全文获取类型
收费全文 | 3053篇 |
免费 | 373篇 |
国内免费 | 11篇 |
专业分类
3437篇 |
出版年
2022年 | 24篇 |
2021年 | 48篇 |
2019年 | 25篇 |
2018年 | 37篇 |
2017年 | 30篇 |
2016年 | 73篇 |
2015年 | 126篇 |
2014年 | 117篇 |
2013年 | 133篇 |
2012年 | 155篇 |
2011年 | 146篇 |
2010年 | 100篇 |
2009年 | 79篇 |
2008年 | 126篇 |
2007年 | 122篇 |
2006年 | 111篇 |
2005年 | 128篇 |
2004年 | 100篇 |
2003年 | 91篇 |
2002年 | 103篇 |
2001年 | 102篇 |
2000年 | 89篇 |
1999年 | 90篇 |
1998年 | 47篇 |
1997年 | 42篇 |
1996年 | 42篇 |
1995年 | 30篇 |
1994年 | 31篇 |
1993年 | 59篇 |
1992年 | 66篇 |
1991年 | 66篇 |
1990年 | 98篇 |
1989年 | 79篇 |
1988年 | 75篇 |
1987年 | 62篇 |
1986年 | 55篇 |
1985年 | 48篇 |
1984年 | 38篇 |
1983年 | 40篇 |
1982年 | 28篇 |
1981年 | 19篇 |
1980年 | 20篇 |
1979年 | 34篇 |
1978年 | 42篇 |
1977年 | 37篇 |
1976年 | 30篇 |
1975年 | 22篇 |
1974年 | 22篇 |
1973年 | 20篇 |
1971年 | 17篇 |
排序方式: 共有3437条查询结果,搜索用时 0 毫秒
991.
992.
J J Sullivan E E Muchnicky B E Davidson G R Jago 《Australian journal of biological sciences》1977,30(6):543-552
Pyrrolidonecarboxylate peptidase (EC 3.4.11.8) from Streptococcus faecium was purified by fractionation with streptomycin sulphate and ammonium sulphate, by chromatography on Sephadex G200 and DEAE-cellulose, and by preparative electrophoresis on Sephadex G25. The purified enzyme on acrylamide gel showed a strong protein band which contained enzyme activity and a very faint band which had no activity. The subunit molecular weight of the purified enzyme was estimated by acrylamide gel electrophoresis in sodium dodecyl sulphate to be 42,000 +/- 1,000. The enzyme showed optimum activity at pH 7.6 and was unstable in the absence of 2-mercaptoethanol. The sensitivity of the enzyme to alkylating agents (N-ethylmaleimide and iodoacetamide) suggested that free sulphydryl groups were essential for enzyme activity. The enzyme was rapidly inactivated above 45 degrees C. The values of the Michaelis constants (Km) obtained with various L-pyrrolidonecarboxylyl dipeptides were similar although there was a 10-fold range in the maximal rates of hydrolysis of these substrates. Inhibition studies showed that the substrate analogues 2-pyrrolidone and pyrrolidonecarboxylate are competitive inhibitors of the enzyme. The binding of substrates and inhibitors to the active site of the enzyme is discussed. 相似文献
993.
994.
W P Sullivan B J Madden D J McCormick D O Toft 《The Journal of biological chemistry》1988,263(29):14717-14723
Progesterone receptors are phosphoproteins, in which phosphorylation has been proposed as a control mechanism for some stages of hormone action. Progesterone administration was shown to increase phosphorylation of the receptor from both cytosol and nuclear extracts of whole cells. We have analyzed the receptor phosphopeptides generated by chemical and proteolytic cleavage to assess the number of phosphorylation sites and their approximate location in the receptor. Progesterone receptor was labeled in situ in the presence or absence of hormone in medium containing [32P] orthophosphate, isolated by immunoprecipitation, and then digested with several proteases. The resulting 32P-labeled peptides were resolved by either two-dimensional electrophoresis:chromatography or by reverse-phase high performance liquid chromatography. Multiple phosphopeptides (3-6) were detected after cleavage with trypsin, chymotrypsin, or V8 protease. Major increases in phosphorylation occurred at existing sites since after hormone treatment no new phosphopeptides were found. Individual phosphopeptides showed variable increases in phosphorylation of 1.5-5-fold. The A and B receptor forms showed identical phosphorylation patterns, indicating similar processing in vivo. The phosphopeptide pattern for receptor in nuclear extracts resembled that of cytosol receptor. Chemical cleavage was used to assess the distribution of phosphorylation sites. Cyanogen bromide produced a large 40-kDa polypeptide which contained all of the phosphorylation sites and comprised the residues 129-449. Hydroxylamine was used to cleave a unique bond, Asn-372-Gly-373, in the 40-kDa polypeptide. All of the phosphorylation sites were located on the amino-terminal side of the cleavage. Thus, all of the phosphorylation sites were localized to a specific region (Met-129 to Asn-372) of the progesterone receptor that does not include either the DNA or steroid binding domains. 相似文献
995.
