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71.
The relationship between the secondary carbide precipitation and transformation of the 3Cr15Mo1V1.5 white iron and abrasion resistance was investigated by using optical microscope (OM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The results show that the properties of secondary carbides precipitated at holding stage play an important role in the abrasion resistance. After certain holding time at 833 K subcritical treatment, the grainy (Fe, Cr)23C6 carbide precipitated and the fresh martensite transformed at the holding stage for 3Cr15Mo1V1.5 white iron improve the bulk hardness and abrasion resistance of the alloy. Prolonging holding time, MoC and (Cr, V)2C precipitations cause the secondary hardening peak and the corresponding better abrasion resistance. Finally, granular (Fe, Cr)23C6 carbide in situ transforms into laminar M3C carbide and the matrix structure transforms into pearlitic matrix. These changes weaken hardness and abrasion resistance of the alloy sharply.  相似文献   
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73.
<正>1.Nanomaterials and device It has been widely accepted that,when a material comes to low dimensions,for example,0D quantum dots and hetero-nanocrystals,1D nanowires and nanotubes,2D nanosheets,and 3D hierarchical or branched nanostructures,the associated physical properties will differ from their bulk counterparts,and subsequently will render enhanced or emergent functions.This has generated a fascinating field of"nanomaterials and devices".It is a  相似文献   
74.
Wu C  Miao X  Huang L  Che X  Jiang G  Yu D  Yang X  Cao G  Hu Z  Zhou Y  Zuo C  Wang C  Zhang X  Zhou Y  Yu X  Dai W  Li Z  Shen H  Liu L  Chen Y  Zhang S  Wang X  Zhai K  Chang J  Liu Y  Sun M  Cao W  Gao J  Ma Y  Zheng X  Cheung ST  Jia Y  Xu J  Tan W  Zhao P  Wu T  Wang C  Lin D 《Nature genetics》2012,44(1):62-66
Pancreatic cancer has the lowest survival rate among human cancers, and there are no effective markers for its screening and early diagnosis. To identify genetic susceptibility markers for this cancer, we carried out a genome-wide association study on 981 individuals with pancreatic cancer (cases) and 1,991 cancer-free controls of Chinese descent using 666,141 autosomal SNPs. Promising associations were replicated in an additional 2,603 pancreatic cancer cases and 2,877 controls recruited from 25 hospitals in 16 provinces or cities in China. We identified five new susceptibility loci at chromosomes 21q21.3, 5p13.1, 21q22.3, 22q13.32 and 10q26.11 (P = 2.24 × 10(-13) to P = 4.18 × 10(-10)) in addition to 13q22.1 previously reported in populations of European ancestry. These results advance our understanding of the development of pancreatic cancer and highlight potential targets for the prevention or treatment of this cancer.  相似文献   
75.
HB(N5)3M (M = Li,Na,K,and Rb) have been investigated as potential high-energy density materials in the present paper by means of density functional theory.They all show kinetic stabilities as to the breakup of N5 ring.Their kinetic stabilities decrease in the order of Li,Na,K,and Rb.Compared to HB(N5)3K and HB(N5)3Rb,HB(N5)3Li and HB(Ns)3Na have higher transition state barriers and are of significantly higher energy content,and thus they are suggested to be more practical and suitable as potential high-energy density materials.  相似文献   
76.
Schizophrenia is a severe mental disorder affecting ~1% of the world population, with heritability of up to 80%. To identify new common genetic risk factors, we performed a genome-wide association study (GWAS) in the Han Chinese population. The discovery sample set consisted of 3,750 individuals with schizophrenia and 6,468 healthy controls (1,578 cases and 1,592 controls from northern Han Chinese, 1,238 cases and 2,856 controls from central Han Chinese, and 934 cases and 2,020 controls from the southern Han Chinese). We further analyzed the strongest association signals in an additional independent cohort of 4,383 cases and 4,539 controls from the Han Chinese population. Meta-analysis identified common SNPs that associated with schizophrenia with genome-wide significance on 8p12 (rs16887244, P = 1.27 × 10(-10)) and 1q24.2 (rs10489202, P = 9.50 × 10(-9)). Our findings provide new insights into the pathogenesis of schizophrenia.  相似文献   
77.
