-
2
-
-
0034133548
-
Idiopathic pulmonary fibrosis: Diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS)
-
American Thoracic Society
-
American Thoracic Society. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS). Am J Respir Crit Care Med 2000;161:646-64.
-
(2000)
Am J Respir Crit Care Med
, vol.161
, pp. 646-64
-
-
-
3
-
-
0037080547
-
This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors June 2001 and by the ERS Executive Committee, June 2001
-
American Thoracic Society/European Respiratory Society. Interna-tional Multidisciplinary Consensus Classification of the Idiopathic In-terstitial Pneumonias
-
American Thoracic Society/European Respiratory Society. Interna-tional Multidisciplinary Consensus Classification of the Idiopathic In-terstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors June 2001 and by the ERS Executive Committee, June 2001. Am J Respir Crit Care Med 2002; 165: 277-304.
-
(2002)
Am J Respir Crit Care Med
, vol.165
, pp. 277-304
-
-
-
4
-
-
22644435878
-
Clinical advances in the diagnosis and therapy of the interstitial lung diseases
-
DOI 10.1164/rccm.200503-483OE
-
King TE Jr. Clinical advances in the diagnosis and therapy of the interstitial lung diseases. Am J Respir Crit Care Med 2005;172:268-79. (Pubitemid 41026138)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.172
, Issue.3
, pp. 268-279
-
-
King Jr., T.E.1
-
5
-
-
30344471883
-
Clinical and pathologic features of familial interstitial pneumonia
-
DOI 10.1164/rccm.200408-1104OC
-
Steele MP, Speer MC, Loyd JE, et al. Clinical and pathologic features of familial interstitial pneumonia. Am J Respir Crit Care Med 2005; 172:1146-52. (Pubitemid 43066651)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.172
, Issue.9
, pp. 1146-1152
-
-
Steele, M.P.1
Speer, M.C.2
Loyd, J.E.3
Brown, K.K.4
Herron, A.5
Slifer, S.H.6
Burch, L.H.7
Wahidi, M.M.8
Phillips III, J.A.9
Sporn, T.A.10
McAdams, H.P.11
Schwarz, M.I.12
Schwartz, D.A.13
-
6
-
-
0036570052
-
Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
-
DOI 10.1164/rccm.200112-123OC
-
Thomas AQ, Lane K, Phillips J III, et al. Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred. Am J Respir Crit Care Med 2002;165:1322-8. (Pubitemid 34461748)
-
(2002)
American Journal of Respiratory and Critical Care Medicine
, vol.165
, Issue.9
, pp. 1322-1328
-
-
Thomas, A.Q.1
Lane, K.2
Phillips III, J.3
Prince, M.4
Markin, C.5
Speer, M.6
Schwartz, D.A.7
Gaddipati, R.8
Marney, A.9
Johnson, J.10
Roberts, R.11
Haines, J.12
Stahlman, M.13
Loyd, J.E.14
-
8
-
-
0036933489
-
The myofibroblast in pulmonary fibrosis
-
Phan SH. The myofibroblast in pulmonary fibrosis. Chest 2002;122: 286S-9S. (Pubitemid 36043014)
-
(2002)
Chest
, vol.122
, Issue.6 SUPPL.
-
-
Phan, S.H.1
-
9
-
-
0025729855
-
The roles of the myofibroblast in idiopathic pulmonary fibrosis. Ultrastructural and immunohistochemical features ofsites ofactive extracellular matrix synthesis
-
Kuhn C, McDonald JA. The roles of the myofibroblast in idiopathic pulmonary fibrosis. Ultrastructural and immunohistochemical features ofsites ofactive extracellular matrix synthesis. Am J Pathol 1991;138:1257-65.