A 90,000-dalton binding protein common to both steroid receptors and the Rous sarcoma virus transforming protein, pp60v-src 总被引:21,自引:0,他引:21
S Schuh W Yonemoto J Brugge V J Bauer R M Riehl W P Sullivan D O Toft 《The Journal of biological chemistry》1985,260(26):14292-14296
Previous studies have shown that the avian progesterone receptor, when in the nontransformed 8 S state, is complexed to another cellular protein having a molecular weight of 90,000. In this report, we show that this receptor-binding protein is indistinguishable from the 90,000-dalton protein which associates in a complex with the Rous sarcoma virus transforming protein, pp60v-src. This identity was established by the following criteria. 1) Monoclonal antibodies directed against the pp60v-src-associated 90-kDa protein recognized the 90-kDa progesterone receptor binding protein in an immunoblot assay. Conversely, monoclonal antibodies that recognize the progesterone receptor binding protein bind to the 90-kDa protein which complexes with pp60v-src. 2) Peptide maps prepared from the 90-kDa proteins immunoprecipitated from chicken cells with monoclonal antibodies directed against either the 90-kDa receptor binding protein or the 90-kDa pp60v-src-associated protein were indistinguishable. 3) Preincubation of the progesterone receptor complex with monoclonal antibodies prepared against the pp60v-src-associated protein caused a shift in the sedimentation of the progesterone receptor. Previous studies have established that the pp60v-src-associated protein is indistinguishable from one of the major heat shock proteins which are induced under a variety of stress conditions in eukaryotic cells. These present studies implicate a new role for this 90-kDa protein in the action of steroid hormones. 相似文献
996.
The transport of L-methionine in human diploid fibroblast strain WI38 was investigated. The uptake of L-methionine was measured in sparse cell cultures in a simple balanced salt solution buffered with either Tris.HCl of N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES). Similar results were obtained with these two buffers. Cultures were allowed to equilibrate with the buffered saline before transport was measured. The presence of glucose in the buffered saline results in a slight reduction in the initial rate of transport for the first 2 h of equilibration in buffered saline. L-Methionine is actively transported in WI38 by saturable, chemicallly specific mechanisms which are temperature, pH and, in part Na+ dependent, and are reactive with both L- and D-stereoisomers. Kinetic analysis of initial rates of transport at substrate concentrations from 0.0005 to 100 mM indicated the presence of two saturable transport systems. System 1 has an apparent KM of 21.7 micrometer and an apparent V of 3.57 nmol/mg per min. System 2 has an apparent KM of 547 micrometer and an apparent V of 22.6 nmol/mg per min. Kinetic analysis of initial rates of transport in Na+-free media or after treatment with ouabain suggested that system 1 is Na+ independent and that system 2 is Na+ dependent. Preloading of cells with unlabeled L-methionine greatly increases the initial rate of uptake. Efflux of transported methionine is temperature dependent, and is greatly increased in the presence of unlabeled L- or D-methionine or L-phenylalanine, but not in the presence of L-arginine. L-Methionine transport is strongly inhibited by other neutral amino acids, and is very weakly inhibited by dibasic amino acids, dicarboxylic amino acids, proline or glycine. 相似文献
997.
998.
999.
The epichloae are ascomycetous fungi in the genera Epichloë and Neotyphodium that live within grasses. Some of these fungi produce alkaloids that can help protect the host from herbivores. The alkaloids may also travel up the food web and affect members of the third trophic level. In this way they can produce trophic cascades which are rippling effects when a trophic level impacts those above or below it. We briefly summarize the general patterns of multitrophic effects of endophytes and highlight the most recent studies on this topic. Further, we report on our study in which we tested if different fungal strains in tall fescue (cultivar Jesup) affect multitrophic interactions involving aphids and their parasitoid natural enemies. Using both the common strain of N. coenophialum and a novel isolate (AR577), we allowed potted plants to be colonized by aphids and parasitoids in a semi-natural setting. We found that endophyte infection of tall fescue resulted in greater vegetative growth of the plant. We also found that N. coenophialum modified bottom-up cascades by depressing both aphid and parasitoid densities. Finally, we found that multitrophic effects were modified by fungal isolate: the common strain had stronger negative impacts on aphid and parasitoid densities than did the novel isolate. 相似文献
1000.