全文获取类型
收费全文 | 627843篇 |
免费 | 63462篇 |
国内免费 | 894篇 |
专业分类
692199篇 |
出版年
2018年 | 6782篇 |
2017年 | 6409篇 |
2016年 | 8710篇 |
2015年 | 11005篇 |
2014年 | 13323篇 |
2013年 | 18357篇 |
2012年 | 21643篇 |
2011年 | 22491篇 |
2010年 | 15160篇 |
2009年 | 13666篇 |
2008年 | 19749篇 |
2007年 | 20422篇 |
2006年 | 19310篇 |
2005年 | 18246篇 |
2004年 | 18373篇 |
2003年 | 17329篇 |
2002年 | 16955篇 |
2001年 | 25916篇 |
2000年 | 25661篇 |
1999年 | 20296篇 |
1998年 | 7350篇 |
1997年 | 7224篇 |
1996年 | 6848篇 |
1995年 | 6477篇 |
1994年 | 6196篇 |
1993年 | 6155篇 |
1992年 | 16666篇 |
1991年 | 16797篇 |
1990年 | 16507篇 |
1989年 | 16034篇 |
1988年 | 14872篇 |
1987年 | 14075篇 |
1986年 | 13267篇 |
1985年 | 13232篇 |
1984年 | 10852篇 |
1983年 | 9310篇 |
1982年 | 6842篇 |
1981年 | 6073篇 |
1980年 | 5766篇 |
1979年 | 10133篇 |
1978年 | 8108篇 |
1977年 | 7289篇 |
1976年 | 6876篇 |
1975年 | 8073篇 |
1974年 | 8846篇 |
1973年 | 8614篇 |
1972年 | 7736篇 |
1971年 | 7201篇 |
1970年 | 6115篇 |
1969年 | 6028篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
61.
S-adenosyl-L-homocysteine (S-AH), a potent inhibitor of biological transmethylation, decreased the response of rat retina adenylate cyclase to dopamine and to 2-amino-6, 7-dihydroxytetrahydronaphtalene (ADTN). This effect appeared for 10?7M of S-adenosyl-L-homocysteine and was linear for concentration ranging to 10?4M. S-adenosyl-L-homocysteine did not decrease the cyclic AMP accumulation with sodium fluoride, a non specific adenylate cyclase activator. On the other hand, the incorporation of methyl group was reduced in rat retina homogenates by S-adenosyl-L-homocysteine. These findings suggest that the activity of the dopamine dependent adenylate cyclase is linked to a methylation process. 相似文献
62.
63.
Protein metal-binding sites. 总被引:2,自引:0,他引:2
Metal ions have a role in a variety of important functions in proteins including protein folding, assembly, stability, conformational change, and catalysis. The presence or absence of a given metal ion is crucial to the conformation or activity of over one third of all proteins. Recent developments have been made in the understanding and design of metal-binding sites in proteins, an important and rapidly advancing area of protein engineering. 相似文献
64.
Maleylated-BSA suppresses IFN-gamma-mediated Ia expression in murine peritoneal macrophages 总被引:1,自引:0,他引:1
T A Hamilton P V Gainey D O Adams 《Journal of immunology (Baltimore, Md. : 1950)》1987,138(12):4063-4068
Maleylated bovine serum albumin (maleyl-BSA) and other polyanionic polymers that are recognized by cell surface receptors on macrophages have been shown to induce chemotaxis, protease secretion, and tumoricidal function in this cell type. In this paper the effect of maleyl-BSA on Ia antigen expression has been evaluated. In a fashion similar to LPS, maleyl-BSA suppressed IFN-gamma-induced expression of Ia in a time- and dose-dependent manner. Also like LPS, maleyl-BSA stimulated the production and secretion of substantial amounts of PGE2 over a 24-hr period. This did not, however, appear to be the primary mechanism by which expression of Ia was suppressed, because co-treatment of the cells with indomethacin, which totally inhibited the production of PGE2, only minimally affected the suppressive activity. Surprisingly, the suppressive activity of both maleyl-BSA and LPS could be largely abrogated by co-treatment of the cells with cyclohexamide during the time period when Ia expression was sensitive to suppression. This effect was selective in that PGE2- or dibutyryl cyclic AMP-induced suppression of Ia expression was not affected by cyclohexamide treatment. The data support the concept that there are multiple molecular mechanisms involved in the negative regulation of IFN-gamma-induced Ia expression in macrophages. Such mechanisms may include, in addition to the synthesis of PGE2 and consequent elevation in intracellular levels of cyclic AMP, one or more proteins made early after treatment with either maleyl-BSA or LPS. Thus the function of some of these early gene products may be to regulate expression of functional genes such as that encoding Ia antigen. 相似文献
65.
