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A. V. Sverdlin G. E. Totten C. Bates L. M. Jarvis 《Metal Science and Heat Treatment》1996,38(6):248-251
The development of methods for evaluating and predicting the variation of the properties of polymer quenching media in operation requires an analysis of the quenching factor, which characterizes the degree of decomposition of the solid solution in quenching, which decreases the strength (hardness) of the alloy by a given value. In the present paper the quenching factorQ is used to compare the properties of aluminum alloys quenched in hot water and aqueous solutions of polymers.Translated from Metallovedenie i Termicheskaya Obrabotka Metallov, No. 6, pp. 14 – 17, June, 1996. 相似文献
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JE is a member of the family of "immediate early" genes induced by growth factors and cytokines. JE encodes a low molecular weight secretory glycoprotein analogous to the human monocyte chemoattractant protein, MCP-1. JE and MCP-1 proteins are thought to play an important role in inflammation and in the recruitment of monocyte/macrophages to the vessel wall during the development of atherosclerosis. We have previously reported that the induction of JE in rat aortic smooth muscle cells (SMC) was specific to platelet-derived growth factor (PDGF) and was not seen with other growth agonists. Using a luciferase reporter system and transient transfection assays of rat aortic SMC, we now report the identification of a region in the proximal rat JE promoter that is responsive to PDGF but not to other growth factors (angiotensin II and alpha-thrombin) or cytokines (interleukin 1-beta and tumor necrosis factor-alpha). The full response to PDGF (approximately 6-fold) requires the cooperative activity of two potentially novel cis-acting elements, at positions -146 to -128 and -84 to -59. While each element produces a different pattern in electrophoretic mobility shift assays, they appear to bind the same PDGF-responsive species. Further analysis of these regions should provide important insights into PDGF-specific responses in vascular SMC. 相似文献
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D. Poteet G. E. Totten L. C. F. Canale 《金属热处理》2006,31(11):88-94
感应淬火冷却系统可能采用各式各样的搅拌方式,包括传统的浸淬、开放式喷雾冷却和浸没状态下的喷射冷却。这些工艺并不等效,而是要根据正确的技术要求来恰当地选用这些方法。本文对这些不同的搅拌系统进行了综述。 相似文献
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BK Ganser S Li VY Klishko JT Finch WI Sundquist 《Canadian Metallurgical Quarterly》1999,283(5398):80-83
The genome of the human immunodeficiency virus (HIV) is packaged within an unusual conical core particle located at the center of the infectious virion. The core is composed of a complex of the NC (nucleocapsid) protein and genomic RNA, surrounded by a shell of the CA (capsid) protein. A method was developed for assembling cones in vitro using pure recombinant HIV-1 CA-NC fusion proteins and RNA templates. These synthetic cores are capped at both ends and appear similar in size and morphology to authentic viral cores. It is proposed that both viral and synthetic cores are organized on conical hexagonal lattices, which by Euler's theorem requires quantization of their cone angles. Electron microscopic analyses revealed that the cone angles of synthetic cores were indeed quantized into the five allowed angles. The viral core and most synthetic cones exhibited cone angles of approximately 19 degrees (the narrowest of the allowed angles). These observations suggest that the core of HIV is organized on the principles of a fullerene cone, in analogy to structures recently observed for elemental carbon. 相似文献
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ER Nekrasova DM Berman RR Rustandi HE Hamm AG Gilman VY Arshavsky 《Canadian Metallurgical Quarterly》1997,36(25):7638-7643
RGS proteins (regulators of G protein signaling) constitute a newly appreciated group of negative regulators of G protein signaling. Several members of this group stimulate the guanosine triphosphatase (GTPase) activity of various G protein alpha-subunits, including the photoreceptor G protein, transducin. In photoreceptor cells transducin GTPase is known to be substantially accelerated by the coordinated action of the gamma-subunit of its effector enzyme, cGMP phosphodiesterase (PDE gamma), and another yet unidentified membrane-associated protein factor. Here we test the possibility that this factor belongs to the RGS family of GTPase stimulators. We report a detailed kinetic analysis of transducin GTPase activation by two members of the RGS family, RGS4 and G alpha interacting protein (GAIP). RGS4, being at least 5-fold more potent than GAIP, stimulates the rate of transducin GTPase by 2 orders of magnitude. Neither RGS4 nor GAIP requires PDE gamma for activating transducin. Rather, PDE gamma causes a partial reversal of transducin GTPase activation by RGS proteins. The effect of PDE gamma is based on a decreased apparent affinity of RGS for the alpha-subunit of transducin. Our observations indicate that GTPase activity of transducin can be activated by at least two distinct mechanisms, one based on the action of RGS proteins alone and another involving the cooperative action of the effector enzyme and another protein. 相似文献