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941.
从一种超声模拟测井记录的井下信号、深度信号送微机处理的实际要求出发,分析井下信号数据采集的工作原理,阐述了与12位A/D转换器实时配套工作的双存储体工作时序。通过对深度信号的解调,提出了一种解决4FSK解调的有效方法。 相似文献
942.
从BP网络对信息存储的分布式特点出发,分析了连接权系数及输入变化对输出的影响,探讨了BP网络的容错性及抗干扰特性,得出了一些有益的结论。 相似文献
943.
第27届Moessbauer效应的应用国际会议于2003年9月2l~25日在阿曼举行.会议有13个专题,本书只收集其中的9个专题的论文。书中给出在Moessbauer光谱学方法论中的新近研究进展,包括在纳米颗粒、纳米线、多层与超点阵、表面和界面等现代领域的进展.也介绍在物理学、化学、生物学、医学、地球科学、矿物学、考古学、材料科学、薄膜、冶金学、腐蚀和催化等工业等各个领域的应用。论文既包括用计算和分子模拟的理论研究,又有用透射分光学、转换电子Moessbauer谱测定法(CEMS)和核共振散射得到的实验结果。 相似文献
944.
提出并分析了任意波形合成系统(AWS)──一种高度智能化的计算机仪器的几种典型结构及其特点,着重讨论了PC总线式任意波形合成系统的系统组成及各部分硬件电路设计的关键技术 相似文献
945.
Mulhern S. A. Stroube W. B. Jacobs R. M. 《Cellular and molecular life sciences : CMLS》1986,42(5):551-553
Summary Second generation mice were exposed to normal (50 ppm, Group I) or excess (2000 ppm, Group II) zinc in the maternal diet during gestation and lactation, then weaned and continued on the mother's diet until sacrifice at 8 weeks. Tibia zinc reflected dietary intake. Group II had reduced plasma copper, body weight, and hematocrit; the second coat of hair appeared late and was lighter in color than Group I, possibly as an effect of copper and pigmentation development and hair growth. 相似文献
946.
S. Benvenuti A. Gagliardo T. Guilford P. Luschi 《Cellular and molecular life sciences : CMLS》1996,52(6):608-612
In order to investigate the pigeon's compass mechanism, a series of overcast tests with clock-shifted birds were run at two familiar release sites. While controls were able to assume a correct homeward direction, the experimental birds' initial orientation cannot be explained either on the basis of a time-compensated sun compass or of a time-independent magnetic compass. Speculative explanations of our paradoxical results are attempted. 相似文献
947.
G. Odierna L. G. Badalucci S. M. Guarino C. Gambardella M. De Nicola 《Cellular and molecular life sciences : CMLS》1996,52(7):652-656
Two mediterranean populations ofIdotea baltica basteri from Messina and Naples showed a set of chromosomes composed by 58 all-biarmed chromosomes. The heterochromatin was located in the pericentromeric region of the chromosomes, and its composition appeared heterogeneous. In fact, not all the homologs showed heterochromatin resistant to digestion with three restriction enzymes (Alu I, Hae III and Sau 3A). Moreover, the two populations showed polymorphism in a band of G+C-rich telomeric heterochromatin, which was present only in the population from Messina. It is hypothesized that chromosomal polymorphism might reflect the geographical isolation of the two populations. It is also suggested that a process of diversification is taking place. 相似文献
948.
949.
Cytochrome c can be modified by [(NH3)5RuII/III-] specifically at the imidazole moiety of histidine 33, and we have recently discussed the thermodynamics and kinetics of electron transfer within this modified protein. X-ray crystal structures of the oxidized and reduced forms of tuna cytochrome c indicate that the separation between the haem group of cytochrome c and the ruthenium label is 12-16 A. Internal electron transfer from the [(NH3)5RuII-] centre to the Fe(III) haem centre occurs with a rate constant k congruent to 53 s-1 (25 degrees C) (delta H = 3.5 kcal mol-1, delta S = -39 EU), as measured by pulse radiolysis. The measured unimolecular rate constant, k congruent to 53 s-1, is on the same timescale as a number of conformational changes that occur within the cytochrome c molecule. These results raise the question of whether electron transfer or protein conformational change is the rate limiting step in this process. We describe here an experiment that probes this intramolecular electron transfer step further. It involves reversing the direction of electron transfer by changing the redox potential of the ruthenium label. Electron transfer in the new ruthenium-cytochrome c derivative described here is from haem(II) to the Ru(III) label, whereas in (NH3)5Ru-cytochrome c the electron transfer is from Ru(II) to haem(III). Intramolecular electron transfer from haem(II) to Ru(III) in the new ruthenium-cytochrome c described here proceeds much slower (greater than 10(5) times) than the electron transfer from Ru(II) to haem(III) in the (NH3)5Ru-cytochrome c. We therefore conclude that electron transfer in cytochrome c is directional, with the protein envelope presumably involved in this directionality. 相似文献
950.
Structure of pre-pro-von Willebrand factor and its expression in heterologous cells 总被引:30,自引:0,他引:30
D T Bonthron R I Handin R J Kaufman L C Wasley E C Orr L M Mitsock B Ewenstein J Loscalzo D Ginsburg S H Orkin 《Nature》1986,324(6094):270-273
Von Willebrand factor (vWF), a multifunctional haemostatic glycoprotein derived from endothelial cells and megakaryocytes, mediates platelet adhesion to injured subendothelium and binds coagulation factor VIII in the circulation. Native vWF is a disulphide-bonded homopolymer; the monomeric subunits, of apparent relative molecular mass (Mr) 220,000 (220K) are derived from an intracellular precursor estimated at 260-275K. Multimer assembly is preceded by the formation of dimers, linked near their C-termini, which then assemble into filamentous polymers. The importance of the removal of the large vWF pro-polypeptide during multimer assembly, and whether this or other stages of the complex post-translational processing require components specific to endothelial cells or megakaryocytes, is unknown. Here we report an analysis of the complete sequence of pre-pro-vWF and expression of the molecule in heterologous cells. The vWF precursor is composed of several repeated subdomains. When expressed in COS and CHO cells, it is cleaved and assembled into biologically active high relative molecular mass disulphide bonded multimers. This suggests that the information for assembly of this complex molecule resides largely within its primary structure. 相似文献