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Volumn 157, Issue 5, 2010, Pages

Quantification of the relative contribution of environmental and genetic factors to variation in cystic fibrosis lung function

Author keywords

Analysis of variance; ANOVA; CF; CFTR; Cystic fibrosis; Cystic fibrosis transmembrane conductance regulator gene; Forced expiratory volume in 1 second

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CYSTIC FIBROSIS; DIZYGOTIC TWINS; ENVIRONMENTAL FACTOR; FEMALE; FORCED EXPIRATORY VOLUME; HEREDITY; HOUSEHOLD; HUMAN; LUNG FUNCTION; MAJOR CLINICAL STUDY; MONOZYGOTIC TWINS; PRESCHOOL CHILD; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SCHOOL CHILD; SIBLING; STOCHASTIC MODEL; COMPARATIVE STUDY; ENVIRONMENT; GENETIC PREDISPOSITION; GENETICS; LUNG; MALE; PATHOPHYSIOLOGY; TWINS; YOUNG ADULT;

EID: 77958034453     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2010.05.018     Document Type: Article
Times cited : (109)

References (26)
  • 3
    • 0035122157 scopus 로고    scopus 로고
    • European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations
    • C. Koch, H. Cuppens, M. Rainisio, U. Madessani, H. Harms, and M. Hodson European Epidemiologic Registry of Cystic Fibrosis (ERCF): comparison of major disease manifestations between patients with different classes of mutations Pediatr Pulmonol 31 2001 1 12
    • (2001) Pediatr Pulmonol , vol.31 , pp. 1-12
    • Koch, C.1    Cuppens, H.2    Rainisio, M.3    Madessani, U.4    Harms, H.5    Hodson, M.6
  • 4
    • 0025241696 scopus 로고
    • The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (deltaF508)
    • E. Kerem, M. Corey, B.-S. Kerem, J. Rommens, D. Markiewicz, and H. Levison The relation between genotype and phenotype in cystic fibrosis-analysis of the most common mutation (deltaF508) N Engl J Med 323 1990 1517 1522
    • (1990) N Engl J Med , vol.323 , pp. 1517-1522
    • Kerem, E.1    Corey, M.2    Kerem, B.-S.3    Rommens, J.4    Markiewicz, D.5    Levison, H.6
  • 5
    • 0027517995 scopus 로고
    • Correlation between genotype and phenotype in cystic fibrosis
    • Cystic Fibrosis Genotype/Phenotype Consortium
    • Cystic Fibrosis Genotype/Phenotype Consortium Correlation between genotype and phenotype in cystic fibrosis N Engl J Med 329 1993 1308 1313
    • (1993) N Engl J Med , vol.329 , pp. 1308-1313
  • 8
    • 0034570596 scopus 로고    scopus 로고
    • Categories of deltaF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics
    • F. Mekus, M. Ballmann, I. Bronsveld, J. Bijman, H. Veeze, and B. Tummler Categories of deltaF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics Twin Res 3 2000 277 293
    • (2000) Twin Res , vol.3 , pp. 277-293
    • Mekus, F.1    Ballmann, M.2    Bronsveld, I.3    Bijman, J.4    Veeze, H.5    Tummler, B.6
  • 9
    • 0028114860 scopus 로고
    • Passive smoking and impaired lung function in cystic fibrosis
    • A. Smyth, U. O'Hea, G. Williams, R. Smyth, and D. Heaf Passive smoking and impaired lung function in cystic fibrosis Arch Dis Child 71 1994 353 354
    • (1994) Arch Dis Child , vol.71 , pp. 353-354
    • Smyth, A.1    O'Hea, U.2    Williams, G.3    Smyth, R.4    Heaf, D.5
  • 11
    • 0026556587 scopus 로고
    • Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion
    • P.W. Campbell III, R.A. Parker, B.T. Roberts, M.R. Krishnamani, and J.A. Phillips III Association of poor clinical status and heavy exposure to tobacco smoke in patients with cystic fibrosis who are homozygous for the F508 deletion J Pediatr 120 1992 261 264
    • (1992) J Pediatr , vol.120 , pp. 261-264
    • Campbell III, P.W.1    Parker, R.A.2    Roberts, B.T.3    Krishnamani, M.R.4    Phillips III, J.A.5
  • 12
    • 0025007903 scopus 로고
    • Exposure of children with cystic fibrosis to environmental tobacco smoke
    • B.K. Rubin Exposure of children with cystic fibrosis to environmental tobacco smoke N Engl J Med 323 1990 782 788
    • (1990) N Engl J Med , vol.323 , pp. 782-788
    • Rubin, B.K.1
