نتایج جستجو برای: فاکتورآلودگی cf

تعداد نتایج: 29477  

2013
Vinciane Saint-Criq Sung Hoon Kim John A. Katzenellenbogen Brian J. Harvey

Male cystic fibrosis (CF) patients survive longer than females and lung exacerbations in CF females vary during the estrous cycle. Estrogen has been reported to reduce the height of the airway surface liquid (ASL) in female CF bronchial epithelium. Here we investigated the effect of 17β-estradiol on the airway surface liquid height and ion transport in normal (NuLi-1) and CF (CuFi-1) bronchial ...

Journal: :The Journal of clinical investigation 1989
I Eichler L Joris Y P Hsu J Van Wye R Bram R Moss

Antibody opsonins from cystic fibrosis (CF) patients were investigated using nonmucoid and mucoid lipopolysaccharide (LPS) immunotype 1 Pseudomonas aeruginosa as bacterial ligands and PMN phagocytes. CF sera were compared to normal sera, polyvalent PA LPS hyperimmune globulin, and isotype switch variant monoclonal antibodies (MAbs) specific for type 1 PA LPS. Sera from PA-infected CF patients (...

2010
David Frear

The value of written corrective feedback (CF) has been an issue of considerable debate in the literature (e.g. Truscott, 1996; Ferris, 1999), and this polemic has lead to a trend in recent studies to draw on second language acquisition (SLA) research as a way to further comprehend the intricacies of this complex issue. Indeed, Ellis, Sheen Murakami and Takashima (2008) delineate between focused...

Journal: :Thorax 2009
C Goubau M Wilschanski V Skalická P Lebecque K W Southern I Sermet A Munck N Derichs P G Middleton L Hjelte R Padoan M Vasar K De Boeck

BACKGROUND In patients with symptoms suggestive of cystic fibrosis (CF) and intermediate sweat chloride values (30-60 mmol/l), extensive CFTR gene mutation analysis and nasal potential difference (NPD) measurement are used as additional diagnostic tests and a positive result in either test provides evidence of CFTR dysfunction. To define the phenotype of such patients and confirm the validity o...

Journal: :Thorax 1999
I Durieu C Amsellem C Paulin M T Chambe J Bienvenu G Bellon Y Pacheco

BACKGROUND Cystic fibrosis (CF) is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and defective expression of CFTR protein in epithelial cells. The main cause of mortality in CF is linked to chronic inflammatory and infectious airway processes. Recent studies have suggested perturbations in the apoptotic process in CF cell lines and ...

Journal: :Thorax 2005
M J Ledson M J Walshaw

survival in CF We read with interest the paper by Jones et al indicating the experience of the Manchester Adult CF Unit in the survival of patients with cystic fibrosis (CF) in the first 5 years following chronic infection with the B cepacia complex (Bcc). The authors appear to have shown that 31 patients with B cenocepacia had a worse prognosis than Pseudomonas aeruginosa infected patients. De...

2007
Yoshitaka Yamamoto Oliver Ray Katsumi Inoue

CF-induction is a sound and complete hypothesis finding procedure for full clausal logic which uses the principle of inverse entailment to compute a hypothesis that logically explains a set of examples with respect to a prior background theory. Currently, CF-induction computes hypotheses by applying combinations of several complex generalisation operators to an intermediate theory called a brid...

Journal: :TRANSACTIONS OF THE JAPAN SOCIETY OF MECHANICAL ENGINEERS Series A 1993

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