메뉴 건너뛰기




Volumn 5, Issue , 2016, Pages

Recent advances in understanding idiopathic pulmonary fibrosis.

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCYSTEINE; BIOLOGICAL MARKER; MATRIX PROTEIN; MICRORNA; NINTEDANIB; PIRFENIDONE;

EID: 85010867816     PISSN: None     EISSN: 20461402     Source Type: Journal    
DOI: 10.12688/F1000RESEARCH.8209.1     Document Type: Review
Times cited : (63)

References (107)
  • 1
    • 84940645409 scopus 로고    scopus 로고
    • Global incidence and mortality of idiopathic pulmonary fibrosis: a systematic review
    • Hutchinson J, Fogarty A, Hubbard R, et al.: Global incidence and mortality of idiopathic pulmonary fibrosis: a systematic review. Eur Respir J. 2015; 46(3): 795-806.
    • (2015) Eur Respir J , vol.46 , Issue.3 , pp. 795-806
    • Hutchinson, J.1    Fogarty, A.2    Hubbard, R.3
  • 2
    • 77951176799 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: a disease with similarities and links to cancer biology
    • Vancheri C, Failla M, Crimi N, et al.: Idiopathic pulmonary fibrosis: a disease with similarities and links to cancer biology. Eur Respir J. 2010; 35(3): 496-504.
    • (2010) Eur Respir J , vol.35 , Issue.3 , pp. 496-504
    • Vancheri, C.1    Failla, M.2    Crimi, N.3
  • 3
    • 84901759236 scopus 로고    scopus 로고
    • A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis
    • King TE Jr, Bradford WZ, Castro-Bernardini S, et al.: A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N Engl J Med. 2014; 370(22): 2083-92.
    • (2014) N Engl J Med , vol.370 , Issue.22 , pp. 2083-2092
    • King, T.E.1    Bradford, W.Z.2    Castro-Bernardini, S.3
  • 4
    • 84901810710 scopus 로고    scopus 로고
    • Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis
    • Richeldi L, du Bois RM, Raghu G, et al.: Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med. 2014; 370(22): 2071-82.
    • (2014) N Engl J Med , vol.370 , Issue.22 , pp. 2071-2082
    • Richeldi, L.1    du Bois, R.M.2    Raghu, G.3
  • 5
    • 84874144193 scopus 로고    scopus 로고
    • Personalized cancer medicine: molecular diagnostics, predictive biomarkers, and drug resistance
    • Gonzalez de Castro D, Clarke PA, Al-Lazikani B, et al.: Personalized cancer medicine: molecular diagnostics, predictive biomarkers, and drug resistance. Clin Pharmacol Ther. 2013; 93(3): 252-9.
    • (2013) Clin Pharmacol Ther , vol.93 , Issue.3 , pp. 252-259
    • Gonzalez de Castro, D.1    Clarke, P.A.2    Al-Lazikani, B.3
  • 6
    • 84899591828 scopus 로고    scopus 로고
    • Integrating omics technologies to study pulmonary physiology and pathology at the systems level
    • Pathak RR, Davé V: Integrating omics technologies to study pulmonary physiology and pathology at the systems level. Cell Physiol Biochem. 2014; 33(5): 1239-60.
    • (2014) Cell Physiol Biochem , vol.33 , Issue.5 , pp. 1239-1260
    • Pathak, R.R.1    Davé, V.2
  • 7
    • 84897499528 scopus 로고    scopus 로고
    • The treatment of idiopathic pulmonary fibrosis
    • Woodcock HV, Maher TM: The treatment of idiopathic pulmonary fibrosis. F1000Prime Rep. 2014; 6: 16.
    • (2014) F1000Prime Rep , vol.6 , pp. 16
    • Woodcock, H.V.1    Maher, T.M.2
  • 8
    • 79952717349 scopus 로고    scopus 로고
    • An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management
    • Raghu G, Collard HR, Egan JJ, et al.: An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011; 183(6): 788-824.
    • (2011) Am J Respir Crit Care Med , vol.183 , Issue.6 , pp. 788-824
    • Raghu, G.1    Collard, H.R.2    Egan, J.J.3
  • 9
    • 84979695447 scopus 로고    scopus 로고
    • In-Hospital Mortality after Surgical Lung Biopsy for Interstitial Lung Disease in the United States
    • Hutchinson JP, Fogarty AW, McKeever TM, et al.: In-Hospital Mortality after Surgical Lung Biopsy for Interstitial Lung Disease in the United States. 2000 to 2011 Am J Respir Crit Care Med. 2016; 193(10): 1161-7.
    • (2016) 2000 to 2011 Am J Respir Crit Care Med , vol.193 , Issue.10 , pp. 1161-1167
    • Hutchinson, J.P.1    Fogarty, A.W.2    McKeever, T.M.3
  • 10
    • 84880571484 scopus 로고    scopus 로고
    • Prevalence and prognosis of unclassifiable interstitial lung disease
    • Ryerson CJ, Urbania TH, Richeldi L, et al.: Prevalence and prognosis of unclassifiable interstitial lung disease. Eur Respir J. 2013; 42(3): 750-7.
    • (2013) Eur Respir J , vol.42 , Issue.3 , pp. 750-757
    • Ryerson, C.J.1    Urbania, T.H.2    Richeldi, L.3
  • 11
    • 84981351583 scopus 로고    scopus 로고
    • Bronchoscopic Lung Cryobiopsy Increases Diagnostic Confidence in the Multidisciplinary Diagnosis of Idiopathic Pulmonary Fibrosis
    • Tomassetti S, Wells AU, Costabel U, et al.: Bronchoscopic Lung Cryobiopsy Increases Diagnostic Confidence in the Multidisciplinary Diagnosis of Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2016; 193(7): 745-52.
    • (2016) Am J Respir Crit Care Med , vol.193 , Issue.7 , pp. 745-752
    • Tomassetti, S.1    Wells, A.U.2    Costabel, U.3
  • 12
    • 38849178850 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: multiple causes and multiple mechanisms?
    • Maher TM, Wells AU, Laurent GJ: Idiopathic pulmonary fibrosis: multiple causes and multiple mechanisms? Eur Respir J. 2007; 30(5): 835-9.
    • (2007) Eur Respir J , vol.30 , Issue.5 , pp. 835-839
    • Maher, T.M.1    Wells, A.U.2    Laurent, G.J.3
  • 13
    • 84918842765 scopus 로고    scopus 로고
    • Combination therapy: the future of management for idiopathic pulmonary fibrosis?
    • Wuyts WA, Antoniou KM, Borensztajn K, et al.: Combination therapy: the future of management for idiopathic pulmonary fibrosis? Lancet Respir Med. 2014; 2(11): 933-42.
