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1.
2.
Acyl carrier proteins (ACPs) from Escherichia coli and Euglena were analyzed on Western blots using rabbit antibodies raised against E. coli ACP. Euglena ACP, unlike that from E. coli, behaves upon electrophoresis under denaturing conditions as its size would predict. Oligomeric forms of both ACPs were evident on Western blots, but the bacterial ACP had more tendency to aggregate. That the oligomeric forms were not due to impurities was shown by their regeneration from low-Mr protein, reaction with antibodies isolated from low-Mr protein, and by molecular weight determination of the ACP by low-angle laser light scattering. 相似文献
3.
John S. Brimacombe Annalee S. Mengech Khandker M. M. Rahman Leslie C. N. Tucker 《Carbohydrate research》1982,110(2)
Methyl 4,6-O-benzylidene-2-deoxy-α-
-erythro-hexopyranosid-3-ulose reacted with potassium cyanide under equilibrating conditions to give, initially, methyl 4,6-O-benzylidene-3-C-cyano-2-deoxy-α-
-ribo-hexopyranoside (7), which, because it reverted slowly to the thermodynamically stable
-arabino isomer, could be crystallised directly from the reaction mixture. The mesylate derived from the kinetic product 7 could be converted by published procedures into methyl 3-acetamido-2,3,6-trideoxy-3-C-methyl-α-
-arabino-hexopyranoside, which was transformed into methyl N-acetyl-α-
-vancosaminide on inversion of the configuration at C-4. A related approach employing methyl 2,6-dideoxy-4-O-methoxymethyl-α-
-erythro-hexopyranosid-3-ulose gave the kinetic cyanohydrin and thence, via the spiro-aziridine 27, methyl 3-acetamido-2,3,6-trideoxy-3-C-methyl-α-
-arabino-hexopyranoside, a known precursor of methyl N-acetyl-α-
-vancosaminide. 相似文献
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Mark A. Tucker Michael S. Bisesi Timothy J. Smith 《Journal of biochemical and molecular toxicology》1989,4(4):267-268
The primary (and inactive) enteric metabolite of 5-aminosalicylate is N-acetyl-5-amino-salicylate. Previous studies have demonstrated acetylation of this anti-inflammatory agent by intestinal and bacterial homogenates. To assess the contribution of anerobic bacteria to the N-acetylation in vivo, we have measured the production of N-acetyl-5-aminosalicylate in anerobic microculture. Our results indicate that enteric bacteria play a minor role in N-acetylation, but may contribute to the production of other metabolites of pharmacologic and toxicological interest. 相似文献
8.
J. W. Breneman P. M. Yau R. R. Swiger R. Teplitz H. A. Smith J. D. Tucker E. M. Bradbury 《Chromosoma》1996,105(1):41-49
The expression of genes in mammalian cells depends on many factors including position in the cell cycle, stage of differentiation,
age, and environmental influences. As different groups of genes are expressed, their packaging within chromatin changes and
may be detected at the chromsomal level. The organization of DNA within a chromosome is determined to a large extent by the
positively charged, highly conserved histones. Histone subtypes and the reversible chemical modifications of histones have
been associated with gene activity. Active or potentially active genes have been associated with hyperacetylated histones
and inactive genes with nonacetylated histones. Sodium butyrate increases the acetylation levels of histones in cell cultures
and acts as both an inducer of gene activity and as a cell-cycle block. We describe a method to label the interphase distribution
of DNA associated with various histone acetylation stages on chromosomes. Nucleosomes from untreated and butyrate-treated
HeLa cells were fractionated by their acetylation level and the associated DNA labeled, and hybridized to normal human chromosomes.
In the sodium butyrate-treated cells the resulting banding patterns of the high- and low-acetylated fractions were strikingly
different. DNA from low-acetylated chromatin labeled several pericentric regions, whereas hybridization with DNA from highly
acetylated chromatin resulted in a pattern similar to inverse G-bands on many chromsomes. The results from noninduced cells
at both high and low acetylation levels were noticeably different from their induced counterparts. The capture and hybridization
of DNA from interphase chromatin at different acetylation states provides a “snap-shot” of the distribution of gene activity
on chromosomes at the time of cell harvest.
Edited by: P.B. Moens 相似文献
9.
Hurricane risk characteristics are examined across the U. S. Gulf of Mexico coastline using a hexagonal tessellation. Using an extreme value model, parameters are collected representing the rate or λ (frequency), the scale or σ (range), and the shape or ξ (intensity) of the extreme wind distribution. These latent parameters and the 30-year return level are visualized across the grid. The greatest 30-year return levels are located toward the center of the Gulf of Mexico, and for inland locations, along the borders of Louisiana, Mississippi, and Alabama. Using a geographically weighted regression model, the relationship of these parameters to sea surface temperature (SST) is found to assess sensitivity to change. It is shown that as SSTs increase near the coast, the frequency of hurricanes in these grids decrease significantly. This reinforces the importance of SST in areas of likely tropical cyclogenesis in determining the number of hurricanes near the coast, along with SSTs along the lifespan of the storm, rather than simply local SST. The range of hurricane wind speeds experienced near Florida is shown to increase with increasing SSTs (insignificant), suggesting that increased temperatures may allow hurricanes to maintain their strength as they pass over the Florida peninsula. The modifiable areal unit problem is assessed using multiple grid sizes. Moran’s I and the local statistic G are calculated to examine spatial autocorrelation in the parameters. This research opens up future questions regarding rapid intensification and decay close to the coast and the relationship to changing SSTs. 相似文献
10.
C Lee L Cordain J Sockler A Tucker 《European journal of applied physiology and occupational physiology》1990,61(3-4):289-293
The intention of this study was to determine the metabolic consequences of reduced frequency breathing (RFB) at total lung capacity (TLC) in competitive cyclists during submaximal exercise at moderate altitude (1520 m; barometric pressure, PB = 84.6 kPa; 635 mm Hg). Nine trained males performed an RFB exercise test (10 breaths.min-1) and a normal breathing exercise test at 75-85% of the ventilatory threshold intensity for 6 min on separate days. RFB exercise induced significant (P less than 0.05) decreases in ventilation (VE), carbon dioxide production (VCO2), respiratory exchange ratio (RER), ventilatory equivalent for O2 consumption (VE/VO2), arterial O2 saturation and increases in heart rate and venous lactate concentration, while maintaining a similar O2 consumption (VO2). During recovery from RFB exercise (spontaneous breathing) a significant (P less than 0.05) decreases in blood pH was detected along with increases in VE, VO2, VCO2, RER, and venous partial pressure of carbon dioxide. The results indicate that voluntary hypoventilation at TLC, during submaximal cycling exercise at moderate altitude, elicits systemic hypercapnia, arterial hypoxemia, tissue hypoxia and acidosis. These data suggest that RFB exercise at moderate altitude causes an increase in energy production from glycolytic pathways above that which occurs with normal breathing. 相似文献