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Efficient techniques for native-labeling of amino acids have been combined successfully with emission tomography to yield significant improvements in pancreatic imaging. Carbon-11-labeled tryptophan appears to be the best agent available currently for imaging the pancreas. Optimum scanning times begin 30 min after tracer administration. Positron emission tomography with 11C-tryptophan is capable of defining both morphological and functional alterations in the pancreas. Tumors as small as 2 cm in diameter can be detected, but reliable differentiation of pancreatic cancer from pancreatis may not be possible even with this improved imaging technique. Longitudinal multiplane emission tomography in single-photon mode with the Pho/Con provides an efficient and satisfactory approach to pancreatic imaging with the positron-emitting radiopharmaceuticals. 相似文献
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Maternal lymphocyte reactivity to human trophoblast antigens was studied in placentas of gestational ages 8 to 14 weeks and 32 to 34 weeks, respectively. Significant trophoblast lysis became apparent after 24 hours' incubation in the latter case compared with a time lag of 72 hours in the terminated gestations. Maternal cellular immunity, therefore, was not detected during the first 3 1/2 months of pregnancy, but was detectable by the time of parturition. The possible significance is discussed with respect to the antigenic stimulus and survival of the fetal allograft. 相似文献
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PURPOSE: To determine if lucanthone crossed the blood-brain barrier in experimental animals; and to determine accelerated tumor regression of human brain metastases treated jointly with lucanthone and whole brain radiation. METHODS AND MATERIALS: The organ distribution of 3H lucanthone in mice and 125I lucanthone in rats was determined to learn if lucanthone crossed the blood-brain barrier. Size determinations were made of patients' brain metastases from magnetic resonance images or by computed tomography before and after treatment with 30 Gy whole brain radiation alone or with lucanthone. RESULTS: The time course of lucanthone's distribution in brain was identical to that in muscle and heart after intraperitoneal or intravenous administration in experimental animals. Lucanthone, therefore, readily crossed the blood-brain barrier in experimental animals. CONCLUSION: Compared with radiation alone, the tumor regression in patients with brain metastases treated with lucanthone and radiation was accelerated, approaching significance using a permutation test at p = 0.0536. 相似文献
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Arabinoxylans (AX) were extracted from Sonalika variety of wheat (whole wheat flour and wheat bran) with barium hydroxide and sodium hydroxide and purified by a combination of alcohol precipitation and glucoamylase digestion. Structural features of purified AX were elucidated by methylation analysis, 13C NMR, FT‐IR, periodate oxidation and optical rotation measurements. The AX showed a backbone of xylose residues with β(1–4) linkages and were branched mainly through O‐3 of xylose residues. Completely branched xylosyl residues were also present. Copyright © 2003 Society of Chemical Industry 相似文献
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Modulation of stability properties of bovine trypsin after in vitro structural changes with a variety of chemical modifiers 总被引:4,自引:0,他引:4
Controlled chemical modification of enzymes, targeting groups not involved
in the active site, can lead to modified catalysts that are intrinsically
more efficient and resistant to heat and denaturing agents. Bovine
pancreatic trypsin was covalently modified up to 75-85% with monomeric
glutaraldehyde (MGA), polymeric glutaraldehyde (PGA), oxidized sucrose and
oxidized sucrose polymers (OSP 70 and OSP 400). Virtually no loss in
activity occurred upon modification. Temperature optima of trypsin shifts
from 45-76 degrees C and T50 from 54-76 degrees C for the best modified
sample made with OSP. The efficiency of the modifiers in stabilization was
ranked in the order: OSP 400-T > OSP 70-T > PGA-T > MGA-T >
Sucrose-T. Half-life of modified enzymes also followed the same trend. Both
stabilization factor and t1/2 decreased with increasing temperatures. The
free energy of activation for inactivation delta(deltaG*) varies from 12-20
kJ/mol and the activation enthalpy delta(deltaH*) of the modified trypsin
by 80-120 kJ/mol indicating stabilization. Inactivation of modified trypsin
by urea is less noticeable. The character of the two-step inactivation
process of trypsin changes with the degree of stabilization in that the
duration of phase I one increased noticeably as stabilization increases.
Native trypsin fluoresces less intensely showing a red shift under the
influence of denaturation. Such a fluorescence change is not so obvious for
the modified enzymes indicating conformational stability acquired by
modification.
相似文献
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