Results 111 to 120 of about 209,966 (285)

Prediction of progression in idiopathic pulmonary fibrosis using CT scans atbaseline: A quantum particle swarm optimization - Random forest approach [PDF]

, 2019
Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease characterized by an unpredictable progressive declinein lung function. Natural history of IPF is unknown and the prediction of disease progression at the time ofdiagnosis is notoriously ...
Brown, Matthew S., Goldin, Jonathan G., Kim, Grace Hyun J., Shi, Yu, Wong, Weng Kee   +4 more
core  

Single Cell RNA-seq reveals ectopic and aberrant lung resident cell populations in Idiopathic Pulmonary Fibrosis

bioRxiv, 2019
We provide a single cell atlas of Idiopathic Pulmonary Fibrosis (IPF), a fatal interstitial lung disease, focusing on resident lung cell populations. By profiling 312,928 cells from 32 IPF, 29 healthy control and 18 chronic obstructive pulmonary disease (
T. Adams, J. Schupp, S. Poli, Ehab A. Ayaub, N. Neumark, F. Ahangari, S. Chu, B. Raby, G. DeIuliis, Michael Januszyk, Qiaonan Duan, H. Arnett, Asim Siddiqui, G. Washko, R. Homer, Xiting Yan, I. Rosas, N. Kaminski   +17 more
semanticscholar   +1 more source

Idiopathic pulmonary fibrosis and intestinal disorders: An observational study

, 2022
Caramaschi Stefania, A. Bertani, Stefania Cerri, Colecchia Antonio, Ambrosini-Spaltro Andrea, Gianrocco Manco, Tiziana Salviato, Luca Reggiani Bonetti   +7 more
openalex   +2 more sources

Idiopathic pulmonary fibrosis: pathogenesis and management

Respiratory Research, 2018
BackgroundIdiopathic pulmonary fibrosis (IPF) is a chronic, progressive disease characterized by the aberrant accumulation of fibrotic tissue in the lungs parenchyma, associated with significant morbidity and poor prognosis.
G. Sgalla, B. Iovene, M. Calvello, Margherita Ori, F. Varone, L. Richeldi   +5 more
semanticscholar   +1 more source

Lung Cancer in Pulmonary Fibrosis: Tales of Epithelial Cell Plasticity [PDF]

, 2011
Lung epithelial cells exhibit a high degree of plasticity. Alterations to lung epithelial cell function are critically involved in several chronic lung diseases such as pulmonary fibrosis.
Adamson IY, Artinian V, Aubry MC, Bai JW, Baumgartner KB, Berschneider B, Brody AR, Chen PP, Chilosi M, Chilosi M, Coalson JJ, Corrin B, Dasari V, Dissanayake SK, Dobbs LG, Flozak AS, Fukuda Y, Ha HY, Haddad R, Herzog EL, Hironaka M, Hu J, Huang CL, Hubbard R, Huber MA, Jayachandran A, Kasai H, Kasper M, Kato N, Kawasaki H, Kawasaki H, Kim J, Kim K, Kim KK, Kuwano K, Königshoff M, Königshoff M, Königshoff M, Lee JM, Liu L, Maher TM, Margalit O, Mason RJ, Matthay MA, Mazieres J, Melanie Königshoff, Moon RT, Nagai A, Pan LH, Park J, Pennison M, Plataki M, Qunn L, Radisky DC, Rosas IO, Sato M, Selman M, Selman M, Soon LL, Sternlicht MD, Thannickal VJ, Thiery JP, Uematsu K, Willis BC, Willis BC, Willis BC, Zavadil J   +66 more
core   +1 more source

Idiopathic Pulmonary Fibrosis: Pathogenesis and the Emerging Role of Long Non-Coding RNAs [PDF]

, 2020
Marina R. Hadjicharalambous, Mark A. Lindsay   +1 more
openalex   +1 more source

Ambulatory Oxygen for Pulmonary Fibrosis (OxyPuF): a randomised controlled trial and acceptability study

Health Technology Assessment
Introduction Idiopathic pulmonary fibrosis is a devastating condition of unknown cause that results in progressive, irreversible scarring of the lung, manifesting as breathlessness and dry cough. Idiopathic pulmonary fibrosis is thought to be responsible
Rachel L Adams, Alisha Maher, Nicola Gale, Anjali Crawshaw, David Thickett, Alice M Turner   +5 more
doaj   +1 more source

Update on diagnosis and treatment of idiopathic pulmonary fibrosis

Jornal Brasileiro de Pneumologia, 2015
Idiopathic pulmonary fibrosis is a type of chronic fibrosing interstitial pneumonia, of unknown etiology, which is associated with a progressive decrease in pulmonary function and with high mortality rates. Interest in and knowledge of this disorder have
José Baddini-Martinez, Bruno Guedes Baldi, Cláudia Henrique da Costa, Sérgio Jezler, Mariana Silva Lima, Rogério Rufino   +5 more
doaj   +1 more source

MicroRNA-124-3p alleviates repetitive bleomycin induced idiopathic pulmonary fibrosis in mouse by repressing Wnt/β-catenin signaling component AXIN1

, 2023
Dharma Jaggi, Kavita Aggarwal, Lavanya Goyal   +2 more
openalex   +2 more sources

Interleukin-11 is a therapeutic target in idiopathic pulmonary fibrosis

Science Translational Medicine, 2019
Interleukin-11 is important for lung fibroblast activation in idiopathic pulmonary fibrosis, and its signaling represents a therapeutic target. Targeting IL-11 in lung fibrosis In idiopathic pulmonary fibrosis (IPF), chronic activation of invasive ...
B. Ng, Jinrui Dong, Giuseppe D’Agostino, S. Viswanathan, A. Widjaja, Wei-Wen Lim, Nicole S. J. Ko, J. Tan, S. Chothani, Benjamin Huang, Chen Xie, C. Pua, A. Chacko, Nuno Guimarães-Camboa, S. Evans, A. Byrne, T. Maher, Jiurong Liang, D. Jiang, P. Noble, S. Schafer, S. Cook   +21 more
semanticscholar   +1 more source