نتایج جستجو برای: cf

تعداد نتایج: 29475  

2016
H. Al-momani A. Perry C. J. Stewart R. Jones A. Krishnan A. G. Robertson S. Bourke S. Doe S. P. Cummings A. Anderson T. Forrest S. M. Griffin M. Brodlie J. Pearson C. Ward

Gastro-Oesophageal Reflux (GOR) is a key problem in Cystic Fibrosis (CF), but the relationship between lung and gastric microbiomes is not well understood. We hypothesised that CF gastric and lung microbiomes are related. Gastric and sputum cultures were obtained from fifteen CF patients receiving percutaneous endoscopic gastrostomy feeding. Non-CF gastric juice data was obtained through endosc...

Journal: :Cardiogenetics 2023

Cell-free nuclear (cf-nDNA) and mitochondrial (cf-mDNA) DNA are released from damaged cells in type 2 diabetes mellitus (T2DM) patients, contributing to adverse cardiac remodeling, vascular dysfunction, inflammation. The purpose of this study was correlate the presence cf-DNAs with HF T2DM patients. A total 612 patients were prescreened by using a local database, 240 (120 non-HF 120 individuals...

Journal: :Journal of Applied Physics 2022

The all-dielectric metasurface-based color filter (CF) has attracted huge interest in many fields due to its excellent optical properties. We present four CFs with different shapes on quartz substrates generate blue (B), green (G), and red (R) spectra high purity. show the maximum reflection intensities of 99.6% 99.7% 95.1% (R), their bandwidths are 14, 16, 13 nm for RGB colors, respectively. T...

Background and Objectives: Pseudomonas aeruginosa isolates from the lungs of cystic fibrosis (CF) patients are often heterogeneous and antibiotic resistant strains. Our work therefore focused on the antibiotic resistance properties of these P. aeruginosa strains isolated from Iranian patients, as well as the genetic diversity analysis by a repetitive-element-based molecular assay. Methods: This ...

Journal: :The European respiratory journal 2001
M Wilschanski H Famini N Strauss-Liviatan J Rivlin H Blau H Bibi L Bentur Y Yahav H Springer M R Kramer A Klar A Ilani B Kerem E Kerem

The diagnosis of cystic fibrosis (CF) is based on characteristic clinical and laboratory findings. However, a subgroup of patients present with an atypical phenotype that comprises partial CF phenotype, borderline sweat tests and one or even no common cystic fibrosis transmembrane conductance regulator (CFTR) mutations. The aim of this study was to evaluate the role of nasal potential differenc...

Journal: :Acta oncologica 2017
Gunhild M Gjerset Jon H Loge Cecilie E Kiserud Sophie D Fosså Sævar B Gudbergsson Line M Oldervoll Torbjørn Wisløff Lene Thorsen

BACKGROUND Knowledge about the user' needs is important to develop targeted rehabilitation for cancer patients with chronic fatigue (CF). The aims of the study were to examine prevalence of CF in cancer survivors attending an one-week inpatient educational program (IEP) and to identify characteristics of those with CF. Further to examine the perceived needs for different components in a rehabil...

Journal: :Molecular plant-microbe interactions : MPMI 2009
Brande B H Wulff Antje Heese Laurence Tomlinson-Buhot David A Jones Marcos de la Peña Jonathan D G Jones

The interaction between tomato and the leaf mold pathogen Cladosporium fulvum is controlled in a gene-for-gene manner by plant Cf genes that encode membrane-anchored extracytoplasmic leucine-rich repeat (LRR) glycoproteins, which confer recognition of their cognate fungal avirulence (Avr) proteins. Cf-9 and Cf-4 are two such proteins that are 91% identical yet recognize the sequence-unrelated f...

2011
D. Wat

Non-cystic fibrosis (CF) bronchiectasis is a complex disorder characterised by recurrent chest infections and poorly regulated respiratory innate and adaptive immunity. These lead to a ‘‘vicious cycle’’ of impaired mucociliary clearance, chronic infection, bronchial inflammation and progressive lung injury. The most prevalent pathogenic bacteria are Haemophilus influenzae, Pseudomonas aeruginos...

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 ...

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