نتایج جستجو برای: genome

تعداد نتایج: 229243  

Journal: :modares journal of medical sciences: pathobiology 2015
sadat dokanehiifard bahram mohamad soltani

although more than 98% of the human genome is transcribed, most of these transcripts are not translated into proteins. rather, they are considered as non-coding rnas. micrornas (mirnas) are very short non-coding rnas approximately 22 nucleotides in length which regulate many key processes of cells such as growth, proliferation, differentiation, cell cycle, apoptosis (programmed cell death) and ...

Abstract Selection not only increases the frequency of new-useful mutations but also remains some signals throughout the genome. Since these areas are often control economically important traits, identifying and tracking these areas is the most important issue in the animal genetics. The aim of this study was to detecting signals of selection in the genome of Turkmen horse using 70K SNP chip...

Journal: :hepatitis monthly 0
samad amini bavil olyaee medical clinic iii, rwth-university hospital aachen, & biotechnology department, pasteur institute of iran, germany christian trautwein medical clinic iii, rwth-university hospital aachen, & biotechnology department, pasteur institute of iran, germany frank tacke medical clinic iii, rwth-university hospital aachen, germany 492418089249, [email protected]; medical clinic iii, rwth-university hospital aachen, germany 492418089249, [email protected]

Journal: :iranian journal of diabetes and obesity 0
ensieh shahvazian department of genetics, faculty of medicine, international campus, shahid sadoughi university of medical sciences, yazd, iran ehsan farashahi yazd stem cell biology research center, yazd reproductive sciences institute, shahid sadoughi university of medical sciences, yazd, iran mohammad hasan sheikhha clinical and research center for infertility, shahid sadoughi university of medical sciences, yazd, iran masoud rahmanian diabetes research center, shahid sadoughi university of medical sciences, yazd, iran

objective: type 2 diabetes (t2d) as a complex disease is the result of genetically heterogeneous factors and environmental issues interaction. linkage and small-scale candidate gene studies were successful in identification of genetic susceptibilities of monogenic form of diseases. however, they were largely unsuccessful while applying to the more common forms of disease. by designing genome wi...

Background: In Archaea, previous studies have revealed the presence of multiple intron-containing tRNAs and split tRNAs. The full unexpurgated analysis of archaeal tRNA genes remains a challenging task in the field of bioinformatics, because of the presence of various types of hidden tRNA genes in archaea. Here, we suggested a computational method that searched for widely separ...

Journal: :Diversity 2023

In this article, we analyzed the origin of wild polyploid oats (Avena L., Poaceae) using region 18S rDNA (partially)–ITS1–5.8S obtained via NGS. There are six tetraploid (2n = 28) and four hexaploid 42) species differing by specific genome combinations: A. barbata, vaviloviana (AB), agadiriana (AB or BB), magna, murphyi, insularis (AC CD), ludoviciana, sterilis, fatua, occidentalis (ACD). We co...

Journal: :iranian journal of applied animal science 2015
a. afsharian m.r. nassiri

in order to perform breeding programs and improve production of native chickens, preserving genetic diversity in different areas of iran is important due to the reduced available population. genome sequencing is considered the most functional approach to determine the phylogeny relation between close populations. the aim of the present study was the evaluation of the phylogeny and genetic nucle...

Journal: :middle east journal of digestive diseases 0
mohammadreza fattahi abdorrasoul malekpour mojtaba mortazavi alireza safarpour nasrin naseri

background recent studies suggest that rare codon clusters are functionally important for protein activity. methods here, for the first time we analyzed and reported rare codon clusters in hepatitis c virus (hcv) genome and then identified the location of these rare codon clusters in the structure of hcv protein. this analysis was performed using the sherlocc program that detects statistically ...

Journal: :jundishapur journal of microbiology 0
mansoureh shahbazi dastjerdeh department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran shirin kouhpayeh department of immunology, school of medicine, isfahan university of medical sciences, isfahan, ir iran faezeh sabzehei department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran hossein khanahmad department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran; department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran. tel: +98-031337922487, fax: +98-031-3668859 mansour salehi department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran zahra mohammadi department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, ir iran

conclusions our findings revealed that the zfn technology could be employed to overcome ampicillin resistance by the targeted disruption of the ampicillin resistance gene, which leads to inactivation of β-lactam synthesis. therefore, zfn technology could be engaged to decrease the antibiotic resistance issue with the construction of a zfn archive against different args. to tackle the resistance...

Voet Th

Recently, we demonstrated chromosome instability (CIN) in human cleavage stage embryogenesis following in vitro fertilization (IVF). CIN not necessarily undermines normal human development (i.e. when remaining normal diploid blastomeres develop the embryo proper), however it can spark a spectrum of conditions, including loss of conception, genetic disease and genetic variation development. To s...

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