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51.
T Sugiyama K Suzue M Okamoto J Inselburg K Tai T Horii 《Canadian Metallurgical Quarterly》1996,14(11):1069-1076
We expressed two regions of the serine repeat antigen (SERA) protein of Plasmodium falciparum in Escherichia coli by synthesizing the genes with a changed codon usage. One of the synthetic gene sequences encodes amino acid residues 17-382 (SE47') and the other encodes amino acid residues 586-802 (SE50A). The products produced by the synthetic gene sequences in E. coli accounted for 15-30% of the total bacterial protein. Antisera against both the purified gene products prepared in rats inhibited malaria parasite growth in vitro. The anti-SE47' serum was significantly more inhibitory than the anti-SE50A serum. The described methods provide a large scale preparation of recombinant antigens for improving and producing malaria vaccine. 相似文献
52.
T Ozawa K Katsumata M Hayakawa M Tanaka S Sugiyama T Tanaka S Itoyama S Nunoda M Sekiguchi 《Canadian Metallurgical Quarterly》1995,207(2):613-620
Comprehensive analyses of mitochondrial (mt)DNA of a recipient of heart transplantation at age 7 because of severe cardiomyopathy revealed three germ line point mutations, each one in the 12S rRNA gene, in the CO1 gene and in the cytochrome b gene, respectively. As the somatic mutation, extensive fragmentation of mtDNA associated with 212 kinds of deletions was detected in contrast to 5 kinds in an age-matched negative control. A recipient's positive control having almost the same base-substitutions and mutations with the recipient except one in the CO1 gene also developed severe cardiomyopathy died at age 20. The close relation between phenotype and mtDNA genotype provides the basis of our understanding of cell death and premature ageing. 相似文献
53.
54.
Kaname Uno Shohei Iyoshi Masato Yoshihara Kazuhisa Kitami Kazumasa Mogi Hiroki Fujimoto Mai Sugiyama Yoshihiro Koya Yoshihiko Yamakita Akihiro Nawa Tomohiro Kanayama Hiroyuki Tomita Atsushi Enomoto Hiroaki Kajiyama 《International journal of molecular sciences》2022,23(8)
Epithelial ovarian cancer (EOC) is the most lethal gynecologic malignancy and has a unique metastatic route using ascites, known as the transcoelomic root. However, studies on ascites and contained cellular components have not yet been sufficiently clarified. In this review, we focus on the significance of accumulating ascites, contained EOC cells in the form of spheroids, and interaction with non-malignant host cells. To become resistant against anoikis, EOC cells form spheroids in ascites, where epithelial-to-mesenchymal transition stimulated by transforming growth factor-β can be a key pathway. As spheroids form, EOC cells are also gaining the ability to attach and invade the peritoneum to induce intraperitoneal metastasis, as well as resistance to conventional chemotherapy. Recently, accumulating evidence suggests that EOC spheroids in ascites are composed of not only cancer cells, but also non-malignant cells existing with higher abundance than EOC cells in ascites, including macrophages, mesothelial cells, and lymphocytes. Moreover, hetero-cellular spheroids are demonstrated to form more aggregated spheroids and have higher adhesion ability for the mesothelial layer. To improve the poor prognosis, we need to elucidate the mechanisms of spheroid formation and interactions with non-malignant cells in ascites that are a unique tumor microenvironment for EOC. 相似文献
55.
56.
Yuka Tarui Takumi Chinen Dr. Yoko Nagumo Dr. Takayuki Motoyama Dr. Toshiaki Hayashi Dr. Hiroshi Hirota Dr. Makoto Muroi Yasuyuki Ishii Hisae Kondo Prof. Dr. Hiroyuki Osada Prof. Dr. Takeo Usui 《Chembiochem : a European journal of chemical biology》2014,15(7):934-938
Terpendole E is first natural product found to inhibit mitotic kinesin Eg5, but its inhibitory mechanism remains to be revealed. Here, we report the effects of terpendole E and 11ketopaspaline (a new natural terpendole E analogue) on the Eg5–microtubule interaction and in several Eg5 mutants. 11‐Ketopaspaline is a shunt product from terpendole E, and it shows potent inhibitory activity against the microtubule‐stimulated ATPase activity of Eg5. Unlike other Eg5 inhibitors, such as S‐trityl‐L ‐cysteine (STLC) and GSK‐1, both terpendole E and 11‐ketopaspaline only partially inhibited Eg5–microtubule interaction. Furthermore, terpendole E and 11‐ketopaspaline inhibited several Eg5 mutants that are resistant to STLC (Eg5D130A, Eg5L214A) or GSK‐1 (Eg5I299F, Eg5A356T), but with the same extent of inhibition against wild‐type Eg5. Because Eg5D130A and Eg5L214A show cross‐resistance to most known Eg5 inhibitors, which bind the L5 loop, these results suggest that terpendole E and its analogues have a different binding site and/or inhibitory mechanism to those for L5 loop‐binding type Eg5 inhibitors. 相似文献
57.
