全文获取类型
收费全文 | 5392篇 |
免费 | 454篇 |
国内免费 | 1篇 |
专业分类
5847篇 |
出版年
2023年 | 22篇 |
2022年 | 46篇 |
2021年 | 80篇 |
2020年 | 57篇 |
2019年 | 61篇 |
2018年 | 105篇 |
2017年 | 102篇 |
2016年 | 138篇 |
2015年 | 211篇 |
2014年 | 229篇 |
2013年 | 295篇 |
2012年 | 337篇 |
2011年 | 359篇 |
2010年 | 235篇 |
2009年 | 217篇 |
2008年 | 290篇 |
2007年 | 296篇 |
2006年 | 283篇 |
2005年 | 262篇 |
2004年 | 270篇 |
2003年 | 265篇 |
2002年 | 250篇 |
2001年 | 146篇 |
2000年 | 151篇 |
1999年 | 119篇 |
1998年 | 52篇 |
1997年 | 34篇 |
1996年 | 42篇 |
1995年 | 42篇 |
1994年 | 49篇 |
1993年 | 40篇 |
1992年 | 70篇 |
1991年 | 66篇 |
1990年 | 50篇 |
1989年 | 53篇 |
1988年 | 57篇 |
1987年 | 43篇 |
1986年 | 54篇 |
1985年 | 38篇 |
1984年 | 20篇 |
1983年 | 34篇 |
1982年 | 28篇 |
1981年 | 17篇 |
1980年 | 21篇 |
1979年 | 26篇 |
1978年 | 19篇 |
1977年 | 18篇 |
1975年 | 19篇 |
1974年 | 13篇 |
1969年 | 21篇 |
排序方式: 共有5847条查询结果,搜索用时 0 毫秒
11.
The polymerase chain reaction for Mycoplasma pulmonis 总被引:2,自引:0,他引:2
R Harasawa K Koshimizu T Uemori O Takeda K Asada I Kato 《Microbiology and immunology》1990,34(4):393-395
In vitro DNA amplification by polymerase chain reaction was examined to detect Mycoplasma pulmonis. A pair of synthetic oligonucleotide primers was constructed, and used to amplify a unique sequence of M. pulmonis DNA. Amplified products were detected by agarose gel electrophoresis and verified by blot hybridization with a synthetic oligonucleotide probe. This system detected cellular DNA of M. pulmonis but not M. arthritidis or M. neurolyticum, and thus appears to be useful for M. pulmonis diagnosis. 相似文献
12.
13.
Production of endothelin-1 from the mesenteric arteries of streptozotocin-induced diabetic rats 总被引:4,自引:0,他引:4
Release of endothelin-1 (ET-1) from the mesenteric arteries of Wistar rats with streptozotocin-induced diabetes (STZ-DM) rats and nondiabetic rats was measured by a specific enzyme immunoassay following purification using an immunoaffinity column. The mesenteric arteries from STZ-DM rats released a significantly higher amount of ET-1 as compared to control rats (35.8 +/- 2.8 vs 14.9 +/- 2.0 pg/1hr, p less than 0.05). The plasma level of ET-1 in STZ-DM rats was also elevated to a significant extent as compared to controls (5.1 +/- 0.4 vs 3.0 +/- 0.4 pg/ml, p less than 0.05). The systolic blood pressure of STZ-DM rats was significantly higher than of the controls (p less than 0.05). The increased level of plasma ET-1 as well as its release from the mesenteric artery of STZ-DM rats may suggest its release following damage to the endothelium caused by diabetes and/or by associated changes in blood pressure. 相似文献
14.
ATP:AMP phosphotransferase (EC 2.7.4.3) (adenylate kinase) has been purified 1746-fold from Mycobacterium marinum (ATCC 927) by successive column chromatography on DEAE-cellulose (DE-53), Reactive Blue agarose, Sephadex G-75, hydroxyapatite and, finally, DEAE-Sephadex A-50. The final enzyme preparation had a specific activity of 576 mumol/min per mg protein with an overall yield of 51%. The preparation was homogeneous by sodium dodecyl sulfate polyacrylamide gel electrophoresis. The enzyme was estimated to have an Mr of 29500 and an isoelectric point of 6.7, properties which generally resemble those of the mitochondrial enzyme. Indeed, the two enzymes failed to separate when subjected to polyacrylamide gel electrophoresis under denaturing conditions. The extinction coefficient (at 276 nm) was calculated to be 3.114 X 10(4) M-1 X cm-1 and E1%1cm = 10.556. Adenylate kinase was present at a concentration of 0.06 mg/g (wet weight) bacteria. Enzyme was stable for months in 60% glycerol in the freezer; at 4 degrees C, less than 5% of the activity was lost over a 7 day period. 相似文献
15.
