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121.
SF Abraham JR Blair-West JP Coghlan DA Denton DR Mouw BA Scoggins 《Canadian Metallurgical Quarterly》1976,81(1):120-132
Conscious sheep with permanent indwelling cannulae in the lateral ventricles and the cisterna magna were Na depleted and then perfused for 9 h with an artificial CSF solution. There were 3 experimental groups: Group I (n=5) received perfusion with aritifical CSF containing NA 170 MEq./1, Group II (n=7) received perfusion with artificial CSF containing Na 145 mEq./1, Group III (n=7) received no perfusion. In Group I the blood aldosterone level fell from 26.4 +/- 7.4 to 8.6 +/- 2.3 ng/100 ml by 9 h after perfusion. There was no significant change in plasma [Na] or [K], blood angiotensin II or plasma renin concentration. Blood cortisol and corticosterone levels rose. There was also a fall in post-perfusion. Group III showed no significant change in blood aldosterone concentration. Multivariate statistical analysis showed that the fall in aldosterone levels during 170 mEq./l Na perfusion could not be accounted for by changes, either alone or together, of ACTH as evidenced by alteration in blood cortisol or corticosterone, or by change of plasma [Na], [K] or renin concentrations. This data supports the hypothesis of an additional factor which may be of CNS origin being involved in the control of aldosterone secretion. 相似文献
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FG Surawicz DR Brightwell WD Weitzel E Othmer 《Canadian Metallurgical Quarterly》1976,133(11):1306-1309
The authors review recent and current literature on the relationship between psychological factors and cancer. They discuss the roles of predisposing personality patterns and emotional stress in the development, site, and course of cancer; the influence of awareness of terminal illness on the behavior of cancer patients; and the management of psychiatric symptoms in these patients. 相似文献
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DR. CHRISTIAN MUELLER-SCHLOER 《Cryptologia》2013,37(3):257-273
Secrecy and authentication are two important features of a secure communication system. Public Key Cryptosystems, based, e.g., on the Rivest-Shamir-Adleman (RSA) algorithm, provide a very elegant solution to the problem of authenticity verification or true electronic signatures. Practical problems, however, mainly the lack of execution speed, prevent a straightforward application. In order to sign a long message it is much faster to first calculate a short digest or checksum and then sign the compressed message. For this checksum calculation the fast, inexpensive and extensively tested Data Encryption Standard (DES) can be used. But care must be taken that this additional processing step does not introduce any weakness into the signature scheme. This paper investigates two DES-based hashing methods. It is shown that neither method seems to introduce any statistical regularities in the generated checksums. The “Cipher/Message to Plain Feedback,” however, is not secure under a modification compensation attack. It is further shown how the second method, the “Cipher to Plain Feedback” proposed by Davies and Price, can be broken by a “meet in the middle attack.” This checksum method, however, can be used safely with a slight modification. 相似文献
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Santoshrupa Dumpala Jacek B. Jasinski Gamini U. Sumanasekera Mahendra K. Sunkara 《Carbon》2011,(8):2725-2734
Conical carbon nanotube (CCNT) arrays were synthesized over a large area of approximately 1 cm2 or more on graphite and tungsten foil substrates. Experimental observations reveal that nucleation is caused by catalyst metal cluster in the initial stages, but the tapered morphology occurs due to the difference in the rates of vertical growth by attachment carbon atoms at edges of growing graphene sheets and radial growth with epitaxial nucleation of new graphene layers near bottom at the substrate. The above mechanism is supported through re-growth experiments on straight multi-walled nanotubes and growth kinetics data, which suggest a linear relationship between the growth rate and ratio of diameter to length (d/l) of CCNT. 相似文献
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We previously reported that substitution of Arg258 within the switch 3 region of Gsalpha impaired activation and increased basal GDP release due to loss of an interaction between the helical and GTPase domains (Warner, D. R., Weng, G., Yu, S., Matalon, R., and Weinstein, L. S. (1998) J Biol. Chem. 273, 23976-23983). The adjacent residue (Glu259) is strictly conserved in G protein alpha-subunits and is predicted to be important in activation. To determine the importance of Glu259, this residue was mutated to Ala (Gsalpha-E259A), Gln (Gsalpha-E259Q), Asp (Gsalpha-E259D), or Val (Gsalpha-E259V), and the properties of in vitro translation products were examined. The Gsalpha-E259V was studied because this mutation was identified in a patient with Albright hereditary osteodystrophy. S49 cyc reconstitution assays demonstrated that Gsalpha-E259D stimulated adenylyl cyclase normally in the presence of GTPgammaS but was less efficient with isoproterenol or AlF4-. The other mutants had more severely impaired effector activation, particularly in response to AlF4-. In trypsin protection assays, GTPgammaS was a more effective activator than AlF4- for all mutants, with Gsalpha-E259D being the least severely impaired. For Gsalpha-E259D, the AlF4--induced activation defect was more pronounced at low Mg2+ concentrations. Gsalpha-E259D and Gsalpha-E259A purified from Escherichia coli had normal rates of GDP release (as assessed by the rate GTPgammaS binding). However, for both mutants, the ability of AlF4- to decrease the rate of GTPgammaS binding was impaired, suggesting that they bound AlF4- more poorly. GTPgammaS bound to purified Gsalpha-E259D irreversibly in the presence of 1 mM free Mg2+, but dissociated readily at micromolar concentrations. Sucrose density gradient analysis of in vitro translates demonstrated that all mutants except Gsalpha-E259V bind to beta gamma at 0 degreesC and were stable at higher temperatures. In the active conformation Glu259 interacts with conserved residues in the switch 2 region that are important in maintaining both the active state and AlF4- in the guanine nucleotide binding pocket. Although both Gsalpha Arg258 and Glu259 are critical for activation, the mechanisms by which these residues affect Gsalpha protein activation are distinct. 相似文献