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排序方式: 共有554条查询结果,搜索用时 15 毫秒
1.
2.
H Imano H Iso T Tanigawa T Sankai T Ohira M Kudo T Shimamoto S Sato T Okamura M Iida 《Canadian Metallurgical Quarterly》1998,45(6):536-551
To investigate the contribution of the platelet aggregation in the development of cardiovascular diseases, we examined the relation of constitutional and lifestyle variables with platelet aggregation for a total of 306 males aged 50 to 70 in Ikawa town, Akita prefecture (n = 163) and Noichi town, Kochi prefecture (n = 143). The examination of platelet aggregation was completed within 3 hours of obtaining blood samples. We used ADP (Adenosine 5'-diphosphate) as an agonist and obtained PATI (the platelet aggregatory threshold index) by nephelometry. Platelet count, mean platelet volume, white blood cell count, serum fatty acid compositions were also examined and dietary intake of fish, seafood and soy bean foods were inquired using one-week dietary records. PATI indicated a logarithmic normal distribution in both Ikawa and Noichi. The mean of logarithmic transformed PATI (log PATI) was higher in Ikawa than in Noichi. Thus platelet aggregation was lower in Ikawa than in Noichi. According to multiple regression analysis, age, platelet count in platelet rich plasma, mean platelet volume in platelet rich plasma, and white blood cell count were inversely associated with log PATI. Serum arachidonic acid composition tended to be inversely related with log PATI. Serum n3-polyunsaturated fatty acid composition was positively related with log PATI, and log gamma-GTP tended to be positively associated with log PATI. Soy protein intake and cigarette smoking showed no consistent associations with log PATI. This cross-sectional study suggests that serum n3-polyunsaturated fatty acid, and gamma-GTP, as an index of alcohol intake, reduce platelet aggregation while age, white blood cell count, platelet count, mean platelet volume, and serum arachidonic acid raise platelet aggregation. 相似文献
3.
H Kusaba J Kudo T Kuruma R Nagashima M Ra T Mori Y Kaji H Ishibashi Y Niho Y Baba 《Canadian Metallurgical Quarterly》1993,84(6):330-333
Cardiotoxicity of interferon-alpha or gamma, such as fatal arrhythmia and myocardial infarction, has been reported. Therefore cardiotoxicity of interferon should be seriously considered before administration for patients with a pre-existing heart disease. We treated a patient with chronic active hepatitis type B, coexisted with Wolff-Parkinson-White syndrome, who has had frequent attacks of paroxysmal atrial fibrillation. To prevent the occurrence of fatal arrhythmia with an interferon therapy in this patient, we performed radiofrequency catheter ablation of the Kent bundle. After the successful ablation, we could safely administered recombinant interferon alpha-2b for chronic hepatitis type B. 相似文献
4.
5.
Inaba S. Okano K. Matsuda S. Fujiwara M. Hokazono A. Adachi K. Ohuchi K. Suto H. Fukui H. Shimizu T. Mori S. Oguma H. Murakoshi A. Itani T. Iinuma T. Kudo T. Shibata H. Taniguchi S. Takayanagi M. Azuma A. Oyamatsu H. Suguro K. Katsumata Y. Toyoshima Y. Ishiuchi H. 《Electron Devices, IEEE Transactions on》2002,49(12):2263-2270
The 35 nm gate length CMOS devices with oxynitride gate dielectric and Ni salicide have been fabricated to study the feasibility of higher performance operation. Nitrogen concentration in gate oxynitride was optimized to reduce gate current I/sub g/ and to prevent boron penetration in the pFET. The thermal budget in the middle of the line (MOL) process was reduced enough to realize shallower junction depth in the S/D extension regions and to suppress gate poly-Si depletion. Finally, the current drives of 676 /spl mu/A//spl mu/m in nFET and 272 /spl mu/A//spl mu/m in pFET at V/sub dd/=0.85 V (at I/sub off/=100 nA//spl mu/m) were achieved and they are the best values for 35 nm gate length CMOS reported to date. 相似文献
6.
Uchiyama K. Arakawa F. Narita S. Aoki H. Kawasaki I. Matsui S. Yamamoto M. Nakagawa N. Kudo I. 《Micro, IEEE》1993,13(5):12-22
The Gmicro/500, which features a RISC-like dual-pipeline structure for high-speed execution of basic instructions and represents a significant advance for the TRON architecture, is presented. Upwardly-object-compatible with earlier members of the Gmicro series, this microprocessor uses resident dedicated branch buffers to greatly enhance branch instruction execution speed. Its microprograms simultaneously use dual execution blocks to execute high-level language instructions effectively. Fabricated with a 0.6-μm CMOS technology on a 10.9-mm×16-mm die, the chip operates at 50/66 MHz and achieves a processing rate of 100/132 MIPS 相似文献
7.
