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61.
建筑用铝合金的疲劳性能试验   总被引:1,自引:0,他引:1  
作为一种建筑金属材料,铝合金对应力集中和裂纹比较敏感。经过固熔热处理、人工时效、挤压成型等处理后,铝合金构件的疲劳强度相对较低,抗疲劳能力差。为研究6061-T 6和6005-T 5两种典型的铝合金材料的疲劳性能,通过常规试验方法分别对这两组铝合金光滑板试件进行了轴向拉伸疲劳试验。在循环次数为104~2×106时测定了两种材料的S-N曲线。试验结果发现:铝合金的疲劳强度大致与抗拉强度成正比,抗拉强度高的疲劳强度也高。  相似文献   
62.
以生姜为原料,采用超临界CO2萃取姜酚类化合物.在强酸性条件下姜酚类化合物脱水成姜烯酚后,与甘氨酸加成生成姜烯酚一甘氨酸复合物以增强姜酚类化合物的稳定性.用紫外分光光度法和差分脉冲伏安法对姜烯酚-甘氨酸进行研究.结果表明:紫外分光光度法测定姜烯酚-甘氨酸,最大特征吸收峰在230、280 nm处.吸光度比值为1.776;差分脉冲伏安法测定姜烯酚-甘氨酸,以玻碳电极为工作电极,在pH=2~8的范围内,姜烯酚-甘氨酸的电化学活性随着pH的降低而减弱;姜烯酚-甘氨酸对N,N-二苯基N'-苦味基肼基自由基(DPPH·自由基)具有良好的清除作用,其对DPPH·自由基的清除率随计量的增加而增加,当加入量为0.125 mg时,其清除率为81.8%.研究发现,姜烯酚-甘氨酸对DPPH·自由基的清除能力高于甘氨酸.  相似文献   
63.
提出了用以处理非线性问题的同伦近似对称法,并利用该方法研究流体动力学中的六阶Boussinesq方程.各阶相似约化解和各阶相似约化方程均可以写出通式,从而导出相应的同伦级数解.零阶相似约化方程等价于Painlevé IV型方程或Weierstrass椭圆方程,高阶相似解可以通过解线性变系数常微分方程得到.辅助参数具有调节同伦级数解的收敛性的作用.由近似对称法得到的级数解和各阶相似约化方程均能够由同伦近似对称法重新得到.  相似文献   
64.
Ion transport proteins must remove an ion's hydration shell to coordinate the ion selectively on the basis of its size and charge. To discover how the K+ channel solves this fundamental aspect of ion conduction, we solved the structure of the KcsA K+ channel in complex with a monoclonal Fab antibody fragment at 2.0 A resolution. Here we show how the K+ channel displaces water molecules around an ion at its extracellular entryway, and how it holds a K+ ion in a square antiprism of water molecules in a cavity near its intracellular entryway. Carbonyl oxygen atoms within the selectivity filter form a very similar square antiprism around each K+ binding site, as if to mimic the waters of hydration. The selectivity filter changes its ion coordination structure in low K+ solutions. This structural change is crucial to the operation of the selectivity filter in the cellular context, where the K+ ion concentration near the selectivity filter varies in response to channel gating.  相似文献   
65.
LEED强度的多重散射分析,进一步确定Zr与氧作用在低覆盖量下(<1ML),形成(2×2)-O结构,是氧吸附后进入Zr表面原子层下,占据八面体空位,形成有两层氧的under layer结构,Zr表面原子层有Fcc重构。分析得到的Zt-O键距为0.232nm,而Zr-Zr间距增大为0.268nm,比原来的距离增大约4.3%,这是由于氧插入的结果。  相似文献   
66.
In vitro ecdysteroid production by dissociated Y-organ cells of the shore crabCarcinus maenas was characterized during short-term incubations. Under optimized conditions (M199 adjusted to crab osmolality and with the addition of 10% foetal calf serum), ecdysteroid production by dispersed cells increased linearly during 4-hour incubations, with little intra-assay variation. 25-deoxyecdysone was mainly produced. PurifiedCarcinus molt inhbiting hormone (CamMIH) produced a dose-dependent inhibition of ecdysteroid production by dispersed cells. The cells were about 50 times more sensitive than whole glands to MIH. Other structurally-related peptides were tested.  相似文献   
67.