-
(1991)
Am J Pathol
, vol.138
, pp. 1257-65
-
-
Kuhn, C.1
McDonald, J.A.2
-
10
-
-
0035895243
-
Idiopathic pulmonary fibrosis: Prevailing and evolving hypotheses about its pathogenesis and implications for therapy
-
Selman M, King TE, Pardo A. Idiopathic pulmonaryfibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med 2001;134:136-51. (Pubitemid 32096342)
-
(2001)
Annals of Internal Medicine
, vol.134
, Issue.2
, pp. 136-151
-
-
Selman, M.1
King Jr., T.E.2
Pardo, A.3
-
11
-
-
4243944861
-
Molecular mechanisms ofpulmonary fibrosis
-
Pardo A, Selman M. Molecular mechanisms ofpulmonary fibrosis. Front Biosci 2002;7:d1743-61.
-
(2002)
Front Biosci
, vol.7
-
-
Pardo, A.1
Selman, M.2
-
12
-
-
0034883331
-
Type II alveolar epithelial cells and interstitial fibroblasts express connective tissue growth factor in IPF
-
DOI 10.1183/09031936.01.00074101
-
Pan LH, Yamauchi K, Uzuki M, et al. Type II alveolar epithelial cells and interstitial fibroblasts express connective tissue growth factor in IPF. Eur Respir J 2001;17:1220-7. (Pubitemid 32717482)
-
(2001)
European Respiratory Journal
, vol.17
, Issue.6
, pp. 1220-1227
-
-
Pan, L.-H.1
Yamauchi, K.2
Uzuki, M.3
Nakanishi, T.4
Takigawa, M.5
Inoue, H.6
Sawai, T.7
-
13
-
-
0025053989
-
Platelet-derived growth factor in idiopathic pulmonary fibrosis
-
Antoniades HN, Bravo MA, Avila RE, et al. Platelet-derived growth factor in idiopathic pulmonary fibrosis. J Clin Invest 1990;86:1055-64. (Pubitemid 20370408)
-
(1990)
Journal of Clinical Investigation
, vol.86
, Issue.4
, pp. 1055-1064
-
-
Antoniades, H.N.1
Bravo, M.A.2
Avila, R.E.3
Galanopoulos, T.4
Neville-Golden, J.5
Maxwell, M.6
Selman, M.7
-
14
-
-
0030076509
-
3, Is Differentially Present in Epithelial Cells of Advanced Pulmonary Fibrosis: An Immunohistochemical Study
-
Khalil N, O'Connor RN, Flanders KC, et al. TGF-beta 1, but not TGF-beta 2 or TGF-beta 3, is differentially present in epithelial cells of advanced pulmonary fibrosis: an immunohistochemical study. Am J Respir Cell Mol Biol 1996;14:131-8. (Pubitemid 126441385)
-
(1996)
American Journal of Respiratory Cell and Molecular Biology
, vol.14
, Issue.2
, pp. 131-138
-
-
Khalil, N.1
O'Connor, R.N.2
Flanders, K.C.3
Unruh, H.4
-
15
-
-
4644344422
-
Apoptosis in lung injury and remodeling
-
DOI 10.1152/japplphysiol.00519.2004
-
Li X, Shu R, Filippatos G, et al. Apoptosis in lung injury and remodeling. J Appl Physiol 2004;97:1535-42. (Pubitemid 39299374)
-
(2004)
Journal of Applied Physiology
, vol.97
, Issue.4
, pp. 1535-1542
-
-
Li, X.1
Shu, R.2
Filippatos, G.3
Uhal, B.D.4
-
16
-
-
0032437815
-
Alveolar epithelial cell death adjacent to underlying myofibroblasts in advanced fibrotic human lung
-
Uhal BD, Joshi I, Hughes WF, et al. Alveolar epithelial cell death adjacent to underlying myofibroblasts in advanced fibrotic human lung. Am J Physiol 1998;275:L1192-9.
-
(1998)
Am J Physiol
, vol.275
-
-
Uhal, B.D.1
Joshi, I.2
Hughes, W.F.3
-
17
-
-
0030638505
-
Apoptosis and Expression of Fas/Fas Ligand mRNA in Bleomycin-induced Pulmonary Fibrosis in Mice
-
Hagimoto N, Kuwano K, Nomoto Y, et al. Apoptosis and expression of Fas/Fas ligand mRNA in bleomycin-induced pulmonary fibrosis in mice. Am J Respir Cell Mol Biol 1997;16:91-101. (Pubitemid 127497440)
-
(1997)
American Journal of Respiratory Cell and Molecular Biology
, vol.16
, Issue.1
, pp. 91-101
-
-
Hagimoto, N.1
Kuwano, K.2
Nomoto, Y.3
Kunitake, R.4
Hara, N.5
-
18
-
-
77957337716
-
Repetitive intratracheal bleomycin models several features of idiopathic pulmonary fibrosis
-
Degryse AL, Tanjore H, Xu XC, et al. Repetitive intratracheal bleomycin models several features of idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol 2010;299:L442-52.
