T. Malling (Aalborg, Denmark), O. Omland (Aalborg, Denmark)
LATE-BREAKING ABSTRACT: Association of GSTT1 & M1 gene polymorphism with ageing in Northern Indian COPD and lung cancer patients
R. K. Shukla, S. Kant, S. Bhattacharya‘, B. Mittal (Lucknow/Uttar Pradesh, India)
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Proteinase activated receptor-1 (F2R) polymorphisms and susceptibility to exacerbations in COPD
M. Plate‘, J.K. Quint, J.A. Wedzicha, R.C. Chambers, J.R. Hurst (London, United Kingdom)
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Heterozygosity for E292V in ABCA3, lung function and COPD in 64,000 individuals
M. Bækvad-Hansen, B. Nordestgaard, M. Dahl (Herlev, Copenhagen, Denmark)
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Estimating the contribution of genetic variants in occupational chronic bronchitis
L. Akhmadishina, G. Korytina, T. Viktorova (Ufa, Russian Federation)
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SNPs in TSPYL-4, NT5DC1 genes are associated with susceptibility to COPD in a southern Chinese Han population
Y. Guo, Y. Gong, G. Shi, K. Yang, C. Pan, M. Li, Q. Li, Q. Cheng, R. Dai, L. Fan, H. Wan (Shanghai, China)
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Genetics of detoxification and oxidative stress pathways in COPD
Q. Pasha, B. Singh, A. Vibhuti, E. Arif (Delhi, New Delhi, India)
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New degradome markers in children and adults with chronic lung disease
O. Tselousova, G. Korytyna, T. Victorova (Ufa, Russian Federation)
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Longitudinal analysis of airway epithelium of COPD subjects reveals unique inflammatory gene networks up-regulated over time
S. Sridhar, J.S. Fine, C.S. Stevenson, H. Bitter, A.E. Tilley, B.G. Harvey, R. Kaner, M.R. Staudt, J. Fuller, J. Salit, N. Hackett, H. Hilton, S. Pillai, G. Wolff, S. Visvanathan, R.G. Crystal (Nutley, New York, Ridgefield, United States Of America)
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Investigation of the role of miRNAs as a biomarker in chronic obstructive pulmonary disease (COPD)
F. Akbas, E. Coskunpinar, E. Aynaci, Y. Musteri Oltulu, P. Yildiz (Istanbul, Turkey)
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Cell-cell variation in expression of blaCTX-M-14
X. Wang, Y. Kang, S. An, T. Zhao, J. Chen, R. Fu, Z. Gao (Beijing, China)
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Polymorphisms of genes involved in extracellular matrix remodeling, xenobiotic metabolism, antioxidant pathways and chronic lung disease in children
G. Korytina, L. Akhmadishina, E. Victorova, T. Victorova (Ufa, Russian Federation; Goettingen, Germany)
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Association of xenobiotic metabolizing gene polymorphisms and chronic obstructive pulmonary disease in Indian population
N. Khan, M. Daga, N. Kamble, G. Mawari, I. Ahmed, S. A. Husain (New Delhi, India)
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Rare alpha-1 antitrypsin mutations in the Irish population
T. Carroll, G. O‘Brien, C. O‘Connor, I. Ferrarotti, S. Ottaviani, M. Luisetti, G. McElvaney (Dublin, Ireland; Pavia, Italy)
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Lung fibroblast function in patients with Birt-Hogg-Dubé syndrome
Y. Hoshika, F. Takahashi, S. Togo, M. Hashimoto, T. Kobayashi, H. Kataoka, M. Kurihara, E. Kobayashi, K. Ando, K. Seyama, K. Takahashi (Tokyo, Japan)
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CCDC103 encodes a novel cilia dynein arm factor that is mutated in primary ciliary dyskinesia
C. Werner, A. Becker-Heck, J.R. Panizzi, V.H. Castleman, D. Al-Mutari, E. Sheridan, N.T. Loges, H. Olbrich, R. Chodhari, C. O‘Callaghan, E.M.K. Chung, R. Reinhardt, H.M. Mitchison, I.A. Drummond, H. Omran (Muenster, Cologne, Germany; Charlestown, United States Of America; Leeds, United Kingdom)
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Recessive HYDIN mutations cause primary ciliary dyskinesia without situs abnomalities
J. Raidt, H. Olbrich, C. Werner, N.T. Loges, N.F. Banki, A. Shoemark, T. Burgoyne, G. Köhler, J. Schroeder, G. Nürnberg, P. Nürnberg, R. Reinhardt, H. Omran (Muenster, , Cologne, Germany; Budapest, Hungary; London, United Kingdom)
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