The morphometric parameters of spermatogenic cells in a mouse strain prone to accelerated senescence (SAM-P), a novel murine model of spontaneously promoted aging, were compared with those of a SAM resistant strain (SAM-R) after birth until 40 weeks (mean life span of SAM-P). A mixture of gonocytes and spermatogonia were present in the testis in 1-week-old mice, and no gonocytes were observed in 2-week-old mice. At 6 weeks of age, the absolute number of spermatogonia in SAM-P was 27% greater than that in SAM-R, whereas the cell number in 40-week-old SAM-P was 17% less than in SAM-R. Primary spermatocytes were first observed in 3-week-old animals, and the cell numbers in SAM-P at 3, 5 and 6 weeks were 78%, 31% and 25%, respectively, greater than in SAM-R, whereas the cell number in SAM-P at 40 weeks was 30% less than SAM-R. Round spermatids were first observed in all SAM-P at 4 weeks old, but 20% of SAM-r had no spermatids and the rest had only a few. At 5 and 6 weeks old, the absolute numbers of round spermatids in SAM-P was about 34% and 41%, respectively, greater than in SAM-R, whereas the cell number in 40-week-old SAM-P was about 34% less than SAM-R. These results indicate that testicular maturation begins at an earlier age in SAM-P than SAM-R. Furthermore, at the age of 40 weeks signs of testicular deterioration are evident in SAM-P mice only  相似文献   
68.
69.
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide. Affected individuals suffer from a progressive degeneration of the photoreceptors, eventually resulting in severe visual impairment. To isolate candidate genes for chorioretinal diseases, we cloned cDNAs specifically or preferentially expressed in the human retina and the retinal pigment epithelium (RPE) through a novel suppression subtractive hybridization (SSH) method. One of these cDNAs (RET3C11) mapped to chromosome 1q31-q32.1, a region harbouring a gene involved in a severe form of autosomal recessive RP characterized by a typical preservation of the para-arteriolar RPE (RP12; ref. 3). The full-length cDNA encodes an extracellular protein with 19 EGF-like domains, 3 laminin A G-like domains and a C-type lectin domain. This protein is homologous to the Drosophila melanogaster protein crumbs (CRB), and denoted CRB1 (crumbs homologue 1). In ten unrelated RP patients with preserved para-arteriolar RPE, we identified a homozygous AluY insertion disrupting the ORF, five homozygous missense mutations and four compound heterozygous mutations in CRB1. The similarity to CRB suggests a role for CRB1 in cell-cell interaction and possibly in the maintenance of cell polarity in the retina. The distinct RPE abnormalities observed in RP12 patients suggest that CRB1 mutations trigger a novel mechanism of photoreceptor degeneration.  相似文献   
70.
The identification of genes that control susceptibility to testicular germ-cell tumours (TGCTs), the most common cancer affecting young men, has been difficult. In laboratory mice, TGCTs arise from primordial germ cells in only the 129 inbred strains, and susceptibility is under multigenic control. The spontaneously arising mutation Ter (ref. 5) on mouse chromosome 18 (Refs 6,7) increases TGCT frequency on a 129/Sv background. We originally used Ter in genetic crosses to identify loci that control tumorigenesis. A genome scan of tumour-bearing progeny from backcrosses between the 129/Sv-Ter/+ and MOLF/Ei strains provided modest evidence that MOLF-derived alleles on chromosome 19 enhance development of bilateral TGCTs (ref. 9). To obtain independent evidence for linkage to the MOLF chromosome, we made an autosomal chromosome substitution strain (CSS; or 'consomic strain') in which chromosome 19 of 129/Sv+/+ was replaced by its MOLF-derived homologue. The unusually high frequency of TGCTs in this CSS (even in the absence of the Ter mutation) provides evidence confirming the genome survey results, identifies linkage for a naturally occurring strain variant allele that confers susceptibility to TGCTs and illustrates the power of CSSs in complex trait analysis.  相似文献   
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