    • (2014) Lancet Respir Med , vol.2 , Issue.11 , pp. 933-942
    • Wuyts, W.A.1    Antoniou, K.M.2    Borensztajn, K.3
  • 14
    • 82755161052 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis
    • King TE Jr, Pardo A, Selman M: Idiopathic pulmonary fibrosis. Lancet. 2011; 378(9807): 1949-61.
    • (2011) Lancet , vol.378 , Issue.9807 , pp. 1949-1961
    • King, T.E.1    Pardo, A.2    Selman, M.3
  • 15
    • 84916231955 scopus 로고    scopus 로고
    • New therapeutic targets in idiopathic pulmonary fibrosis. Aiming to rein in runaway wound-healing responses
    • Ahluwalia N, Shea BS, Tager AM: New therapeutic targets in idiopathic pulmonary fibrosis. Aiming to rein in runaway wound-healing responses. Am J Respir Crit Care Med. 2014; 190(8): 867-78.
    • (2014) Am J Respir Crit Care Med , vol.190 , Issue.8 , pp. 867-878
    • Ahluwalia, N.1    Shea, B.S.2    Tager, A.M.3
  • 16
    • 84923882858 scopus 로고    scopus 로고
    • Cellular interactions in the pathogenesis of interstitial lung diseases
    • Bagnato G, Harari S: Cellular interactions in the pathogenesis of interstitial lung diseases. Eur Respir Rev. 2015; 24(135): 102-14.
    • (2015) Eur Respir Rev , vol.24 , Issue.135 , pp. 102-114
    • Bagnato, G.1    Harari, S.2
  • 18
    • 84901022861 scopus 로고    scopus 로고
    • Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model
    • Selman M, Pardo A: Revealing the pathogenic and aging-related mechanisms of the enigmatic idiopathic pulmonary fibrosis. an integral model. Am J Respir Crit Care Med. 2014; 189(10): 1161-72.
    • (2014) Am J Respir Crit Care Med , vol.189 , Issue.10 , pp. 1161-1172
    • Selman, M.1    Pardo, A.2
  • 19
    • 84877097869 scopus 로고    scopus 로고
    • The pathogenesis of pulmonary fibrosis: a moving target
    • Wuyts WA, Agostini C, Antoniou KM, et al.: The pathogenesis of pulmonary fibrosis: a moving target. Eur Respir J. 2013; 41(5): 1207-18.
    • (2013) Eur Respir J , vol.41 , Issue.5 , pp. 1207-1218
    • Wuyts, W.A.1    Agostini, C.2    Antoniou, K.M.3
  • 20
    • 79951844263 scopus 로고    scopus 로고
    • Clinical course and prediction of survival in idiopathic pulmonary fibrosis
    • Ley B, Collard HR, King TE Jr: Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011; 183(4): 431-40.
    • (2011) Am J Respir Crit Care Med , vol.183 , Issue.4 , pp. 431-440
    • Ley, B.1    Collard, H.R.2    King, T.E.3
  • 21
    • 84881639762 scopus 로고    scopus 로고
    • Beyond the diagnosis of idiopathic pulmonary fibrosis; the growing role of systems biology and stratified medicine
    • Maher TM: Beyond the diagnosis of idiopathic pulmonary fibrosis; the growing role of systems biology and stratified medicine. Curr Opin Pulm Med. 2013; 19(5): 460-5.
    • (2013) Curr Opin Pulm Med , vol.19 , Issue.5 , pp. 460-465
    • Maher, T.M.1
  • 22
    • 84455168726 scopus 로고    scopus 로고
    • Forced vital capacity in patients with idiopathic pulmonary fibrosis: test properties and minimal clinically important difference
    • du Bois RM, Weycker D, Albera C, et al.: Forced vital capacity in patients with idiopathic pulmonary fibrosis: test properties and minimal clinically important difference. Am J Respir Crit Care Med. 2011; 184(12): 1382-9.
    • (2011) Am J Respir Crit Care Med , vol.184 , Issue.12 , pp. 1382-1389
    • du Bois, R.M.1    Weycker, D.2    Albera, C.3
  • 23
    • 84862826491 scopus 로고    scopus 로고
    • Relative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosis
    • Richeldi L, Ryerson CJ, Lee JS, et al.: Relative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosis. Thorax. 2012; 67(5): 407-11.
    • (2012) Thorax , vol.67 , Issue.5 , pp. 407-411
    • Richeldi, L.1    Ryerson, C.J.2    Lee, J.S.3
  • 24
    • 84899830690 scopus 로고    scopus 로고
    • 6-Minute walk distance is an independent predictor of mortality in patients with idiopathic pulmonary fibrosis
    • du Bois RM, Albera C, Bradford WZ, et al.: 6-Minute walk distance is an independent predictor of mortality in patients with idiopathic pulmonary fibrosis. Eur Respir J. 2014; 43(5): 1421-9.
    • (2014) Eur Respir J , vol.43 , Issue.5 , pp. 1421-1429
    • du Bois, R.M.1    Albera, C.2    Bradford, W.Z.3
  • 25
    • 0037383987 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: a composite physiologic index derived from disease extent observed by computed tomography
    • Wells AU, Desai SR, Rubens MB, et al.: Idiopathic pulmonary fibrosis: a composite physiologic index derived from disease extent observed by computed tomography. Am J Respir Crit Care Med. 2003; 167(7): 962-9.
    • (2003) Am J Respir Crit Care Med , vol.167 , Issue.7 , pp. 962-969
    • Wells, A.U.1    Desai, S.R.2    Rubens, M.B.3
  • 26
    • 80051819865 scopus 로고    scopus 로고
    • Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis
    • du Bois RM, Weycker D, Albera C, et al.: Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011; 184(4): 459-66.
    • (2011) Am J Respir Crit Care Med , vol.184 , Issue.4 , pp. 459-466
    • du Bois, R.M.1    Weycker, D.2    Albera, C.3
  • 27
    • 84861162888 scopus 로고    scopus 로고
    • A multidimensional index and staging system for idiopathic pulmonary fibrosis
    • Ley B, Ryerson CJ, Vittinghoff E, et al.: A multidimensional index and staging system for idiopathic pulmonary fibrosis. Ann Intern Med. 2012; 156(10): 684-91.
    • (2012) Ann Intern Med , vol.156 , Issue.10 , pp. 684-691
    • Ley, B.1    Ryerson, C.J.2    Vittinghoff, E.3
  • 28
    • 84928995228 scopus 로고    scopus 로고
    • Unified baseline and longitudinal mortality prediction in idiopathic pulmonary fibrosis
    • Ley B, Bradford WZ, Weycker D, et al.: Unified baseline and longitudinal mortality prediction in idiopathic pulmonary fibrosis. Eur Respir J. 2015; 45(5): 1374-81.
