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Philip Morris

Genetic Risk Factors for Chronic Obstructive Pulmonary Disease

Date: 19970000/P
Length: 12 pages
2063633573-2063633584
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Author
Pare, P.D.
Sandford, A.J.
Weir, T.D.
Type
PSCI, PUBLICATION SCIENTIFIC
BIBL, BIBLIOGRAPHY
Area
CARCHMAN,RICHARD/OFFICE
Litigation
Iwoh/Produced
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EXTR, EXTRA
MARG, MARGINALIA
Site
R530
Named Organization
St Pauls Hospital
Ubc Pulmonary Research Lab
European Respiratory Journal
Munksgaard Int Pub
Author (Organization)
Respiratory Network of Centers of Excell
St Pauls Hospital
Ubc Pulmonary Research Lab
European Respiratory Journal
Ers Journals
Named Person
Pare, P.D.
Sandford, A.J.
Master ID
2063633486/4072
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1390 A.J. SANDFORD ET AL. RA, Fick RB. Independent mutations in the flanking sequence of the alphal-antitrypsin gene are associated with chronic obstructive airways disease. Dis Markers 1990; 8: 151-157. 66. Billingsley GD, Walter MA, Hammond GL, Cox DW. Physical mapping of four serpin genes: at-antit~psin, txl-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280 kb region on chro- mosome 14q32.1. AmJHura Genet 1993; 52: 343-353. 67. Cruickshank AM, Hansell DT, Bums HJG, Shenkin A. Effect of nutritional status on acute phase protein res- ponse to elective surgery. BrJSurg 1989; 76: 165-168. 68. Morgan K, Scobie G, Kalsheker N. The characterization of a mutation of the 3' flanking sequence of the a: antitrypsin gene commonly associated with chronic ob- structive airways disease. Eur J Clin Invest 1992; 22: 134-137. 69. Morgan K, Scobie G, Kalsheker NA. 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A leucine-to- proline substitution causes a defective ctt-antichymotryp- sin allele associated with familial obstructive lung ~.sease. Genomics 1993; 17: 740-743. 80. Samilchuk EI, Chuchalin AG. Mis-sense mutation of a:antichymotrypsin gene and chronic lung disease. Lancet 1993; 342: 624. 81. Welch MJ, Tsui L-T, Boat TF, Beaudet AL. The Metabolic Basis of Inherited Disease. In: Scriver CL, Beaudel AL, Sly WS, Valle D, eds. New York, McGraw- Hill Inc., 1995; pp. 3799-3876. 82. Meindl RS. Hypothesis: a selective advantage for cys- tic fibrosis heterozygotes. Am J Phys Anthropol 1987; 74: 39-45. 83. Shier WT. Increased resistance to influenza as a poss~le source ofheterozygote advantage in cystic fibrosis. Med Hypotheses 1979; 5: 661-667. 84. Quinton PM. Fluid and Electrolyte Abnormalities in Exocrine Glands in Cystic Fibrosis. In: Quinton PM, Martinez R J, Hopfer U, eds. San Francisco, San Francisco Press, 1982; pp. 53-76. 85. Gabriel SE, Brigman KN, Koiler BH, Boucher RC,. Stutts MJ. 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AF508 mutation of cystic fibrosis gene is not found in chronic bronchitis with severe obstruction in Japan. Am Rev Respir Dis 1992; 146: 781-783. 97. Artlich A, Boysen A, Bunge S, Entzian P, Schlaak M, Schwinger E. Common CFrR mutations are not likely to predispose to chronic bronchitis in Northern Germany. Hum Genet 1995; 95: 226-228. 98. Entzian P, Mtiller E, Boysen A, Artlich A, Schwinger E, Schlaak M. Frequency of common cystic fibrosis gene mutations in chronic bronchitis patients. Scand J Lab Invest 1995; 55: 263-266. 99. Pignatti PF, Bombied C, Marigo C, Benetazzo M, Luisetti M. Increased incidence of cystic fibrosis gene muta- tions in adults with disseminated bronchiectasis. Hum Mol Genet 1995; 4: 635-636. 100. Pignatti PF, Bombieri C, Benetazzo M, et al. CIzTR gene variant IVS8-5T in disseminated bronchiectasis. Am J Hum Genet 1996; 58: 889-892. I01. Gasparini P, Savoia A, Luisetti M, Peona V, Pignatti PF. The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary disease. Am J Respir Cell Mol Biol 1990; 2: 297-299. 102. Kew R.R, Webster RO. Gc-globulin (vitamin D-binding
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GENETICS OF COPD 1391 protein) enhances the neutrophil chemotactic activity of CSa and C5a des Arg../Clin Invest 1988; 82: 36~-369. 103. Yamamoto N, Homma S. Vitamin D-binding protein (group-specific component) is a precursor for the mac- rophage-activating signal factor from lysophosphatidyl- choline-treated lymphocytes. Proc Natl Acad Sci USA 1991; 88: 8539-8543. 104. Horue SL, Cockcroft DW, Dosman JA. Possible pro- tective effect against chronic obstructive airways dis- ease by the GC 2 allele. Hum Hered 1990; 40: 173-176. 105. Kauffmann F, Kleisbauer J-P, Cambon-de-Mouzon A, et al. Genetic markers in chronic airflow limitation: a genetic epidemiologic study. Am Rev Respir Dis 1983; 127: 263-269. I06. White R, Janoff A, Godfrey HP. Secretion of alphaz- macroglobulin by alveolar macrophages. Lung 1980; 158: 9-14. I07. Mosher DF, Wing WA. Synthesis and secretion of c~a- macroglobulin by cultured human fibroblasts. J Exp Med 1976; 143: 462-467. I08. 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