| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Edwin K Silverman | |
| P2860 | cites work | Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN) | Q22008606 |
| Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol | Q22337068 | ||
| An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa | Q24314373 | ||
| Genome-wide association studies for common diseases and complex traits | Q29615822 | ||
| Case-control association studies for the genetics of complex respiratory diseases | Q33933058 | ||
| The SERPINE2 gene is associated with chronic obstructive pulmonary disease | Q34398902 | ||
| Inducible targeting of IL-13 to the adult lung causes matrix metalloproteinase- and cathepsin-dependent emphysema | Q34457903 | ||
| Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease | Q34521964 | ||
| Transforming growth factor-beta1 genotype and susceptibility to chronic obstructive pulmonary disease | Q34544941 | ||
| Quantitative relationships between cigarette smoking and ventilatory function | Q34730271 | ||
| Association between polymorphism in gene for microsomal epoxide hydrolase and susceptibility to emphysema | Q34742826 | ||
| Tumor necrosis factor-alpha gene polymorphism in chronic bronchitis | Q34743595 | ||
| Chronic obstructive pulmonary disease in alpha1-antitrypsin PI MZ heterozygotes: a meta-analysis | Q35536217 | ||
| Congenital cutis laxa with a dominant inheritance and early onset emphysema | Q36573905 | ||
| Attempted replication of reported chronic obstructive pulmonary disease candidate gene associations | Q37273821 | ||
| A functional mutation in the terminal exon of elastin in severe, early-onset chronic obstructive pulmonary disease | Q37273940 | ||
| Frequency of glutathione S-transferase M1 deletion in smokers with emphysema and lung cancer | Q38474281 | ||
| Familial prevalence of chronic obstructive pulmonary disease in a matched pair study | Q40656485 | ||
| Chronic obstructive pulmonary disease: a challenge in genetic epidemiology | Q41612123 | ||
| Genotypic and phenotypic similarities in pulmonary function among family members of adult monozygotic and dizygotic twins | Q42651323 | ||
| Glutathione S-transferase P1 (GSTP1) polymorphism in patients with chronic obstructive pulmonary disease | Q43060845 | ||
| Possible protective effect against chronic obstructive airways disease by the GC2 allele | Q44418780 | ||
| Glutathione S-transferase variants and their interaction with smoking on lung function | Q44926988 | ||
| The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD). | Q47401096 | ||
| The development of emphysema in cigarette smoke-exposed mice is strain dependent | Q47949544 | ||
| Risk and severity of COPD is associated with the group-specific component of serum globulin 1F allele | Q48032587 | ||
| A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease | Q48104043 | ||
| Peculiarities of the GSTM1 0/0 genotype in French heavy smokers with various types of chronic bronchitis. | Q50951067 | ||
| Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes. | Q51722853 | ||
| Genome-wide linkage analysis of bronchodilator responsiveness and post-bronchodilator spirometric phenotypes in chronic obstructive pulmonary disease | Q57253805 | ||
| Genetic and environmental determinants of level of pulmonary function | Q70606727 | ||
| Association of tumor necrosis factor alpha gene promoter polymorphism with the presence of chronic obstructive pulmonary disease | Q73442209 | ||
| Susceptibility genes for rapid decline of lung function in the lung health study | Q73442228 | ||
| Further evidence for the role of genes on chromosome 2 and chromosome 5 in the inheritance of pulmonary function | Q73490247 | ||
| Requirement for macrophage elastase for cigarette smoke-induced emphysema in mice | Q73709481 | ||
| Association between alpha-1-antichymotrypsin polymorphism and susceptibility to chronic obstructive pulmonary disease | Q73883775 | ||
| Surfactant protein gene A, B, and D marker alleles in chronic obstructive pulmonary disease of a Mexican population | Q74598084 | ||
| Genome-wide linkage of forced mid-expiratory flow in chronic obstructive pulmonary disease | Q80526285 | ||
| Smoke and mirrors: Mouse models as a reflection of human chronic obstructive pulmonary disease | Q80907521 | ||
| P433 | issue | 5 | |
| P921 | main subject | chronic obstructive pulmonary disease | Q199804 |
| P304 | page(s) | 405-408 | |
| P577 | publication date | 2006-07-01 | |
| P1433 | published in | Proceedings of the American Thoracic Society | Q7247176 |
