ALOX15 gene polymorphisms in Japanese patients with aspirin-exacerbated respiratory disease (AERD) Source: International Congress 2016 – Role of genetics and exposures in COPD and asthma Year: 2016
Polymorphisms of the vitamin D-binding protein (DBP) gene in Japanese patients with aspirin-exacerbated respiratory disease (AERD) Source: International Congress 2014 – Allergy and asthma: novel findings based on human cell biology Year: 2014
Genetic Polymorphisms of the glutation-s-transferase (GST) gene family in patients with bronchial asthma Source: Eur Respir J 2003; 22: Suppl. 45, 421s Year: 2003
Replication association study IREB2, CHRNA5, CHRNA3, CHRNB4, FAM13A, HTR4, and HHIP genes polymorphisms with chronic obstructive pulmonary disease in Tatar population from Russia Source: International Congress 2016 – Role of genetics and exposures in COPD and asthma Year: 2016
Polymorphic variants of genes ADRB2, NR3C1, MDR1 in patients with chronic obstructive pulmonary disease and obesity Source: International Congress 2015 – Genetics and environmental factors in phenotypes of asthma and COPD Year: 2015
-82 A>G promoter polymorphism in the gene of human macrophage elastase (MMP-12) as a risk factor for COPD and bronchial asthma Source: International Congress 2014 – Basic and translational research in asthma and COPD Year: 2014
Investigating tensin1 expression and the presence of SNP identified in GWAS in COPD Source: International Congress 2016 – Mechanisms of disease Year: 2016
The role of histone deacetylase 2 (HDAC2) and glucocorticoid receptor (GR) isoforms α, β in patients with asthma–COPD overlap syndrome (ACOS) Source: International Congress 2016 – Molecular targets in pulmonary disease Year: 2016
Repeat polymorphisms (pol.) in the NOS-1 gene and its association with the clinical severity of cystic fibrosis (CF) Source: Annual Congress 2010 - Cystic fibrosis: clinical and laboratory studies Year: 2010
Plasma uteroglobin-related protein 1 (Ugrp1) levels is associated with Ugrp1 -112G/A polymorphism and the severity of asthma Source: Eur Respir J 2006; 28: Suppl. 50, 592s Year: 2006
CARD15 gene mutations in sarcoidosis Source: Eur Respir J 2003; 22: 748-754 Year: 2003
Determination of a single nucleotide polymorphism (SNP) of the TNFalpha-R1 region (TNFRSF1A) in patients with lung sarcoidosis: Preliminary results Source: International Congress 2015 – Sarcoidosis: pathogenesis Year: 2015
MiR-320c regulates SERPINA1 expression and is associated with pulmonary disease in alpha-1-antitrypsin deficiency Source: International Congress 2016 – How the understanding og molecular and genomic crosstalk is helping to diagnose lung disease Year: 2016
Association of single nucleotide polymorphisms in 4 genes (VDR, COL1A1, CALCR and BGLAP) with susceptibility to steroid osteoporosis in patients with idiopathic pulmonary fibrosis (IPF) Source: Annual Congress 2011 - Genetic and molecular background in pulmonary fibrosis Year: 2011
SNPs in SPINK5 gene region are associated with asthma severity: Preliminary results from the gene environment interactions in respiratory diseases (GEIRD) study Source: Annual Congress 2013 –Genetic factors in airway development and disease Year: 2013
DPP10 protein expression is associated with the pathogenesis of asthma and COPD Source: Eur Respir J 2005; 26: Suppl. 49, 231s Year: 2005
A single nucleotide polymorphism in NOD2 gene was associated with pathogenesis and severity of COPD Source: Annual Congress 2010 - Genetics of obstruction Year: 2010
Single nucleotide polymorphism of PSMA6 gene in Lithuanian patients with asthma Source: Annual Congress 2013 –Genetics and genomics of lung disease Year: 2013
The role of genetic polymorphisms of glutation-S-transferase μ1 (GSTM1) and gelatinase B (MMP9) in the risk of COPD development Source: Annual Congress 2003 - Alpha-1 antitrypsin deficiency and COPD Year: 2003
Genetic association studies of interleukin-13 receptor α1 subunit gene polymorphisms in asthma and atopy Source: Eur Respir J 2007; 30: 40-47 Year: 2007