    • (2015) Eur Respir J , vol.45 , Issue.5 , pp. 1374-1381
    • Ley, B.1    Bradford, W.Z.2    Weycker, D.3
  • 29
    • 84910069392 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: CT and risk of death
    • Ley B, Elicker BM, Hartman TE, et al.: Idiopathic pulmonary fibrosis: CT and risk of death. Radiology. 2014; 273(2): 570-9.
    • (2014) Radiology , vol.273 , Issue.2 , pp. 570-579
    • Ley, B.1    Elicker, B.M.2    Hartman, T.E.3
  • 30
    • 84958040637 scopus 로고    scopus 로고
    • Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function Decline
    • Salisbury ML, Xia M, Zhou Y, et al.: Idiopathic Pulmonary Fibrosis: Gender-Age-Physiology Index Stage for Predicting Future Lung Function Decline. Chest. 2016; 149(2): 491-8.
    • (2016) Chest , vol.149 , Issue.2 , pp. 491-498
    • Salisbury, M.L.1    Xia, M.2    Zhou, Y.3
  • 31
    • 84901817527 scopus 로고    scopus 로고
    • Staging of idiopathic pulmonary fibrosis: past, present and future
    • Kolb M, Collard HR: Staging of idiopathic pulmonary fibrosis: past, present and future. Eur Respir Rev. 2014; 23(132): 220-4.
    • (2014) Eur Respir Rev , vol.23 , Issue.132 , pp. 220-224
    • Kolb, M.1    Collard, H.R.2
  • 32
    • 84859640369 scopus 로고    scopus 로고
    • 18F-Fluorodeoxyglucose positron emission tomography pulmonary imaging in idiopathic pulmonary fibrosis is reproducible: implications for future clinical trials
    • Win T, Lambrou T, Hutton BF, et al.: 18F-Fluorodeoxyglucose positron emission tomography pulmonary imaging in idiopathic pulmonary fibrosis is reproducible: implications for future clinical trials. Eur J Nucl Med Mol Imaging. 2012; 39(3): 521-8.
    • (2012) Eur J Nucl Med Mol Imaging , vol.39 , Issue.3 , pp. 521-528
    • Win, T.1    Lambrou, T.2    Hutton, B.F.3
  • 33
    • 84897088450 scopus 로고    scopus 로고
    • Areas of normal pulmonary parenchyma on HRCT exhibit increased FDG PET signal in IPF patients
    • Win T, Thomas BA, Lambrou T, et al.: Areas of normal pulmonary parenchyma on HRCT exhibit increased FDG PET signal in IPF patients. Eur J Nucl Med Mol Imaging. 2014; 41(2): 337-42.
    • (2014) Eur J Nucl Med Mol Imaging , vol.41 , Issue.2 , pp. 337-342
    • Win, T.1    Thomas, B.A.2    Lambrou, T.3
  • 35
    • 84942884150 scopus 로고    scopus 로고
    • Personalized medicine in idiopathic pulmonary fibrosis: facts and promises
    • Spagnolo P, Tzouvelekis A, Maher TM: Personalized medicine in idiopathic pulmonary fibrosis: facts and promises. Curr Opin Pulm Med. 2015; 21(5): 470-8.
    • (2015) Curr Opin Pulm Med , vol.21 , Issue.5 , pp. 470-478
    • Spagnolo, P.1    Tzouvelekis, A.2    Maher, T.M.3
  • 36
    • 77953522852 scopus 로고    scopus 로고
    • What can biomarkers tell us about the pathogenesis of acute exacerbations of idiopathic pulmonary fibrosis?
    • Huie TJ, Moss M, Frankel SK: What can biomarkers tell us about the pathogenesis of acute exacerbations of idiopathic pulmonary fibrosis? Am J Physiol Lung Cell Mol Physiol. 2010; 299(1): L1-2.
    • (2010) Am J Physiol Lung Cell Mol Physiol , vol.299 , Issue.1 , pp. L1-L2
    • Huie, T.J.1    Moss, M.2    Frankel, S.K.3
  • 37
    • 84871320910 scopus 로고    scopus 로고
    • Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis
    • Naik PK, Bozyk PD, Bentley JK, et al.: Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2012; 303(12): L1046-56.
    • (2012) Am J Physiol Lung Cell Mol Physiol , vol.303 , Issue.12 , pp. L1046-L1056
    • Naik, P.K.1    Bozyk, P.D.2    Bentley, J.K.3
  • 38
    • 84903993583 scopus 로고    scopus 로고
    • Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study
    • Han MK, Zhou Y, Murray S, et al.: Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET study. Lancet Respir Med. 2014; 2(7): 548-56.
    • (2014) Lancet Respir Med , vol.2 , Issue.7 , pp. 548-556
    • Han, M.K.1    Zhou, Y.2    Murray, S.3
  • 39
    • 84878454973 scopus 로고    scopus 로고
    • PROFILEing idiopathic pulmonary fibrosis: rethinking biomarker discovery
    • Maher TM: PROFILEing idiopathic pulmonary fibrosis: rethinking biomarker discovery. Eur Respir Rev. 2013; 22(128): 148-52.
    • (2013) Eur Respir Rev , vol.22 , Issue.128 , pp. 148-152
    • Maher, T.M.1
  • 40
    • 84930865108 scopus 로고    scopus 로고
    • Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study
    • Jenkins RG, Simpson JK, Saini G, et al.: Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study. Lancet Respir Med. 2015; 3(6): 462-72.
    • (2015) Lancet Respir Med , vol.3 , Issue.6 , pp. 462-472
    • Jenkins, R.G.1    Simpson, J.K.2    Saini, G.3
  • 41
    • 84878686854 scopus 로고    scopus 로고
    • Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
    • Fingerlin TE, Murphy E, Zhang W, et al.: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. Nat Genet. 2013; 45(6): 613-20.
    • (2013) Nat Genet , vol.45 , Issue.6 , pp. 613-620
    • Fingerlin, T.E.1    Murphy, E.2    Zhang, W.3
  • 42
    • 84880043679 scopus 로고    scopus 로고
    • Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study
    • Noth I, Zhang Y, Ma SF, et al.: Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. Lancet Respir Med. 2013; 1(4): 309-17.
    • (2013) Lancet Respir Med , vol.1 , Issue.4 , pp. 309-317
    • Noth, I.1    Zhang, Y.2    Ma, S.F.3
  • 43
    • 84892563951 scopus 로고    scopus 로고
    • Muc5b is required for airway defence
    • Roy MG, Livraghi-Butrico A, Fletcher AA, et al.: Muc5b is required for airway defence. Nature. 2014; 505(4783): 412-6.
