2:
IL10 polymorphisms are associated with airflow obstruction in severe alpha1-antitrypsin deficiency.
Demeo DL, Campbell EJ, Barker AF, Brantly ML, Eden E, McElvaney NG, Rennard SI, Sandhaus RA, Stocks JM, Stoller JK, Strange C, Turino G, Silverman EK.
Am J Respir Cell Mol Biol. 2008 Jan;38(1):114-20. Epub 2007 Aug 9.
PMID: 17690329 [PubMed - indexed for MEDLINE]
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Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations.
Hersh CP, Demeo DL, Lange C, Litonjua AA, Reilly JJ, Kwiatkowski D, Laird N, Sylvia JS, Sparrow D, Speizer FE, Weiss ST, Silverman EK.
Am J Respir Cell Mol Biol. 2005 Jul;33(1):71-8. Epub 2005 Apr 7.
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[The variability of clinical presentation of chronic obstructive pulmonary disease in patients with hereditary alpha-1 antitrypsin deficiency]
Kuca P, Kamiński D, Campbell E, Kołakowski J, Goljan-Geremek A, Puścińska E, Bieleń P, Nowiński A, Wojda E, Hawryłkiewicz I, Sliwiński P, Górecka D.
Pneumonol Alergol Pol. 2004;72(9-10):420-3. Polish.
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Development of a novel microarray methodology for the study of SNPs in the promoter region of the TNF-alpha gene: their association with obstructive pulmonary disease in Greek patients.
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Genetic association analysis of functional impairment in chronic obstructive pulmonary disease.
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Am J Respir Crit Care Med. 2006 May 1;173(9):977-84. Epub 2006 Feb 2.
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