-
(2010)
Am J Physiol Lung Cell Mol Physiol
, vol.299
-
-
Degryse, A.L.1
Tanjore, H.2
Xu, X.C.3
-
19
-
-
0033862955
-
Abrogation of bleomycin-induced epithelial apoptosis and lung fibrosis by captopril or by a caspase inhibitor
-
Wang R, Ibarra-Sunga O, Verlinski L, et al. Abrogation ofbleomy-cin-induced epithelial apoptosis and lung fibrosis by captopril or by a caspase inhibitor. Am J Physiol Lung Cell Mol Physiol 2000;279: L143-51. (Pubitemid 30619534)
-
(2000)
American Journal of Physiology - Lung Cellular and Molecular Physiology
, vol.279
, Issue.1
-
-
Wang, R.1
Ibarra-Sunga, O.2
Verlinski, L.3
Pick, R.4
Uhal, B.D.5
-
20
-
-
14344283933
-
Attenuation of bleomy-cin-induced pneumopathy in mice by a caspase inhibitor
-
Kuwano K, Kunitake R, Maeyama T, et al. Attenuation of bleomy-cin-induced pneumopathy in mice by a caspase inhibitor. Am J Physiol Lung Cell Mol Physiol 2001;280:L316-25.
-
(2001)
Am J Physiol Lung Cell Mol Physiol
, vol.280
-
-
Kuwano, K.1
Kunitake, R.2
Maeyama, T.3
-
21
-
-
3543109115
-
1-induced pulmonary fibrosis
-
DOI 10.1084/jem.20040104
-
Lee CG, Cho SJ, Kang MJ, et al. Early growth response gene 1-mediated apoptosis is essential for transforming growth factor beta1-induced pulmonary fibrosis. J Exp Med 2004;200:377-89. (Pubitemid 39031256)
-
(2004)
Journal of Experimental Medicine
, vol.200
, Issue.3
, pp. 377-389
-
-
Lee, C.G.1
Cho, S.J.2
Kang, M.J.3
Chapoval, S.P.4
Lee, P.J.5
Noble, P.W.6
Yehualaeshet, T.7
Lu, B.8
Flavell, R.A.9
Milbrandt, J.10
Homer, R.J.11
Elias, J.A.12
-
22
-
-
76749165460
-
Targeted injury of type II alveolar epithelial cells induces pulmonary fibrosis
-
Sisson TH, Mendez M, Choi K, et al. Targeted injury of type II alveolar epithelial cells induces pulmonary fibrosis. Am J Respir Crit Care Med 2010;181:254-63.
-
(2010)
Am J Respir Crit Care Med
, vol.181
, pp. 254-63
-
-
Sisson, T.H.1
Mendez, M.2
Choi, K.3
-
23
-
-
0035931973
-
A mutation in the surfactant protein C gene associated with familial interstitial lung disease
-
DOI 10.1056/NEJM200102223440805
-
Nogee LM, Dunbar AE III, Wert SE, et al. A mutation in the surfactant protein C gene associated with familial interstitial lung disease. N Engl J Med 2001;344:573-9. (Pubitemid 32167871)
-
(2001)
New England Journal of Medicine
, vol.344
, Issue.8
, pp. 573-579
-
-
Nogee, L.M.1
Dunbar, A.E.2
Wert, S.E.3
Askin, F.4
Hamvas, A.5
Whitsett, J.A.6
-
24
-
-
48949119341
-
Endoplasmic retic-ulum 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 retic-ulum 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:L1119-26.