| P1476 | title | Progress in chronic obstructive pulmonary disease genetics | |
| P478 | volume | 3 |
| Q36321481 | A predictive model for the development of chronic obstructive pulmonary disease |
| Q36293942 | Altered regulation and expression of genes by BET family of proteins in COPD patients |
| Q37783859 | An Official American Thoracic Society Public Policy Statement: Novel Risk Factors and the Global Burden of Chronic Obstructive Pulmonary Disease |
| Q37211184 | Analysis of exonic elastin variants in severe, early-onset chronic obstructive pulmonary disease |
| Q90132747 | Animal Models Reflecting Chronic Obstructive Pulmonary Disease and Related Respiratory Disorders: Translating Pre-Clinical Data into Clinical Relevance |
| Q37041236 | Association of Functional Variants of Phase I and II Genes with Chronic Obstructive Pulmonary Disease in a Serbian Population |
| Q35990449 | Association of TNF-α -308G/A, SP-B 1580 C/T, IL-13 -1055 C/T gene polymorphisms and latent adenoviral infection with chronic obstructive pulmonary disease in an Egyptian population |
| Q34522806 | Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case-control study |
| Q34584449 | Autoantibodies in patients with chronic obstructive pulmonary disease |
| Q49148594 | C-reactive protein levels, haplotypes, and the risk of incident chronic obstructive pulmonary disease. |
| Q34399667 | CFTR regulates early pathogenesis of chronic obstructive lung disease in βENaC-overexpressing mice |
| Q28752596 | COPD and the risk of tuberculosis--a population-based cohort study |
| Q33591899 | Canadian Thoracic Society recommendations for management of chronic obstructive pulmonary disease - 2007 update |
| Q37287153 | Chronic obstructive pulmonary disease: a view from the NHLBI. |
| Q33541285 | Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation |
| Q34004971 | Common genetic determinants of lung function, subclinical atherosclerosis and risk of coronary artery disease |
| Q34014161 | Effect of heme oxygenase-1 polymorphisms on lung function and gene expression |
| Q36389310 | Emerging genetics of COPD. |
| Q39704546 | Gene-environment interaction between the MMP9 C-1562T promoter variant and cigarette smoke in the pathogenesis of chronic obstructive pulmonary disease. |
| Q36025785 | Gene-environment interaction testing in family-based association studies with phenotypically ascertained samples: a causal inference approach |
| Q37070366 | Gene-environment interactions in chronic obstructive pulmonary disease |
| Q34003674 | Genetic associations with hypoxemia and pulmonary arterial pressure in COPD |
| Q36609353 | Glutathione S-transferase and microsomal epoxide hydrolase gene polymorphisms and risk of chronic obstructive pulmonary disease in Slovak population |
| Q35542366 | Immunology, genetics and microbiota in the COPD pathophysiology: potential scope for patient stratification |
| Q34374230 | Improving the differential diagnosis of chronic obstructive pulmonary disease in primary care. |
| Q33324460 | Increased prevalence of multiple sclerosis among COPD patients and their first-degree relatives: a population-based study |
| Q33323178 | Increased risk of both ulcerative colitis and Crohn's disease in a population suffering from COPD. |
| Q48273700 | Integrative Genomics of Emphysema-Associated Genes: Are We Closer to Identifying the Genetic Determinants of Lung Function? |
| Q37334890 | Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population |
| Q37168317 | Markers of early disease and prognosis in COPD. |
| Q41898716 | Molecular biomarkers for quantitative and discrete COPD phenotypes. |
| Q34118461 | Multistudy fine mapping of chromosome 2q identifies XRCC5 as a chronic obstructive pulmonary disease susceptibility gene |
| Q41838638 | Natural histories of chronic obstructive pulmonary disease |
| Q47985603 | Passive smoking and chronic obstructive pulmonary disease mortality: findings from the Japan collaborative cohort study. |
| Q37008634 | Phenotypes of chronic obstructive pulmonary disease |
| Q36162231 | Role of GSTM1 in resistance to lung inflammation |
| Q36640817 | Second hand smoke and COPD: lessons from animal studies. |
| Q26824019 | Transposable elements and their potential role in complex lung disorder |
| Q36784448 | Variability in small airway epithelial gene expression among normal smokers. |
| Q33687879 | Variants in FAM13A are associated with chronic obstructive pulmonary disease |
| Q36443195 | Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility |
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