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991.
PB Moore 《Canadian Metallurgical Quarterly》1997,7(3):R179-R181
Using image reconstruction methods, electron microscopists can now visualize ribosomes at resolutions so high that the changes in the positions of ribosome-bound tRNAs which occur during protein synthesis can be seen. 相似文献
992.
These experiments were designed to test the hypothesis that glides in frequency are detected and discriminated by monitoring changes in excitation level on the low-frequency side of the excitation pattern. Thresholds were measured for detecting an increase in the extent of a frequency glide, for various standard extents (transition spans). The center frequency of each stimulus was roved, to prevent subjects from using the start or endpoint frequencies of the stimuli as cues. The level was either fixed at 70 dB SPL, or changed linearly in dB/s by an amount that varied randomly in extent and direction, keeping the level at the midpoint of the glide at 70 dB SPL. These random changes in level were intended to disrupt cues based on monitoring changes in excitation level on one side of the excitation pattern. For some conditions, performance was too good to be explained by subjects monitoring the start or endpoint frequencies of the stimuli. Performance was also too good to be explained in terms of the discrimination of changes in excitation level on one side of the excitation pattern. Thresholds, expressed as a proportion of the equivalent rectangular bandwidth (ERB) of the auditory filter, did not vary greatly with center frequency (0.5, 2, or 6 kHz), suggesting that discrimination did not depend strongly on information derived from phase locking. Glide duration (50 or 400 ms) and glide direction (upward or downward) also had little effect. Thresholds increased with increasing standard transition span, when that span was increased beyond 0.5 ERB. It is concluded that changes in glide extent per se can be discriminated, but this is not done by monitoring just one side of the excitation pattern. 相似文献
993.
994.
The avidity of antibodies for antigens can be measured by determining what remains bound after exposing the antibody-antigen complex to a chaotropic agent such as urea. This method has been gaining popularity for assessing the immune response to the human immunodeficiency virus type 1 (HIV-1) surface glycoprotein gp120 (or its counterpart from simian immunodeficiency virus), during natural infection or after subunit vaccination. High-avidity antibodies have been considered to be a possible correlate of protection. We have examined the avidity assay to determine what it, in fact, measures. First, we studied the development of the anti-gp120 response in seroconverting individuals. Urea elution reduced the polyclonal anti-gp120 titers by 3- to 10-fold. After allowing for the consequent reduction in assay sensitivity, there was no obvious change in the rate of development of the high-avidity and unfractionated antibody responses. Furthermore, in the one individual who developed a strong autologous, virus-neutralizing response, the appearance of neutralizing antibodies and high-avidity antibodies did not coincide. Antibodies to the V3 loop, when present, comprised a major fraction of the polyclonal response that survives urea elution. We next examined the effect of urea elution on the binding to gp120 of a panel of monoclonal antibodies (MAbs). Urea treatment preferentially eluted MAbs to discontinuous rather than continuous epitopes, independent of their affinities. Furthermore, these patterns of epitope stability were unaltered by the presence of polyclonal anti-gp120 antibodies. As most broadly neutralizing anti-gp120 antibodies recognize discontinuous epitopes, this skewing effect must be taken into account when interpreting studies using polyclonal sera. 相似文献
995.
SD Brown RC Twells PJ Hey RD Cox ER Levy AR Soderman ML Metzker CT Caskey JA Todd JF Hess 《Canadian Metallurgical Quarterly》1998,248(3):879-888
A novel member of the low density lipoprotein receptor (LDLR) gene family has been identified and characterized. This gene, termed LDL receptor-related protein 6 (LRP6), encodes a transmembrane protein which has 71% identity and is structurally similar to the protein encoded by LRP5, a proposed candidate gene for type 1 diabetes located on human chromosome 11q13. LRP6 maps to human chromosome 12p11-p13. Mouse Lrp6 encodes a protein that has 98% identity to human LRP6 and maps to chromosome 6. Unlike other members of the LDLR family, LRP6 and LRP5 display a unique pattern of four epidermal growth factor (EGF) and three LDLR repeats in the extracellular domain. The cytoplasmic domain of LRP6 is not similar to other members of the LDLR family, while comparison with LRP5 reveals proline-rich motifs that may mediate protein-protein interactions. Thus, it is likely that LRP6 and LRP5 comprise a new class of the LDLR family. 相似文献
996.
MR Paley P Farrant P Kane ND Heaton ER Howard JB Karani 《Canadian Metallurgical Quarterly》1997,7(9):1377-1382
The purpose of this study was to evaluate the role of radiological techniques in the diagnosis and management of developmental intrahepatic shunts. Hepatic vascular fistulae are recognised sequelae of liver trauma and intrahepatic tumours. However, there are rare developmental malformations which may present in childhood or later life and which may carry life-threatening complications. Retrospective analysis of clinical and radiological data was carried out in 24 patients. Anomalies evaluated were: (a) direct communication between hepatic artery and hepatic veins; (b) congenital hepatoportal arteriovenous malformations; and (c) congenital portocaval anastomosis with persistent flow through the ductus venosus. Although rare, the prompt recognition of these vascular anomalies allows early surgical or radiological intervention and reversal of the haemodynamic complications. 相似文献
997.
