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Respiratory Research|October 22, 2011
Activated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosisCecilia K Andersson, Annika Andersson-Sjöland, Michiko Mori, et al.Proceedings of the National Academy of Sciences of the United States of America|May 2, 2002
Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humansFengrong Zuo, Naftali Kaminski, Elsie Eugui, et al.ERJ Open Research|September 1, 2020
Determination of the phenotypic age in residents of Mexico City: effect of accelerated ageing on lung function and structureIvette Buendía-Roldan, Rosario Fernández-Plata, Abigail Valdes-Bartolo, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|January 24, 2012
Allele-specific transactivation of matrix metalloproteinase 7 by FOXA2 and correlation with plasma levels in idiopathic pulmonary fibrosisThomas J Richards, Chunghyun Park, Yiliang Chen, et al.Archivos De Bronconeumologia|December 1, 2019
An Open-label Study With Pirfenidone on Chronic Hypersensitivity PneumonitisHeidegger Mateos-Toledo, Mayra Mejía-Ávila, Óscar Rodríguez-Barreto, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 7, 2011
Role of von Hippel-Lindau protein in fibroblast proliferation and fibrosisQiyuan Zhou, Annie Pardo, Melanie Königshoff, et al.Chest|October 3, 2014
The MUC5B promoter polymorphism is associated with idiopathic pulmonary fibrosis in a Mexican cohort but is rare among Asian ancestriesAnna L Peljto, Moises Selman, Dong Soon Kim, et al.American Journal of Respiratory Cell and Molecular Biology|March 26, 2013
Telomerase and telomere length in pulmonary fibrosisTianju Liu, Matthew Ullenbruch, Yoon Young Choi, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 22, 2012
CXCL17 is a mucosal chemokine elevated in idiopathic pulmonary fibrosis that exhibits broad antimicrobial activityAmanda M Burkhardt, Kenneth P Tai, Juan P Flores-Guiterrez, et al.Human Genetics|September 19, 2003
Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosisMoises Selman, Hung-Mo Lin, Martha Montaño, et al.Pageof 8