The H2 evolution reaction from an aqueous Na2SO3 solution proceeded with 3.7% quantum yield under visible light irradiation (λ > 420 nm) on a Zn0.957Cu0.043S solid solution photocatalyst without co‐catalysts such as Pt.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
8.
Ichiro Kudo Shoshichi Nojima Hyeun Wook Chang Ryohei Yanoshita Hidetoshi Hayashi Eri Kondo Hiroaki Nomura Keizo Inoue 《Lipids》1987,22(11):862-867
1-O-Octadecyl-2-O-methyl-sn-glycero-3-phosphocholine (ET-18-OMe) has been reported to possess definite antitumor activity in vivo. Twenty-two alkyl lysophospholipid analogs were chemically synthesized, and their antitumor activity against mouse experimental tumors (Sarcoma 180, MM46, P388) was examined. Among them, 1-O-octadecyl-2-O-acetoacetyl-rac-glycerol-3-phosphocholine was found to show antitumor activity similar to ET-18-OMe with less acute toxicity. Intravenous injection of the ET-18-OMe withsn-3 configuration retarded the subcutaneous growth of Sarcoma 180 cells effectively, while the growth inhibition by thesn-1 isomer was much less effective. This stereospecificity was similar to that observed in their activities as platelet-activating factor (PAF) agonists. The acetoacetyl compound, another PAF agonist, showed similar stereospecific antitumor action in vivo. These findings suggest that some alkyl lysophospholipids may activate host cells to a cytostatic stage against tumor cells in vivo through binding to a PAF receptor. Our preliminary results indicated that the responsible cells under these conditions might be primarily immature macrophages present in the bone marrow. No appreciable or even adverse stereospecificity was observed in the different sets of experiments where the activity of ET-18-OMe against MM46 tumor cells in vivo or the direct cytotoxicity against human promyelocytic leukemia HL-60 cells in vitro was examined. Under, some conditions, the antitumor activity of ET-18-OMe in vivo may be revealed through direct cytotoxicity and/or modulation of the host defense system by “nonspecific” mechanisms. Some alkylphospholipids without PAF activity may also show antitumor activity through similar, “nonspecific” mechanisms. 相似文献
9.
Zhaoxia Song Hiroyasu Nishiguchi Wei Liu Hiroshi Yamada Akihide Takami Kumiko Kudo Katsutoshi Nagaoka Yusaku Takita 《Catalysis Letters》2006,111(3-4):169-171
Redox properties of CeO2 and Pt-Rh/CeO2 were studied by temporal analysis of products (TAP) method using alternative pulses of CO and O2. A portion of pulsed CO was oxidized to CO2 and a portion of CO was adsorbed on the surface. Pulsing 18O2 onto the catalyst which has surface species derived from CO, evolved CO2 contained no 18O suggesting that the surface species will be carbonate ions. 相似文献
10.
Ichiro Kudo Toshiyuki Kato Hidetoshi Hayashi Ryohei Yanoshita Koichi Ikizawa Hiroko Uda Keizo Inoue 《Lipids》1991,26(12):1065-1070
We have previously reported that platelet-activating factor (PAF) induces proliferation and microbicidal activity of guinea
pig bone marrow cells. In the present study, we have found that the conditioned medium of PAF- or nonmetabolizable PAF agonist-treated
guinea pig bone marrow cells augmented DNA synthesis and induced microbicial activity of bone marrow cells. A PAF specific
antagonist, CV-6209, inhibited generation of the active conditioned medium by PAF. Addition of the PAF antagonist only partially
suppressed the augmentative effect of the active conditioned medium on DNA synthesis; this is consistent with the fact that,
because of the rapid breakdown, no appreciable amount of PAF remained in the conditioned medium of PAF-treated cells. Although
mouse bone marrow cells did not respond to PAF unlike guinea pig cells, their DNA synthesis was significantly enhanced by
the conditioned medium of PAF-treated guinea pig bone marrow cells. Thus, some newly generated factor(s) distinct from the
originally inoculated PAF seemed to modulate the bioactions of PAF on bone marrow cells. An appreciable amount of PAF was
produced by calcium ionophore-treated guinea pig bone marrow cells. These findings indicate that PAF synthesized in guinea
pig bone marrow cells induces generation in the cells of some factor(s) which affects proliferation or microbicidal activity.
Presented at The Third International Conference on Platelet-Activating Factor and Structurally Related Ether Lipids, Tokyo,
Japan, May 1989. 相似文献