全文获取类型
收费全文 | 95157篇 |
免费 | 148374篇 |
国内免费 | 40317篇 |
出版年
2021年 | 2463篇 |
2020年 | 2543篇 |
2019年 | 4177篇 |
2018年 | 3138篇 |
2017年 | 2968篇 |
2016年 | 3128篇 |
2015年 | 3847篇 |
2014年 | 4753篇 |
2013年 | 4274篇 |
2012年 | 5681篇 |
2011年 | 6130篇 |
2010年 | 7271篇 |
2009年 | 12515篇 |
2008年 | 6658篇 |
2007年 | 6319篇 |
2006年 | 5439篇 |
2005年 | 4894篇 |
2004年 | 4222篇 |
2003年 | 3493篇 |
2002年 | 4183篇 |
2001年 | 5295篇 |
2000年 | 3037篇 |
1999年 | 7268篇 |
1998年 | 9141篇 |
1997年 | 9203篇 |
1996年 | 8583篇 |
1995年 | 8825篇 |
1994年 | 8221篇 |
1993年 | 7868篇 |
1992年 | 7792篇 |
1991年 | 7828篇 |
1990年 | 8645篇 |
1989年 | 7911篇 |
1988年 | 7196篇 |
1987年 | 6278篇 |
1986年 | 5811篇 |
1985年 | 5256篇 |
1984年 | 4050篇 |
1983年 | 3268篇 |
1982年 | 3604篇 |
1981年 | 3234篇 |
1980年 | 3155篇 |
1979年 | 3247篇 |
1978年 | 2967篇 |
1977年 | 2897篇 |
1976年 | 2722篇 |
1974年 | 2459篇 |
1973年 | 2464篇 |
1972年 | 2811篇 |
1971年 | 2590篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
1.
2.
Imaging in five dimensions: time-dependent membrane potentials in individual mitochondria. 总被引:13,自引:2,他引:11
Because of its importance in the chemiosmotic theory, mitochondrial membrane potential has been the object of many investigations. Significantly, however, quantitative data on how energy transduction might be regulated or perturbed by the physiological state of the cell has only been gathered via indirect studies on isolated mitochondrial suspensions; quantitative studies on individual mitochondria in situ have not been possible because of their small size, their intrinsic motility, and the absence of appropriate analytical reagents. In this article, we combine techniques for rapid, high resolution, quantitative three-dimensional imaging microscopy and mathematical modeling to determine accurate distributions of a potentiometric fluorescent probe between the cytosol and individual mitochondria inside a living cell. Analysis of this distribution via the Nernst equation permits assignment of potentials to each of the imaged mitochondrial membranes. The mitochondrial membrane potentials are distributed over a narrow range centered at -150 mV within the neurites of differentiated neuroblastoma cells. We find that the membrane potential of a single mitochondrion is generally remarkably stable over times of 40-80 s, but significant fluctuations can occasionally be seen. The motility of individual mitochondria is not directly correlated to membrane potential, but mitochondria do become immobile after prolonged treatment with respiratory inhibitors or uncouplers. Thus, three spatial dimensions, a key physiological parameter, and their changes over time are all quantitated for objects at the resolution limit of light microscopy. The methods described may be readily extended to permit investigations of how mitochondrial function is integrated with other processes in the intact cell. 相似文献
3.
4.
E. Smyk-Randall O. R. Brown A. Wilke A. Eisenstark D. H. Flint 《Free radical biology & medicine》1993,14(6):609-613
The effects of near ultraviolet (NUV) light on a NUV chromophore-containing oxidant-sensitive enzyme, dihydroxyacid dehydratase (DHAD), were measured in seven strains of Escherichia coli. The strains differed in production of the oxidant-defense enzymes, superoxide dismutases (Fe-SOD and Mn-SOD), and catalases HPI and HPII. With the stress of aerobic growth but without NUV exposure, the strains lacking either Fe or Mn SOD or both SODs had 57%, 25%, and 12%, respectively, of the DHAD-specific activity of the parent (K12) strain. Under the same conditions, the catalase strains that were wild type, overproducing, and deficient had comparable DHAD-specific activities. When aerobic cultures were exposed for 30 min to NUV with a fluence of 216 J/m2/s at 310–400 nm, the percentage decreases in DHAD-specific activities were similar (ranging from 75% to 89%) in strains with none, either, or both SODs missing, and in the catalase-overproducing strain. However, the decreases were only 58% and 52% in the strain with catalase missing and in its parent, respectively. The NUV-induced loss of DHAD enzyme activity was not accompanied by any detectable loss of the DHAD protein as measured by polyclonal antibody to DHAD. 相似文献
5.
The ADP/ATP carrier is the 32-kilodalton receptor for an NH2-terminally myristylated src peptide but not for pp60src polypeptide. 总被引:2,自引:0,他引:2 下载免费PDF全文
Membrane binding of pp60src is initiated via its myristylated NH2 terminus. To identify a candidate pp60src docking protein or receptor in the membrane, a radiolabelled peptide corresponding to the pp60src NH2-terminal membrane binding domain was cross-linked to fibroblast membranes and found to specifically label a 32-kDa protein. This protein was purified by appending an affinity tag to the peptide probe so that the cross-linked complex could be isolated via affinity chromatography. Microsequencing indicated that the 32-kDa protein was the mitochondrial ADP/ATP carrier (AAC). This result was further confirmed by the ability of an antibody to the AAC to immunoprecipitate the cross-linked complex, by the ability of certain inhibitors of the AAC to block cross-linking, and by membrane fractionation to show that complex formation occurred essentially exclusively in the mitochondrial fraction. While the AAC bound the myristyl-src peptide in a specific manner both in vitro and in vivo, its localization to the inner membrane of the mitochondrion precludes its being a pp60src binding protein. An analysis of pp60v-src binding in vitro was consistent with this expectation. Thus, use of a myristyl-src peptide revealed an unexpected and previously unidentified binding capacity of the AAC, most likely related to the ability of long-chain fatty acyl coenzyme As to serve as AAC inhibitors. The amphipathic nature of the pp60src NH2 terminus suggests alternative strategies for uncovering pp60src membrane binding species. 相似文献
6.
7.
Regulation of Escherichia coli secA mRNA translation by a secretion-responsive element. 总被引:6,自引:2,他引:4 下载免费PDF全文
The Escherichia coli secA gene, whose translation is responsive to the proficiency of protein export within the cell, is the second gene in a three-gene operon and is flanked by gene X and mutT. By using gene fusion and oligonucleotide-directed mutagenesis techniques, we have localized this translationally regulated site to a region at the end of gene X and the beginning of secA. This region has been shown to bind SecA protein in vitro. These studies open the way for a direct investigation of the mechanism of secA regulation and its coupling to the protein secretion capability of the cell. 相似文献
8.
Maternal serum alpha-fetoprotein screening activities of state health agencies: a survey. 总被引:5,自引:5,他引:0 下载免费PDF全文
Maternal serum alpha-fetoprotein (MSAFP) screening has been demonstrated to be cost-effective on a population basis and is becoming standard practice. The American Society of Human Genetics has twice published policy statements to define the essential elements of a quality screening program. The present study reviewed the impact of these policy statements on state public-health agencies with respect to regulation or provision of MSAFP screening in their jurisdictions. With a few exceptions, states have not elected to play a major role in provision or regulation of this test. There is need to address issues of funding, standards, and data collection in a collaborative effort, if policy statements on genetic services are to be translated into effective state population screening. 相似文献
9.
10.