全文获取类型
收费全文 | 517篇 |
免费 | 40篇 |
国内免费 | 1篇 |
专业分类
558篇 |
出版年
2023年 | 4篇 |
2021年 | 17篇 |
2020年 | 6篇 |
2019年 | 3篇 |
2018年 | 9篇 |
2017年 | 14篇 |
2016年 | 17篇 |
2015年 | 18篇 |
2014年 | 24篇 |
2013年 | 28篇 |
2012年 | 27篇 |
2011年 | 29篇 |
2010年 | 20篇 |
2009年 | 22篇 |
2008年 | 23篇 |
2007年 | 24篇 |
2006年 | 22篇 |
2005年 | 19篇 |
2004年 | 15篇 |
2003年 | 14篇 |
2002年 | 15篇 |
2001年 | 12篇 |
2000年 | 21篇 |
1999年 | 14篇 |
1998年 | 5篇 |
1997年 | 6篇 |
1995年 | 5篇 |
1994年 | 5篇 |
1992年 | 7篇 |
1991年 | 5篇 |
1990年 | 3篇 |
1989年 | 3篇 |
1988年 | 5篇 |
1987年 | 5篇 |
1986年 | 4篇 |
1985年 | 4篇 |
1984年 | 6篇 |
1983年 | 6篇 |
1982年 | 5篇 |
1981年 | 3篇 |
1980年 | 4篇 |
1979年 | 5篇 |
1978年 | 6篇 |
1974年 | 4篇 |
1973年 | 5篇 |
1972年 | 5篇 |
1971年 | 4篇 |
1969年 | 4篇 |
1968年 | 6篇 |
1965年 | 3篇 |
排序方式: 共有558条查询结果,搜索用时 15 毫秒
1.
2.
3.
Methyl mercury uptake in free cells and different immobilizates of the cyanobacteriumNostoc calcicola has been examined. The general growth of the immobilized cyanobacterial cells could be negatively correlated with methyl mercury uptake. Alginate spheres proved most efficient in terms of uptake rate (0.48 nmol mg protein–1 min–1, 10 min) and total bioaccumulation (10.71 nmol mg protein–1, 1 h) with a bioconcentration factor of 3.3×103. Alginate biofilms showed a faster methyl mercury accumulation rate (0.83 nmol mg protein–1 min–1, 10 min) with a saturation of 10.28 nmol mg protein–1 reached within only 30 min (bioconcentration factor, 3.1×103). Foam preparations with a slow initial uptake approximated biofilms but were characterized by a lower bioconcentration factor (2.8×103). Free cells, in comparison, maintained the initial slow rate of uptake (0.62 nmol mg protein–1 min–1, 10 min), saturating at 30 min (8.81 nmol mg protein–1), and the resultant lowest bioconcentration factor (2.7×103). Cell ageing (30 days) brought a drastic reduction (3-fold) in organomercury uptake by free cells while alginate spheres maintained the same potential. Foam preparations of the same age showed a significant improvement in methyl mercury uptake followed by only a marginal decline in alginate biofilms. Data are discussed in the light of the physiological efficiency and longevity of immobilized cells. 相似文献
4.
Thirty-six cases of solitary and scintigraphically "cold" thyroid nodules were studied by fine needle aspiration (FNA) cytology, ultrasonography, radionuclide perfusion study (RPS) and xeroradiography with the aim of differentiating the neoplastic from the nonneoplastic nodules. Histologic study of the excised specimens provided the definitive diagnosis in all cases. Of the techniques used in this study, FNA cytology and RPS had the highest sensitivities and specificities. Ultrasonography and xeroradiography were of limited use due to their low sensitivity rates. 相似文献
5.
Summary The susceptibility of 50 drug resistant strains of Escherichia coli of human gut was determined against ciprofloxacin, acridine orange (AO) and sodium dodecyl sulphate (SDS). Curing efficacy of these agents were worked out at subminimal inhibitory concentrations. Ciprofloaxacin was found a better curing agent for E coli R-plasmids, eliminating R-factors from 48% of the strains followed by SDS and AO which eliminated 24% and 20% of the drug resistance determinants, respectively. Elimination of R-plasmids was found dependent on the concentrations of curing agents and nature of R-plasmids. 相似文献
6.
