e-learning
resources
Amsterdam 2011
Monday, 26.09.2011
Genes, environment and obstruction
Login
Search all ERS
e-learning
resources
Disease Areas
Airways Diseases
Interstitial Lung Diseases
Respiratory Critical Care
Respiratory Infections
Paediatric Respiratory Diseases
Pulmonary Vascular Diseases
Sleep and Breathing Disorders
Thoracic Oncology
Events
International Congress
Courses
Webinars
Conferences
Research Seminars
Journal Clubs
Publications
Breathe
Monograph
ERJ
ERJ Open Research
ERR
European Lung White Book
Handbook Series
Guidelines
All ERS guidelines
e-learning
CME Online
Case reports
Short Videos
SpirXpert
Procedure Videos
CME tests
Reference Database of Respiratory Sounds
Radiology Image Challenge
Brief tobacco interventions
EU Projects
VALUE-Dx
ERN-LUNG
ECRAID
UNITE4TB
Disease Areas
Events
Publications
Guidelines
e-learning
EU Projects
Login
Search
Detection of specific mitochondrial RNA gene mutations in asthma patients: Contribution of haplogroup U
F. Malli, E. Zifa, K. Gourgoulianis, Z. Mamuris, Z. Daniil (Larissa, Greece)
Source:
Annual Congress 2011 - Genes, environment and obstruction
Session:
Genes, environment and obstruction
Session type:
Oral Presentation
Number:
1735
Disease area:
Airway diseases, Paediatric lung diseases
Rating:
You must
login
to grade this presentation.
Share or cite this content
Citations should be made in the following way:
F. Malli, E. Zifa, K. Gourgoulianis, Z. Mamuris, Z. Daniil (Larissa, Greece). Detection of specific mitochondrial RNA gene mutations in asthma patients: Contribution of haplogroup U. Eur Respir J 2011; 38: Suppl. 55, 1735
You must
login
to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
No comment yet.
You must
Login
to comment this presentation.
Related content which might interest you:
Panel discussion: Lung function in epidemiological studies from infancy to childhood with focus on urban environment
Late Breaking Abstract - Implications of treatable traits and treatment choices on exacerbation risk in moderate-severe asthma
Observational cohort study of pulmonary exacerbations in alpha-1 antitrypsin deficiency
Related content which might interest you:
The lueokocyte telomere length, single nucleotide polymorphisms near TERC gene and risk of COPD
Source: International Congress 2016 – Molecular targets in pulmonary disease
Year: 2016
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
Novel genetic variants in alpha-1 antitripsin deficiency cases carrying S alleles and discordant genotype and serum levels
Source: International Congress 2015 – Promising novel findings in translational pulmonary research
Year: 2015
A common deletion encompassing
ADAM
genes is associated with lung function in the ECRHS cohort
Source: Annual Congress 2010 - Genetics of asthma
Year: 2010
Study of gene expression control elements of the human SP-A genes: Role of the 5‘UTR exon B
Source: Annual Congress 2010 - Recent developments of molecular pathology and functional genomics in chronic and acute airway diseases
Year: 2010
Genetic variation in human RHS7 of the T
H
2 locus control region influences DNA methylation and is associated with IgE
Source: International Congress 2014 – Paediatric asthma: pathogenesis and immunology
Year: 2014
Single nucleotide polymorphism and asthma: A study on the genetic basis of asthma
Source: International Congress 2015 – Genetics and environmental factors in phenotypes of asthma and COPD
Year: 2015
Altered circulating exosomal RNA profiles detected by next-generation sequencing in patients with severe asthma
Source: International Congress 2016 – How the understanding og molecular and genomic crosstalk is helping to diagnose lung disease
Year: 2016
Analyses of genetic association and DNA methylation in the ORMDL3/GSDMB locus
Source: Annual Congress 2013 –Genetic factors in airway development and disease
Year: 2013
Cytotoxicity molecules expression in COPD patients with acquired somatic DNA mutations
Source: Annual Congress 2010 - Novel markers of lung injury
Year: 2010
Tumour necrosis factor family genes in a phenotype of COPD associated with emphysema
Source: Eur Respir J 2003; 21: 444-449
Year: 2003
Single nucleotide polymorphism of
PSMA6
gene in Lithuanian patients with asthma
Source: Annual Congress 2013 –Genetics and genomics of lung disease
Year: 2013
Analysis of the human SP-A 5‘UTR exon B: Identification of regulatory regions
Source: Annual Congress 2010 - Recent developments of molecular pathology and functional genomics in chronic and acute airway diseases
Year: 2010
Expression of prohibitin 1 mitochondrial protein in non-COPD and COPD smokers
Source: Annual Congress 2011 - Phenotyping airway diseases
Year: 2011
Replication study for a locus modulating total serum IgE on chromosome 14q13-24 in families with asthma
Source: Eur Respir J 2002; 20: Suppl. 38, 421s
Year: 2002
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
LSC 2010 Abstract: Perforin expression in COPD patients with microsatellite DNA instability
Source: Annual Congress 2010 - Novel mechanisms in COPD
Year: 2010
Topological data analysis (TDA) of U-BIOPRED paediatric peripheral blood gene expression identified asthma phenotypes characterised by alternative splicing of glucocorticoid receptor (GR) mRNA
Source: International Congress 2018 – New developments in paediatric asthma
Year: 2018
Mutation and functional analysis of the IL-18 promoter in sarcoidosis: a potential role for single nucleotide polymorphisms in cytokine expression regulation
Source: Eur Respir J 2003; 22: Suppl. 45, 180s
Year: 2003
Gene expression in CD4+ T-cells reflects heterogeneity in infant wheezing phenotypes
Source: Eur Respir J 2008; 32: 1203-1212
Year: 2008
We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. By clicking "Accept", you consent to the use of the cookies.
Accept