메뉴 건너뛰기




Volumn 25, Issue 5, 2005, Pages 915-927

Genetics of fibrosing lung diseases

Author keywords

Familial; Genetics; Interstitial lung disease; Pulmonary fibrosis

Indexed keywords

AUTOANTIBODY; CENTROMERE ANTIBODY; COMPLEMENT RECEPTOR; DNA TOPOISOMERASE; HLA DP ANTIGEN; HLA DR ANTIGEN; INTERLEUKIN 1 RECEPTOR BLOCKING AGENT; INTERLEUKIN 6; SURFACTANT PROTEIN C; TRANSFORMING GROWTH FACTOR BETA1; TUMOR NECROSIS FACTOR; TUMOR NECROSIS FACTOR RECEPTOR 2;

EID: 18744374226     PISSN: 09031936     EISSN: None     Source Type: Journal    
DOI: 10.1183/09031936.05.00133404     Document Type: Review
Times cited : (95)

References (94)
  • 1
    • 0033036715 scopus 로고    scopus 로고
    • The diagnosis, assessment and treatment of diffuse parenchymal lung disease in adults
    • British Thoracic Society recommendations
    • Cushley MJ, Davison AG, du Bois RM, et al. The diagnosis, assessment and treatment of diffuse parenchymal lung disease in adults. British Thoracic Society recommendations. Thorax 1999; 54: Suppl. 1, S1-S30.
    • (1999) Thorax , vol.54 , Issue.SUPPL. 1
    • Cushley, M.J.1    Davison, A.G.2    du Bois, R.M.3
  • 2
    • 0037080547 scopus 로고    scopus 로고
    • American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias
    • American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. Am J Respir Crit Care Med 2002; 165: 277-304.
    • (2002) Am. J. Respir. Crit. Care Med. , vol.165 , pp. 277-304
  • 3
    • 18744389254 scopus 로고    scopus 로고
    • Familial pulmonary fibrosis (FPF) in the United States: Clinical characteristics and patterns of inheritance
    • Steele MP, Speer MC, Loyd JE, et al. Familial pulmonary fibrosis (FPF) in the United States: clinical characteristics and patterns of inheritance. Am J Respir Crit Care Med 2004; 169: A550.
    • (2004) Am. J. Respir. Crit. Care Med. , vol.169
    • Steele, M.P.1    Speer, M.C.2    Loyd, J.E.3
  • 5
    • 0034018105 scopus 로고    scopus 로고
    • Adult familial cryptogenic fibrosing alveolitis in the United Kingdom
    • Marshall RP, Puddicombe A, Cookson WO, Laurent GJ. Adult familial cryptogenic fibrosing alveolitis in the United Kingdom. Thorax 2000; 55: 143-146.
    • (2000) Thorax , vol.55 , pp. 143-146
    • Marshall, R.P.1    Puddicombe, A.2    Cookson, W.O.3    Laurent, G.J.4
  • 6
    • 0042328231 scopus 로고    scopus 로고
    • Pulmonary fibrosis in families
    • Loyd JE. Pulmonary fibrosis in families. Am J Respir Cell Mol Biol 2003; 29: Suppl. 3, S47-S50.
    • (2003) Am. J. Respir. Cell Mol. Biol. , vol.29 , Issue.SUPPL. 3
    • Loyd, J.E.1
  • 7
    • 0036214069 scopus 로고    scopus 로고
    • Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: Evidence of founder effect among multiplex families in Finland
    • Hodgson U, Laitinen T, Tukiainen P. Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: evidence of founder effect among multiplex families in Finland. Thorax 2002; 57: 338-342.
    • (2002) Thorax , vol.57 , pp. 338-342
    • Hodgson, U.1    Laitinen, T.2    Tukiainen, P.3
  • 8
    • 0036570052 scopus 로고    scopus 로고
    • Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred
    • 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: 1322-1328.
    • (2002) Am. J. Respir. Crit. Care Med. , vol.165 , pp. 1322-1328
    • Thomas, A.Q.1    Lane, K.2    Phillips III, J.3
  • 10
    • 0022654849 scopus 로고
    • Genetic studies in familial fibrosing alveolitis. Possible linkage with immunoglobulin allotypes (Gm)
    • Musk AW, Zilko PJ, Manners P, Kay PH, Kamboh MI. Genetic studies in familial fibrosing alveolitis. Possible linkage with immunoglobulin allotypes (Gm). Chest 1986; 89: 206-210.
    • (1986) Chest , vol.89 , pp. 206-210
    • Musk, A.W.1    Zilko, P.J.2    Manners, P.3    Kay, P.H.4    Kamboh, M.I.5
  • 12
    • 0037442389 scopus 로고    scopus 로고
    • Deletion of exon 4 from human surfactant protein C results in aggresome formation and generation of a dominant negative
    • Wang WJ, Mulugeta S, Russo SJ, Beers MF. Deletion of exon 4 from human surfactant protein C results in aggresome formation and generation of a dominant negative. J Cell Sci 2003; 116: 683-692.
