Nasal polyposis (NP) is an inflammatory disease of the upper nasal airways frequently present in CF patients. Interferon-Related Developmental Regulator 1 (IFRD1) gene was reported as a possible modifier of CF lung disease severity. Three IFRD1 SNPs were analyzed to investigate a possible effect on the development of NP in CF patients. The DNA of 143 patients with CF (40 with and 103 without NP) was purified from peripheral blood samples. IFRD1 SNPs (rs7817, rs3807213, rs6968084) were genotyped by restriction enzyme analysis. The T allele of the common polymorphism rs7817 and the rs7817-rs3807213 haplotype were associated with NP(p=0.002 and 0.004 respectively). These results showed the association of the IFRD1-rs7817 polymorphism with NP i...
Background The dysfunction of the mucosal interface of the upper respiratory tract in cystic fibrosi...
BPI fold containing family A, member 1 (BPIFA1) and BPIFB1 are putative innate immune molecules expr...
AbstractThe variation in cystic fibrosis (CF) lung disease and development of CF related complicatio...
Lung disease is the major cause of morbidity and mortality in cystic fibrosis, an autosomal recessiv...
A genome-wide association study identified interferon-related de-velopment regulator–1 (IFRD1), a pr...
A genome-wide association study identified interferon-related development regulator-1 (IFRD1), a pro...
A wide range of clinical phenotypes are associated with mutations in the cystic fibrosis transmembra...
SummaryAlthough the cytokine profile in nasal polyposis is well documented, little is known about cy...
Aim of the study was to analyse IFRD1 gene as a possible modifier gene for Cystic Fibrosis Lung Dise...
Cystic Fibrosis is one of the most common genetic recessive diseases among Caucasians and is caused ...
There is growing evidence that the great phenotypic variability in patients with cystic fibrosis (CF...
International audienceCystic fibrosis may be revealed by nasal polyposis (NP) starting early in life...
Cystic fibrosis (CF) is a monogenic syndrome determined by over 2000 mutations in the CF Transmembra...
Includes bibliographical references (p. 32-34)Cystic fibrosis (CF) is the most common monogenic diso...
Cystic fibrosis (CF) is a single gene Mendelian disorder characterized by pulmonary disease and panc...
Background The dysfunction of the mucosal interface of the upper respiratory tract in cystic fibrosi...
BPI fold containing family A, member 1 (BPIFA1) and BPIFB1 are putative innate immune molecules expr...
AbstractThe variation in cystic fibrosis (CF) lung disease and development of CF related complicatio...
Lung disease is the major cause of morbidity and mortality in cystic fibrosis, an autosomal recessiv...
A genome-wide association study identified interferon-related de-velopment regulator–1 (IFRD1), a pr...
A genome-wide association study identified interferon-related development regulator-1 (IFRD1), a pro...
A wide range of clinical phenotypes are associated with mutations in the cystic fibrosis transmembra...
SummaryAlthough the cytokine profile in nasal polyposis is well documented, little is known about cy...
Aim of the study was to analyse IFRD1 gene as a possible modifier gene for Cystic Fibrosis Lung Dise...
Cystic Fibrosis is one of the most common genetic recessive diseases among Caucasians and is caused ...
There is growing evidence that the great phenotypic variability in patients with cystic fibrosis (CF...
International audienceCystic fibrosis may be revealed by nasal polyposis (NP) starting early in life...
Cystic fibrosis (CF) is a monogenic syndrome determined by over 2000 mutations in the CF Transmembra...
Includes bibliographical references (p. 32-34)Cystic fibrosis (CF) is the most common monogenic diso...
Cystic fibrosis (CF) is a single gene Mendelian disorder characterized by pulmonary disease and panc...
Background The dysfunction of the mucosal interface of the upper respiratory tract in cystic fibrosi...
BPI fold containing family A, member 1 (BPIFA1) and BPIFB1 are putative innate immune molecules expr...
AbstractThe variation in cystic fibrosis (CF) lung disease and development of CF related complicatio...