نتایج جستجو برای: فاکتورآلودگی cf

تعداد نتایج: 29477  

Journal: :The Laryngoscope 2014
Maaike C Berkhout Cornelis J van Rooden Ralph C Aalbers Lahssan H el Bouazzaoui Wytske J Fokkens Evert Rijntjes Harry G M Heijerman

OBJECTIVES/HYPOTHESIS Paranasal sinus pneumatization in patients with cystic fibrosis (CF) is less extensive compared to the general population and seems to be correlated to CF genotype. Interestingly, in CF patients temporal bone pneumatization (TBP) is more extensive compared to the general population, and middle ear pathology is generally uncommon in CF. It is debated whether TBP is influenc...

2014
Kaivon Assani Mia F. Tazi Amal O. Amer Benjamin T. Kopp

Burkholderia cenocepacia is a virulent pathogen that causes significant morbidity and mortality in patients with cystic fibrosis (CF), survives intracellularly in macrophages, and uniquely causes systemic infections in CF. Autophagy is a physiologic process that involves engulfing non-functional organelles and proteins and delivering them for lysosomal degradation, but also plays a role in elim...

Journal: :Circulation. Arrhythmia and electrophysiology 2015
Andrea Sarkozy Dipen Shah Johan Saenen Juan Sieira Thomas Phlips Wim Boris Mehdi Namdar Christiaan Vrints

BACKGROUND In an experimental model, variable and intermittent contact force (CF) resulted in a significant decrease in lesion volume. In humans, variability of CF during pulmonary vein isolation has not been characterized. METHODS AND RESULTS In 20 consecutive patients undergoing CF-guided circumferential pulmonary vein isolation, 914 radiofrequency applications (530 in sinus rhythm and 384 ...

Journal: :Physiological genomics 2003
Christina K Haston Lap-Chee Tsui

The strain-dependent survival of cystic fibrosis (CF) knockout mice has been used to map a modifier of CF, Cfm1, in mice and, subsequently, in humans. To identify additional modifiers of the CF phenotype, in this study, the survival of F2 CF mice derived from a cross between congenic C57BL/6J CF and BALB/cJ CF heterozygotes was followed up to 12 wk of age. A genome-wide linkage scan completed i...

Background:Cystic Fibrosis (CF) is a systemic disease affecting extra pulmonary dysfunction as a result of CF-related lung disease. Because of lack of enough studies in this field and utilization of TDE in this field, we aimed to evaluate t...

Journal: :Neuron 2003
Kouichi Hashimoto Masanobu Kano

We studied how physiological properties of cerebellar climbing fiber (CF) to Purkinje cell (PC) synapses change during developmental transition from multiple to mono CF innervation onto each PC. From P3 to P6, differences in the strengths of multiple CFs became larger. Around P10, each PC was either monoinnervated by one strong CF (CF-mono) or multiply innervated by one strong CF (CF-multi-S) p...

Journal: :به زراعی کشاورزی 0
سید مجید موسوی دانشجوی دکتری، گروه مهندسی علوم خاک، دانشگاه تهران، پردیس کشاورزی و منابع طبیعی، کرج ـ ایران زهرا احمدآبادی کارشناس ارشد، گروه علوم خاک، دانشگاه علوم کشاورزی و منابع طبیعی ساری، ساری ـ ایران

to compare potential of two organic materials including sewage sludge (ss) and municipal solid wastecompost (msw) on micronutrients entry to soil, a research was conducted as split-plot arrangement basedon randomized complete block design with three replications in research field of sari agriculturaluniversity. main-plot (fertilizer treatments) included 20 and 40 ton/ha ss, 20 and 40 ton/ha ss ...

Journal: :The Plant cell 2001
R A Van der Hoorn R Roth P J De Wit

The tomato resistance genes Cf-4 and Cf-9 confer specific, hypersensitive response-associated recognition of Cladosporium carrying the avirulence genes Avr4 and Avr9, respectively. Cf-4 and Cf-9 encode type I transmembrane proteins with extracellular leucine-rich repeats (LRRs). Compared with Cf-9, Cf-4 lacks two LRRs and differs in 78 amino acid residues. To investigate the relevance of these ...

2008
M. Eshaghi Gordji H. Khodaie

In this paper, we achieve the general solution and the generalized Hyers-UlamRassias stability for the quadratic type functional equation f(x+ y + 2cz) + f(x+ y − 2cz) + cf(2x) + cf(2y) = 2[f(x+ y) + cf(x+ z) + cf(x− z) + cf(y + z) + cf(y − z)] for fixed integers c with c 6= 0,±1, by using the fixed point alternative.

Cystic fibrosis (CF) is the most common autosomal recessive disorder in white skinned individuals. Chronic lung infection is the main cause of mortality in this disease. Approximately 60–75 % of adult CF patients frequently suffer from Pseudomonas aeruginosa (PA) infection that is strongly associated with inflammation, lung destruction, and increased mortality. Therefore, CF patients should be ...

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