نتایج جستجو برای: rare populations
تعداد نتایج: 470522 فیلتر نتایج به سال:
Abstract Background: NOD2 gene located on chromosome 16 (IBD1) is known to have a strong association with Crohn’s disease. Three common polymorphisms of this gene including R702W, G908R, 1007fsinsC, were reported to be frequent in many western populations while rare occurrence of them was observed in eastern countries. The aim of this study was to assess the frequency of these polymorphisms ...
A major focus in population ecology is understanding factors that limit rare species. We used stable isotope approaches to diet to determine whether remaining rare antelope populations in Kruger National Park (KNP), South Africa experience i) nutritional stress; ii) competition with sympatric bulk grazers; iii) reduced habitat heterogeneity. Rare species consumed near-pure C4 grass-based diets ...
The black-striped pipefish, Syngnathus abaster, is a species of the Syngnathidae family. This study provides data on the morphometric, meristic and genetic structuring of the Caspian Sea pipefish, Syngnathus abaster. Eight morphometric characteristics based on total length and five morphometric characteristics based on standard length were analyzed. A total of 50 specimens were collected in bra...
Congenital diaphragmatic hernia (CDH) is a rare anomaly with a reported incidence of 1 in 16,000 populations. It may be associated with herniation of stomach, intestinal loops, spleen, and kidney through a chest wall defect. We report a case of a 1 year old male child who presented with recurrent fever, occasional chills and rigor of 4 months duration. Left kidney was non visualised on ultrasou...
BACKGROUND AND AIMS The effects of habitat fragmentation on quantitative genetic variation in plant populations are still poorly known. Saxifraga sponhemica is a rare endemic of Central Europe with a disjunct distribution, and a stable and specialized habitat of treeless screes and cliffs. This study therefore used S. sponhemica as a model species to compare quantitative and molecular variation...
Linkage disequilibrium has been a powerful tool in identifying rare disease alleles in human populations. To date, most research has been directed to isolated populations which have undergone a bottleneck followed by rapid exponential expansion. While this strategy works well for rare diseases in which all disease alleles in the population today are clonal copies of some common ancestral allele...
Next-generation sequencing technologies have been designed to discover rare and de novo variants and are an important tool for identifying rare disease variants. Many statistical methods have been developed to test, using next-generation sequencing data, for rare variants that are associated with a trait. However, many of these methods make assumptions that rare variants are in linkage equilibr...
The seed production of the rare species Gueldenstaedtia monophylla has been investigated in 19 coenotic populations territories Russia (Central Altai) and Mongolia (the north-western part). G. reproduces exclusively by seeds is characterized low number density plants populations. Its have a high proportion generative plants: from 31 to 84% total plants. small shoots, varying 1 6 per plant. flow...
background: cytokines are cell signaling molecules which upon release by cells facilitate the recruitment of immune-modulatory cells towards the sites of inflammation. genetic variations in cytokine genes are shown to regulate their production and affect the risk of infectious as well as autoimmune diseases. intron-3 of interleukin-4 gene (il-4) harbors 70-bp variable number of tandem repeats (...
Objective: Although metabolic diseases individually are rare ,but overall have an incidence of 1/2000 and can cause devastating and irreversible effect if not diagnosed early and treated promptly. selective screening is an acceptable method for detection of these multi presentation diseases.Method: using panel neonatal screening for detection of metabolic diseases in 650 high risk Iranian patie...
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