V K Khugaeva E D Klimenko P N Aleksandrov G F Leskova M I Reutov 《Biulleten' eksperimental'no? biologii i meditsiny》1985,100(7):15-19
Experiments were made on rabbit fed an atherogenic diet (0.5 g/kg cholesterol) singly for 15 and 24 h and repeatedly for 3, 9 and 30 days. At early stages of lipid metabolism distress the interrelationship was established between blood rheological disorders and microcirculatory abnormalities. The dependence of the initial reaction of some rheological characteristics on their initial level was marked. 相似文献
66.
67.
68.
Puerto Rican populations of two species of sea anemones (Bunodosoma cavernata and B. granulifera) which had previously been considered one were assayed electrophoretically for enzymes encoded by 12 loci. The two species shared no common allozymes at 6 of the 12 loci. Genetic distance and identity values based on these allozymes were computed for the Puerto Rican populations and for B. cavernata from Florida and B. granulifera from Panama. The Puerto Rican populations of both species had much higher genetic identities for their geographically distant conspecifics than for each other. These results indicate that the two species are reproductively isolated and should be considered as separate valid species. Average heterozygosities are presented which are the first published for coelenterate species. 相似文献
69.
(+)-2,9 alpha-Dimethyl-5-(m-hydroxyphenyl)morphan is the only phenylmorphan analog whose affinity for opioid kappa-receptors is greater than its affinity for opioid mu-receptors. Pharmacologically, the compound is a pure opioid antagonist devoid of agonist activity in in vivo assays of antinociception. The absolute configuration of the compound has been determined to be (1R,5S,9R) from an X-ray crystallographic study of the chloride salt. Thus, the absolute configuration corresponds to that of the atypical opioid agonist (-)-phenylmorphan while the weak atypical agonist (-)-2,9 alpha-dimethyl-5-(m- hydroxyphenyl)morphan corresponds to the potent morphine-like (+)-phenylmorphan. The preferred orientations of the phenyl ring for the two stereoisomers were determined using the molecular mechanics program MM2-87 and found to vary from that of the two parent compounds. The atypical properties of the two 9 alpha-methyl analogs is consistent with an opioid ligand model which proposes that morphine-like properties require a particular range of phenyl orientations. There was good agreement between the structure obtained from X-ray crystallography and computed with the MM2-87 program. 相似文献
70.
Content of red blood-cell sialic acid in BW 35 blood donors. Relation to magnesium concentration and pyruvate kinase activity 总被引:1,自引:0,他引:1
Previous studies have shown that the concentration of red blood cell (RBC) magnesium is significantly lower in subjects carrying an HLA-BW 35 antigen (p less than 0.001) than in non-carriers. As this finding might be related to modifications of the RBC membrane sialoglycoconjugates, RBC sialic acid was comparatively determined in BW 35+ and BW 35- subjects. Pyruvate-kinase activity mean RBC volume, and reticulocyte count have also been determined in order to estimate whether some significant variations in the level of these age markers could be detected between the HLA BW 35+ and BW 35- subjects. A significant negative correlation between sialic acid and RBC magnesium concentrations was observed for the whole population tested (n 57, p less than 0.005), 61% of the BW 35+ and only 25% of the BW 35- individuals having sialic acid values above, and magnesium values below the overall mean (p less than 0.01). The variance of mean RBC volume was also larger for the BW 35+ group. Other determinations did not show any significant variations, suggesting that the results are not related to RBC age. 相似文献