نتایج جستجو برای: iran polymorphism
تعداد نتایج: 208521 فیلتر نتایج به سال:
The Clara cell protein (CC16) is a small and readily diffusible protein of 16 kDa secreted by bronchiolar Clara cells in the distal airspaces. Mutation detection methods identified an adenine to guanine substitution in the CC16 gene at position 38 (A38G) downstream from the transcription initiation site within the non-coding region of exon 1. In the present study, the genetic polymorphism of CC...
lstituto Beni Culturali (Institute for Cultural Heritage) is the cultural institution of Regione Emilia Romagna. IBC web site [6] has been completely revised in cooperation with Hypermedia Open Center [S], the laboratory of the Electronics and Information Department at Politecnico di Milano. We adopted W2000 model for requirements analysis and for the analysis and organization of the applicatio...
Background and purpose: The human multidrug resistance gene (MDR1) encodes for P-glycoprotein (P-gp) which is a transmembrane transporter protein acts as an efflux pump for a number of xenobiotics. It plays a protective role for cells against DNA damage caused by toxins and drugs. The wobble C3435T polymorphism at exon 26 has been associated with different expression levels and activities of th...
objective(s) the sst-i polymorphic site on the 3' untranslated region of the apo ciii gene, has been previously reported to be associated with hypertriglyceridemia. the aim of the present study was to explore the association between sst-i polymorphism with plasma lipid and lipoprotein levels in hyperlipidemic (hlp) patients from semnan province, iran. materials and methods genomic dna was ...
ava ii site as a marker of β-globin gene polymorphism, among normal and sickle cell patients in iran
the restriction enzyme ava ii detects the base change of the intervening sequence ii (ivs ii) which is used as one of the markers of β-globin gene polymorphism. this study was conducted to determine the frequency of the ava ii site on the β-globin gene among normal people and patients with sickle cell syndrome (scs) in iran. dna fragments containing the ivs ii region of the β-globin gene from 3...
Background and Aim: Breast cancer is the most common type leading cause of cancer-induced deaths in women, worldwide. The Fibroblast Growth Factor Receptor 2 (FGFR2) a tyrosine kinase receptor that plays an essential role growth, invasion, movement, angiogenesis tumor cells. Several single nucleotide polymorphisms have been found intron FGFR2 gene, i.e., associated with high risk breast cancer....
Snezana Mladenovic Drinic, Editor of the journal Genetika request from Xiaohui Qian to remove name paper DETECTING DNA POLYMORPHISM AND GENETIC DIVERSITY IN A WIDE PISTACHIO GERMPLASM BY RAPD MARKERS QIAN1* and Shahram MEHRI2 1Department Tourism Culture, Anhui Finance Trade Vocational College, Hefei, China 2Department Agronomy Plant Breeding, ParsAbad Moghan Branch, Islamic Azad University, Mog...
multiple sclerosis (ms) is a chronic inflammatory disorder of the central nervous system, with a complex etiology that includes a strong genetic component. the chromosome 19q 13 region surrounding the apolipoprotein e (apoe) gene has shown consistent evidence of involvement in ms. in a cross-sectional study, to show the apoe genotype and allele frequency in the ms population of iran in comparis...
in this report, β-tubulin gene polymorphism was investigated in haemonchus contortus populations isolated from sheep flocks in different regions of khouzestan province, southwestern iran. the samples were chosen on the basis of regional variation in benzimidazole treatment background of sheep flocks. our objective was to study the relationship between treatment background andβ -tubulin gene po...
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