    • (2003) J. Cell Sci. , vol.116 , pp. 683-692
    • Wang, W.J.1    Mulugeta, S.2    Russo, S.J.3    Beers, M.F.4
  • 13
    • 0023724623 scopus 로고
    • The gene encoding the hydrophobic surfactant protein SP-C is located on 8p and identifies an EcoRI RFLP
    • Fisher JH, Emrie PA, Drabkin HA, et al. The gene encoding the hydrophobic surfactant protein SP-C is located on 8p and identifies an EcoRI RFLP. Am J Hum Genet 1988; 43: 436-441.
    • (1988) Am. J. Hum. Genet. , vol.43 , pp. 436-441
    • Fisher, J.H.1    Emrie, P.A.2    Drabkin, H.A.3
  • 15
    • 3442875930 scopus 로고    scopus 로고
    • Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene
    • Brasch F, Griese M, Tredano M, et al. Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene. Eur Respir J 2004; 24: 30-39.
    • (2004) Eur. Respir. J. , vol.24 , pp. 30-39
    • Brasch, F.1    Griese, M.2    Tredano, M.3
  • 16
    • 11144354727 scopus 로고    scopus 로고
    • Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease
    • Tredano M, Griese M, Brasch F, et al. Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease. Am J Med Genet 2004; 126A: 18-26.
    • (2004) Am. J. Med. Genet. , vol.126 A , pp. 18-26
    • Tredano, M.1    Griese, M.2    Brasch, F.3
  • 17
    • 0036948098 scopus 로고    scopus 로고
    • SNPper: Retrieval and analysis of human SNPs
    • Version 118. Date last accessed: October 6 2004
    • Riva A, Kohane IS. SNPper: retrieval and analysis of human SNPs. Bioinformatics 2002; 18: 1681-1685. Version 118. http://snpper.chip.org/bio/show-sequence/?TYPE=U&GENE=18686. Date last accessed: October 6 2004.
    • (2002) Bioinformatics , vol.18 , pp. 1681-1685
    • Riva, A.1    Kohane, I.S.2
  • 18
    • 0036569894 scopus 로고    scopus 로고
    • Genetic basis of familial interstitial lung disease: Misfolding or function of surfactant protein C?
    • Whitsett JA. Genetic basis of familial interstitial lung disease: misfolding or function of surfactant protein C? Am J Respir Crit Care Med 2002; 165: 1201-1202.
    • (2002) Am. J. Respir. Crit. Care Med. , vol.165 , pp. 1201-1202
    • Whitsett, J.A.1
  • 19
    • 0027090063 scopus 로고
    • Structure and functions of a dimeric form of surfactant protein SP-C: A Fourier transform infrared and surfactometry study
    • Baatz JE, Smyth KL, Whitsett JA, Baxter C, Absolom DR. Structure and functions of a dimeric form of surfactant protein SP-C: a Fourier transform infrared and surfactometry study. Chem Phys Lipids 1992; 63: 91-104.
    • (1992) Chem. Phys. Lipids , vol.63 , pp. 91-104
    • Baatz, J.E.1    Smyth, K.L.2    Whitsett, J.A.3    Baxter, C.4    Absolom, D.R.5
  • 20
    • 0034968955 scopus 로고    scopus 로고
    • Surfactant protein deficiency in familial interstitial lung disease
    • Amin RS, Wert SE, Baughman RP, et al. Surfactant protein deficiency in familial interstitial lung disease. J Pediatr 2001; 139: 85-92.
    • (2001) J. Pediatr. , vol.139 , pp. 85-92
    • Amin, R.S.1    Wert, S.E.2    Baughman, R.P.3
  • 21
    • 0037666799 scopus 로고    scopus 로고
    • Hermansky-Pudlak syndrome type 4 (HPS-4): Clinical and molecular characteristics
    • Anderson PD, Huizing M, Claassen DA, White J, Gahl WA. Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics. Hum Genet 2003; 113: 10-17.
    • (2003) Hum. Genet. , vol.113 , pp. 10-17
    • Anderson, P.D.1    Huizing, M.2    Claassen, D.A.3    White, J.4    Gahl, W.A.5
  • 22
    • 0031566379 scopus 로고    scopus 로고
    • β3A-adaptin, a subunit of the adaptor-like complex AP-3
    • Dell'Angelica EC, Ooi CE, Bonifacino JS. β3A-adaptin, a subunit of the adaptor-like complex AP-3. J Biol Chem 1997; 272: 15078-15084.
    • (1997) J. Biol. Chem. , vol.272 , pp. 15078-15084
    • Dell'Angelica, E.C.1    Ooi, C.E.2    Bonifacino, J.S.3
  • 24
    • 0033829367 scopus 로고    scopus 로고
    • Interstitial pneumonia in Hermansky-Pudlak syndrome: Significance of florid foamy swelling/degeneration (giant lamellar body degeneration) of type-2 pneumocytes
    • Nakatani Y, Nakamura N, Sano J, et al. Interstitial pneumonia in Hermansky-Pudlak syndrome: significance of florid foamy swelling/degeneration (giant lamellar body degeneration) of type-2 pneumocytes. Virchows Arch 2000; 437: 304-313.
    • (2000) Virchows Arch. , vol.437 , pp. 304-313
    • Nakatani, Y.1    Nakamura, N.2    Sano, J.3
  • 25
    • 0035895243 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: Prevailing and evolving hypotheses about its pathogenesis and implications for therapy
    • Selman M, King TE, Pardo A. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med 2001; 134: 136-151.
