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排序方式: 共有1619条查询结果,搜索用时 31 毫秒
61.
孔锐  谢玮  雷泰 《系统仿真学报》2020,32(4):601-611
自动识别和描述图像的内容是人工智能中一个重要的研究方向,它涉及计算机视觉和自然语言处理技术。针对这一难题,提出了一种由深层神经网络模型生成自然语言句子来描述图像内容的方法。该方法提出的模型由卷积神经网络(Convolution Neural Network,CNN)和循环神经网络(Recurrent Neural Network,RNN)组成,其中,CNN用来提取输入图像的特征生成固定长度的特征向量,该特征向量初始化RNN来生成句子。在MSCOCO图像描述数据集上的实验结果表明了该模型所生成句子的语法准确性和语义准确性,且优于先前的基线模型。  相似文献   
62.
We tested 16 million SNPs, identified through whole-genome sequencing of 457 Icelanders, for association with gout and serum uric acid levels. Genotypes were imputed into 41,675 chip-genotyped Icelanders and their relatives, for effective sample sizes of 968 individuals with gout and 15,506 individuals for whom serum uric acid measurements were available. We identified a low-frequency missense variant (c.1580C>G) in ALDH16A1 associated with gout (OR = 3.12, P = 1.5 × 10(-16), at-risk allele frequency = 0.019) and serum uric acid levels (effect = 0.36 s.d., P = 4.5 × 10(-21)). We confirmed the association with gout by performing Sanger sequencing on 6,017 Icelanders. The association with gout was stronger in males relative to females. We also found a second variant on chromosome 1 associated with gout (OR = 1.92, P = 0.046, at-risk allele frequency = 0.986) and serum uric acid levels (effect = 0.48 s.d., P = 4.5 × 10(-16)). This variant is close to a common variant previously associated with serum uric acid levels. This work illustrates how whole-genome sequencing data allow the detection of associations between low-frequency variants and complex traits.  相似文献   
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64.
Cardiac fibrosis is characterized by net accumulation of extracellular matrix proteins in the cardiac interstitium, and contributes to both systolic and diastolic dysfunction in many cardiac pathophysiologic conditions. This review discusses the cellular effectors and molecular pathways implicated in the pathogenesis of cardiac fibrosis. Although activated myofibroblasts are the main effector cells in the fibrotic heart, monocytes/macrophages, lymphocytes, mast cells, vascular cells and cardiomyocytes may also contribute to the fibrotic response by secreting key fibrogenic mediators. Inflammatory cytokines and chemokines, reactive oxygen species, mast cell-derived proteases, endothelin-1, the renin/angiotensin/aldosterone system, matricellular proteins, and growth factors (such as TGF-β and PDGF) are some of the best-studied mediators implicated in cardiac fibrosis. Both experimental and clinical evidence suggests that cardiac fibrotic alterations may be reversible. Understanding the mechanisms responsible for initiation, progression, and resolution of cardiac fibrosis is crucial to design anti-fibrotic treatment strategies for patients with heart disease.  相似文献   
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66.
We conducted a genome-wide association study for androgenic alopecia in 1,125 men and identified a newly associated locus at chromosome 20p11.22, confirmed in three independent cohorts (n = 1,650; OR = 1.60, P = 1.1 x 10(-14) for rs1160312). The one man in seven who harbors risk alleles at both 20p11.22 and AR (encoding the androgen receptor) has a sevenfold-increased odds of androgenic alopecia (OR = 7.12, P = 3.7 x 10(-15)).  相似文献   
67.
Chan TL  Yuen ST  Kong CK  Chan YW  Chan AS  Ng WF  Tsui WY  Lo MW  Tam WY  Li VS  Leung SY 《Nature genetics》2006,38(10):1178-1183
Epimutations in the germline, such as methylation of the MLH1 gene, may contribute to hereditary cancer syndrome in human, but their transmission to offspring has never been documented. Here we report a family with inheritance, in three successive generations, of germline allele-specific and mosaic hypermethylation of the MSH2 gene, without evidence of DNA mismatch repair gene mutation. Three siblings carrying the germline methylation developed early-onset colorectal or endometrial cancers, all with microsatellite instability and MSH2 protein loss. Clonal bisulfite sequencing and pyrosequencing showed different methylation levels in different somatic tissues, with the highest level recorded in rectal mucosa and colon cancer tissue, and the lowest in blood leukocytes. This mosaic state of germline methylation with different tissue distribution could act as the first hit and provide a mechanism for genetic disease inheritance that may deviate from the mendelian pattern and be overlooked in conventional leukocyte-based genetic diagnosis strategy.  相似文献   
68.
从"教师专业自我"出发,通过调查分析,从教师自我认识、教师自我体验、教师自我控制三方面描述民族地区双语教师专业自我发展现状。分析了民族地区双语教师专业自我发展问题,探讨了影响双语教师专业自我发展的因素,提出了提升双语教师专业自我发展的策略和路径。  相似文献   
69.
在翻译中,英语的否定结构是一个常见的语言现象.由于英汉两种语言在表达方法上存在很大差异,尤其在表达否定概念上,英语在用词、语法和逻辑等方面与汉语都有很大不同.如何将英语否定句的确切含义准确地用汉语表达出来,是一个较为复杂的事.本文就英语转移否定句的理解与翻译从3个方面进行了探讨.  相似文献   
70.
简述了切削用量对刀具耐用度的影响程度,叙述了在零件加工过程中合理的选取切削用量和合适的刀具耐用度,对于提高机械加工的效率有很大的作用.  相似文献   
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