Browsing by Sponsor/Funder Action for Pulmonary Fibrosis

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Showing results 1 to 20 of 34  next >
Issue DateTitleAuthor(s)
1-Jul-202150-gene risk profiles in peripheral blood predict COVID-19 outcomes: A retrospective, multicenter cohort studyJuan Guardela, BM; Sun, J; Zhang, T; Xu, B; Balnis, J, et al
26-Mar-2020A positron emission tomography imaging study to confirm target engagement in the lungs of patients with idiopathic pulmonary fibrosis following a single dose of a novel inhaled αvβ6 integrin inhibitorMaher, TM; Simpson, JK; Porter, JC; Wilson, FJ; Chan, R, et al
3-Apr-2020Bacterial burden in the lower airways predicts disease progression in idiopathic pulmonary fibrosis and is independent of radiological disease extentInvernizzi, R; Barnett, J; Rawal, B; Nair, A; Ghai, P, et al
9-Mar-2021Blood transcriptomic predicts progression of pulmonary fibrosis and associates natural killer cells.Huang, Y; Oldham, JM; Ma, S-F; Unterman, A; Liao, S-Y, et al
28-Aug-2020Bronchoalveolar lavage is safe and well tolerated in individuals with idiopathic pulmonary fibrosis: an analysis of the PROFILE studyMolyneaux, PL; Smith, JJ; Saunders, P; Chua, F; Wells, AU, et al
5-Jan-2022Candidate role for toll-like receptor 3 L412F polymorphism and infection in acute exacerbation of idiopathic pulmonary fibrosisMcElroy, AN; Invernizzi, R; Laskowska, JW; O'Neill, A; Doroudian, M, et al
7-Jan-2022Common idiopathic pulmonary fibrosis risk variants are associated with hypersensitivity pneumonitisFurusawa, H; Peljto, AL; Walts, AD; Cardwell, J; Molyneaux, PL, et al
15-Jun-2022CYFRA 21-1 predicts progression in IPF: a prospective longitudinal analysis of the PROFILE cohortMolyneaux, PL; Fahy, WA; Byrne, AJ; Braybrooke, R; Saunders, P, et al
1-Apr-2020Defining genetic risk factors for scleroderma-associated interstitial lung disease : IRF5 and STAT4 gene variants are associated with scleroderma while STAT4 is protective against scleroderma-associated interstitial lung diseaseStock, CJW; De Lauretis, A; Visca, D; Daccord, C; Kokosi, M, et al
15-Oct-2021DNA methylome alterations are associated with airway macrophage differentiation and phenotype during lung fibrosis.McErlean, P; Bell, CG; Hewitt, RJ; Busharat, Z; Ogger, PP, et al
2021Enhanced IL-1β Release Following NLRP3 and AIM2 Inflammasome Stimulation Is Linked to mtROS in Airway Macrophages in Pulmonary Fibrosis.Trachalaki, A; Tsitoura, E; Mastrodimou, S; Invernizzi, R; Vasarmidi, E, et al
1-Mar-2020Genome-wide association study of susceptibility to idiopathic pulmonary fibrosisAllen, RJ; Guillen-Guio, B; Oldham, JM; Ma, S-F; Dressen, A, et al
1-Oct-2022Genome-wide enrichment of TERT rare variants in Idiopathic Pulmonary Fibrosis patients of Latino ancestryZhang, D; Povysil, G; Newton, CA; Maher, TM; Molyneaux, PL, et al
1-Mar-2022Immuno-proteomic profiling reveals aberrant immune cell regulation in the airways of individuals with ongoing post-COVD-19 respiratory diseaseVijayakumar, B; Boustani, K; Ogger, P; Papadaki, A; Tonkin, J, et al
15-Sep-2020Interaction between the promoter MUC5B polymorphism and mucin expression: is there a difference according to ILD subtype?Stock, CJ; Conti, C; Montero-Fernandez, Á; Caramori, G; Molyneaux, PL, et al
11-Jul-2022Interstitial lung disease incidence and mortality in the United Kingdom and the European Union: an observational study, 2001-2017Salciccioli, J; Marshall, D; Goodall, R; Crowley, C; Shalhoub, J, et al
-Lung function trajectory in progressive fibrosing interstitial lung diseaseOldham, JM; Lee, CT; Wu, Z; Bowman, WS; Pugashetti, JV, et al
1-Nov-2019Modelling forced vital capacity in idiopathic pulmonary fibrosis: optimising trial design.Santermans, E; Ford, P; Kreuter, M; Verbruggen, N; Meyvisch, P, et al
1-Jul-2021Monocyte count as a prognostic biomarker in patients with idiopathic pulmonary fibrosisKreuter, M; Lee, JS; Tzouvelekis, A; Oldham, JM; Molyneaux, PL, et al
2-Oct-2020Outcome of hospitalization for COVID-19 in patients with interstitial lung disease: an international multicenter study.Drake, TM; Docherty, AB; Harrison, EM; Quint, JK; Adamali, H, et al