نتایج جستجو برای: alamut
تعداد نتایج: 47 فیلتر نتایج به سال:
In general, the figurines belonging to the Neolithic (the New Stone Age) have rarely been under functional analysis. Nevertheless, three studies undertaken on the figurines unearthed from some places in the Middle East have presented some classifications for them, and attempted to study different results in terms of their application (Voight, M., 1983, pp.186-192). The first one is the publishe...
wild boar is distributed throughout iran except highly arid areas. in recent years, however, population size of wild boar has increased primarily because of reduction in population size of natural predators such as leopard. conversely, changes in land-use practices and increase in foraging of livestock in natural habitats has led to reduction of food resources and consequently, has forced the s...
OBJECTIVE We report a novel lamin A/C (LMNA) mutation, p.Glu223Lys, in a family with extensive atherosclerosis, diabetes mellitus and steatosis hepatis. METHODS Sequence analysis of LMNA (using Alamut version 2.2), co-segregation analysis, electron microscopy, extensive phenotypic evaluation of the mutation carriers and literature comparison were used to determine the loss of function of this...
Background: Medicinal plants have been used for treatment of diseases and finding of new drugs. Botanical valuable traditional methods, offer finding new medicinal plants and herbal medicines. Objective: The aim of this study was the identification of important medicinal plants that widely were used by local inhabitants, in the treatment of skin diseases in the area of Alamut-Qazvin, Iran. M...
Background. Most genetic disorders are caused by single nucleotide variations (SNVs) or small insertion/deletions (indels). High throughput sequencing has broadened the catalogue of human variation, including common polymorphisms, rare variations or disease causing mutations. However, identifying one variation among hundreds or thousands of others is still a complex task for biologists, genetic...
Galactosemia is a metabolic disorder caused by mutations in the GALT gene [1,2]. We encountered a patient heterozygous for a known pathogenic H132Q mutation and a novel S222N variant of unknown significance [3]. Reminiscent of patients with the S135L mutation, our patient had loss of GALT enzyme activity in erythrocytes but a very mild clinical phenotype [3-8]. We performed splicing experiments...
This experiment was conducted in a greenhouse at Isfahan University of Technology, Isfahan, Iran in 2014 to evaluate 20 wheat cultivars (Navid, Pishtaz, Karaj, Kavir, Tajan, Karun, sholeh, Bahar, Khoshki 11, Gasparood, Sepahan, Sorkh tokhm, Chamran, Ghods, Shariar, Omid, Sistan, Alamut, Marvdasht and Shiraz) under two carbon dioxide concentrations (the ambient 360 and the enriched 700 µM) and t...
Nepeta is one of the biggest geniuses of Lamiaceae family which N. pungens, N. binaludensis, N. isphanica, N. pogonosperma and N. bracteata has been used traditionally in Iran. Nepeta pogonesperma is one of the endemic Nepeta species in Alamut region (Qazvin Province ). So in this research the aerial parts of Nepeta pogonesperma in full flowering stage were collected from Kheshchal altitudes of...
The ryanodine receptor 1-related congenital myopathies (RYR1-RM) comprise a spectrum of slow, rare neuromuscular diseases. Affected individuals present with a mild-to-severe symptomatology ranging from proximal muscle weakness, hypotonia and joint contractures to scoliosis, ophthalmoplegia, and respiratory involvement. Although there is currently no FDA-approved treatment for RYR1-RM, our group...
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