نتایج جستجو برای: variants
تعداد نتایج: 108401 فیلتر نتایج به سال:
background: as a dna repair protein, flap endonuclease 1 is a key enzyme in maintaining genomic instability and preventing carcinogenesis. two single nucleotide polymorphisms (snps), -69g>a and 4150g>t are associated with dna damage. this meta-analysis is to evaluate the genetic effects of fen1 gene snps (-69g/a and 4150g/t) and the susceptibility to diseases, including glioma risk, breast canc...
regarding the large number of developed particle swarm optimization (pso) algorithms and the various applications for which pso has been used, selecting the most suitable variant of pso for solving a particular optimization problem is a challenge for most researchers. in this paper, using a comprehensive survey and taxonomy on different types of pso, an expert system (es) is designed to identif...
Introduction: Long QT syndrome (LQTS) is a type of ventricular arrhythmia characterized by prolonged QT intervals on electrocardiogram or delay in ventricular repolarization and it can lead to syncope, seizure and sudden cardiac death. Here, KCNE1 and KCNE2 variants are studied among Iranian affected families with this syndrome. Materials and Methods: Fifty patients referring to Rajaei Cardiov...
Introduction: The precision and time required for analysis of data in next-generation sequencing (NGS) depends on many factors including the tools utilized for alignment, variant calling, annotation and filtering of variants, personnel expertise in data analysis and interpretation, and computational capacity of the lab and its optimization is a challenging task. Method: An application software...
Introduction: The precision and time required for analysis of data in next-generation sequencing (NGS) depends on many factors including the tools utilized for alignment, variant calling, annotation and filtering of variants, personnel expertise in data analysis and interpretation, and computational capacity of the lab and its optimization is a challenging task. Method: An application software...
background: variants in the candidate genes enos, cyp11b2 and ace have been implicated as liable biomarkers that can predict complications like hypertension and preeclampsia. studies on the impact and distribution of these variants on healthy pregnancy have not been done so far in south indian or in any of the native indian population. examining these variants could lay a strong basis in unders...
numerous problems encountered in real life cannot be actually formulated as a single objective problem; hence the requirement of multi-objective optimization (moo) had arisen several years ago. due to the complexities in such type of problems powerful heuristic techniques were needed, which has been strongly satisfied by swarm intelligence (si) techniques. particle swarm optimization (pso) has ...
conclusions the distribution of amino acid mutations as well as the ratio between missense and silent nucleotide mutations (dn/ds) showed that a narrowly focused immune pressure had already been on the surface protein (especially ctl epitopes) which led to the emergence of escape mutants in these patients who were in tolerance phase of chronicity. materials and methods the surface genes from 17...
This study investigatesvariability in English yes/no questions as well as the commonalities among yes/no question variants produced by members of two different varieties of English: Canadian English native speakers and Iranian EFL learners.Further, it probes the role of gender in theEnglish yes/no question variants produced by Canadian English native speakers and those produced by Iranian EFL l...
Amelogenin gene (AMEL-X) encodes an enamel protein called amelogenin, which plays a vital role in tooth development. Any mutations in this gene or the associated pathway lead to developmental abnormalities of the tooth. The present study aims to analyze functional missense mutations in AMEL-X genes and derive an association with amelogenesis imperfecta. The information on miss...
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