EJ DeSchepper Y Oshida BK Moore NB Cook H Eggertson 《Canadian Metallurgical Quarterly》1997,22(5):209-216
Concerns of mercury toxicity have led to the development of gallium-based restorative materials to replace dental amalgam. A new gallium-based dental restorative, Galloy, was compared with a high-copper amalgam, Permite, for anodic polarization behavior in deoxygenated Ringer's solution and by immersion testing in normal Ringer's solution at 37 degrees C. Corrosion products were analyzed using energy dispersive X-ray spectrometry and transmission electron diffraction. The data from both sources were consistent with the presence of alpha-Ga2O3 and SnO2 as the primary corrosion products of Galloy. Anodic polarization behavior of Galloy- and Permite-coupled specimens suggests that coupling Galloy with the more noble Permite amalgam may cause accelerated electrochemical corrosion and that Galloy is more corrosion prone than Permite. 相似文献
998.
The circadian timing of the suprachiasmatic nucleus (SCN) is modulated by its neural inputs. In the present study, we examine the organization of the neural inputs to the rat SCN using both retrograde and anterograde tracing methods. After Fluoro-Gold injections into the SCN, retrogradely labeled neurons are present in a number of brain areas, including the infralimbic cortex, the lateral septum, the medial preoptic area, the subfornical organ, the paraventricular thalamus, the subparaventricular zone, the ventromedial hypothalamic nucleus, the posterior hypothalamic area, the intergeniculate leaflet, the olivary pretectal nucleus, the ventral subiculum, and the median raphe nuclei. In the anterograde tracing experiments, we observe three patterns of afferent termination within the SCN that correspond to the photic/raphe, limbic/hypothalamic, and thalamic inputs. The median raphe projection to the SCN terminates densely within the ventral subdivision and sparsely within the dorsal subdivision. Similarly, areas that receive photic input, such as the retina, the intergeniculate leaflet, and the pretectal area, densely innervate the ventral SCN but provide only minor innervation of the dorsal SCN. A complementary pattern of axonal labeling, with labeled fibers concentrated in the dorsal SCN, is observed after anterograde tracer injections into the hypothalamus and into limbic areas, such as the ventral subiculum and infralimbic cortex. A third, less common pattern of labeling, exemplified by the paraventricular thalamic afferents, consists of diffuse axonal labeling throughout the SCN. Our results show that the SCN afferent connections are topographically organized. These hodological differences may reflect a functional heterogeneity within the SCN. 相似文献
999.
Torsion of an accessory spleen is a rare entity that can have a variable clinical presentation. We report the computed tomographic (CT) findings of an acute torsion of an accessory spleen in a 13-year-old girl. CT disclosed a hypodense mesenteric mass with peripheral inflammatory changes. 相似文献
1000.
NJ Hoeldtke PG Napolitano KH Moore BC Calhoun RF Hume 《Canadian Metallurgical Quarterly》1997,177(5):1088-1092
OBJECTIVES: Our purpose was to determine the effects of acidosis and acidosis-hypoxia on fetoplacental perfusion pressure and its response to angiotensin II. STUDY DESIGN: Perfused cotyledons from 14 placentas were studied with either an acidotic fetal circuit perfusate (n = 7) or an acidotic-hypoxic fetal circuit perfusate (n = 7). Each cotyledon's fetal vasculature was initially perfused under standard conditions and bolus injected with 1 x 10(-10) moles of angiotensin II. Fetoplacental perfusate was then replaced with either an acidotic medium (pH 6.90 to 7.00 and Po2 516 to 613 mm Hg) or an acidotic-hypoxic medium (pH 6.90 to 7.00 and Po2 20 to 25 mm Hg) followed by an angiotensin II injection. The vasculature was subsequently recovered with standard perfusate and again injected with angiotensin II. Perfusion pressures within each group were compared by one-way analysis of variance, and results were expressed as mean pressure +/- SEM. RESULTS: Resting fetoplacental perfusion pressure did not change when the fetal circuit perfusate was made acidotic (28 +/- 1 mm Hg vs 25 +/- 2 mm Hg) or acidotic-hypoxic (26 +/- 2 mm Hg vs 25 +/- 2 mm Hg). The maximal fetoplacental perfusion pressure achieved in response to angiotensin II did not differ with an acidotic perfusate (41 +/- 2 mm Hg vs 38 +/- 1 mm Hg) or with an acidotic-hypoxic perfusate (39 +/- 2 mm Hg vs 36 +/- 2 mm Hg). CONCLUSIONS: In the perfused placental cotyledon fetoplacental perfusion pressure and pressor response to angiotensin II are not affected by fetal circuit acidosis or acidosis-hypoxia. This suggests that neither fetal acidosis nor fetal acidosis combined with hypoxia has a direct effect on fetoplacental vascular tone. 相似文献