    • (2001) Ann. Intern. Med. , vol.134 , pp. 136-151
    • Selman, M.1    King, T.E.2    Pardo, A.3
  • 26
    • 0041827226 scopus 로고    scopus 로고
    • The epithelial/fibroblastic pathway in the pathogenesis of idiopathic pulmonary fibrosis
    • Selman M, Pardo A. The epithelial/fibroblastic pathway in the pathogenesis of idiopathic pulmonary fibrosis. Am J Respir Cell Mol Biol 2003; 29: Suppl. 3, S93-S97.
    • (2003) Am. J. Respir. Cell Mol. Biol. , vol.29 , Issue.SUPPL. 3
    • Selman, M.1    Pardo, A.2
  • 27
    • 0037426052 scopus 로고    scopus 로고
    • Problems of reporting genetic associations with complex outcomes
    • Colhoun HM, McKeigue PM, Davey SG. Problems of reporting genetic associations with complex outcomes. Lancet 2003; 361: 865-872.
    • (2003) Lancet , vol.361 , pp. 865-872
    • Colhoun, H.M.1    McKeigue, P.M.2    Davey, S.G.3
  • 28
    • 0036128213 scopus 로고    scopus 로고
    • The genetic predisposition to interstitial lung disease: Functional relevance
    • du Bois RM. The genetic predisposition to interstitial lung disease: functional relevance. Chest 2002; 121: Suppl. 3, 14S-20S.
    • (2002) Chest , vol.121 , Issue.SUPPL. 3
    • du Bois, R.M.1
  • 29
    • 0037080545 scopus 로고    scopus 로고
    • Interleukin-1 gene cluster polymorphisms in sarcoidosis and idiopathic pulmonary fibrosis
    • Hutyrova B, Pantelidis P, Drabek J, et al. Interleukin-1 gene cluster polymorphisms in sarcoidosis and idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2002; 165: 148-151.
    • (2002) Am. J. Respir. Crit. Care Med. , vol.165 , pp. 148-151
    • Hutyrova, B.1    Pantelidis, P.2    Drabek, J.3
  • 30
    • 0033837130 scopus 로고    scopus 로고
    • Increased risk of fibrosing alveolitis associated with interleukin-1 receptor antagonist and tumor necrosis factor-α gene polymorphisms
    • Whyte M, Hubbard R, Meliconi R, et al. Increased risk of fibrosing alveolitis associated with interleukin-1 receptor antagonist and tumor necrosis factor-α gene polymorphisms. Am J Respir Crit Care Med 2000; 162: 755-758.
    • (2000) Am. J. Respir. Crit. Care Med. , vol.162 , pp. 755-758
    • Whyte, M.1    Hubbard, R.2    Meliconi, R.3
  • 32
    • 0034993072 scopus 로고    scopus 로고
    • Analysis of tumor necrosis factor-α, lymphotoxin-α, tumor necrosis factor receptor II, and interleukin-6 polymorphisms in patients with idiopathic pulmonary fibrosis
    • Pantelidis P, Fanning GC, Wells AU, Welsh KI, du Bois RM. Analysis of tumor necrosis factor-α, lymphotoxin-α, tumor necrosis factor receptor II, and interleukin-6 polymorphisms in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2001; 163: 1432-1436.
    • (2001) Am. J. Respir. Crit. Care Med. , vol.163 , pp. 1432-1436
    • Pantelidis, P.1    Fanning, G.C.2    Wells, A.U.3    Welsh, K.I.4    du Bois, R.M.5
  • 34
    • 0033923117 scopus 로고    scopus 로고
    • Distribution of novel polymorphisms of the interleukin-8 and CXC receptor 1 and 2 genes in systemic sclerosis and cryptogenic fibrosing alveolitis
    • Renzoni E, Lympany P, Sestini P, et al. Distribution of novel polymorphisms of the interleukin-8 and CXC receptor 1 and 2 genes in systemic sclerosis and cryptogenic fibrosing alveolitis. Arthritis Rheum 2000; 43: 1633-1640.
    • (2000) Arthritis Rheum. , vol.43 , pp. 1633-1640
    • Renzoni, E.1    Lympany, P.2    Sestini, P.3
  • 35
    • 11144308883 scopus 로고    scopus 로고
    • Analysis of IL-12 p40 subunit gene and IFN-γ G5644A polymorphisms in idiopathic pulmonary fibrosis
    • Latsi P, Pantelidis P, Vassilakis D, Sato H, Welsh KI, du Bois RM. Analysis of IL-12 p40 subunit gene and IFN-γ G5644A polymorphisms in idiopathic pulmonary fibrosis. Respir Res 2003; 4: 6. http://respiratory-research.com/content/4/1/6.
    • (2003) Respir. Res. , vol.4 , pp. 6
    • Latsi, P.1    Pantelidis, P.2    Vassilakis, D.3    Sato, H.4    Welsh, K.I.5    du Bois, R.M.6
  • 37
    • 0242690510 scopus 로고    scopus 로고
    • Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis
    • Selman M, Lin HM, Montano M, et al. Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis. Hum Genet 2003; 113: 542-550.
