全文获取类型
收费全文 | 4589篇 |
免费 | 352篇 |
出版年
2021年 | 31篇 |
2020年 | 19篇 |
2019年 | 32篇 |
2018年 | 41篇 |
2017年 | 43篇 |
2016年 | 75篇 |
2015年 | 110篇 |
2014年 | 128篇 |
2013年 | 195篇 |
2012年 | 238篇 |
2011年 | 231篇 |
2010年 | 154篇 |
2009年 | 161篇 |
2008年 | 243篇 |
2007年 | 235篇 |
2006年 | 246篇 |
2005年 | 242篇 |
2004年 | 230篇 |
2003年 | 289篇 |
2002年 | 301篇 |
2001年 | 81篇 |
2000年 | 43篇 |
1999年 | 89篇 |
1998年 | 100篇 |
1997年 | 83篇 |
1996年 | 73篇 |
1995年 | 60篇 |
1994年 | 58篇 |
1993年 | 64篇 |
1992年 | 81篇 |
1991年 | 54篇 |
1990年 | 34篇 |
1989年 | 47篇 |
1988年 | 48篇 |
1987年 | 33篇 |
1986年 | 27篇 |
1985年 | 41篇 |
1984年 | 42篇 |
1983年 | 36篇 |
1982年 | 60篇 |
1981年 | 55篇 |
1980年 | 48篇 |
1979年 | 43篇 |
1978年 | 40篇 |
1977年 | 38篇 |
1976年 | 41篇 |
1975年 | 28篇 |
1974年 | 21篇 |
1973年 | 20篇 |
1971年 | 18篇 |
排序方式: 共有4941条查询结果,搜索用时 46 毫秒
41.
Claude Lefevre 《Bulletin of mathematical biology》1983,45(1):11-20
This paper is concerned with a generalization of the simple epidemic model in which the infective population is partitioned
intom classes, each of specific infectiousness. Attention is restricted, however, to the case where all the meeting rates between
two individuals are equal to each other. Both deterministic and stochastic versions are examined. In either case the development
in time of the epidemic process is investigated by exploiting a connection with the standard simple epidemic model. Finally,
it is shown that the technique used also applies to a similar model for the spread of information. 相似文献
42.
An alpha-amylase gene from Bacillus coagulans has previously been cloned in Escherichia coli and shown to direct the synthesis of an enzymically active protein of 60,000 Dal (Cornelis et al., 1982). In one particular E. coli host, strain HB101, amylase was found to accumulate in the periplasmic space. To study the processing and the location of the amylase, plasmid pAMY2 was introduced into E. coli 188 which is a strain constitutive for alkaline phosphatase, a periplasmic marker, and for beta-galactosidase, a cytoplasmic marker. Abnormally large amounts of both alpha-amylase and beta-galactosidase were found in the culture fluid of cells grown in rich medium. Furthermore a severe growth defect was found when cells containing pAMY2 were grown in maltose and glycerol media, while the ability to grow on glucose remained normal. This defect could be reversed by two types of spontaneous mutations. Mutations in the first class are located on the plasmid and correspond to the insertional inactivation of the amylase gene by IS1. Mutations in the second class are located on the host chromosome. These results suggest that the synthesis and export of B. coagulans alpha-amylase is deleterious to E. coli, especially in media containing maltose or glycerol as sole carbon source. 相似文献
43.
44.
Michel GuerineauClaude Grandchamp Claude PaolettiPiotr Slonimski 《Biochemical and biophysical research communications》1971
This paper describes the isolation of a pure population of covalently closed circular twisted DNA molecules from yeast. These molecules are homogeneous in size, that is consist of monomers of 2.2μ and of multiple length oligomers of n x 2.2μ. While no data rule out the mitochondrial origin of this DNA, its actual intracellular localization remains unknown; it displays the same buoyant density as the main nuclear DNA and therefore is not the heavy nuclear satellite DNA (γ-DNA described by Moustacchi and Williamson (1966)); although circular molecules represent only 1 to 5 % of the total DNA, they can be prepared in sizable and reproducible amounts by a method based on the use of mechanical disruption of yeast cells rather than lysis by snail gut juice. 相似文献
45.
