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21.
通过对锯齿调频连续测距系统的差频信号分析可知,由于观测时间的随机性导致同一距离上对应两个不同的差频频率。对差频信号进行时域和频域分析发现,利用两次混频的方法能够解决这种测距模糊问题,使信号处理单元的输出信号频率和距离一一对应。利用仿真软件,得到信号处理过程中的时频关系曲线,验证了这种信号处理方法的有效性。 相似文献
22.
LI Xiao ZHANG JianQing LIU Wei LI XiaoNa ZHANG Xin JIANG YouSheng ZHOU Jian & JIN YiHe Key Laboratory of Industrial Ecology Environmental Engineering Ministry of Education School of Environmental Science Technology Dalian University of Technology Dalian China Shenzhen Center for Disease Control Prevention Shenzhen 《科学通报(英文版)》2011,(Z2):3092-3099
Perfluorinated compounds (PFCs) have been detected in many environmental matrices, biota, and nonoccupationally exposed populations in China recently. However, little is known about the distribution and levels of various PFCs in the general population living in areas where there is PFC exposure. In the present study, the levels and prevalence of ten target PFCs were determined in 227 serum samples from a population of nonoccupationally exposed individuals in Shenzhen, China. Results indicated that human exposure to PFCs was prevalent in Shenzhen. Perfluorooctanoate (PFOA) was the dominant PFC contaminant in the serum samples, with a median concentration of 6.72 ng/mL, followed by perfluorooctane sulfonate (PFOS) with a median concentration of 2.07 ng/mL. Other PFCs were detected at much lower concentrations, with median concentrations ranging from 0.02 to 0.87 ng/mL. Statistically, no significant (P>0.05) gender differences were observed for any of the PFCs. Significant (P<0.01) positive correlations were found between age and serum concentrations of the target PFCs, except for perfluorobutane sulfonate (R = 0.16, P = 0.01), perfluorohexanoic acid (R = 0.08, P = 0.22), and perfluoroheptanoic acid (R = 0.11, P = 0.10). Based on the one-compartment pharmacokinetic model, the total daily intakes of PFOA and PFOS for the general population in Shenzhen were calculated as 0.63 and 0.20 ng/kg body weight/day, respectively. 相似文献
23.
Genome sequence and analysis of the tuber crop potato 总被引:11,自引:0,他引:11
Potato Genome Sequencing Consortium Xu X Pan S Cheng S Zhang B Mu D Ni P Zhang G Yang S Li R Wang J Orjeda G Guzman F Torres M Lozano R Ponce O Martinez D De la Cruz G Chakrabarti SK Patil VU Skryabin KG Kuznetsov BB Ravin NV Kolganova TV Beletsky AV Mardanov AV Di Genova A Bolser DM Martin DM Li G Yang Y Kuang H Hu Q Xiong X Bishop GJ Sagredo B Mejía N Zagorski W Gromadka R Gawor J Szczesny P Huang S Zhang Z Liang C He J Li Y He Y Xu J Zhang Y Xie B Du Y Qu D Bonierbale M Ghislain M 《Nature》2011,475(7355):189-195
Potato (Solanum tuberosum L.) is the world's most important non-grain food crop and is central to global food security. It is clonally propagated, highly heterozygous, autotetraploid, and suffers acute inbreeding depression. Here we use a homozygous doubled-monoploid potato clone to sequence and assemble 86% of the 844-megabase genome. We predict 39,031 protein-coding genes and present evidence for at least two genome duplication events indicative of a palaeopolyploid origin. As the first genome sequence of an asterid, the potato genome reveals 2,642 genes specific to this large angiosperm clade. We also sequenced a heterozygous diploid clone and show that gene presence/absence variants and other potentially deleterious mutations occur frequently and are a likely cause of inbreeding depression. Gene family expansion, tissue-specific expression and recruitment of genes to new pathways contributed to the evolution of tuber development. The potato genome sequence provides a platform for genetic improvement of this vital crop. 相似文献
24.
International Consortium for Blood Pressure Genome-Wide Association Studies Ehret GB Munroe PB Rice KM Bochud M Johnson AD Chasman DI Smith AV Tobin MD Verwoert GC Hwang SJ Pihur V Vollenweider P O'Reilly PF Amin N Bragg-Gresham JL Teumer A Glazer NL Launer L Zhao JH Aulchenko Y Heath S Sõber S Parsa A Luan J Arora P Dehghan A Zhang F Lucas G Hicks AA Jackson AU Peden JF Tanaka T Wild SH Rudan I Igl W Milaneschi Y Parker AN Fava C Chambers JC Fox ER Kumari M Go MJ van der Harst P Kao WH 《Nature》2011,478(7367):103-109
Blood pressure is a heritable trait influenced by several biological pathways and responsive to environmental stimuli. Over one billion people worldwide have hypertension (≥140?mm?Hg systolic blood pressure or ≥90?mm?Hg diastolic blood pressure). Even small increments in blood pressure are associated with an increased risk of cardiovascular events. This genome-wide association study of systolic and diastolic blood pressure, which used a multi-stage design in 200,000 individuals of European descent, identified sixteen novel loci: six of these loci contain genes previously known or suspected to regulate blood pressure (GUCY1A3-GUCY1B3, NPR3-C5orf23, ADM, FURIN-FES, GOSR2, GNAS-EDN3); the other ten provide new clues to blood pressure physiology. A genetic risk score based on 29 genome-wide significant variants was associated with hypertension, left ventricular wall thickness, stroke and coronary artery disease, but not kidney disease or kidney function. We also observed associations with blood pressure in East Asian, South Asian and African ancestry individuals. Our findings provide new insights into the genetics and biology of blood pressure, and suggest potential novel therapeutic pathways for cardiovascular disease prevention. 相似文献
25.