    • (2003) Hum. Genet. , vol.113 , pp. 542-550
    • Selman, M.1    Lin, H.M.2    Montano, M.3
  • 38
    • 0037530490 scopus 로고    scopus 로고
    • A plasminogen activator inhibitor-1 promoter polymorphism and idiopathic interstitial pneumonia
    • Kim KK, Flaherty KR, Long Q, et al. A plasminogen activator inhibitor-1 promoter polymorphism and idiopathic interstitial pneumonia. Mol Med 2003; 9: 52-56.
    • (2003) Mol. Med. , vol.9 , pp. 52-56
    • Kim, K.K.1    Flaherty, K.R.2    Long, Q.3
  • 39
    • 0041326688 scopus 로고    scopus 로고
    • Transforming growth factor-β1 gene polymorphisms are associated with disease progression in idiopathic pulmonary fibrosis
    • Xaubet A, Marin-Arguedas A, Lario S, et al. Transforming growth factor-β1 gene polymorphisms are associated with disease progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2003; 168: 431-435.
    • (2003) Am. J. Respir. Crit. Care Med. , vol.168 , pp. 431-435
    • Xaubet, A.1    Marin-Arguedas, A.2    Lario, S.3
  • 40
    • 0034991863 scopus 로고    scopus 로고
    • Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosis
    • Morrison CD, Papp AC, Hejmanowski AQ, Addis VM, Prior TW. Increased D allele frequency of the angiotensin-converting enzyme gene in pulmonary fibrosis. Hum Pathol 2001; 32: 521-528.
    • (2001) Hum. Pathol. , vol.32 , pp. 521-528
    • Morrison, C.D.1    Papp, A.C.2    Hejmanowski, A.Q.3    Addis, V.M.4    Prior, T.W.5
  • 41
    • 0029952585 scopus 로고    scopus 로고
    • Co-expression of TNF alpha and IL-1 beta in human acute pulmonary fibrotic diseases: An immunohistochemical analysis
    • Pan LH, Ohtani H, Yamauchi K, Nagura H. Co-expression of TNF alpha and IL-1 beta in human acute pulmonary fibrotic diseases: an immunohistochemical analysis. Pathol Int 1996; 46: 91-99.
    • (1996) Pathol. Int. , vol.46 , pp. 91-99
    • Pan, L.H.1    Ohtani, H.2    Yamauchi, K.3    Nagura, H.4
  • 42
    • 0027231698 scopus 로고
    • Expression of tumour necrosis factor-α in cryptogenic fibrosing alveolitis
    • Nash JR, McLaughlin PJ, Butcher D, Corrin B. Expression of tumour necrosis factor-α in cryptogenic fibrosing alveolitis. Histopathology 1993; 22: 343-347.
    • (1993) Histopathology , vol.22 , pp. 343-347
    • Nash, J.R.1    McLaughlin, P.J.2    Butcher, D.3    Corrin, B.4
  • 43
    • 0027724235 scopus 로고
    • Expression and localization of tumor necrosis factor-α and its mRNA in idiopathic pulmonary fibrosis
    • Piguet PF, Ribaux C, Karpuz V, Grau GE, Kapanci Y. Expression and localization of tumor necrosis factor-α and its mRNA in idiopathic pulmonary fibrosis. Am J Pathol 1993; 143: 651-655.
    • (1993) Am. J. Pathol. , vol.143 , pp. 651-655
    • Piguet, P.F.1    Ribaux, C.2    Karpuz, V.3    Grau, G.E.4    Kapanci, Y.5
  • 46
    • 0035020567 scopus 로고    scopus 로고
    • Fibrosis of the lung and other tissues: New concepts in pathogenesis and treatment
    • Sime PJ, O'Reilly KM. Fibrosis of the lung and other tissues: new concepts in pathogenesis and treatment. Clin Immunol 2001; 99: 308-319.
    • (2001) Clin. Immunol. , vol.99 , pp. 308-319
    • Sime, P.J.1    O'Reilly, K.M.2
  • 47
    • 0033385544 scopus 로고    scopus 로고
    • Interleukin-4-producing cells in idiopathic pulmonary fibrosis: An immunohistochemical study
    • Ando M, Miyazaki E, Fukami T, Kumamoto T, Tsuda T. Interleukin-4-producing cells in idiopathic pulmonary fibrosis: an immunohistochemical study. Respirology 1999; 4: 383-391.
    • (1999) Respirology , vol.4 , pp. 383-391
    • Ando, M.1    Miyazaki, E.2    Fukami, T.3    Kumamoto, T.4    Tsuda, T.5
  • 48
    • 0029113474 scopus 로고
    • A type 2 (Th2-like) pattern of immune response predominates in the pulmonary interstitium of patients with cryptogenic fibrosing alveolitis (CFA)
    • Wallace WA, Ramage EA, Lamb D, Howie SE. A type 2 (Th2-like) pattern of immune response predominates in the pulmonary interstitium of patients with cryptogenic fibrosing alveolitis (CFA). Clin Exp Immunol 1995; 101: 436-441.
    • (1995) Clin. Exp. Immunol. , vol.101 , pp. 436-441
    • Wallace, W.A.1    Ramage, E.A.2    Lamb, D.3    Howie, S.E.4
  • 49
    • 0026550854 scopus 로고
    • In vivo levels and in vitro production of interferon-gamma in fibrosing interstitial lung diseases
    • Prior C, Haslam PL. In vivo levels and in vitro production of interferon-gamma in fibrosing interstitial lung diseases. Clin Exp Immunol 1992; 88: 280-287.
