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181.
The interactions of chymotrypsin, subtilisin and trypsin with a low MW proteinase inhibitor from potatoes were investigated. The Ki value calculated for the binding of inhibitor to chymotrypsin was 1.6 ± 0.9 × 10?10M, while the second-order rate constant for association was 6 × 105 M?1/sec. Although binding was not observed to chymotrypsin which had been treated with diisopropyl fluorophosphate or with l-tosylamide-2-phenylethyl chloromethyl ketone, the 3-methylhistidine-57 derivative bound inhibitor with a Ki value of 9.6 × 10?9 M. The inhibitor also exhibited a tight association with subtilisin (Ki < 4 × 10?9 M). In contrast, little inhibition of trypsin was observed, and this was believed to be due to low levels of a contaminant in our preparations. No evidence for reactive site cleavage was observed after incubation of the inhibitor with catalytic amounts of chymotrypsin or subtilisin at acid pH. 相似文献
182.
Manfred Klaus Grossmann 《Archives of microbiology》1980,124(2-3):293-295
Catabolite inactivation of fructose-1,6-bisphosphatase, isocitrate lyase, phosphoenolpruvate carboxykinase and malate dehydrogenase in intact cells could be prevented by phenylmethylsulfonyl fluoride added 40 min prior to the addition of glucose. Protein synthesis, fermentative and respiratory activity and catabolite repression were not affected. Elimination of catabolite inactivation by the addition of PMSF revealed that catabolite repression started at different times for different enzyme.Abbreviation PMSF
phenylmethylsulfonyl fluoride 相似文献
183.
Characterization of an inhibitor of the intracellular protease from Bacillus subtilis. 总被引:4,自引:0,他引:4
A specific inhibitor of intracellular serylprotease from Bacillus subtilis has been isolated from both growing and sporulating cells. Like other protease inhibitors isolated from eukaryotic cells, the inhibitor from B. subtilis is a thermostable protein. A purification method is described. The molecular weight estimated by Biogel filtration and SDS gel electrophoresis is about 15,500. Both proteolytic and esterolytic activities of intracellular protease are equally sensitive to inhibition. With azocoll or Z-tyrosine p-nitrophenylester as substrates, noncompetitive inhibition patterns are observed. The inhibitor has no effect on the proteolytic or esterolytic activities of the extracellular serylprotease. A similar thermostable inhibitor is also present in Bacillus megaterium. 相似文献
184.
S. R. Akruk A. A. Farooqui William L. Williams P. N. Srivastava 《Molecular reproduction and development》1979,2(1):1-13
Significant release of the acrosomal enzymes arylsulfatase, β-N-acetylhexosaminidase and hyaluronidase was observed following the treatment of ejaculated rabbit spermatozoa for 12 hours in 20% rabbit serum for inducing in vitro capacitation, and these sperm were capable of in vivo fertilization; however, the treatment of sperm for 15 minutes in high ionic strength (380 mOsm/kg) or low ionic strength medium (305 mOsm/kg) for in vitro capacitation did not result in any significant release of the above enzymes nor were the sperm capable of in vivo fertilization. Serum-treated spermatozoa remained significantly motile following the 12 hour treatment, 51% underwent the acrosome reaction and were capable of fertilizing 66% of the ova in vivo. Identical serum treatment of lysosomes from rabbit liver resulted in a comparable release of the lysosomal enzymes. Serum treatment for in vitro capacitation resulted in vesiculation of the anterior margin of half the spermatozoa, but left their inner acrosomal membranes and equatorial segments intact. A biochemical relationship between the release of acrosomal enzymes and capacitation is suggested. 相似文献
185.
186.
Hiroki Nakagawa Shinji Ishigami Kiyoshi Sekiguchi Kunio Kurata Nagao Ogura 《Phytochemistry》1981,20(6):1229-1230
Evidence is presented for the selective breakdown of altered tomato β-fructofuranosidase molecules by a neutral protease from Bacillus subtilis. 相似文献
187.
T. Friedel F. G. Barth 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1997,180(3):223-233
Spiders can use air particle movements to localize moving prey. We studied the responses of 32 wind-sensitive interneurones
in the hunting spider Cupiennius salei to prey stimuli.
Stimulation with a tethered flying fly or with artificial air pulses activated plurisegmental interneurones that responded
to changes in air movement velocity and were thus well suited to represent the highly fluctuating air stream typical of prey
stimuli. In most interneurones (n = 18) the responses to the stimulation of different legs were not significantly different from each other.
Different interneurones had different response characteristics and their latencies largely overlapped suggesting that there
is parallel processing of the signals by populations of interneurones with different response characteristics.
In two interneurones the number of spikes and the spiking pattern elicited by stimulation of each of the eight legs markedly
differed depending on the leg stimulated. These neurones may play an important role in directional information processing.
Stimulation of the adjacent legs from front to back or from back to front revealed two interneurones sensitive to the direction
of successive stimulation of the legs. These neurones may be able to detect the motion of an air movement source in a preferred
direction and thus act as nearfield motion detectors to localize a moving prey item.
Accepted: 28 September 1996 相似文献
188.
189.
《Bioscience, biotechnology, and biochemistry》2013,77(5):1262-1264
Fungal protease inhibitor F (FPI-F) from silkworm inhibits subtilisin and fungal proteases. FPI-F mutants P1 residues of which, Thr29, were replaced with Glu, Phe, Gly, Leu, Met, and Arg, were prepared. The inhibitory activities of mutated FPI-F against subtilisin and other mammalian proteases indicated that FPI-F might be a specific inhibitor toward subtilisin-type protease. 相似文献
190.
Keigo Gohda 《Journal of enzyme inhibition and medicinal chemistry》2013,28(5):609-615
In this study, we investigated by linear regression model the SAR data of the 15 HIV-1 protease inhibitors possessing structurally diverse scaffolds. First, a regression model was developed only using the enzyme-inhibitor interaction energy as a term of the model, but did not provide a good correlation with the inhibitory activity (R2 = 0.580 and Q2 = 0.500). Then, we focused on the conformational flexibility of the inhibitors which may represent the diversity of the inhibitors, and added two conformational parameters into the model, respectively: the number of rotatable bonds of ligands (ΔSrot) and the distortion energy of ligands (ΔElig). The regression model by adding ΔElig successfully improved the quality of the model (R2 = 0.771 and Q2 = 0.713) while the model with ΔSrot was unsuccessful. The prediction for a training inhibitor by the ΔElig model also showed good agreement with experimental activity. These results suggest that the conformational flexibility of HIV-1 protease inhibitors directly contributes to the enzyme inhibition. 相似文献