Tsuyoshi Honma Yasuhiko Benino Takumi Fujiwara Takayuki Komatsu Ryuji Sato 《Journal of the American Ceramic Society》2005,88(4):989-992
The glass formation region, crystalline phases, second harmonic (SH) generation, and Nd:yttrium aluminum garnet (YAG) laser-induced crystallization in the Sm2 O3 –Bi2 O3 –B2 O3 system were clarified. The crystalline phases of Bi4 B2 O9 , Bi3 B5 O12 , BiBO3 , Sm x Bi1− x BO3 , and SmB3 O6 were formed through the usual crystallization in an electric furnace. The crystallized glasses consisting of BiBO3 and Sm x Bi1− x BO3 showed SH generations. The formation of the nonlinear optical BiB3 O6 phase was not confirmed. The formation (writing) region of crystal lines consisting of Sm x Bi1− x BO3 by YAG laser irradiation was determined, in which Sm2 O3 contents were∼10 mol%. The present study demonstrates that Sm2 O3 –Bi2 O3 –B2 O3 glasses are promising materials for optical functional applications. 相似文献
58.
微波活化法从甲烷合成乙烯 总被引:1,自引:0,他引:1
利用微波活化法从甲烷催化偶合合成了乙烯。在5% Pt/c Lot 86111催化剂情况下得到了3.65%甲烷转化率和近100%的乙烯选择性。同一催化剂在热反应条件下完全没有反应活性。 相似文献
59.
N Sugiyama P Marchot C Kawanishi H Osaka B Molles SM Sine P Taylor 《Canadian Metallurgical Quarterly》1998,53(4):787-794
The two binding sites in the pentameric nicotinic acetylcholine receptor of subunit composition alpha2 beta gamma delta are formed by nonequivalent alpha-gamma and alpha-delta subunit interfaces, which produce site selectivity in the binding of agonists and antagonists. We show by sedimentation analysis that 125I-alpha-conotoxin M1 binds with high affinity to the alpha-delta subunit dimers, but not to alpha-gamma dimers, nor to alpha, gamma, and delta monomers, a finding consistent with alpha-conotoxin M1 selectivity for the alpha delta interface in the intact receptor measured by competition against alpha-bungarotoxin binding. We also extend previous identification of alpha-conotoxin M1 determinants in the gamma and delta subunits to the alpha subunit interface by mutagenesis of conserved residues in the alpha subunit. Most mutations of the alpha subunit affect affinity similarly at the two sites, but Tyr93Phe, Val188Lys, Tyr190Thr, Tyr198Thr, and Asp152Asn affect affinity in a site-selective manner. Mutant cycle analysis reveals only weak or no interactions between mutant alpha and non-alpha subunits, indicating that side chains of the alpha subunit do not interact with those of the gamma or delta subunits in stabilizing alpha-conotoxin M1. The overall findings suggest different binding configurations of alpha-conotoxin M1 at the alpha-delta and alpha-gamma binding interfaces. 相似文献
60.
K Sugiyama 《Canadian Metallurgical Quarterly》1998,35(10):757-764
Modification of DNA with aging has been proposed as a mechanism of cellular senescence. To test this hypothesis, we measured fluorescence of the DNA-Ethidium bromide (EB) complex in human peripheral lymphocytes. Lymphocytes were incubated in a medium containing phytohemagglutinin (PHA-P). EB was linked to lymphoblast-DNA. Healthy adults of three age groups were examined: 40-49 (N = 14), 50-59 (N = 16), 60-69 (N = 8). Moreover, we studied lymphocytes from 17 patients (47-74 years old) with probable Alzheimer's disease. An aged-related linear decrease in fluorescence intensity was found in healthy controls (r = 0.135, p < 0.05), and for Alzheimer's disease patients (r = 0.443, P < 0.10). The regression equation are: Y = -0.0405X + 7.164 (Healthy Controls) Y = -0.121X + 11.258 (Alzheimer's disease patients) where X and Y are age and fluorescence, respectively. These results indicate that the analysis of DNA-EB fluorescence in lymphocytes may be useful in the study of changes associated with aging, and also in the evaluation of the clinical diagnosis of Alzheimer's disease. 相似文献