46.
Agar Plate Method for Detecting Microorganisms Which Produce Equilin and Other Estrogens from Various Steroids 总被引:1,自引:1,他引:0
下载免费PDF全文
![点击此处可从《Applied microbiology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The intense red color produced by a reagent specific for xi(7)-estrogens is used to directly detect microorganisms which produce these estrogens from various steroids. 相似文献
47.
48.
49.
Tarek Bisat Terry R. Brown Claude J. Migeon Gary D. Berkovitz 《In vitro cellular & developmental biology. Plant》1989,25(9):806-812
Summary Because the measurement of aromatase activity in cultured human genital skin fibroblasts has been proposed as a means of studying
estrogen production in men, we investigated the influence of culture conditions on aromatase activity.
Genital skin fibroblasts were seeded onto culture plates at a density of 1×106 cells/plate and aromatase activity was determined over a 1-mo. period. Enzyme activity rose slowly over the first 14 d but
then rose rapidly to a 10-fold higher plateau by Day 28. The rise in aromatase activity was similar whether activity was normalized
for protein or for DNA content. When cells were seeded at the usual density of 1×106 or at 0.25×106 cells/plate, aromatase activity was consistently lower during the first 2 wk in cells plated at lower density, but thereafter
the levels of enzyme activity in the two groups converged. In cells plated at the lower density, the lower activity observed
in the first 2 wk was associated with a lower V
max
. Preincubation of cells plated at one density with conditoned medium from cells plated at the other density did not change
the relatve levels of activity in the two groups. By contrast, dihydrotestosterone (DHT) receptor binding and 5α-reductase
activity were similar at all time points, despite differences in plating density.
In additional experiments, the culture medium was replaced daily rather than every 3rd d, and aromatase activity was assayed
on Day 7. In cells fed daily, DNA and protein content were twice that of cells fed every 3rd d. By contrast, aromatase activity
declined to 30% of the in the latter group. DHT and dexamethasone receptor binding and 5α-reductase activity were similar
in the two groups.
In summary, factors such as plating density, culture density, and frequency of media replacement dramatically influence aromatase
activity in cultured human genital skin fibroblasts. Therefore, the interpretation of aromatase activity data obtained from
cultured cells in relation to physiologic or pathologic states should be viewed with appropriate caution.
The work was supported in part by grants R01 DK 35339 and R01 DK 00180 from the National Institutes of Health, Bethesda, MD,
and by RR 00035 from CLINFO Systems at the Johns Hopkins University School of Medicine, Baltimore, MD. 相似文献
50.
Philip W. Beesley Toni Paladino Irene Hill Claude Gravel Richard B. Hawkes James W. Gurd 《Journal of neurochemistry》1990,54(2):505-512
Glycoprotein gp50 is a neurone-specific, granule cell-enriched glycoprotein that is also a major component of isolated synaptic membranes. Here, we describe the use of a monoclonal antibody, mab SM gp50, to study the postnatal development of gp50 in the brain of normal and thyroid-deficient rats. Radioimmunoassay, enzyme-linked immunosorbent assay, and Western blotting show that gp50 is not detectable in brain until postnatal day 4 (P4) in both forebrain and cerebellum. In forebrain, the rate of increase of gp50 levels is maximal between P12 and P20. It is somewhat later in cerebellum, where peak levels are attained between P30 and P35. Immunocytochemical studies show little detectable gp50-like immunoreactivity before P16, and the staining is still weak, relative to adult tissue, at P25. The intense staining of the granule cell layer characteristic of adult cerebellum predominantly appears after P25. Development of gp50 is severely retarded in the cerebellum of thyroid-deficient rats, particularly during the second and third postnatal weeks. However, by the fourth postnatal week, gp50 levels in normal and hypothyroid animals are comparable. The results indicate that significant alterations in the pattern of gp50 expression continue to occur at a late stage of cerebellar development. In particular, the increase in immunocytochemical staining of the granule cells after P25 is striking in that by this time most major events associated with cerebellar development are essentially complete. 相似文献