-
(2008)
Am J Physiol Lung Cell Mol Physiol
, vol.294
-
-
Lawson, W.E.1
Crossno, P.F.2
Polosukhin, V.V.3
-
25
-
-
58149159548
-
Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer
-
Wang Y, Kuan PJ, Xing C, et al. Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet 2009;84:52-9.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 52-9
-
-
Wang, Y.1
Kuan, P.J.2
Xing, C.3
-
26
-
-
20044378690
-
A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation
-
DOI 10.1165/rcmb.2005-0009OC
-
Mulugeta S, Nguyen V, Russo SJ, et al. A surfactant protein C precursor protein BRICHOS domain mutation causes endoplasmic reticulum stress, proteasome dysfunction, and caspase 3 activation Am J Respir Cell Mol Biol 2005;32:521-30. (Pubitemid 40770130)
-
(2005)
American Journal of Respiratory Cell and Molecular Biology
, vol.32
, Issue.6
, pp. 521-530
-
-
Mulugeta, S.1
Nguyen, V.2
Russo, S.J.3
Muniswamy, M.4
Beers, M.F.5
-
27
-
-
34548388834
-
Misfolded BRICHOS SP-C mutant proteins induce apoptosis via caspase-4- and cytochrome c-related mechanisms
-
DOI 10.1152/ajplung.00025.2007
-
Mulugeta S, Maguire JA, Newitt JL, et al. Misfolded BRICHOS SP-C mutant proteins induce apoptosis via caspase-4-and cytochrome c-related mechanisms. Am J Physiol Lung Cell Mol Physiol 2007;293: L720-9. (Pubitemid 47358835)
-
(2007)
American Journal of Physiology - Lung Cellular and Molecular Physiology
, vol.293
, Issue.3
-
-
Mulugeta, S.1
Maguire, J.A.2
Newitt, J.L.3
Russo, S.J.4
Kotorashvili, A.5
Beers, M.F.6
-
28
-
-
0034604129
-
The acute respiratory distress syndrome
-
DOI 10.1056/NEJM200005043421806
-
Ware LB, Matthay MA. The acute respiratory distress syndrome. N Engl J Med 2000;342:1334-49. (Pubitemid 30408719)
-
(2000)
New England Journal of Medicine
, vol.342
, Issue.18
, pp. 1334-1349
-
-
Ware, L.B.1
Matthay, M.A.2
-
30
-
-
0042831333
-
Role of repeated lung injury and genetic background in bleomycin-induced fibrosis
-
DOI 10.1165/rcmb.2003-0029OC
-
Chung MP, Monick MM, Hamzeh NY, et al. Role ofrepeated lung injury and genetic background in bleomycin-induced fibrosis. Am J Respir Cell Mol Biol 2003;29:375-80. (Pubitemid 37093996)
-
(2003)
American Journal of Respiratory Cell and Molecular Biology
, vol.29
, Issue.3 I
, pp. 375-380
-
-
Chung, M.P.1
Monick, M.M.2
Hamzeh, N.Y.3
Butler, N.S.4
Powers, L.S.5
Hunninghake, G.W.6
-
31
-
-
27544476860
-
Increased and prolonged pulmonary fibrosis in surfactant protein C-deficient mice following intratracheal bleomycin
-
Lawson WE, Polosukhin VV, Stathopoulos GT, et al. Increased and prolonged pulmonary fibrosis in surfactant protein C-deficient mice following intratracheal bleomycin. Am J Pathol 2005;167:1267-77. (Pubitemid 41541413)
-
(2005)
American Journal of Pathology
, vol.167
, Issue.5
, pp. 1267-1277
-
-
Lawson, W.E.1
Polosukhin, V.V.2
Stathopoulos, G.T.3
Zoia, O.4
Han, W.5
Lane, K.B.6
Li, B.7
Donnelly, E.F.8
Holburn, G.E.9
Lewis, K.G.10
Collins, R.D.11
Hull, W.M.12
Glasser, S.W.13
Whitsett, J.A.14
Blackwell, T.S.15
-
32
-
-
34047188508