表面等离激元光子学是研究光和金属表面自由电子耦合所引起金属表面电荷密度振荡的性质及其应用的一门学科. 金属中的自由电子在入射光的作用下产生集体振荡. 在垂直表面的方向上强度呈指数衰减, 使得亚波长金属结构中光场高度局域. 由于独特的光学性质, 使得其具有广泛的应用, 其中两个重要的分支为: 表面增强光谱和表面等离激元共振传感器. 表面增强光谱传感器是利用纳米结构的巨大表面增强效应来直接探测表面分子,表面等离激元共振传感器通过检测目标分子对等离激元共振峰的影响进行定性定量检测.这两种优势互补的传感器技术都可以达到单细胞甚至单分子的检测水平. 本文将论述表面等离激元光子学的原理、表面增强光谱和表面增强光谱传感器研究领域的国内外最新进展和发展趋势. 相似文献
26.
Yang J Ferreira T Morris AP Medland SE;Genetic Investigation of ANthropometric Traits 《Nature genetics》2012,44(4):369-75, S1-3
We present an approximate conditional and joint association analysis that can use summary-level statistics from a meta-analysis of genome-wide association studies (GWAS) and estimated linkage disequilibrium (LD) from a reference sample with individual-level genotype data. Using this method, we analyzed meta-analysis summary data from the GIANT Consortium for height and body mass index (BMI), with the LD structure estimated from genotype data in two independent cohorts. We identified 36 loci with multiple associated variants for height (38 leading and 49 additional SNPs, 87 in total) via a genome-wide SNP selection procedure. The 49 new SNPs explain approximately 1.3% of variance, nearly doubling the heritability explained at the 36 loci. We did not find any locus showing multiple associated SNPs for BMI. The method we present is computationally fast and is also applicable to case-control data, which we demonstrate in an example from meta-analysis of type 2 diabetes by the DIAGRAM Consortium. 相似文献
27.
ZHANG Rui WU Min WANG Qiang GENG JinJu & YANG XiaoDi School of Chemistry Environmental Science Nanjing Normal University Nanjing China National Marine Environmental Monitoring Centre Dalian College of Environmental Science Engineering Peking University Beijing State Key Laboratory of Pollution Control Resource Reuse Nanjing University Nanjing 《科学通报(英文版)》2010,(16)
Phoshpine (PH3), a volatile and toxic gas, has been proved to commonly exist in the environment.The determination of gaseous phosphine and its emission fluxes in Ny-lesund is reported in this paper.Results showed that gaseous phosphine exist in Arctic atmosphere commonly and the concentration of phosphine ranged from 16.3-600.2 ng/m3, with the maximum concentration of phosphine in tundra areas and the minimum in surface air of ocean.The concentration of phosphine ranged from 65.79-1259 ng/m3 in colliery at... 相似文献
28.
MC Turchin CW Chiang CD Palmer S Sankararaman D Reich;Genetic Investigation of ANthropometric Traits 《Nature genetics》2012,44(9):1015-1019
Strong signatures of positive selection at newly arising genetic variants are well documented in humans, but this form of selection may not be widespread in recent human evolution. Because many human traits are highly polygenic and partly determined by common, ancient genetic variation, an alternative model for rapid genetic adaptation has been proposed: weak selection acting on many pre-existing (standing) genetic variants, or polygenic adaptation. By studying height, a classic polygenic trait, we demonstrate the first human signature of widespread selection on standing variation. We show that frequencies of alleles associated with increased height, both at known loci and genome wide, are systematically elevated in Northern Europeans compared with Southern Europeans (P < 4.3 × 10(-4)). This pattern mirrors intra-European height differences and is not confounded by ancestry or other ascertainment biases. The systematic frequency differences are consistent with the presence of widespread weak selection (selection coefficients ~10(-3)-10(-5) per allele) rather than genetic drift alone (P < 10(-15)). 相似文献
29.
LIU HongJia ZHENG HuaKun WANG Hua GUO Peng ZUO JianRu & TAO YueZhi State Key Laboratory Breeding Base for Zhejiang Sustainable Pest Disease Control 《科学通报(英文版)》2011,(31)
Three allelic short root mutants were identified by screening mutants with defective root elongation of the rice japonica cultivar Nipponbare mutant library generated via 60 Co γ-ray irradiation mutagenesis. These mutants, designated srt7-1 (short root 7-1), srt7-2 and srt7-3, respectively, had an extremely short seminal root, adventitious roots and lateral roots. Histological observation revealed the cell length of srt7 mutant roots was significantly shorter than that of wild-type roots. Genetic analysis i... 相似文献
30.
酮麝香是化妆品中的限用物质,对人体有致癌作用,因此,有必要对其含量进行分析。采用超声辅助提取法对不同基质类型的化妆品样品进行预处理。利用反相高效液相色谱法测定化妆品中的酮麝香。色谱条件为Kromasil C18(250mm×4.6mm i.d.,5μm)色谱柱,流动相V(乙腈):V(水)= 80:20,流速1.0mL/min,检测波长235nm。结果表明,在此条件下,酮麝香在0.5-150 μg/mL范围内与相应的峰面积具有良好的线性关系(相关系数r为0.9998),线性回归方程为A=13500ρ-4829,回收率为90.5%-102.5%,RSD为0.45%-0.98%。因此,研究建立的利用反相高效液相色谱法测定化妆品中的酮麝香的方法准确、可靠、适用性广,可为酮麝香的分析及国家相关法规的制定提供一定的参考。 相似文献