis" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1980 | 3 | 0 | 3 | 1981 | 3 | 0 | 3 | 1982 | 2 | 0 | 2 | 1983 | 5 | 0 | 5 | 1984 | 5 | 0 | 5 | 1985 | 3 | 0 | 3 | 1986 | 10 | 0 | 10 | 1987 | 5 | 1 | 6 | 1988 | 7 | 1 | 8 | 1989 | 9 | 0 | 9 | 1990 | 9 | 2 | 11 | 1991 | 9 | 1 | 10 | 1992 | 8 | 1 | 9 | 1993 | 7 | 2 | 9 | 1994 | 3 | 1 | 4 | 1995 | 3 | 1 | 4 | 1996 | 6 | 1 | 7 | 1997 | 7 | 1 | 8 | 1998 | 8 | 0 | 8 | 1999 | 13 | 1 | 14 | 2000 | 11 | 3 | 14 | 2001 | 10 | 2 | 12 | 2002 | 16 | 3 | 19 | 2003 | 12 | 0 | 12 | 2004 | 13 | 3 | 16 | 2005 | 22 | 0 | 22 | 2006 | 22 | 1 | 23 | 2007 | 17 | 2 | 19 | 2008 | 14 | 4 | 18 | 2009 | 21 | 2 | 23 | 2010 | 16 | 5 | 21 | 2011 | 22 | 4 | 26 | 2012 | 30 | 1 | 31 | 2013 | 33 | 3 | 36 | 2014 | 33 | 0 | 33 | 2015 | 42 | 1 | 43 | 2016 | 23 | 5 | 28 | 2017 | 32 | 4 | 36 | 2018 | 28 | 1 | 29 | 2019 | 27 | 2 | 29 | 2020 | 16 | 4 | 20 |
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Below are the most recent publications written about "Cystic Fibrosis" by people in Profiles.
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Dang H, Polineni D, Pace RG, Stonebraker JR, Corvol H, Cutting GR, Drumm ML, Strug LJ, O'Neal WK, Knowles MR. Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation. PLoS One. 2020; 15(11):e0239189.
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Panjwani N, Wang F, Mastromatteo S, Bao A, Wang C, He G, Gong J, Rommens JM, Sun L, Strug LJ. LocusFocus: Web-based colocalization for the annotation and functional follow-up of GWAS. PLoS Comput Biol. 2020 10; 16(10):e1008336.
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Stanojevic S, Filipow N, Ratjen F. Paediatric reproducibility limits for the forced expiratory volume in 1 s. Thorax. 2020 10; 75(10):891-896.
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Gupta S, Batt J, Bourbeau J, Chapman KR, Gershon A, Granton J, Hambly N, Hernandez P, Kolb M, Mehta S, Mielniczuk L, Provencher S, Stephenson AL, Swiston J, Tullis DE, Vozoris NT, Wald J, Weatherald J, Bhutani M. Triaging Access to Critical Care Resources in Patients With Chronic Respiratory Diseases in the Event of a Major COVID-19 Surge: Key Highlights From the Canadian Thoracic Society (CTS) Position Statement. Chest. 2020 12; 158(6):2270-2274.
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Jackson L, DePas W, Morris AJ, Guttman K, Yau YCW, Waters V. Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients. J Vis Exp. 2020 07 16; (161).
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Degrugillier F, Aissat A, Prulière-Escabasse V, Bizard L, Simonneau B, Decrouy X, Jiang C, Rotin D, Fanen P, Simon S. Phosphorylation of the Chaperone-Like HspB5 Rescues Trafficking and Function of F508del-CFTR. Int J Mol Sci. 2020 Jul 08; 21(14).
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Kouri A, Gupta S, Yadollahi A, Ryan CM, Gershon AS, To T, Tarlo SM, Goldstein RS, Chapman KR, Chow CW. Addressing Reduced Laboratory-Based Pulmonary Function Testing During a Pandemic. Chest. 2020 12; 158(6):2502-2510.
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Gold A, Young JM, Solomon M, Grasemann H. Neuropsychological outcomes following pediatric lung transplantation. Pediatr Pulmonol. 2020 09; 55(9):2427-2436.
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Smith S, Waters V, Jahnke N, Ratjen F. Standard versus biofilm antimicrobial susceptibility testing to guide antibiotic therapy in cystic fibrosis. Cochrane Database Syst Rev. 2020 06 10; 6:CD009528.
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Waters V, Ratjen F. Antibiotic treatment for nontuberculous mycobacteria lung infection in people with cystic fibrosis. Cochrane Database Syst Rev. 2020 06 10; 6:CD010004.
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