نتایج جستجو برای: and c individual

تعداد نتایج: 16985603  

2013
Kate M. Scott Karestan C. Koenen Sergio Aguilar-Gaxiola Jordi Alonso Matthias C. Angermeyer Corina Benjet Ronny Bruffaerts Jose Miguel Caldas-de-Almeida Giovanni de Girolamo Silvia Florescu Noboru Iwata Daphna Levinson Carmen C. W. Lim Sam Murphy Johan Ormel Jose Posada-Villa Ronald C. Kessler

BACKGROUND Associations between lifetime traumatic event (LTE) exposures and subsequent physical ill-health are well established but it has remained unclear whether these are explained by PTSD or other mental disorders. This study examined this question and investigated whether associations varied by type and number of LTEs, across physical condition outcomes, or across countries. METHODS Cro...

2013
Mark Lucanic Jill Graham Gary Scott Dipa Bhaumik Christopher C. Benz Alan Hubbard Gordon J. Lithgow Simon Melov

Non-coding small RNAs of the micro-RNA class (miRNA) are conserved regulators of gene function with a broad impact on biological processes. We screened miRNA levels for age-related changes in individual worms and investigated their influence on the lifespan of the nematode C. elegans. We measured the abundance of 69 miRNAs expressed in individual animals at different ages with over thirty five ...

ژورنال: طب کار 2013
بابایی مزرعه‌نو, علیرضا, شریفی, غلامرضا , کیخسروی, فریده ,

Background: Fatigue is an important inhibiting factor in human performance, so with rising aerobic power could be overcome individual fatigue. Based on the importance of maximum oxygen consumption at fatigue threshold, the purpose of this study was to evaluate changes in temperature of the maximum rate of oxygen consumption and time to exhaustion in workers of spinning factory. Methods: In thi...

E Rezaei , H Dastsooz , H Faraji , J Manoochehri , Kh Sadeghi , M Fardaei , R Masoumi Dehshiri , S Mohammadi , T Moradi ,

Background Wilson disease (WD) is a rare autosomal recessive disorder, which leads to copper metabolism, due to mutations in ATP7B gene. The gene responsible for WD consists of 21 exons that span a genomic region of about 80 kb and encodes a copper transporting P-type ATPase (ATP7B), a protein consisting of 1465 amino acids. Identifying mutation in ATP7B gene is important to find carrier i...

Recent pre-clinical and clinical studies have revealed the C-reactive protein gene (CRP) is related to the degree of acute rise in plasma C-reactive protein (CRP) levels. Moreover, single nucleotide polymorphisms (SNPs) in the CRP gene could associate with increased risk of cancer, atherosclerosis, diabetes mellitus, bowel disease, rheumatoid arthritis, psoriasis, obstructive pulmonary disease,...

Amir Masoomi, Javad Kojuri, Negar Azarpira, Niusha Behdad, Soha Namazi,

Background:  Atorvastatin is prescribed for the primary and the secondary prevention of coronary artery diseases. A wide variation in inter-individual statin response suggests that genetic differences may contribute to this variation. This study investigated the association of ABCB1 (C3435T) and ABCC1 (G2012T) polymorphisms with clinical response to atorvastatin in Iranian primary hyperlip...

Journal: :IDEAS: Journal on English Language Teaching and Learning, Linguistics and Literature 2020

Journal: :journal of sciences islamic republic of iran 0

in this paper, the ultrasonic absorption of amino acids was measured using a small cylindrical resonator at physiological ph and 25°c and a concentration of 0.1. m. the absorption of mixtures of some amino acids was also measured. in the case of cysteine-histidine, the absorption of mixtures is much larger (more than twice) than the summation of absorption of the individual amino acid. this may...

Journal: :journal of research in medical sciences 0
majid motovali-bashi department of biology, genetic division, faculty of sciences, university of isfahan, isfahan, iran zohreh hojati department of biology, genetic division, faculty of sciences, university of isfahan, , isfahan, iran samaneh hajihoseiny department of biology, genetic division, faculty of sciences, university of isfahan, , isfahan, iran simin hemmati department of oncology and radiotherapy, school of medicine, isfahan university of medical sciences, isfahan, iran

background: matrix metalloproteinases comprise a family of enzyme degrade components of extra cellular matrix. there are single nucleotide polymorphisms in the promoter regions of several genes with ability to influence cancer susceptibility. the aim of this study was to analyze association between mmp 3 promoter polymorphisms and colorectal cancer occurrence and progression. materials and meth...

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