  • 13
    • 38749090611 scopus 로고    scopus 로고
    • Interactions between secondhand smoke and genes that affect cystic fibrosis lung disease
    • J.M. Collaco, L. Vanscoy, L. Bremer, K. McDougal, S.M. Blackman, and A. Bowers Interactions between secondhand smoke and genes that affect cystic fibrosis lung disease JAMA 299 2008 417 424
    • (2008) JAMA , vol.299 , pp. 417-424
    • Collaco, J.M.1    Vanscoy, L.2    Bremer, L.3    McDougal, K.4    Blackman, S.M.5    Bowers, A.6
  • 15
    • 0031916045 scopus 로고    scopus 로고
    • Relationship between socioeconomic status and disease severity in cystic fibrosis
    • M.S. Schechter, and P.A. Margolis Relationship between socioeconomic status and disease severity in cystic fibrosis J Pediatr 132 1998 260 264
    • (1998) J Pediatr , vol.132 , pp. 260-264
    • Schechter, M.S.1    Margolis, P.A.2
  • 16
    • 0034987271 scopus 로고    scopus 로고
    • The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States
    • M.S. Schechter, B.J. Shelton, P.A. Margolis, and S.C. Fitzsimmons The association of socioeconomic status with outcomes in cystic fibrosis patients in the United States Am J Respir Crit Care Med 163 2001 1331 1337
    • (2001) Am J Respir Crit Care Med , vol.163 , pp. 1331-1337
    • Schechter, M.S.1    Shelton, B.J.2    Margolis, P.A.3    Fitzsimmons, S.C.4
  • 17
    • 0030916094 scopus 로고    scopus 로고
    • Absence of health insurance is associated with decreased life expectancy in patients with cystic fibrosis
    • J.R. Curtis, W. Burke, A.W. Kassner, and M.L. Aitken Absence of health insurance is associated with decreased life expectancy in patients with cystic fibrosis Am J Respir Crit Care Med 155 1997 1921 1924
    • (1997) Am J Respir Crit Care Med , vol.155 , pp. 1921-1924
    • Curtis, J.R.1    Burke, W.2    Kassner, A.W.3    Aitken, M.L.4
  • 19
    • 12144288251 scopus 로고    scopus 로고
    • Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
    • N.S. Wexler, J. Lorimer, J. Porter, F. Gomez, C. Moskowitz, and E. Shackell Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset Proc Natl Acad Sci U S A 101 2004 3498 3503
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 3498-3503
    • Wexler, N.S.1    Lorimer, J.2    Porter, J.3    Gomez, F.4    Moskowitz, C.5    Shackell, E.6
  • 20
    • 0031900652 scopus 로고    scopus 로고
    • The diagnosis of cystic fibrosis: A consensus statement
    • B.J. Rosenstein, and G.R. Cutting The diagnosis of cystic fibrosis: a consensus statement J Pediatr 132 1998 589 595
    • (1998) J Pediatr , vol.132 , pp. 589-595
    • Rosenstein, B.J.1    Cutting, G.R.2
  • 23
    • 85047690027 scopus 로고
    • The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitus
    • D.S. Falconer The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitus Ann Hum Genet 31 1967 1 20
    • (1967) Ann Hum Genet , vol.31 , pp. 1-20
    • Falconer, D.S.1
  • 24
    • 40549083327 scopus 로고    scopus 로고
    • Complex two-gene modulation of lung disease severity in children with cystic fibrosis
    • R. Dorfman, A. Sandford, C. Taylor, B. Huang, D. Frangolias, and Y. Wang Complex two-gene modulation of lung disease severity in children with cystic fibrosis J Clin Invest 118 2008 1040 1049
    • (2008) J Clin Invest , vol.118 , pp. 1040-1049
    • Dorfman, R.1    Sandford, A.2    Taylor, C.3    Huang, B.4    Frangolias, D.5    Wang, Y.6
  • 25
    • 33745953585 scopus 로고    scopus 로고
    • Association between mannan-binding lectin and impaired lung function in cystic fibrosis may be age-dependent
    • M.S. Muhlebach, S.L. MacDonald, B. Button, J.J. Hubbard, M.L. Turner, and R.C. Boucher Association between mannan-binding lectin and impaired lung function in cystic fibrosis may be age-dependent Clin Exp Immunol 145 2006 302 307
    • (2006) Clin Exp Immunol , vol.145 , pp. 302-307
    • Muhlebach, M.S.1    MacDonald, S.L.2    Button, B.3    Hubbard, J.J.4    Turner, M.L.5    Boucher, R.C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.