نتایج جستجو برای: gene frequency

تعداد نتایج: 1580534  

دیهم, بهناز, فرخی, عفت, کریمی, علی, زمان زاد, بهنام , نفیسی, محمدرضا ,

Introduction & Objective: TEM-1 beta lactamase gene is one of the important plasmidic genes in Enterobacteriaceae which is the cause of over 90% of Escherichia coli isolates resistance to beta lactam antibiotics. In this study, the frequency of TEM-1 gene in nosocomial strains of Escherichia coli, Klebsiella pneumoniae and Enterobacter was investigated using PCR. Materials & Methods: In th...

Journal: :research in molecular medicine 0
mohammad bokaeian 1. infectious disease and tropical medicine research center zahedan university of medical sciences saeide saeidi 2. institute of plant biotechnology, university of zabol, 98616, iran mehdi hassanshahian : department of biology, faculty of sciences, shahid bahonar university of kerman, kerman, iran.

background: in this study we aimed at detecting the enterotoxin a and b gene of s. aureus in clinical samples of patients attending health centers in zahedan using molecular methods. materials and methods: a cross-sectional study was carried out in which 40 samples of s. aureus were obtained from patients in a hospital in zahedan, iran. following the biochemical tests, identifications were conf...

ژورنال: Anatomical Sciences Journal 2016
Ghajavand, Hassan, Johari, Behrooz, Sangarifar, Samira, Yari, Abazar,

Introduction: There are various virulence factors encoded by Staphylococcus Aureus, which enable them to cause nosocomial infections and mastitis in dairy cattle. The clf-A gene mediates the bacterial colonization through binding to the extracellular matrix of the host. Treatment of such infections becomes more difficult due to increased resistance to methicillin. The current study aimed at inv...

ژورنال: پژوهش در پزشکی 2012
ابراهیمی دریانی, ناصر, بالایی, هدیه, حبیبی, منیژه, زالی, محمد رضا, زجاجی, همایون, شریفیان, افسانه, فرنود, آلما, نادری, نصرت اله,

Abstract Background: NOD2 gene located on chromosome 16 (IBD1) is known to have a strong association with Crohn’s disease. Three common polymorphisms of this gene including R702W, G908R, 1007fsinsC, were reported to be frequent in many western populations while rare occurrence of them was observed in eastern countries. The aim of this study was to assess the frequency of these polymorphisms ...

Background and Aims: Helicobacter pylori (H. pylori) is a gram-negative, microaerophilic, spiral-shaped flagellated bacterium that is urease, catalase and oxidase positive. One of its pathogenicity factors is the iceA gene. H. pylori has recently been recognized as a genetic indicator for the development and evolution of duodenal ulcer disease in the East. This study aimed to determine the pres...

ژورنال: پیاورد سلامت 2018
امینی, کیومرث, رنجبر, الهام,

Background and Aim: Pseudomonas aeruginosa is one of the most important factors in hospital infections, especially in patients with immune deficiency and Childhood diseases. The Virulence of bacteria are due to the presence of the Pyoverdine gene, which has many effects on the wild type of bacteria during the pathogenic pathway. Identification of different classes of PVD gene is necessary for t...

Background and aims:  Gastric malignancies have the fourth place among the most prevalent cancers. In many cancers, overexpressing of HER2/neu gene has been observed with a poor prediction. Up to now, there is a little information about the duplication of HER2/neu gene in gastric cancer using MLPA method. The present study aimed to investigate the frequency of mutations resulting from ampl...

Journal: :genetics in the 3rd millennium 0
محمد تقی اکبری mohammad taghi akbari no.98, akbari medical genetics laboratory, taleghani street, tehran, iranآزمایشگاه ژنتیک پزشکی دکتر اکبری، خیابان طالقانی، شماره 98، تهران، ایران./ تلفن: 8896868 شهره زارع کاریزی shohreh zare karizi akbari medical genetics laboratory, tehran, iran1- آزمایشگاه ژنتیک پزشکی دکتر اکبری، تهران، ایران شهریار نفیسی shahriai nafisi department of neurology, tehran university of medical science, tehran, iranبخش مغز و اعصاب، دانشگاه علوم پزشکی تهران، تهران، ایران زهرا بهمنی zahra bahmani akbari medical genetics laboratory, tehran, iran1- آزمایشگاه ژنتیک پزشکی دکتر اکبری، تهران، ایران

duchene and becker muscular dystrophy (dmd and bmd) are x-linked conditions that result from a defect in the dystrophin gene located on xp21. dmd is the most frequent neuromuscular disease in humans (1/3500 male newborns). in approximately 65% of dmd and bmd patients, deletions in the dystrophin gene have been identified as the molecular determinant. population-based variations in frequency and...

Journal: :genetics in the 3rd millennium 0
حسین نجم ابادی hossein najmabadi welfare & rehabilitation university of medical sciences, tehran, irankariminejad-najmabadi pathology & genetics centetel: +98218836952-5 r ماندانا حسن زاد mandana hasanzad genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran.tehran medical unit, islamic azad university, tehran, iran مریم آزاد maryam azad kariminejad-najmabadi pathology & genetics center, tehran, iran کیمیا کهریزی kimia kahrizi genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran واله هادوی valeh hadavi kariminejad-najmabadi pathology & genetics center, tehran, iran بهاره شجاع صفار bahareh shoja saffar genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran شهریار نفیسی

spinal muscular atrophy (sma) is a common autosomal recessive neuromuscular disorder caused by the loss of α-motor neurons in the spinal cord. the survival motor neuron (smn) protein is encoded by 2 genes, smn1 and smn2. the most frequent mutation is the biallelic deletion of exon 7 of the smn1 gene. smn2 cannot compensate for the loss of smn1, due to the exclusion of exon 7. carrier frequency ...

ژورنال: پژوهش در پزشکی 2008
بیژن مقیمی دهکردی, , دکتر سمیه غیاثی, , دکتر سیدرضا محبی, , دکتر محمدرضا زالی, , روح‌ا... نجارصادقی, , فاطمه خاتمی, , مهدی منتظرحقیقی, ,

Background and Aim: Colorectal cancer is one of the most common malignancies in worldwide. Because the gene 5, 10-methylene-tetrahydrofolate reductase (MTHFR) plays a key role in methylation, synthesis and repair of DNA, numerous studies have focused on evaluating the correlation between polymorphisms of this gene and sporadic colorectal cancer. This study was carried out to examine the associa...

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