全文获取类型
收费全文 | 6991篇 |
免费 | 846篇 |
国内免费 | 6篇 |
出版年
2021年 | 70篇 |
2020年 | 45篇 |
2019年 | 73篇 |
2018年 | 76篇 |
2017年 | 77篇 |
2016年 | 97篇 |
2015年 | 230篇 |
2014年 | 176篇 |
2013年 | 281篇 |
2012年 | 398篇 |
2011年 | 392篇 |
2010年 | 230篇 |
2009年 | 229篇 |
2008年 | 282篇 |
2007年 | 300篇 |
2006年 | 343篇 |
2005年 | 279篇 |
2004年 | 314篇 |
2003年 | 312篇 |
2002年 | 271篇 |
2001年 | 127篇 |
2000年 | 112篇 |
1999年 | 119篇 |
1998年 | 99篇 |
1997年 | 86篇 |
1996年 | 73篇 |
1995年 | 68篇 |
1994年 | 71篇 |
1993年 | 57篇 |
1992年 | 107篇 |
1991年 | 88篇 |
1990年 | 90篇 |
1989年 | 77篇 |
1988年 | 88篇 |
1987年 | 69篇 |
1986年 | 82篇 |
1985年 | 70篇 |
1984年 | 80篇 |
1983年 | 63篇 |
1982年 | 92篇 |
1981年 | 86篇 |
1980年 | 78篇 |
1979年 | 84篇 |
1978年 | 54篇 |
1977年 | 79篇 |
1976年 | 65篇 |
1975年 | 62篇 |
1974年 | 68篇 |
1973年 | 64篇 |
1969年 | 46篇 |
排序方式: 共有7843条查询结果,搜索用时 31 毫秒
21.
Structure of the tetragonal surface virulence array protein and gene of Aeromonas salmonicida 总被引:17,自引:0,他引:17
S Chu S Cavaignac J Feutrier B M Phipps M Kostrzynska W W Kay T J Trust 《The Journal of biological chemistry》1991,266(23):15258-15265
The paracrystalline surface protein array of the pathogenic bacterium Aeromonas salmonicida is a primary virulence factor with novel binding capabilities. The species-specific structural gene (vapA) for this array protein (A-protein) was cloned into lambda gt11 but was unstable when expressed in Escherichia coli, undergoing an 816-base pair deletion due to a 21-base pair direct repeat within the gene. However, the gene was stable in cosmid pLA2917 as long as expression was poor. A-protein was located in the cytoplasmic, inner membrane and periplasmic fractions in E. coli. The DNA sequence revealed a 1,506-base pair open reading frame encoding a protein consisting of a 21-amino acid signal peptide, and a 481-residue 50,778 molecular weight protein containing considerable secondary structure. When assembled into a paracrystalline protein array on Aeromonas the cell surface A-protein was totally refractile to cleavage by trypsin, but became trypsin sensitive when disassembled. Trypsin cleavage of the isolated protein provided evidence that both the NH2- and COOH-terminal regions form distinct structural domains, consistent with three-dimensional ultrastructural evidence. The NH2-terminal 274-residue domain remained refractile to trypsin activity. This segment connects by a trypsin and CNBr-sensitive 78-residue linker region to a COOH-terminal 129-residue fragment which could apparently refold into a partially trypsin-resistant structure after cleavage at residue 323. 相似文献
22.
23.
24.
25.
26.
27.
28.
King Frederick D.; Cucci Terry L.; Townsend David W. 《Journal of plankton research》1987,9(2):277-289
Ammonium regeneration by micro- (35153 µm) andmacrozooplankton (> 153 µm) was determined in the Gulfof Maine by measuring the activity of the excretory enzyme glutamatedehydrogenase (GDH) in various size fractions. GDH maxima weregenerally observed to correspond to the depth of the chlorophyllmaximum as previously reported in the Gulf of Mexico and inthe vicinity of the Nantucket Shoals. GDH activity of the microzooplanktonwas considerably lower than the macrazooplankton, suggestingthe microzooplankton made only a minor contribution (111%) to the total ammonium regenerated. These results were confirmedby biomass estimates made from counts of individual species.Ammonium excretion by both zooplankton fractions was estimatedto supply 531 % of the nitrogen requirements for primaryproduction, with an estimated 5963% supplied by the verticaltransport of nitrate (new nitrogen) into the euphoric zone. 相似文献
29.
L P Solomonson M J McCreery C J Kay M J Barber 《The Journal of biological chemistry》1987,262(18):8934-8939
Recently we demonstrated that target sizes for the partial activities of nitrate reductase were considerably smaller than the 100-kDa subunit which corresponded to the target size of the full (physiologic) activity NADH:nitrate reductase. These results suggested that the partial activities resided on functionally independent domains and that radiation inactivation may be due to localized rather than extensive damage to protein structure. The present study extends these observations and addresses several associated questions. Monophasic plots were observed over a wide range of radiation doses, suggesting a single activity component in each case. No apparent differences were observed over a 10-fold range of concentration for each substrate, suggesting that the observed slopes were not due to marked changes in Km values. Apparent target sizes estimated for partial activities associated with native enzyme and with limited proteolysis products of native enzyme suggested that the functional size obtained by radiation inactivation analysis is independent of the size of the polypeptide chain. The presence of free radical scavengers during irradiation reduced the apparent target size of both the physiologic and partial activities by an amount ranging from 24 to 43%, suggesting that a free radical mechanism is at least partially responsible for the inactivation. Immunoblot analysis of nitrate reductase irradiated in the presence of free radical scavengers revealed formation of distinct bands at 90, 75, and 40 kDa with increasing doses of irradiation rather than complete destruction of the polypeptide chain. 相似文献
30.
L E Kay J M Pascone B D Sykes J W Shriver 《The Journal of biological chemistry》1987,262(5):1984-1988
An 19F NMR probe has been attached to the reactive sulfhydryl SH1 of the globular heads of rabbit skeletal heavy meromyosin. It serves as a sensitive monitor of the conformational state of the heads of heavy meromyosin in a manner similar to that seen for subfragment-1 (Shriver, J.W., and Sykes, B.D. (1982) Biochemistry 21, 3022-3028; Tollemar, U., Cunningham, K., and Shriver, J.W. (1986) Biochim. Biophys. Acta 873, 243-251). The NMR spectra indicate that there are at least two states for the heads in the SH1 region. The energetics of the interconversion of the two states of heavy meromyosin (HMM) differs significantly from that of S-1. In HMM in the absence of divalent cations, there are two reversible paths between the low temperature and high temperature states with a hysteresis-like behavior. One path is consistent with the head groups behaving independently and similar to S-1 alone. The second path indicates a coupling of the globular head region observed in S-1 with a second region forming a distinctly different cooperative unit. Upon addition of Ca(II) the hysteresis effect is lost and only the second cooperative unit is observed. Two explanations are offered for these results: the globular heads in HMM may couple with the S-2 segment, or the two globular heads of HMM may couple to form a larger cooperative unit. The ability to stabilize the larger cooperative unit with a divalent metal ion implicates a role for the LC2 light chain in coupling regions of the myosin molecule. 相似文献