نتایج جستجو برای: incorrect deletion
تعداد نتایج: 99820 فیلتر نتایج به سال:
In this paper, we introduce a novel self-supervised learning (SSL) loss for image representation learning. There is growing belief that generalization in deep neural networks linked to their ability discriminate object shapes. Since shape related the location of its parts, propose detect those have been artificially misplaced. We represent parts with tokens and train ViT which token has combine...
Background and Aim:-thalassemia is the most common inherited disorder of hemoglobin (Hb) synthesis in the world. Alpha thalassemia most frequently results from the loss of one (- ) or both (- -) of the duplicated genes () on chromosome 16. Carriers of deletional forms of -thalassemia (-/- /-, or --/) are clinically normal but have a mild hypochromic, microcytic anemia. C...
Background and Aim: A peptic ulcer is a breach in the gastric or duodenal mucosa down to the submucosa. There is evidence concerning the role of Reactive Oxygen Species (ROS) in the genesis of such ulcers production of intracellular ROS along mitochondria oxidative phosphorylation (OXPHOS) predisposes the deletion of 4977 bp mtDNA. The aim of the present study was to evaluate the association of...
In order to study the effect of incomplete sire's pedigree on genetic trend (bBv,y) and gain (R) of quantitative trait, two population were simulated with the heritability 0.15 and 0.30. For each population, information resulted from ten years of selection were saved in different files. In generated data files, the sire numbers were eliminated from pedigree file with 0, 10, 20, …, 100 percentag...
Objective Globozoospermia is a rare syndrome with an incidence of less than 0.1% among infertile men. Researchers have recently identified a large deletion, about 200 kbp, encompassing the whole length of DPY19L2 or mutations in SPATA16 and PICK1 genes associated with globozoospermia. The aim of this study was to analyze the DPY19L2 gene deletion using polymerase chain reaction technique for th...
Colorectal cancer (CRC) is the third leading cause of cancer-related death worldwide, and its occurrence can be ascribed to genetic susceptibility. Mitochondrial DNA 4977-bp (mtDNA 4977), as the most described mtDNA deletion, has been long proposed to be involved in various types of cancers. However, a few studies on mtDNA 4977-bp deletion in Iranian patients with CRC have been reported. The cu...
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