    • (2014) Nature , vol.505 , Issue.4783 , pp. 412-416
    • Roy, M.G.1    Livraghi-Butrico, A.2    Fletcher, A.A.3
  • 44
    • 79955146233 scopus 로고    scopus 로고
    • A common MUC5B promoter polymorphism and pulmonary fibrosis
    • Seibold MA, Wise AL, Speer MC, et al.: A common MUC5B promoter polymorphism and pulmonary fibrosis. N Engl J Med. 2011; 364(16): 1503-12.
    • (2011) N Engl J Med , vol.364 , Issue.16 , pp. 1503-1512
    • Seibold, M.A.1    Wise, A.L.2    Speer, M.C.3
  • 45
    • 84878600828 scopus 로고    scopus 로고
    • Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
    • Peljto AL, Zhang Y, Fingerlin TE, et al.: Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis. JAMA. 2013; 309(21): 2232-9.
    • (2013) JAMA , vol.309 , Issue.21 , pp. 2232-2239
    • Peljto, A.L.1    Zhang, Y.2    Fingerlin, T.E.3
  • 46
    • 84876281483 scopus 로고    scopus 로고
    • Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis
    • Stock CJ, Sato H, Fonseca C, et al.: Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis. Thorax. 2013; 68(5): 436-41.
    • (2013) Thorax , vol.68 , Issue.5 , pp. 436-441
    • Stock, C.J.1    Sato, H.2    Fonseca, C.3
  • 47
    • 84930412885 scopus 로고    scopus 로고
    • The genetic basis of idiopathic pulmonary fibrosis
    • Kropski JA, Blackwell TS, Loyd JE: The genetic basis of idiopathic pulmonary fibrosis. Eur Respir J. 2015; 45(6): 1717-27.
    • (2015) Eur Respir J , vol.45 , Issue.6 , pp. 1717-1727
    • Kropski, J.A.1    Blackwell, T.S.2    Loyd, J.E.3
  • 48
    • 84922948913 scopus 로고    scopus 로고
    • Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease
    • Kropski JA, Pritchett JM, Zoz DF, et al.: Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease. Am J Respir Crit Care Med. 2015; 191(4): 417-26.
    • (2015) Am J Respir Crit Care Med , vol.191 , Issue.4 , pp. 417-426
    • Kropski, J.A.1    Pritchett, J.M.2    Zoz, D.F.3
  • 49
    • 84903995680 scopus 로고    scopus 로고
    • Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation
    • Stuart BD, Lee JS, Kozlitina J, et al.: Effect of telomere length on survival in patients with idiopathic pulmonary fibrosis: an observational cohort study with independent validation. Lancet Respir Med. 2014; 2(7): 557-65.
    • (2014) Lancet Respir Med , vol.2 , Issue.7 , pp. 557-565
    • Stuart, B.D.1    Lee, J.S.2    Kozlitina, J.3
  • 50
    • 84952037891 scopus 로고    scopus 로고
    • TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis
    • Oldham JM, Ma SF, Martinez FJ, et al.: TOLLIP, MUC5B, and the Response to N-Acetylcysteine among Individuals with Idiopathic Pulmonary Fibrosis. Am J Respir Crit Care Med. 2015; 192(12): 1475-82.
    • (2015) Am J Respir Crit Care Med , vol.192 , Issue.12 , pp. 1475-1482
    • Oldham, J.M.1    Ma, S.F.2    Martinez, F.J.3
  • 51
    • 31944436620 scopus 로고    scopus 로고
    • Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis
    • Selman M, Pardo A, Barrera L, et al.: Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis. Am J Respir Crit Care Med. 2006; 173(2): 188-98.
    • (2006) Am J Respir Crit Care Med , vol.173 , Issue.2 , pp. 188-198
    • Selman, M.1    Pardo, A.2    Barrera, L.3
  • 52
    • 84930871576 scopus 로고    scopus 로고
    • Classification of usual interstitial pneumonia in patients with interstitial lung disease: assessment of a machine learning approach using high-dimensional transcriptional data
    • Kim SY, Diggans J, Pankratz D, et al.: Classification of usual interstitial pneumonia in patients with interstitial lung disease: assessment of a machine learning approach using high-dimensional transcriptional data. Lancet Respir Med. 2015; 3(6): 473-82.
    • (2015) Lancet Respir Med , vol.3 , Issue.6 , pp. 473-482
    • Kim, S.Y.1    Diggans, J.2    Pankratz, D.3
  • 53
    • 64649089804 scopus 로고    scopus 로고
    • Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF)
    • Boon K, Bailey NW, Yang J, et al.: Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF). PLoS One. 2009; 4(4): e5134.
    • (2009) PLoS One , vol.4 , Issue.4
    • Boon, K.1    Bailey, N.W.2    Yang, J.3
  • 54
    • 84862677507 scopus 로고    scopus 로고
    • The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosis
    • Yang IV, Luna LG, Cotter J, et al.: The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosis. PLoS One. 2012; 7(6): e37708.
    • (2012) PLoS One , vol.7 , Issue.6
    • Yang, I.V.1    Luna, L.G.2    Cotter, J.3
  • 55
    • 84928723451 scopus 로고    scopus 로고
    • Familial and sporadic idiopathic pulmonary fibrosis: making the diagnosis from peripheral blood
    • Meltzer EB, Barry WT, Yang IV, et al.: Familial and sporadic idiopathic pulmonary fibrosis: making the diagnosis from peripheral blood. BMC Genomics. 2014; 15(1): 902.
    • (2014) BMC Genomics , vol.15 , Issue.1 , pp. 902
    • Meltzer, E.B.1    Barry, W.T.2    Yang, I.V.3
  • 56
    • 84905728335 scopus 로고    scopus 로고
    • The mitochondrial cardiolipin remodeling enzyme lysocardiolipin acyltransferase is a novel target in pulmonary fibrosis
    • Huang LS, Mathew B, Li H, et al.: The mitochondrial cardiolipin remodeling enzyme lysocardiolipin acyltransferase is a novel target in pulmonary fibrosis. Am J Respir Crit Care Med. 2014; 189(11): 1402-15.
    • (2014) Am J Respir Crit Care Med , vol.189 , Issue.11 , pp. 1402-1415
    • Huang, L.S.1    Mathew, B.2    Li, H.3
  • 57
    • 84866069730 scopus 로고    scopus 로고
    • Altered DNA methylation profile in idiopathic pulmonary fibrosis
    • Sanders YY, Ambalavanan N, Halloran B, et al.: Altered DNA methylation profile in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2012; 186(6): 525-35.
