نتایج جستجو برای: i gene

تعداد نتایج: 2077523  

Journal: :iranian journal of microbiology 0
farzan modarresi department of microbiology and virology, afzalipuor school of medicine, kerman, iran omid azizi department of microbiology and virology, afzalipuor school of medicine, kerman, iran. mohammadreza shakibaie department of microbiology and virology, afzalipuor school of medicine, kerman, iran and research center for infectious diseases and tropical medicine, kerman, iran and environmental health engineering research center, kerman university of medical sciences, kerman, iran. mohammad motamedifar departments of bacteriology and virology, school of medicine, shiraz university of medical sciences, shiraz, iran. shala mansouri department of microbiology and virology, afzalipuor school of medicine, kerman, iran.

objectives: in present study we aimed to clone the lux i gene encoding n-acyl-homoserine synthase detected in biofilm forming clinical isolates of acinetobacter baumannii and study its expression in escherichia coli transformants. materials and methods: four a. baumannii hospital strains which demonstrated strong biofilm activity were selected in this investigation. the presence of lux i gene w...

I-cell disease is a rare inherited metabolic disorder resulting from a defective phosphotransferase, characterized by coarse facial features, skeletal abnormalities and mental retardation. As clinical features of this condition mimic that of Hurler disease mutation studies help in the diagnosis. We present a case of I-cell disease in a neonate with GNPTAB gene mutation.

M. Sadeghi P. Zamani R. Abdoli S. Behzadi, S.R. Miraei-Ashtiani

Molecular genetics selection on individual genes is a promising method to genetically improve economically important traits in livestock. The insulin like growth factor-I (IGF-I) gene may play important roles in growth of multiple tissues, including muscle cells, cartilage and bone. The objectives of the present study were the estimate the haplotype frequencies of the IGF-I gene polymorphisms i...

صالحی, رسول, صالحی, منصور, نصر اصفهانی, بهرام,

Introduction: Mucopolysaccharidosis I (MPS-I) is an autosomal recessive lysosomal storage diseases, caused by α-L-iduronidase (IDUA) enzyme deficiency. The clinical manifestations of MPS-I patients are variable ranging from severe to mild, and therefore prediction of disease severity is difficult. From when IDUA gene has been cloned more than 109 distinct mutations have been identified in it an...

Ahmadi MR Ararooti T, Kadivar A Mirzaei A Rowshan Ghasrodashti A Sharifiyazdi H

Background: One of the most important metabolic factors affecting the reproductive activity is insulin-like growth factor-I (IGFI) concentration changes after calving. Recently, Maj et al. (2008) discovered a significant association between the IGF-I genotypes based on the 5'-untranslatedregion (5'-UTR) of IGF-I gene and the IGF-I blood level. The objective of this study is to investi...

Background: Hepatic ischemia/reperfusion injury (I/RI) is a multifactorial pathophysiologic process which can lead to liver damage and dysfunction. This study examined the protective effect of dexamethasone on the gene expression of endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) and on the liver tissue damage during warm hepatic I/R. Materials and Methods: A total of 32 mal...

آیرملو, هرمز, امین بخش, محمد, برزگر, محمد, جبارپور بنیادی, مرتضی, خندقی, رضا, شیمیا, محمد, عمرانی, امید, نداف نیا, حسین,

Background: Spinal muscular atrophy includes a group of neuromuscular disorders characterized by degeneration of anterior horn cells in the spinal cord, and leads to progressive muscular weakness. NAIP is one of the genes that inhibits motor neuron apoptosis. Deletion of this gene is usually observed in type I SMI. The aim of this study was to investigate the frequency and pathogenicity of NAIP...

Ali Forouzanfar

Background  Recent investigations show that both proliferation and secretion of macromolecules by cells can be regulated by low level laser therapy (LLLT). The aim of this study was to determine whether LLLT could induce a bio-stimulatory effects on human gingival fibroblasts (HGF3-PI 53). Therefore, the effect of laser irradiation on human gingival cell proliferation and collagen type I gene ...

Journal: :acta medica iranica 0
a nikzamir department of biochemistry, school of medicine, ahwaz jondi shapour university of medical sciences, m nakhjavani endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic t golmohammadi department of biochemistry, school of medicine, tehran university of medical sciences, tehran, iran l dibai endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic r saffary endocrinology and metabolism research center (emrc), vali-e-asr hospital, tehran university of medic

diabetes mellitus is a multifactorial disease. it has recently been shown that an insertion (i)/deletion (d) polymorphism exists in the angiotensin-converting enzyme (ace) gene that can affect the serum ace level. there are three genotypes: dd, di, and ii, with the ace level being highest in dd, intermediate in di, and lowest in ii. in the present investigation, 170 patients with type 2 diabete...

خنکدار طارسی, عباس, عزیزی, سهیل, قناعت, کسری, ملک زاده شفارودی, مجید, ولیزاده دیزجیکان, امیر,

Background and purpose: Damage caused by ischemia/reperfusion (I/R) is one of the major causes of liver failure during surgeries. Endothelin as the main vasoconstrictor has two receptors; ETA and ETB. Increased number of ETB during ischemia-reperfusion, reduces tissue damages by sinusoidal dilation. This study investigated the effects of dexamethasone against liver endothelial glycocalyx injury...

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