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National Emphysema Treatment Trial state of the art: genetics of emphysema

Published in: Proceedings of the American Thoracic Society

Date of publication: May 1, 2008

Main subject: pulmonary emphysema

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Cites articles 121

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James Jackson, Jr., the young pulmonologist who described familial emphysema. An historical footnote
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The mechanism of Z alpha 1-antitrypsin accumulation in the liver
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Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease
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Association between polymorphism in gene for microsomal epoxide hydrolase and susceptibility to emphysema
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Frequency of glutathione S-transferase M1 deletion in smokers with emphysema and lung cancer
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Does alpha1-antitrypsin augmentation therapy slow the annual decline in FEV1 in patients with severe hereditary alpha1-antitrypsin deficiency? Wissenschaftliche Arbeitsgemeinschaft zur Therapie von Lungenerkrankungen (WATL) alpha1-AT study group
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Lung function after bilateral lower lobe lung volume reduction surgery for alpha1-antitrypsin emphysema
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Use of unlinked genetic markers to detect population stratification in association studies
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Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN)
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A randomized clinical trial of alpha(1)-antitrypsin augmentation therapy
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Glutathione S-transferase P1 (GSTP1) polymorphism in patients with chronic obstructive pulmonary disease
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alpha 1-antitrypsin TAQ I polymorphism and alpha 1-antichymotrypsin mutations in patients with obstructive pulmonary disease
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Molecular mechanisms of alpha1-antitrypsin null alleles
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Genetic susceptibility to chronic obstructive pulmonary disease in Koreans: combined analysis of polymorphic genotypes for microsomal epoxide hydrolase and glutathione S-transferase M1 and T1.
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Microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with susceptibility to emphysema
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Gene polymorphism for microsomal epoxide hydrolase and susceptibility to emphysema in a Japanese population

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