    • (2012) Am J Respir Crit Care Med , vol.186 , Issue.6 , pp. 525-535
    • Sanders, Y.Y.1    Ambalavanan, N.2    Halloran, B.3
  • 58
    • 84925156003 scopus 로고    scopus 로고
    • Lung fibroblasts from patients with idiopathic pulmonary fibrosis exhibit genome-wide differences in DNA methylation compared to fibroblasts from nonfibrotic lung
    • Huang SK, Scruggs AM, McEachin RC, et al.: Lung fibroblasts from patients with idiopathic pulmonary fibrosis exhibit genome-wide differences in DNA methylation compared to fibroblasts from nonfibrotic lung. PLoS One. 2014; 9(9): e107055.
    • (2014) PLoS One , vol.9 , Issue.9
    • Huang, S.K.1    Scruggs, A.M.2    McEachin, R.C.3
  • 59
    • 67651232689 scopus 로고    scopus 로고
    • Defective histone acetylation is responsible for the diminished expression of cyclooxygenase 2 in idiopathic pulmonary fibrosis
    • Coward WR, Watts K, Feghali-Bostwick CA, et al.: Defective histone acetylation is responsible for the diminished expression of cyclooxygenase 2 in idiopathic pulmonary fibrosis. Mol Cell Biol. 2009; 29(15): 4325-39.
    • (2009) Mol Cell Biol , vol.29 , Issue.15 , pp. 4325-4339
    • Coward, W.R.1    Watts, K.2    Feghali-Bostwick, C.A.3
  • 60
    • 77953449840 scopus 로고    scopus 로고
    • Repression of IP-10 by interactions between histone deacetylation and hypermethylation in idiopathic pulmonary fibrosis
    • Coward WR, Watts K, Feghali-Bostwick CA, et al.: Repression of IP-10 by interactions between histone deacetylation and hypermethylation in idiopathic pulmonary fibrosis. Mol Cell Biol. 2010; 30(12): 2874-86.
    • (2010) Mol Cell Biol , vol.30 , Issue.12 , pp. 2874-2886
    • Coward, W.R.1    Watts, K.2    Feghali-Bostwick, C.A.3
  • 61
    • 84873978112 scopus 로고    scopus 로고
    • Epigenetic regulation of miR-17~92 contributes to the pathogenesis of pulmonary fibrosis
    • Dakhlallah D, Batte K, Wang Y, et al.: Epigenetic regulation of miR-17~92 contributes to the pathogenesis of pulmonary fibrosis. Am J Respir Crit Care Med. 2013; 187(4): 397-405.
    • (2013) Am J Respir Crit Care Med , vol.187 , Issue.4 , pp. 397-405
    • Dakhlallah, D.1    Batte, K.2    Wang, Y.3
  • 62
    • 84919876731 scopus 로고    scopus 로고
    • Epigenetics of idiopathic pulmonary fibrosis
    • Yang IV, Schwartz DA: Epigenetics of idiopathic pulmonary fibrosis. Transl Res. 2015; 165(1): 48-60.
    • (2015) Transl Res , vol.165 , Issue.1 , pp. 48-60
    • Yang, I.V.1    Schwartz, D.A.2
  • 63
    • 84916200736 scopus 로고    scopus 로고
    • Relationship of DNA methylation and gene expression in idiopathic pulmonary fibrosis
    • Yang IV, Pedersen BS, Rabinovich E, et al.: Relationship of DNA methylation and gene expression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2014; 190(11): 1263-72.
    • (2014) Am J Respir Crit Care Med , vol.190 , Issue.11 , pp. 1263-1272
    • Yang, I.V.1    Pedersen, B.S.2    Rabinovich, E.3
  • 64
    • 84870508377 scopus 로고    scopus 로고
    • Profibrotic role of miR-154 in pulmonary fibrosis
    • Milosevic J, Pandit K, Magister M, et al.: Profibrotic role of miR-154 in pulmonary fibrosis. Am J Respir Cell Mol Biol. 2012; 47(6): 879-87.
    • (2012) Am J Respir Cell Mol Biol , vol.47 , Issue.6 , pp. 879-887
    • Milosevic, J.1    Pandit, K.2    Magister, M.3
  • 65
    • 77955399498 scopus 로고    scopus 로고
    • Inhibition and role of let-7d in idiopathic pulmonary fibrosis
    • Pandit KV, Corcoran D, Yousef H, et al.: Inhibition and role of let-7d in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2010; 182(2): 220-9.
    • (2010) Am J Respir Crit Care Med , vol.182 , Issue.2 , pp. 220-229
    • Pandit, K.V.1    Corcoran, D.2    Yousef, H.3
  • 66
    • 79959338409 scopus 로고    scopus 로고
    • A micro RNA processing defect in rapidly progressing idiopathic pulmonary fibrosis
    • Oak SR, Murray L, Herath A, et al.: A micro RNA processing defect in rapidly progressing idiopathic pulmonary fibrosis. PLoS One. 2011; 6(6): e21253.
    • (2011) PLoS One , vol.6 , Issue.6
    • Oak, S.R.1    Murray, L.2    Herath, A.3
  • 67
    • 84940467245 scopus 로고    scopus 로고
    • The code of non-coding RNAs in lung fibrosis
    • Cui H, Xie N, Thannickal VJ, et al.: The code of non-coding RNAs in lung fibrosis. Cell Mol Life Sci. 2015; 72(18): 3507-19.
    • (2015) Cell Mol Life Sci , vol.72 , Issue.18 , pp. 3507-3519
    • Cui, H.1    Xie, N.2    Thannickal, V.J.3
  • 68
    • 84925086698 scopus 로고    scopus 로고
    • Discovery and validation of extracellular/circulating microRNAs during idiopathic pulmonary fibrosis disease progression
    • Yang G, Yang L, Wang W, et al.: Discovery and validation of extracellular/circulating microRNAs during idiopathic pulmonary fibrosis disease progression. Gene. 2015; 562(1): 138-44.
    • (2015) Gene , vol.562 , Issue.1 , pp. 138-144
    • Yang, G.1    Yang, L.2    Wang, W.3
  • 69
    • 84899531719 scopus 로고    scopus 로고
    • Expression analysis of serum microRNAs in idiopathic pulmonary fibrosis
    • Li P, Li J, Chen T, et al.: Expression analysis of serum microRNAs in idiopathic pulmonary fibrosis. Int J Mol Med. 2014; 33(6): 1554-62.
