全文获取类型
收费全文 | 157篇 |
免费 | 25篇 |
出版年
2017年 | 2篇 |
2015年 | 2篇 |
2013年 | 26篇 |
2012年 | 2篇 |
2011年 | 7篇 |
2009年 | 6篇 |
2008年 | 2篇 |
2007年 | 8篇 |
2006年 | 5篇 |
2005年 | 9篇 |
2004年 | 7篇 |
2003年 | 3篇 |
2002年 | 6篇 |
2000年 | 3篇 |
1999年 | 2篇 |
1998年 | 2篇 |
1997年 | 2篇 |
1996年 | 4篇 |
1993年 | 2篇 |
1992年 | 5篇 |
1990年 | 3篇 |
1989年 | 5篇 |
1987年 | 7篇 |
1985年 | 2篇 |
1980年 | 2篇 |
1975年 | 2篇 |
1926年 | 1篇 |
1925年 | 1篇 |
1924年 | 1篇 |
1921年 | 1篇 |
1920年 | 1篇 |
1915年 | 2篇 |
1914年 | 1篇 |
1909年 | 1篇 |
1902年 | 1篇 |
1901年 | 1篇 |
1897年 | 2篇 |
1892年 | 1篇 |
1891年 | 1篇 |
1889年 | 1篇 |
1888年 | 1篇 |
1887年 | 1篇 |
1883年 | 3篇 |
1882年 | 5篇 |
1881年 | 2篇 |
1880年 | 1篇 |
1879年 | 6篇 |
1878年 | 2篇 |
1877年 | 2篇 |
1876年 | 1篇 |
排序方式: 共有182条查询结果,搜索用时 187 毫秒
1.
The demonstration that activators of the Ca2+-activated, phospholipid-dependent protein kinase (protein kinase C), such as phorbol esters and diacylglycerols, can provoke luteinizing hormone (LH) release from pituitary gonadotropes, suggests a possible role for protein kinase C in stimulus-release coupling. We now report that administration of phorbol myristate acetate (PMA) to pituitary cell cultures causes a sustained reduction in Triton X-100-extracted protein kinase C activity. Further, phorbol ester- and diacylglycerol-stimulated LH release, as well as inhibition by PMA of gonadotropin-releasing hormone (GnRH)-stimulated inositol phosphate production, were reduced by pretreatment with PMA. The effects of phorbol ester pretreatment on PMA-stimulated LH release and protein kinase C activity were dose-dependent, sustained (greater than or equal to 24 h) and specific (no measurable effect with 4 alpha-phorbol didecanoate). The effect on PMA-stimulated LH release was apparently Ca2+-independent. In pituitary cell cultures with reduced protein kinase C activity, the gonadotropes have reduced responsiveness to PMA but release a similar proportion of cellular LH in response to Ca2+-mobilizing secretagogues (GnRH and A23187) as do control cells. The normal responsiveness to GnRH of cells with reduced responsiveness to protein kinase C activators calls into question the requirement for this enzyme for GnRH-stimulated LH release. 相似文献
2.
Expression of a Clostridium thermocellum endoglucanase gene in Lactobacillus plantarum 总被引:1,自引:0,他引:1
E E Bates H J Gilbert G P Hazlewood J Huckle J I Laurie S P Mann 《Applied and environmental microbiology》1989,55(8):2095-2097
Recombinant plasmid pM25 containing the celE gene of Clostridium thermocellum, which codes for an enzymatically active endoglucanase, was transformed into Lactobacillus plantarum by electroporation. Strains harboring pM25 expressed thermostable endoglucanase, which was found predominantly in the culture medium. Two other plasmids, pGK12 and pSA3, were transformed into L. plantarum, and the stability of each plasmid was evaluated. 相似文献
3.
4.
To investigate the physical and kinetic properties of sperm carnitine acetyltransferase, the enzyme was purified from bovine spermatozoa and heart muscle. Carnitine acetyltransferase was purified 580-fold from ejaculated bovine spermatozoa to a specific activity of 85 units/mg protein (95% homogeneity). Sperm carnitine acetyltransferase was characterized as a single polypeptide of Mr 62,000 and pI 8.2. Heart carnitine acetyltransferase was purified 650-fold by the same procedure to a final specific activity of 71 units/mg protein. The kinetic properties of purified bovine sperm carnitine acetyltransferase were consistent with the proposed function of this enzyme in acetylcarnitine pool formation. Product inhibition by either acetyl-l-carnitine or CoASH was not sufficient to predict significant in vivo inhibition of acetyl transfer. At high concentrations of l-carnitine, bovine sperm and heart carnitine acetyltransferases were most active with propionyl- and butyryl-CoA substrates, although octanoyl-, iso-butyryl-, and iso-valeryl-CoA were acceptable substrates. Binding of one substrate was enhanced by the presence of the second substrate. Carnitine analogs that have significance in reproduction, such as phosphorylcholine and taurine, did not inhibit carnitine acetyltransferase. Bovine sperm and heart carnitine acetyltransferases were indistinguishable on the basis of purification behavior, pI, pH optima, kinetic properties, acyl-CoA specificity, and sensitivity to sulfhydryl reagents and divalent cations; thus there was no indication that bovine sperm carnitine acetyltransferase is a sperm-specific isozyme. 相似文献
5.
6.
7.
8.
J.?M.?Huckle R.?H.?MarrsEmail author J.?A.?Potter 《Wetlands Ecology and Management》2004,12(5):483-498
Vegetation changes in salt marsh communities of the Dee estuary, northwest England, were analysed with a combination of remote sensing techniques using data dating back to the 1950s. The distribution of communities in 1997 was classified using Airborne Thematic Mapper data and used to develop a methodology for the analysis of black and white photographs of the marsh. These methods were then applied retrogressively to a time sequence of monochrome photographs running from 1955 to 1975. At the apex of the salt marshes on the English shore of the Dee estuary, the marsh expanded dramatically to 1975, and consisted predominantly of pioneer and low marsh vegetation types. Between 1975 and 1997, however, there was only a slight increase in salt marsh area, but with an increase in mid and high marsh vegetation, replacing pioneer marsh. In a second area of the salt marsh on the English shore, a different pattern of salt marsh expansion was observed. The area occupied by marsh continued to increase right up to 1997, with extensive pioneer vegetation suggesting a process of continuing expansion. However, the pattern of marsh colonisation appeared to be different in 1997 compared to 1975. The significance of the changes in salt marsh distribution within the Dee estuary are discussed in relation to the historical pattern of salt marsh colonisation, the importance of Spartina anglica in the process and the implications for strategic management of the estuarine resources. 相似文献
9.
10.