7.
Glycollic acid, supplied at a concentration of 1 mg l?1, increased the relative growth rate of Skeletonema costatum (Grev.) Cleve growing in bacterized culture at limiting light intensities. There was little or no such effect at intensities approaching saturation. The presence in the medium of alumina, an adsorbent for glycollate, prolonged the lag phase, the cells remaining viable for up to 5 days. Uptake of glycollate was not appreciably affected by the bicarbonate concentration of the medium. After 3 h, 80–92% of the glycollate carbon assimilated was found in the alcohol and benzene insoluble fraction of the cells. This is in agreement with the supposition that glycollate carbon is as-similated directly by the diatom rather than after degradation by bacteria to carbon dioxide. 相似文献
8.
miR-497 and miR-302b regulate ethanol-induced neuronal cell death through BCL2 protein and cyclin D2 总被引:1,自引:0,他引:1
Yadav S Pandey A Shukla A Talwelkar SS Kumar A Pant AB Parmar D 《The Journal of biological chemistry》2011,286(43):37347-37357
In chronic alcoholism, brain shrinkage and cognitive defects because of neuronal death are well established, although the sequence of molecular events has not been fully explored yet. We explored the role of microRNAs (miRNAs) in ethanol-induced apoptosis of neuronal cells. Ethanol-sensitive miRNAs in SH-SY5Y, a human neuroblastoma cell line, were identified using real-time PCR-based TaqMan low-density arrays. Long-term exposure to ethanol (0.5% v/v for 72 h) produced a maximum increase in expression of miR-497 (474-fold) and miR-302b (322-fold). Similar to SH-SY5Y, long-term exposure to ethanol induced miR-497 and miR-302b in IMR-32, another human neuroblastoma cell line. Using in silico approaches, BCL2 and cyclin D2 (CCND2) were identified as probable target genes of these miRNAs. Cotransfection studies with 3'-UTR of these genes and miRNA mimics have demonstrated that BCL2 is a direct target of miR-497 and that CCND2 is regulated negatively by either miR-302b or miR-497. Overexpression of either miR-497 or miR-302b reduced expression of their identified target genes and increased caspase 3-mediated apoptosis of SH-SY5Y cells. However, overexpression of only miR-497 increased reactive oxygen species formation, disrupted mitochondrial membrane potential, and induced cytochrome c release (mitochondria-related events of apoptosis). Moreover, ethanol induced changes in miRNAs, and their target genes were substantially prevented by pre-exposure to GSK-3B inhibitors. In conclusion, our studies have shown that ethanol-induced neuronal apoptosis follows both the mitochondria-mediated (miR-497- and BCL2-mediated) and non-mitochondria-mediated (miR-302b- and CCND2-mediated) pathway. 相似文献
9.
Calcium-Dependent 4-aminopyridine stimulation of protein phosphorylation in squid optic lobe synaptosomes 总被引:1,自引:0,他引:1
Harish C. Pant Paul E. Gallant Rochelle Cohen Joseph T. Neary Harold Gainer 《Cellular and molecular neurobiology》1983,3(3):223-238
When intact synaptosomes were incubated with [gamma-32P]ATP, maximal protein phosphorylation was attained 2 min after the start of incubation. Protein phosphorylation under basal conditions was dependent on external Ca2+, and the dominant peak of phosphorylation was a 50-kd protein. Incubation of intact synaptosomes in the presence of 3-6 mM 4-aminopyridine (4-AP) caused a markedly enhanced phosphorylation of high molecular weight proteins of 90, 100, 130, and 180 kd, with no increase in the 50 or 38 kd proteins. This effect of 4-AP was dependent on external calcium ions in the incubation medium. The 4-AP effect on the high molecular weight proteins was also found in synaptosomal plasma membranes isolated from the synaptosomes. Tetraethylammonium (TEA) ions did not produce this enhancement of phosphorylation. 相似文献
10.