    • (2014) Int J Mol Med , vol.33 , Issue.6 , pp. 1554-1562
    • Li, P.1    Li, J.2    Chen, T.3
  • 70
    • 84908087700 scopus 로고    scopus 로고
    • MicroRNA mimicry blocks pulmonary fibrosis
    • Montgomery RL, Yu G, Latimer PA, et al.: MicroRNA mimicry blocks pulmonary fibrosis. EMBO Mol Med. 2014; 6(10): 1347-56.
    • (2014) EMBO Mol Med , vol.6 , Issue.10 , pp. 1347-1356
    • Montgomery, R.L.1    Yu, G.2    Latimer, P.A.3
  • 71
    • 63849228099 scopus 로고    scopus 로고
    • Serum surfactant protein-A is a strong predictor of early mortality in idiopathic pulmonary fibrosis
    • Kinder BW, Brown KK, McCormack FX, et al.: Serum surfactant protein-A is a strong predictor of early mortality in idiopathic pulmonary fibrosis. Chest. 2009; 135(6): 1557-63.
    • (2009) Chest , vol.135 , Issue.6 , pp. 1557-1563
    • Kinder, B.W.1    Brown, K.K.2    McCormack, F.X.3
  • 72
    • 77649263746 scopus 로고    scopus 로고
    • Surfactant protein-D predicts survival in patients with idiopathic pulmonary fibrosis
    • Barlo NP, van Moorsel CH, Ruven HJ, et al.: Surfactant protein-D predicts survival in patients with idiopathic pulmonary fibrosis. Sarcoidosis Vasc Diffuse Lung Dis. 2009; 26(2): 155-61.
    • (2009) Sarcoidosis Vasc Diffuse Lung Dis , vol.26 , Issue.2 , pp. 155-161
    • Barlo, N.P.1    van Moorsel, C.H.2    Ruven, H.J.3
  • 73
    • 33644828168 scopus 로고    scopus 로고
    • Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis
    • Yokoyama A, Kondo K, Nakajima M, et al.: Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis. Respirology. 2006; 11(2): 164-8.
    • (2006) Respirology , vol.11 , Issue.2 , pp. 164-168
    • Yokoyama, A.1    Kondo, K.2    Nakajima, M.3
  • 74
    • 65249160219 scopus 로고    scopus 로고
    • Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis
    • Prasse A, Probst C, Bargagli E, et al.: Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2009; 179(8): 717-23.
    • (2009) Am J Respir Crit Care Med , vol.179 , Issue.8 , pp. 717-723
    • Prasse, A.1    Probst, C.2    Bargagli, E.3
  • 75
    • 84898934902 scopus 로고    scopus 로고
    • C-X-C motif chemokine 13 (CXCL13) is a prognostic biomarker of idiopathic pulmonary fibrosis
    • Vuga LJ, Tedrow JR, Pandit KV, et al.: C-X-C motif chemokine 13 (CXCL13) is a prognostic biomarker of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2014; 189(8): 966-74.
    • (2014) Am J Respir Crit Care Med , vol.189 , Issue.8 , pp. 966-974
    • Vuga, L.J.1    Tedrow, J.R.2    Pandit, K.V.3
  • 76
    • 84919768376 scopus 로고    scopus 로고
    • Heterogeneous gene expression signatures correspond to distinct lung pathologies and biomarkers of disease severity in idiopathic pulmonary fibrosis
    • DePianto DJ, Chandriani S, Abbas AR, et al.: Heterogeneous gene expression signatures correspond to distinct lung pathologies and biomarkers of disease severity in idiopathic pulmonary fibrosis. Thorax. 2015; 70(1): 48-56.
    • (2015) Thorax , vol.70 , Issue.1 , pp. 48-56
    • DePianto, D.J.1    Chandriani, S.2    Abbas, A.R.3
  • 77
    • 84871320910 scopus 로고    scopus 로고
    • Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis
    • Naik PK, Bozyk PD, Bentley JK, et al.: Periostin promotes fibrosis and predicts progression in patients with idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2012; 303(12): L1046-56.
    • (2012) Am J Physiol Lung Cell Mol Physiol , vol.303 , Issue.12 , pp. L1046-L1056
    • Naik, P.K.1    Bozyk, P.D.2    Bentley, J.K.3
  • 78
    • 84907919354 scopus 로고    scopus 로고
    • Fibulin-1 predicts disease progression in patients with idiopathic pulmonary fibrosis
    • Jaffar J, Unger S, Corte TJ, et al.: Fibulin-1 predicts disease progression in patients with idiopathic pulmonary fibrosis. Chest. 2014; 146(4): 1055-63.
    • (2014) Chest , vol.146 , Issue.4 , pp. 1055-1063
    • Jaffar, J.1    Unger, S.2    Corte, T.J.3
  • 79
    • 43249084804 scopus 로고    scopus 로고
    • MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis
    • Rosas IO, Richards TJ, Konishi K, et al.: MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis. PLoS Med. 2008; 5(4): e93.
    • (2008) PLoS Med , vol.5 , Issue.4
    • Rosas, I.O.1    Richards, T.J.2    Konishi, K.3
  • 80
    • 84855264195 scopus 로고    scopus 로고
    • Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis
    • Richards TJ, Kaminski N, Baribaud F, et al.: Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2012; 185(1): 67-76.
    • (2012) Am J Respir Crit Care Med , vol.185 , Issue.1 , pp. 67-76
    • Richards, T.J.1    Kaminski, N.2    Baribaud, F.3
  • 81
    • 84899870174 scopus 로고    scopus 로고
    • Serum lysyl oxidase-like 2 levels and idiopathic pulmonary fibrosis disease progression
    • Chien JW, Richards TJ, Gibson KF, et al.: Serum lysyl oxidase-like 2 levels and idiopathic pulmonary fibrosis disease progression. Eur Respir J. 2014; 43(5): 1430-8.
    • (2014) Eur Respir J , vol.43 , Issue.5 , pp. 1430-1438
    • Chien, J.W.1    Richards, T.J.2    Gibson, K.F.3
  • 82
    • 84902370988 scopus 로고    scopus 로고
    • Baseline KL-6 predicts increased risk for acute exacerbation of idiopathic pulmonary fibrosis
    • Ohshimo S, Ishikawa N, Horimasu Y, et al.: Baseline KL-6 predicts increased risk for acute exacerbation of idiopathic pulmonary fibrosis. Respir Med. 2014; 108(7): 1031-9.
    • (2014) Respir Med , vol.108 , Issue.7 , pp. 1031-1039
    • Ohshimo, S.1    Ishikawa, N.2    Horimasu, Y.3
  • 83
    • 65249098301 scopus 로고    scopus 로고
    • Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis
    • Moeller A, Gilpin SE, Ask K, et al.: Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2009; 179(7): 588-94.