-
Telomerase mutations in families with idiopathic pulmonary fibrosis
-
DOI 10.1056/NEJMoa066157
-
Armanios MY, Chen JJ, Cogan JD, et al. Telomerase mutations in families with idiopathic pulmonary fibrosis. N Engl J Med 2007;356: 1317-26. (Pubitemid 46513297)
-
(2007)
New England Journal of Medicine
, vol.356
, Issue.13
, pp. 1317-1326
-
-
Armanios, M.Y.1
Chen, J.J.-L.2
Cogan, J.D.3
Alder, J.K.4
Ingersoll, R.G.5
Markin, C.6
Lawson, W.E.7
Xie, M.8
Vulto, I.9
Phillips III, J.A.10
Lansdorp, P.M.11
Greider, C.W.12
Loyd, J.E.13
-
33
-
-
34250614359
-
Adult-onset pulmonary fibrosis caused by mutations in telomerase
-
DOI 10.1073/pnas.0701009104
-
Tsakiri KD, Cronkhite JT, Kuan PJ, et al. Adult-onset pulmonary fibrosis caused by mutations in telomerase. Proc Natl Acad Sci USA 2007;104:7552-7. (Pubitemid 47185944)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.18
, pp. 7552-7557
-
-
Tsakiri, K.D.1
Cronkhite, J.T.2
Kuan, P.J.3
Xing, C.4
Raghu, G.5
Weissler, J.C.6
Rosenblatt, R.L.7
Shay, J.W.8
Garcia, C.K.9
-
34
-
-
70349441112
-
Contribution ofepithelial-derived fibroblasts to bleomycin-induced lung fibrosis
-
Tanjore H, Xu XC, Polosukhin VV, et al. Contribution ofepithelial-derived fibroblasts to bleomycin-induced lung fibrosis. Am J Respir Crit Care Med 2009;180:657-65.
-
(2009)
Am J Respir Crit Care Med
, vol.180
, pp. 657-65
-
-
Tanjore, H.1
Xu, X.C.2
Polosukhin, V.V.3
-
35
-
-
33744935773
-
The genetic approach in pulmonary fibrosis: Can it provide clues to this complex disease?
-
DOI 10.1513/pats.200512-137TK
-
Lawson WE, Loyd JE. The genetic approach in pulmonary fibrosis: can it provide clues to this complex disease? Proc Am Thorac Soc 2006;3:345-9. (Pubitemid 43845411)
-
(2006)
Proceedings of the American Thoracic Society
, vol.3
, Issue.4
, pp. 345-349
-
-
Lawson, W.E.1
Loyd, J.E.2
-
36
-
-
21844478279
-
Familial idiopathic pulmonary fibrosis: Clinical features and outcome
-
Lee HL, Ryu JH, Wittmer MH, et al. Familial idiopathic pulmonary fibrosis: clinical features and outcome. Chest 2005;127:2034-41.
-
(2005)
Chest
, vol.127
, pp. 2034-41
-
-
Lee, H.L.1
Ryu, J.H.2
Wittmer, M.H.3
-
37
-
-
8544245673
-
Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
-
DOI 10.1136/thx.2004.026336
-
Lawson WE, Grant SW, Ambrosini V, et al. Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF. Thorax 2004;59:977-80. (Pubitemid 39490784)
-
(2004)
Thorax
, vol.59
, Issue.11
, pp. 977-980
-
-
Lawson, W.E.1
Grant, S.W.2
Ambrosini, V.3
Womble, K.E.4
Dawson, E.P.5
Lane, K.B.6
Markin, C.7
Renzoni, E.8
Lympany, P.9
Thomas, A.Q.10
Roldan, J.11
Scott, T.A.12
Blackwell, T.S.13
Phillips III, J.A.14
Loyd, J.E.15
Du Bois, R.M.16
-
38
-
-
77950815362
-
Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC
-
Crossno PF, Polosukhin VV, Blackwell TS, et al. Identification of early interstitial lung disease in an individual with genetic variations in ABCA3 and SFTPC Chest 2010;137:969-73.
-
(2010)
Chest
, vol.137
, pp. 969-73
-
-
Crossno, P.F.1
Polosukhin, V.V.2
Blackwell, T.S.3
|