    • (1992) Clin. Exp. Immunol. , vol.88 , pp. 280-287
    • Prior, C.1    Haslam, P.L.2
  • 50
    • 0346877501 scopus 로고    scopus 로고
    • A TaqI polymorphism in the 3′UTR of the IL-12 p40 gene correlates with increased IL-12 secretion
    • Seegers D, Zwiers A, Strober W, Pena AS, Bouma G. A TaqI polymorphism in the 3′UTR of the IL-12 p40 gene correlates with increased IL-12 secretion. Genes Immun 2002; 3: 419-423.
    • (2002) Genes Immun. , vol.3 , pp. 419-423
    • Seegers, D.1    Zwiers, A.2    Strober, W.3    Pena, A.S.4    Bouma, G.5
  • 51
    • 25444468816 scopus 로고    scopus 로고
    • Surfactant gene polymorphisms and interstitial lung diseases
    • Pantelidis P, Veeraraghavan S, du Bois RM. Surfactant gene polymorphisms and interstitial lung diseases. Respir Res 2002; 3: 14. http://respiratory-research.com/content/3/1/14.
    • (2002) Respir. Res. , vol.3 , pp. 14
    • Pantelidis, P.1    Veeraraghavan, S.2    du Bois, R.M.3
  • 52
    • 17944363930 scopus 로고    scopus 로고
    • Surfactant protein gene A, B, and D marker alleles in chronic obstructive pulmonary disease of a Mexican population
    • Guo X, Lin HM, Lin Z, et al. Surfactant protein gene A, B, and D marker alleles in chronic obstructive pulmonary disease of a Mexican population. Eur Respir J 2001; 18: 482-490.
    • (2001) Eur. Respir. J. , vol.18 , pp. 482-490
    • Guo, X.1    Lin, H.M.2    Lin, Z.3
  • 53
    • 8544245673 scopus 로고    scopus 로고
    • Genetic mutations in surfactant protein C are a rare cause of sporadic cases of IPF
    • 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: 977-980.
    • (2004) Thorax , vol.59 , pp. 977-980
    • Lawson, W.E.1    Grant, S.W.2    Ambrosini, V.3
  • 54
    • 0024578662 scopus 로고
    • Glutathione deficiency in the epithelial lining fluid of the lower respiratory tract in idiopathic pulmonary fibrosis
    • Cantin AM, Hubbard RC, Crystal RG. Glutathione deficiency in the epithelial lining fluid of the lower respiratory tract in idiopathic pulmonary fibrosis. Am Rev Respir Dis 1989; 139: 370-372.
    • (1989) Am. Rev. Respir. Dis. , vol.139 , pp. 370-372
    • Cantin, A.M.1    Hubbard, R.C.2    Crystal, R.G.3
  • 55
    • 13644273518 scopus 로고
    • Oxidants and respiratory tract epithelial injury: Pathogenesis and strategies for therapeutic intervention
    • Crystal RG. Oxidants and respiratory tract epithelial injury: pathogenesis and strategies for therapeutic intervention. Am J Med 1991; 91: Suppl. 3C, 39S-44S.
    • (1991) Am. J. Med. , vol.91 , Issue.SUPPL. 3C
    • Crystal, R.G.1
  • 56
    • 0022135836 scopus 로고
    • Pathogenesis of "fibrosis" in interstitial pneumonia: An electron microscopic study
    • Katzenstein AL. Pathogenesis of "fibrosis" in interstitial pneumonia: an electron microscopic study. Hum Pathol 1985; 16: 1015-1024.
    • (1985) Hum. Pathol. , vol.16 , pp. 1015-1024
    • Katzenstein, A.L.1
  • 57
    • 0028929665 scopus 로고
    • Increased procoagulant and antifibrinolytic activities in the lungs with idiopathic pulmonary fibrosis
    • Kotani I, Sato A, Hayakawa H, Urano T, Takada Y, Takada A. Increased procoagulant and antifibrinolytic activities in the lungs with idiopathic pulmonary fibrosis. Thromb Res 1995; 77: 493-504.
    • (1995) Thromb. Res. , vol.77 , pp. 493-504
    • Kotani, I.1    Sato, A.2    Hayakawa, H.3    Urano, T.4    Takada, Y.5    Takada, A.6
  • 58
    • 0030791559 scopus 로고    scopus 로고
    • Tissue factor expression and fibrin deposition in the lungs of patients with idiopathic pulmonary fibrosis and systemic sclerosis
    • Imokawa S, Sato A, Hayakawa H, Kotani M, Urano T, Takada A. Tissue factor expression and fibrin deposition in the lungs of patients with idiopathic pulmonary fibrosis and systemic sclerosis. Am J Respir Crit Care Med 1997; 156: 631-636.
    • (1997) Am. J. Respir. Crit. Care Med. , vol.156 , pp. 631-636
    • Imokawa, S.1    Sato, A.2    Hayakawa, H.3    Kotani, M.4    Urano, T.5    Takada, A.6
  • 59
    • 0034661333 scopus 로고    scopus 로고
    • Relevance of tissue factor and tissue factor pathway inhibitor for hypercoagulable state in the lungs of patients with idiopathic pulmonary fibrosis
    • Fujii M, Hayakawa H, Urano T, et al. Relevance of tissue factor and tissue factor pathway inhibitor for hypercoagulable state in the lungs of patients with idiopathic pulmonary fibrosis. Thromb Res 2000; 99: 111-117.