Samples of human milk obtained from lactating women in the early postpartum period were assayed for oxytocin concentrations by specific RIA, following extraction procedures with Florisil. Mean oxytocin concentrations in human milk at postpartum day 1 to 5 were 4.5 +/- 1.1, 4.7 +/- 1.1, 4.0 +/- 1.3, 3.2 +/- 0.4, 3.3 +/- 0.6 microunits/ml (+/- SE), respectively. Oxytocin levels in milk were significantly increased by nursing (3.1 +/- 0.6, 5.3 +/- 1.0 microunits/ml, respectively). 3H-oxytocin in human milk was stable even after incubation at 37 degrees C for 2 hours. The dilution curve for milk was parallel to the curve for the standard oxytocin. The chromatographic fraction of immunoreactive oxytocin was identical to that of 3H-oxytocin. 3H-oxytocin was administered to lactating rats. Radioactivity in the neonatal gastric contents and plasma were 12.8% and 4.4% of the counts in the maternal plasma. It was made clear that oxytocin is stable in milk and that oxytocin in maternal blood can be transferred to mik and then to neonates. 相似文献
16.
Isolation, and catalytic and immunochemical properties of cathepsin D-like acid proteinase from rat erythrocytes 总被引:1,自引:0,他引:1
An erythrocyte membrane-associated cathepsin D-like acid proteinase, termed "EMAP," was purified to homogeneity from freshly collected rat blood in a yield of 60-65%. The molecular weight of the enzyme was determined to be 80,000-82,000 by Sephadex G-100 gel filtration. The enzyme was inhibited strongly by pepstatin and partially by HgCl2, Pb(NO3)2, and iodoacetic acid. The preferred substrate for the enzyme was hemoglobin. The enzyme also hydrolyzed serum albumin and casein, but to lesser extents, with an optimum pH of 3.5-4.0. However, it could not hydrolyze leucyl-2-naphthylamide, benzyloxycarbonyl-Phe-Arg-4-methyl-7-coumarylamide or other synthetic substrates at pH values ranging from 3.5 to 9.5. The enzyme was very similar to human EMAP in a number of enzymatic properties, whereas it differed from rat cathepsin D in several respects, such as pH stability, molecular weight, isoelectric point, and chromatographic properties. Immunologically, the enzyme cross-reacted with the rabbit antibody prepared against human EMAP. The patterns of immunoelectrophoresis, immunoblotting, and immunoprecipitation of the enzyme were remarkably similar, if not identical, to those of human EMAP. In contrast, rat EMAP showed no reaction with the rabbit antibody raised to rat spleen cathepsin D. These results indicate that EMAP is a unique cathepsin D-like acid proteinase different from ordinary cathepsin D. 相似文献
17.
Bile acid metabolism in partially hepatectomized rats 总被引:2,自引:0,他引:2
The bile flow and the bile acid secretion, calculated on liver weight basis, increased 12 H and 24 H after 60-70% hepatectomy and returned to the initial levels thereafter. The biliary phospholipid secretion much more increased than bile acids, but the cholesterol secretion decreased. Bile acid composition changed with an increase of the cholic acid group and a decrease of the chenodeoxycholic acid group in both bile and feces. These changes almost disappeared on Day 14. The pool size of bile acid decreased maximally on Day 4 to about 40% of the initial, but the distribution of bile acids in the enterohepatic circulation was not changed. The fecal cholesterol and coprostanol markedly decreased on Day 2 but gradually returned to the initial levels according to the recovery of diet intake. The fecal bile acids decreased on Day 2, increased on Day 4, and returned to the normal range after Day 7. In conclusion, the regenerating liver secretes more bile, bile acids and phospholipids, and less cholesterol than the normal liver. Cholic acid predominates in the bile acids. These changes restored to the initial levels by about one week after the operation. 相似文献
18.
19.
20.
Isolation of virus causing hemorrhagic fever with renal syndrome (HFRS) through a cell culture system 总被引:4,自引:0,他引:4
T Kitamura C Morita T Komatsu K Sugiyama J Arikawa S Shiga H Takeda Y Akao K Imaizumi A Oya N Hashimoto S Urasawa 《Japanese journal of medical science & biology》1983,36(1):17-25
Twenty-three rat lung specimens collected in outbreaks of hemorrhagic fever with renal syndrome (HFRS) in three medical institutions were inoculated onto the VERO-E6 cell monolayers. After several blind passages, an agent growing serially in the cell cultures and reacting specifically with known HFRS-positive sera was isolated from two of these specimens. The two isolates were antigenically identical each other. The agent, named strain SR-11, was identified as the causative virus of HFRS by its antigenic identity with E6 cell-adapted HFRS virus, Hantaan 76-118 strain, and the specific reactions with sera from various HFRS cases. 相似文献