全文获取类型
收费全文 | 57649篇 |
免费 | 4617篇 |
国内免费 | 4452篇 |
出版年
2024年 | 100篇 |
2023年 | 692篇 |
2022年 | 1660篇 |
2021年 | 3032篇 |
2020年 | 2077篇 |
2019年 | 2507篇 |
2018年 | 2348篇 |
2017年 | 1812篇 |
2016年 | 2553篇 |
2015年 | 3632篇 |
2014年 | 4391篇 |
2013年 | 4442篇 |
2012年 | 5297篇 |
2011年 | 4772篇 |
2010年 | 2891篇 |
2009年 | 2600篇 |
2008年 | 2944篇 |
2007年 | 2641篇 |
2006年 | 2267篇 |
2005年 | 1891篇 |
2004年 | 1513篇 |
2003年 | 1420篇 |
2002年 | 1075篇 |
2001年 | 909篇 |
2000年 | 889篇 |
1999年 | 810篇 |
1998年 | 501篇 |
1997年 | 454篇 |
1996年 | 479篇 |
1995年 | 422篇 |
1994年 | 414篇 |
1993年 | 326篇 |
1992年 | 446篇 |
1991年 | 324篇 |
1990年 | 284篇 |
1989年 | 260篇 |
1988年 | 210篇 |
1987年 | 194篇 |
1986年 | 176篇 |
1985年 | 154篇 |
1984年 | 115篇 |
1983年 | 122篇 |
1982年 | 81篇 |
1981年 | 45篇 |
1980年 | 51篇 |
1979年 | 63篇 |
1976年 | 46篇 |
1974年 | 54篇 |
1973年 | 45篇 |
1972年 | 53篇 |
排序方式: 共有10000条查询结果,搜索用时 140 毫秒
291.
证候空间和方剂空间的数学结构 总被引:2,自引:0,他引:2
本文考察了中医理、法、方、药原理,给出了证候空间和方剂空间的数学结构,以利于中医现代化和中医临床中应用电子计算机诊疗技术。 相似文献
292.
293.
经N-乙酰氨基葡萄糖交联琼脂糖亲和层析及以交联琼脂糖介质的高效液相分子筛层析,从中国鲎细胞溶解物中分离纯化了一种凝集素,其活性比原料鲎试剂提高128倍。鲎凝集素SDS电泳时表现出分子量为69000,和72000的二个亚基。N-乙酰氨基葡萄糖、D-半乳糖,D-甘露糖及岩藻糖等对鲎凝集素凝集鸡红细胞的活性有显著抑制作用,加热60℃,10分钟可使凝集素活性基本丧失。CaCl_2为凝集素活性所必需。鲎凝集素与肺炎球菌C多糖有沉淀反应。 相似文献
294.
本文研究了不同底物(N_2,H_2,N_2O,NaN_3,C_2H_2)对棕色固氮菌固氮酶及其钼铁蛋白荧光光谱的影响。结果表明,上述底物均能络合在钼铁蛋白及固氮酶上,但络合程度不同,从而为固氮酶系统有多个不同的底物络合中心,底物络合中心在钼铁蛋白分子上,铁蛋白对钼铁蛋白有变构作用,提供了光谱学证据。 相似文献
295.
296.
297.
An effort to identify the major general esterases of rat liver cytosol that are insensitive to the serine esterase inhibitor paraoxon (diethyl 4-nitrophenyl phosphate) has led to the isolation of a dozen enzymes. Four of these are electrophoretically homogeneous. Although purified on the basis of their hydrolytic activity toward 4-nitrophenyl acetate, each of the enzymes has a very broad and overlapping substrate specificity for aromatic esters. Thiol esters serve as substrates but, within the limits of the methods used, amides are not hydrolyzed. 相似文献
298.
Protein kinase FA (an activating factor of ATP·Mg-dependent protein phosphatase) has been characterized to exist in two forms in the purified brain myelin. One form of kinase FA is spontaneously active and trypsin-labile, whereas the other form of kinase FA is inactive and trypsin-resistant, suggesting a different membrane topography with active FA exposed on the outer face of the myelin membrane and inactivu FQ buried within the myelin membrane. When myelin was solubilized in 1% Triton X-100, all kinase FA became active and trypsin-labile. Phospholipid reconstitution studies further indicated that when kinase FA was reconstituted in acidic phospholipids, such as phosphatidylinositol and phosphatidylserine, the enzyme activity was inhibited in a dose-dependent manner, suggesting that kinase FA interacts with acidic phospholipids which inhibit its activity. Furthermore, when myelin was incubated with exogenous phospholipase C, the inactive/trypsin-resistant FA could be converted to the active/trypsin-labile FA in a time- and dose-dependent manner. Taken together, it is concluded that membrane phospholipids play an important role in modulating the activity of kinase FA in the brain myelin. It is suggested that phospholipase C may mediate the activation-sequestration of inactive/trypsin-resistant kinase FA in the brain myelin through the phospholipase C-katalyzed degradation of acidic membrane phospholipids. The activation-sequestration of protein Kinase FA may represent one mode of control modulating the activity of kinase FA in the central nervous system myelin. 相似文献
299.
杨扬 《分子细胞生物学报》1990,(3)
本文报道了一组新的核仁组织者区蛋白(ANOP)。这些蛋白由三种多肽组成,分子量分别为65,76和78KD。它们集中分布在核纤丝中心周围的高密度纤维组分中。研究表明ANOP广泛地分布于各种脊椎动物细胞中,有较强的抗原保守性。但在两栖类的红细胞和原肠期以前的早期胚胎细胞中则缺乏此种抗原。而在原肠形成过程中,ANOP开始出现并逐渐增加,表明ANOP可能与rRNA基因的活性有关。 相似文献
300.
Role of viral antigens in destructive cellular immune responses to adenovirus vector-transduced cells in mouse lungs. 总被引:8,自引:3,他引:5 下载免费PDF全文
Adenoviruses missing E1 have been used as gene delivery vectors to the lungs for the treatment of cystic fibrosis. Transient expression of the recombinant gene and the development of inflammation have been two major limitations to the application of first-generation recombinant adenoviruses for gene therapy. Studies with mouse models of liver- and lung-directed gene therapy suggested that CD8+ cytotoxic T lymphocytes (CTLs) are effectors that contribute to extinction of transgene expression. The precise antigens responsible for activation of CTLs have not been identified. In this study, we examine the relative contributions of viral proteins versus the transgene product to the activation of CTLs which eliminate transgene-containing cells in mouse lungs. Instillation of a lacZ-expressing virus into the lungs of C57BL/6 mice elicited CTL responses to both viral proteins and the transgene product, beta-galactosidase, which collectively contribute to loss of trans-gene expression in mouse airways. Similar results were obtained in two experimental models in which the animals should be tolerant to the transgene, i.e., lacZ virus delivered to an animal transgenic for lacZ and a virus expressing the liver-specific enzyme ornithine transcarbamylase administered to the lungs of various strains of immune-competent mice. These data confirm the hypothesis that CTLs specific for viral antigens contribute to the problem of transgene instability in mouse lungs and indicate that CTLs specific for transgene product alone cannot account for the observed problem. 相似文献