    • (2000) Thromb. Res. , vol.99 , pp. 111-117
    • Fujii, M.1    Hayakawa, H.2    Urano, T.3
  • 60
    • 0042829360 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis. New insights into classification and pathogenesis usher in a new era therapeutic approaches
    • Noble PW. Idiopathic pulmonary fibrosis. New insights into classification and pathogenesis usher in a new era therapeutic approaches. Am J Respir Cell Mol Biol 2003; 29, Suppl. 3, S27-S31.
    • (2003) Am. J. Respir. Cell Mol. Biol. , vol.29 , Issue.SUPPL. 3
    • Noble, P.W.1
  • 61
    • 0030800795 scopus 로고    scopus 로고
    • Adenovector-mediated gene transfer of active transforming growth factor-β1 induces prolonged severe fibrosis in rat lung
    • Sime PJ, Xing Z, Graham FL, Csaky KG, Gauldie J. Adenovector-mediated gene transfer of active transforming growth factor-β1 induces prolonged severe fibrosis in rat lung. J Clin Invest 1997; 100: 768-776.
    • (1997) J. Clin. Invest. , vol.100 , pp. 768-776
    • Sime, P.J.1    Xing, Z.2    Graham, F.L.3    Csaky, K.G.4    Gauldie, J.5
  • 62
    • 18744374273 scopus 로고    scopus 로고
    • TGFβ3 has differential effects in the lung dependent on the underlying pathogenetic condition
    • Kolb M, Bonniaud P, Ask K, et al. TGFβ3 has differential effects in the lung dependent on the underlying pathogenetic condition. Eur Respir J 2003; 24: Suppl. 48, 481s.
    • (2003) Eur. Respir. J. , vol.24 , Issue.SUPPL. 48
    • Kolb, M.1    Bonniaud, P.2    Ask, K.3
  • 63
    • 0032958714 scopus 로고    scopus 로고
    • Genetic control of the circulating concentration of transforming growth factor type β1
    • Grainger DJ, Heathcote K, Chiano M, et al. Genetic control of the circulating concentration of transforming growth factor type β1. Hum Mol Genet 1999; 8: 93-97.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 93-97
    • Grainger, D.J.1    Heathcote, K.2    Chiano, M.3
  • 64
    • 0346057802 scopus 로고    scopus 로고
    • Reduction of bleomycin induced lung fibrosis by candesartan cilexetil, an angiotensin II type 1 receptor antagonist
    • Otsuka M, Takahashi H, Shiratori M, Chiba H, Abe S. Reduction of bleomycin induced lung fibrosis by candesartan cilexetil, an angiotensin II type 1 receptor antagonist. Thorax 2004; 59: 31-38.
    • (2004) Thorax , vol.59 , pp. 31-38
    • Otsuka, M.1    Takahashi, H.2    Shiratori, M.3    Chiba, H.4    Abe, S.5
  • 65
    • 0028296772 scopus 로고
    • Captopril inhibits proliferation of human lung fibroblasts in culture: A potential antifibrotic mechanism
    • Nguyen L, Ward WF, Ts'ao CH, Molteni A. Captopril inhibits proliferation of human lung fibroblasts in culture: a potential antifibrotic mechanism. Proc Soc Exp Biol Med 1994; 205: 80-84.
    • (1994) Proc. Soc. Exp. Biol. Med. , vol.205 , pp. 80-84
    • Nguyen, L.1    Ward, W.F.2    Ts'ao, C.H.3    Molteni, A.4
  • 66
    • 4143091523 scopus 로고    scopus 로고
    • Impact of angiotensin-converting enzyme inhibitors and statins on survival in idiopathic pulmonary fibrosis
    • Nadrous HF, Ryu JH, Douglas WW, Decker PA, Olson EJ. Impact of angiotensin-converting enzyme inhibitors and statins on survival in idiopathic pulmonary fibrosis. Chest 2004; 126: 438-446.
    • (2004) Chest , vol.126 , pp. 438-446
    • Nadrous, H.F.1    Ryu, J.H.2    Douglas, W.W.3    Decker, P.A.4    Olson, E.J.5
  • 67
    • 0023797003 scopus 로고
    • Familial resemblance of plasma angiotensin-converting enzyme level: The Nancy Study
    • Cambien F, Alhenc-Gelas F, Herbeth B, et al. Familial resemblance of plasma angiotensin-converting enzyme level: the Nancy Study. Am J Hum Genet 1988; 43: 774-780.
    • (1988) Am. J. Hum. Genet. , vol.43 , pp. 774-780
    • Cambien, F.1    Alhenc-Gelas, F.2    Herbeth, B.3
  • 68
    • 0025165779 scopus 로고
    • An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
    • Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest 1990; 86: 1343-1346.
    • (1990) J. Clin. Invest. , vol.86 , pp. 1343-1346
    • Rigat, B.1    Hubert, C.2    Alhenc-Gelas, F.3    Cambien, F.4    Corvol, P.5    Soubrier, F.6
  • 69
    • 0036094293 scopus 로고    scopus 로고
    • High prevalence of polymorphisms of angiotensin-converting enzyme (I/D) and endothelial nitric oxide synthase (Glu298Asp) in patients with systemic sclerosis
    • Fatini C, Gensini F, Sticchi E, et al. High prevalence of polymorphisms of angiotensin-converting enzyme (I/D) and endothelial nitric oxide synthase (Glu298Asp) in patients with systemic sclerosis. Am J Med 2002; 112: 540-544.