To identify genetic variants influencing plasma lipid concentrations, we first used genotype imputation and meta-analysis to combine three genome-wide scans totaling 8,816 individuals and comprising 6,068 individuals specific to our study (1,874 individuals from the FUSION study of type 2 diabetes and 4,184 individuals from the SardiNIA study of aging-associated variables) and 2,758 individuals from the Diabetes Genetics Initiative, reported in a companion study in this issue. We subsequently examined promising signals in 11,569 additional individuals. Overall, we identify strongly associated variants in eleven loci previously implicated in lipid metabolism (ABCA1, the APOA5-APOA4-APOC3-APOA1 and APOE-APOC clusters, APOB, CETP, GCKR, LDLR, LPL, LIPC, LIPG and PCSK9) and also in several newly identified loci (near MVK-MMAB and GALNT2, with variants primarily associated with high-density lipoprotein (HDL) cholesterol; near SORT1, with variants primarily associated with low-density lipoprotein (LDL) cholesterol; near TRIB1, MLXIPL and ANGPTL3, with variants primarily associated with triglycerides; and a locus encompassing several genes near NCAN, with variants strongly associated with both triglycerides and LDL cholesterol). Notably, the 11 independent variants associated with increased LDL cholesterol concentrations in our study also showed increased frequency in a sample of coronary artery disease cases versus controls.  相似文献   
78.
Wu C  Hu Z  He Z  Jia W  Wang F  Zhou Y  Liu Z  Zhan Q  Liu Y  Yu D  Zhai K  Chang J  Qiao Y  Jin G  Liu Z  Shen Y  Guo C  Fu J  Miao X  Tan W  Shen H  Ke Y  Zeng Y  Wu T  Lin D 《Nature genetics》2011,43(7):679-684
Esophageal squamous-cell carcinoma (ESCC) is one of the most prevalent cancers worldwide and occurs at a relatively high frequency in China. To identify genetic susceptibility loci for ESCC, we conducted a genome-wide association study on 2,031 individuals with ESCC (cases) and 2,044 controls of Chinese descent using 666,141 autosomal SNPs. We evaluated promising associations in an additional 6,276 cases and 6,165 controls of Chinese descent from different areas of China. We identified seven susceptibility loci on chromosomes 5q11, 6p21, 10q23, 12q24 and 21q22 (ranging from P = 7.48 × 10(-12) to P = 2.44 × 10(-31)); among these loci, 5q11, 6p21 and 21q22 were newly identified. Three variants in high linkage disequilibrium on 12q24 confer their risks to ESCC in a gene-lifestyle interaction manner, with more pronounced risk enhancement seen in tobacco and alcohol users. Furthermore, the identified variants had a cumulative association with ESCC risk (P(trend) = 7.92 × 10(-56)). These findings highlight the involvement of multiple genetic loci and gene-environment interaction in the development of esophageal cancer.  相似文献   
79.
Structural redundancy elimination in case resource pools (CRP) is critical for avoiding performance bottlenecks and maintaining robust decision capabilities in cloud computing services. For these purposes, this paper proposes a novel approach to ensure redundancy elimination of a reasoning system in CRP. By using α entropy and mutual information, functional measures to eliminate redundancy of a system are developed with respect to a set of outputs. These measures help to distinguish both the optimal feature and the relations among the nodes in reasoning networks from the redundant ones with the elimination criterion. Based on the optimal feature and its harmonic weight, a model for knowledge reasoning in CRP (CRPKR) is built to complete the task of query matching, and the missing values are estimated with Bayesian networks. Moreover, the robustness of decisions is verified through parameter analyses. This approach is validated by the simulation with benchmark data sets using cloud SQL. Compared with several state-of-the-art techniques, the results show that the proposed approach has a good performance and boosts the robustness of decisions.  相似文献   
80.
第二次数学危机爆发至今一直都存在不同的意见,无穷小分析这套微积分工具对问题的解决颇具启发性,但其理论基础备受质疑;而现今极限理论框架下的微积分失去了无穷小分析的简明直观性。该文修正了极限理论中微分和无穷小量的定义,根据“Bolzano连续性赋值”建立微商引理,统一了无穷小分析与极限理论;举例推证了部分微分学公式,揭示了无穷小分析和极限理论之间内在的蕴含关系,指出了L’Hospital法则、等价无穷小代换本质上就是求出函数在0/0处的值,和Euler的观点吻合。同时用纯粹数学描述Marx的数学手稿,证明其“微分为特定的0”的观点的正确性,表明可以从本质上彻底解决第二次数学危机。  相似文献   
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