    • (2009) Am J Respir Crit Care Med , vol.179 , Issue.7 , pp. 588-594
    • Moeller, A.1    Gilpin, S.E.2    Ask, K.3
  • 84
    • 84872588648 scopus 로고    scopus 로고
    • Semaphorin 7a+ regulatory T cells are associated with progressive idiopathic pulmonary fibrosis and are implicated in transforming growth factor-β1-induced pulmonary fibrosis
    • Reilkoff RA, Peng H, Murray LA, et al.: Semaphorin 7a+ regulatory T cells are associated with progressive idiopathic pulmonary fibrosis and are implicated in transforming growth factor-β1-induced pulmonary fibrosis. Am J Respir Crit Care Med. 2013; 187(2): 180-8.
    • (2013) Am J Respir Crit Care Med , vol.187 , Issue.2 , pp. 180-188
    • Reilkoff, R.A.1    Peng, H.2    Murray, L.A.3
  • 85
    • 84938890295 scopus 로고    scopus 로고
    • αvβ6 integrin may be a potential prognostic biomarker in interstitial lung disease
    • Saini G, Porte J, Weinreb PH, et al.: αvβ6 integrin may be a potential prognostic biomarker in interstitial lung disease. Eur Respir J. 2015; 46(2): 486-94.
    • (2015) Eur Respir J , vol.46 , Issue.2 , pp. 486-494
    • Saini, G.1    Porte, J.2    Weinreb, P.H.3
  • 86
    • 84857922118 scopus 로고    scopus 로고
    • S100A9 in BALF is a candidate biomarker of idiopathic pulmonary fibrosis
    • Hara A, Sakamoto N, Ishimatsu Y, et al.: S100A9 in BALF is a candidate biomarker of idiopathic pulmonary fibrosis. Respir Med. 2012; 106(4): 571-80.
    • (2012) Respir Med , vol.106 , Issue.4 , pp. 571-580
    • Hara, A.1    Sakamoto, N.2    Ishimatsu, Y.3
  • 87
    • 84946552488 scopus 로고    scopus 로고
    • Increased alveolar soluble annexin V promotes lung inflammation and fibrosis
    • Buckley S, Shi W, Xu W, et al.: Increased alveolar soluble annexin V promotes lung inflammation and fibrosis. Eur Respir J. 2015; 46(5): 1417-29.
    • (2015) Eur Respir J , vol.46 , Issue.5 , pp. 1417-1429
    • Buckley, S.1    Shi, W.2    Xu, W.3
  • 88
    • 84877629067 scopus 로고    scopus 로고
    • Blood biomarkers MMP-7 and SP-A: predictors of outcome in idiopathic pulmonary fibrosis
    • Song JW, Do KH, Jang SJ, et al.: Blood biomarkers MMP-7 and SP-A: predictors of outcome in idiopathic pulmonary fibrosis. Chest. 2013; 143(5): 1422-9.
    • (2013) Chest , vol.143 , Issue.5 , pp. 1422-1429
    • Song, J.W.1    Do, K.H.2    Jang, S.J.3
  • 89
    • 84921759167 scopus 로고    scopus 로고
    • The metabolomics of airway diseases, including COPD, asthma and cystic fibrosis
    • Nobakht M Gh BF, Aliannejad R, Rezaei-Tavirani M, et al.: The metabolomics of airway diseases, including COPD, asthma and cystic fibrosis. Biomarkers. 2015; 20(1): 5-16.
    • (2015) Biomarkers , vol.20 , Issue.1 , pp. 5-16
    • Nobakht, M.G.B.F.1    Aliannejad, R.2    Rezaei-Tavirani, M.3
  • 90
    • 84867604212 scopus 로고    scopus 로고
    • Lactic acid is elevated in idiopathic pulmonary fibrosis and induces myofibroblast differentiation via pH-dependent activation of transforming growth factor-β
    • Kottmann RM, Kulkarni AA, Smolnycki KA, et al.: Lactic acid is elevated in idiopathic pulmonary fibrosis and induces myofibroblast differentiation via pH-dependent activation of transforming growth factor-β. Am J Respir Crit Care Med. 2012; 186(8): 740-51.
    • (2012) Am J Respir Crit Care Med , vol.186 , Issue.8 , pp. 740-751
    • Kottmann, R.M.1    Kulkarni, A.A.2    Smolnycki, K.A.3
  • 91
    • 84952063696 scopus 로고    scopus 로고
    • Glycolytic Reprogramming in Myofibroblast Differentiation and Lung Fibrosis
    • Xie N, Tan Z, Banerjee S, et al.: Glycolytic Reprogramming in Myofibroblast Differentiation and Lung Fibrosis. Am J Respir Crit Care Med. 2015; 192(12): 1462-74.
    • (2015) Am J Respir Crit Care Med , vol.192 , Issue.12 , pp. 1462-1474
    • Xie, N.1    Tan, Z.2    Banerjee, S.3
  • 92
    • 0031030088 scopus 로고    scopus 로고
    • Cigarette smoking: a risk factor for idiopathic pulmonary fibrosis
    • Baumgartner KB, Samet JM, Stidley CA, et al.: Cigarette smoking: a risk factor for idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 1997; 155(1): 242-8.
    • (1997) Am J Respir Crit Care Med , vol.155 , Issue.1 , pp. 242-248
    • Baumgartner, K.B.1    Samet, J.M.2    Stidley, C.A.3
  • 93
    • 30344471883 scopus 로고    scopus 로고
    • Clinical and pathologic features of familial interstitial pneumonia
    • Steele MP, Speer MC, Loyd JE, et al.: Clinical and pathologic features of familial interstitial pneumonia. Am J Respir Crit Care Med. 2005; 172(9): 1146-52.
    • (2005) Am J Respir Crit Care Med , vol.172 , Issue.9 , pp. 1146-1152
    • Steele, M.P.1    Speer, M.C.2    Loyd, J.E.3
  • 94
    • 38349039634 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: outcome in relation to smoking status
    • Antoniou KM, Hansell DM, Rubens MB, et al.: Idiopathic pulmonary fibrosis: outcome in relation to smoking status. Am J Respir Crit Care Med. 2008; 177(2): 190-4.
    • (2008) Am J Respir Crit Care Med , vol.177 , Issue.2 , pp. 190-194
    • Antoniou, K.M.1    Hansell, D.M.2    Rubens, M.B.3
  • 95
    • 33744908816 scopus 로고    scopus 로고
    • Is idiopathic pulmonary fibrosis an environmental disease?
    • Taskar VS, Coultas DB: Is idiopathic pulmonary fibrosis an environmental disease? Proc Am Thorac Soc. 2006; 3(4): 293-8.