    • (2002) Am. J. Med. , vol.112 , pp. 540-544
    • Fatini, C.1    Gensini, F.2    Sticchi, E.3
  • 70
    • 18344396051 scopus 로고    scopus 로고
    • Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans
    • Zuo F, Kaminski N, Eugui E, et al. Gene expression analysis reveals matrilysin as a key regulator of pulmonary fibrosis in mice and humans. Proc Natl Acad Sci U S A 2002; 99: 6292-6297.
    • (2002) Proc. Natl. Acad. Sci. U. S. A. , vol.99 , pp. 6292-6297
    • Zuo, F.1    Kaminski, N.2    Eugui, E.3
  • 71
    • 0041827284 scopus 로고    scopus 로고
    • Microarray analysis of idiopathic pulmonary fibrosis
    • Kaminski N. Microarray analysis of idiopathic pulmonary fibrosis. Am J Respir Cell Mol Biol 2003; 29: Suppl. 3, S32-S36.
    • (2003) Am. J. Respir. Cell Mol. Biol. , vol.29 , Issue.SUPPL. 3
    • Kaminski, N.1
  • 72
    • 0036310631 scopus 로고    scopus 로고
    • Metalloproteinase and growth factor interactions: Do they play a role in pulmonary fibrosis?
    • Winkler MK, Fowlkes JL. Metalloproteinase and growth factor interactions: do they play a role in pulmonary fibrosis? Am J Physiol Lung Cell Mol Physiol 2002; 283: L1-L11.
    • (2002) Am. J. Physiol. Lung Cell Mol. Physiol. , vol.283
    • Winkler, M.K.1    Fowlkes, J.L.2
  • 73
    • 0035026949 scopus 로고    scopus 로고
    • Fibroblasts from idiopathic pulmonary fibrosis and normal lungs differ in growth rate, apoptosis, and tissue inhibitor of metalloproteinases expression
    • Ramos C, Montano M, Garcia-Alvarez J, et al. Fibroblasts from idiopathic pulmonary fibrosis and normal lungs differ in growth rate, apoptosis, and tissue inhibitor of metalloproteinases expression. Am J Respir Cell Mol Biol 2001; 24: 591-598.
    • (2001) Am. J. Respir. Cell Mol. Biol. , vol.24 , pp. 591-598
    • Ramos, C.1    Montano, M.2    Garcia-Alvarez, J.3
  • 74
    • 0041827227 scopus 로고    scopus 로고
    • Fibroblast phenotypes in pulmonary fibrosis
    • Phan SH. Fibroblast phenotypes in pulmonary fibrosis. Am J Respir Cell Mol Biol 2003; 29: Suppl. 3, S87-S92.
    • (2003) Am. J. Respir. Cell Mol. Biol. , vol.29 , Issue.SUPPL. 3
    • Phan, S.H.1
  • 75
    • 0035448128 scopus 로고    scopus 로고
    • Sarcoidosis: Do our genes really matter?
    • du Bois RM. Sarcoidosis: do our genes really matter? Am J Respir Crit Care Med 2001; 164: 725-726.
    • (2001) Am. J. Respir. Crit. Care Med. , vol.164 , pp. 725-726
    • du Bois, R.M.1
  • 76
    • 0032427870 scopus 로고    scopus 로고
    • Heterogeneous point mutations of the p53 gene in pulmonary fibrosis
    • Hojo S, Fujita J, Yamadori I, et al. Heterogeneous point mutations of the p53 gene in pulmonary fibrosis. Eur Respir J 1998; 12: 1404-1408.
    • (1998) Eur. Respir. J. , vol.12 , pp. 1404-1408
    • Hojo, S.1    Fujita, J.2    Yamadori, I.3
  • 77
    • 0031201212 scopus 로고    scopus 로고
    • The CXC chemokines, IL-8 and IP-10, regulate angiogenic activity in idiopathic pulmonary fibrosis
    • Keane MP, Arenberg DA, Lynch JP III, et al. The CXC chemokines, IL-8 and IP-10, regulate angiogenic activity in idiopathic pulmonary fibrosis. J Immunol 1997; 159: 1437-1443.
    • (1997) J. Immunol. , vol.159 , pp. 1437-1443
    • Keane, M.P.1    Arenberg, D.A.2    Lynch III, J.P.3
  • 78
    • 2542436942 scopus 로고    scopus 로고
    • Neovascularization in idiopathic pulmonary fibrosis: Too much or too little?
    • Renzoni EA. Neovascularization in idiopathic pulmonary fibrosis: too much or too little? Am J Respir Crit Care Med 2004; 169: 1179-1180.
    • (2004) Am. J. Respir. Crit. Care Med. , vol.169 , pp. 1179-1180
    • Renzoni, E.A.1
  • 79
    • 2542481862 scopus 로고    scopus 로고
    • Heterogeneous increase in CD34-positive alveolar capillaries in idiopathic pulmonary fibrosis
    • Ebina M, Shimizukawa M, Shibata N, et al. Heterogeneous increase in CD34-positive alveolar capillaries in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2004; 169: 1203-1208.
