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1.
Immunoglobulin-containing cells in lungs of hamsters infected with Mycoplasma pneumoniae 总被引:17,自引:0,他引:17
G W Fernald W A Clyde J Bienenstock 《Journal of immunology (Baltimore, Md. : 1950)》1972,108(5):1400-1408
2.
Alan M. Nevill Roger Ramsbottom Clyde Williams 《European journal of applied physiology and occupational physiology》1992,65(2):110-117
This paper examines how selected physiological performance variables, such as maximal oxygen uptake, strength and power, might best be scaled for subject differences in body size. The apparent dilemma between using either ratio standards or a linear adjustment method to scale was investigated by considering how maximal oxygen uptake (l.min-1), peak and mean power output (W) might best be adjusted for differences in body mass (kg). A curvilinear power function model was shown to be theoretically, physiologically and empirically superior to the linear models. Based on the fitted power functions, the best method of scaling maximum oxygen uptake, peak and mean power output, required these variables to be divided by body mass, recorded in the units kg 2/3. Hence, the power function ratio standards (ml.kg-2/3.min-1) and (W.kg-2/3) were best able to describe a wide range of subjects in terms of their physiological capacity, i.e. their ability to utilise oxygen or record power maximally, independent of body size. The simple ratio standards (ml.kg-1.min-1) and (W.kg-1) were found to best describe the same subjects according to their performance capacities or ability to run which are highly dependent on body size. The appropriate model to explain the experimental design effects on such ratio standards was shown to be log-normal rather than normal. Simply by taking logarithms of the power function ratio standard, identical solutions for the design effects are obtained using either ANOVA or, by taking the unscaled physiological variable as the dependent variable and the body size variable as the covariate, ANCOVA methods. 相似文献
3.
The topographical distribution of genetically defined alloantigens of the bovine erythrocyte was investigated by a serological absorption procedure known as the blocking test. Blocking was observed between the E′1 and Y2 antigens in theB system when these occurred in the same phenogroup. E′1 was also blocked by G and Q′ in the same phenogroup and Y2 was blocked by G. No blocking was observed between specificities residing either in different phenogroups or in different systems. We conclude that the several specificities in a givenB-system phenogroup are carried on a single molecule having multiple antigenic determinants, and that this arrangement is entirely consistent with the hypothesis that these factors are controlled by multiple alleles at a single locus. 相似文献
4.
The results presented here indicate that mitochondrial DNA (mtDNA) synthesis occurs on the inner mitochondrial membrane and that a membrane-DNA complex, enriched in newly synthesized DNA, can be isolated. The complex is able to synthesize DNA in vitro. Enrichment studies demonstrated that mtDNA synthesis occurs on an intact membrane-DNA complex in vitro and that pulse-labeled mtDNA could be chased from the membrane-DNA complex to the top fraction of the discontinuous sucrose gradient. The membrane-DNA complex was also shown to carry out replicative synthesis of mtDNA in vitro. Replication was shown to be asynchronous with heavy-strand synthesis preceding light-strand synthesis. The progression of mtDNA replication by the membrane-DNA complex was shown to be from small fragments (<13 S) to larger fragments (14–24 S) liberated from closed circular molecules, to a heat-stable 27 S molecule, and finally to a 38 S heat-stable molecule. The time estimated to progress from small fragments to the 38 S molecule is 120 min. 相似文献
5.
The metabolic rates of laboratory mice were compared in three conditions: isolated mice, mice paired together over six days (stable groups), and mice paired with strange partners daily (unstable groups). Stable pairs had 15% lower metabolic rates than either isolated or unstable pairs. In other experiments when two mice were placed in separate metabolic chambers and connected together via an air flow, the metabolic rate of the recipient in the series was 35% lower than the donor. The data suggest that a ‘factor’ produced by the donor mouse was passed via the air supply into the recipient's chamber. 相似文献
6.
Concentrations of calcium and magnesium were determined for 39 lots of media, including broth and agar media used for susceptibility
tests and plain agar. In addition, the effect that media with and without physiological levels of these divalent cations would
have on the disk diffusion susceptibility of 21 strains ofPseudomonas aeruginosa to four antimicrobics was also ascertained. Mueller-Hinton agar showed a wide variation in calcium and magnesium content.
Mueller-Hinton broth contained lower concentrations of calcium and magnesium, and there was little lot-to-lot variation. Lots
of Mueller-Hinton agar with higher concentrations of calcium and magnesium yielded smaller zone diamaters than those with
lower concentrations. Even at equal cation concentration, zones of inhibition varied from lot to lot. Since the addition of
calcium and magnesium to Mueller-Hinton agar to obtain a predetermined level did not result in equivalent zone diameters,
performance testing of susceptibility media is recommended. 相似文献
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