    • (2006) Proc Am Thorac Soc , vol.3 , Issue.4 , pp. 293-298
    • Taskar, V.S.1    Coultas, D.B.2
  • 96
    • 84897452881 scopus 로고    scopus 로고
    • Acute exacerbation of idiopathic pulmonary fibrosis associated with air pollution exposure
    • Johannson KA, Vittinghoff E, Lee K, et al.: Acute exacerbation of idiopathic pulmonary fibrosis associated with air pollution exposure. Eur Respir J. 2014; 43(4): 1124-31.
    • (2014) Eur Respir J , vol.43 , Issue.4 , pp. 1124-1131
    • Johannson, K.A.1    Vittinghoff, E.2    Lee, K.3
  • 97
    • 84887263711 scopus 로고    scopus 로고
    • Gastro-oesophageal reflux and gastric aspiration in idiopathic pulmonary fibrosis patients
    • Savarino E, Carbone R, Marabotto E, et al.: Gastro-oesophageal reflux and gastric aspiration in idiopathic pulmonary fibrosis patients. Eur Respir J. 2013; 42(5): 1322-31.
    • (2013) Eur Respir J , vol.42 , Issue.5 , pp. 1322-1331
    • Savarino, E.1    Carbone, R.2    Marabotto, E.3
  • 98
    • 84455201657 scopus 로고    scopus 로고
    • Gastroesophageal reflux therapy is associated with longer survival in patients with idiopathic pulmonary fibrosis
    • Lee JS, Ryu JH, Elicker BM, et al.: Gastroesophageal reflux therapy is associated with longer survival in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011; 184(12): 1390-4.
    • (2011) Am J Respir Crit Care Med , vol.184 , Issue.12 , pp. 1390-1394
    • Lee, J.S.1    Ryu, J.H.2    Elicker, B.M.3
  • 99
    • 84881367867 scopus 로고    scopus 로고
    • Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials
    • Lee JS, Collard HR, Anstrom KJ, et al.: Anti-acid treatment and disease progression in idiopathic pulmonary fibrosis: an analysis of data from three randomised controlled trials. Lancet Respir Med. 2013; 1(5): 369-76.
    • (2013) Lancet Respir Med , vol.1 , Issue.5 , pp. 369-376
    • Lee, J.S.1    Collard, H.R.2    Anstrom, K.J.3
  • 100
    • 84938125365 scopus 로고    scopus 로고
    • An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of Idiopathic Pulmonary Fibrosis. An Update of the 2011 Clinical Practice Guideline
    • Raghu G, Rochwerg B, Zhang Y, et al.: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of Idiopathic Pulmonary Fibrosis. An Update of the 2011 Clinical Practice Guideline. Am J Respir Crit Care Med. 2015; 192(2): e3-19.
    • (2015) Am J Respir Crit Care Med , vol.192 , Issue.2 , pp. e3-e19
    • Raghu, G.1    Rochwerg, B.2    Zhang, Y.3
  • 101
    • 84883341999 scopus 로고    scopus 로고
    • The role of infection in the pathogenesis of idiopathic pulmonary fibrosis
    • Molyneaux PL, Maher TM: The role of infection in the pathogenesis of idiopathic pulmonary fibrosis. Eur Respir Rev. 2013; 22(129): 376-81.
    • (2013) Eur Respir Rev , vol.22 , Issue.129 , pp. 376-381
    • Molyneaux, P.L.1    Maher, T.M.2
  • 102
    • 48949119341 scopus 로고    scopus 로고
    • Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection
    • Lawson WE, Crossno PF, Polosukhin VV, et al.: Endoplasmic reticulum stress in alveolar epithelial cells is prominent in IPF: association with altered surfactant protein processing and herpesvirus infection. Am J Physiol Lung Cell Mol Physiol. 2008; 294(6): L1119-26.
    • (2008) Am J Physiol Lung Cell Mol Physiol , vol.294 , Issue.6 , pp. L1119-L1126
    • Lawson, W.E.1    Crossno, P.F.2    Polosukhin, V.V.3
  • 103
    • 84857758730 scopus 로고    scopus 로고
    • Right place, right time: the evolving role of herpesvirus infection as a "second hit" in idiopathic pulmonary fibrosis
    • Kropski JA, Lawson WE, Blackwell TS: Right place, right time: the evolving role of herpesvirus infection as a "second hit" in idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2012; 302(5): L441-4.
    • (2012) Am J Physiol Lung Cell Mol Physiol , vol.302 , Issue.5 , pp. L441-L444
    • Kropski, J.A.1    Lawson, W.E.2    Blackwell, T.S.3
  • 104
    • 84857760659 scopus 로고    scopus 로고
    • Ganciclovir antiviral therapy in advanced idiopathic pulmonary fibrosis: an open pilot study
    • Egan JJ, Adamali HI, Lok SS, et al.: Ganciclovir antiviral therapy in advanced idiopathic pulmonary fibrosis: an open pilot study. Pulm Med. 2011; 2011: 240805.
    • (2011) Pulm Med , vol.2011
    • Egan, J.J.1    Adamali, H.I.2    Lok, S.S.3
  • 105
    • 84919361154 scopus 로고    scopus 로고
    • Influenza promotes collagen deposition via αvβ6 integrin-mediated transforming growth factor β activation
    • Jolly L, Stavrou A, Vanderstoken G, et al.: Influenza promotes collagen deposition via αvβ6 integrin-mediated transforming growth factor β activation. J Biol Chem. 2014; 289(51): 35246-63.
    • (2014) J Biol Chem , vol.289 , Issue.51 , pp. 35246-35263
    • Jolly, L.1    Stavrou, A.2    Vanderstoken, G.3
  • 106
    • 84918777951 scopus 로고    scopus 로고
    • The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
    • Molyneaux PL, Cox MJ, Willis-Owen SA, et al.: The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2014; 190(8): 906-13.
    • (2014) Am J Respir Crit Care Med , vol.190 , Issue.8 , pp. 906-913
    • Molyneaux, P.L.1    Cox, M.J.2    Willis-Owen, S.A.3
  • 107
    • 84872677109 scopus 로고    scopus 로고
    • Treating idiopathic pulmonary fibrosis with the addition of co-trimoxazole: a randomised controlled trial
    • Shulgina L, Cahn AP, Chilvers ER, et al.: Treating idiopathic pulmonary fibrosis with the addition of co-trimoxazole: a randomised controlled trial. Thorax. 2013; 68(2): 155-62.
    • (2013) Thorax , vol.68 , Issue.2 , pp. 155-162
    • Shulgina, L.1    Cahn, A.P.2    Chilvers, E.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.