    • (2004) Am. J. Respir. Crit. Care Med. , vol.169 , pp. 1203-1208
    • Ebina, M.1    Shimizukawa, M.2    Shibata, N.3
  • 80
    • 3242754119 scopus 로고    scopus 로고
    • Pigment epithelium-derived factor in idiopathic pulmonary fibrosis: A role in aberrant angiogenesis
    • Cosgrove GP, Brown KK, Schiemann WP, et al. Pigment epithelium-derived factor in idiopathic pulmonary fibrosis: a role in aberrant angiogenesis. Am J Respir Crit Care Med 2004; 170: 242-251.
    • (2004) Am. J. Respir. Crit. Care Med. , vol.170 , pp. 242-251
    • Cosgrove, G.P.1    Brown, K.K.2    Schiemann, W.P.3
  • 81
    • 0037098050 scopus 로고    scopus 로고
    • Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome
    • Bouros D, Wells AU, Nicholson AG, et al. Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome. Am J Respir Crit Care Med 2002; 165: 1581-1586.
    • (2002) Am. J. Respir. Crit. Care Med. , vol.165 , pp. 1581-1586
    • Bouros, D.1    Wells, A.U.2    Nicholson, A.G.3
  • 82
    • 0346727461 scopus 로고    scopus 로고
    • Following the molecular pathways toward an understanding of the pathogenesis of systemic sclerosis
    • Jimenez SA, Derk CT. Following the molecular pathways toward an understanding of the pathogenesis of systemic sclerosis. Ann Intern Med 2004; 140: 37-50.
    • (2004) Ann. Intern. Med. , vol.140 , pp. 37-50
    • Jimenez, S.A.1    Derk, C.T.2
  • 84
    • 0035320790 scopus 로고    scopus 로고
    • Class II HLA associations with autoantibodies in scleroderma: A highly significant role for HLA-DP
    • Gilchrist FC, Bunn C, Foley PJ, et al. Class II HLA associations with autoantibodies in scleroderma: a highly significant role for HLA-DP. Genes Immun 2001; 2: 76-81.
    • (2001) Genes Immun. , vol.2 , pp. 76-81
    • Gilchrist, F.C.1    Bunn, C.2    Foley, P.J.3
  • 88
    • 10744224410 scopus 로고    scopus 로고
    • The TNF-863A allele strongly associates with anticentromere antibody positivity in scleroderma
    • Sato H, Lagan AL, Alexopoulou C, et al. The TNF-863A allele strongly associates with anticentromere antibody positivity in scleroderma. Arthritis Rheum 2004; 50: 558-564.
    • (2004) Arthritis Rheum. , vol.50 , pp. 558-564
    • Sato, H.1    Lagan, A.L.2    Alexopoulou, C.3
  • 89
    • 0038505528 scopus 로고    scopus 로고
    • Transforming growth factor β1 gene polymorphism in patients with systemic sclerosis
    • Sugiura Y, Banno S, Matsumoto Y, et al. Transforming growth factor β1 gene polymorphism in patients with systemic sclerosis. J Rheumatol 2003; 30: 1520-1523.
    • (2003) J. Rheumatol. , vol.30 , pp. 1520-1523
    • Sugiura, Y.1    Banno, S.2    Matsumoto, Y.3
  • 90
    • 0035997478 scopus 로고    scopus 로고
    • Analysis of transforming growth factor β1 gene polymorphisms in patients with systemic sclerosis
    • Crilly A, Hamilton J, Clark CJ, Jardine A, Madhok R. Analysis of transforming growth factor β1 gene polymorphisms in patients with systemic sclerosis. Ann Rheum Dis 2002; 61: 678-681.
    • (2002) Ann. Rheum. Dis. , vol.61 , pp. 678-681
    • Crilly, A.1    Hamilton, J.2    Clark, C.J.3    Jardine, A.4    Madhok, R.5
  • 92
    • 0036846150 scopus 로고    scopus 로고
    • Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma
    • Zhou X, Tan FK, Reveille JD, et al. Association of novel polymorphisms with the expression of SPARC in normal fibroblasts and with susceptibility to scleroderma. Arthritis Rheum 2002; 46: 2990-2999.
    • (2002) Arthritis Rheum. , vol.46 , pp. 2990-2999
    • Zhou, X.1    Tan, F.K.2    Reveille, J.D.3
  • 93
    • 0035052163 scopus 로고    scopus 로고
    • Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations
    • Tan FK, Wang N, Kuwana M, et al. Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations. Arthritis Rheum 2001; 44: 893-901.
    • (2001) Arthritis Rheum. , vol.44 , pp. 893-901
    • Tan, F.K.1    Wang, N.2    Kuwana, M.3
  • 94
    • 0034459681 scopus 로고    scopus 로고
    • Functional consequences of a polymorphism affecting NF-κB p50-p50 binding to the TNF promoter region
    • Udalova IA, Richardson A, Denys A, et al. Functional consequences of a polymorphism affecting NF-κB p50-p50 binding to the TNF promoter region. Mol Cell Biol 2000; 20: 9113-9119.
    • (2000) Mol. Cell Biol. , vol.20 , pp. 9113-9119
    • Udalova, I.A.1    Richardson, A.2    Denys, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.