全文获取类型
收费全文 | 1220篇 |
免费 | 102篇 |
出版年
2023年 | 13篇 |
2021年 | 15篇 |
2020年 | 21篇 |
2019年 | 22篇 |
2018年 | 37篇 |
2017年 | 27篇 |
2016年 | 35篇 |
2015年 | 64篇 |
2014年 | 73篇 |
2013年 | 54篇 |
2012年 | 86篇 |
2011年 | 65篇 |
2010年 | 41篇 |
2009年 | 38篇 |
2008年 | 65篇 |
2007年 | 77篇 |
2006年 | 45篇 |
2005年 | 66篇 |
2004年 | 55篇 |
2003年 | 36篇 |
2002年 | 35篇 |
2001年 | 23篇 |
2000年 | 17篇 |
1999年 | 14篇 |
1998年 | 6篇 |
1997年 | 13篇 |
1996年 | 7篇 |
1995年 | 13篇 |
1994年 | 14篇 |
1993年 | 8篇 |
1992年 | 8篇 |
1991年 | 15篇 |
1990年 | 13篇 |
1989年 | 11篇 |
1988年 | 19篇 |
1987年 | 7篇 |
1982年 | 7篇 |
1979年 | 6篇 |
1978年 | 9篇 |
1977年 | 10篇 |
1976年 | 8篇 |
1975年 | 8篇 |
1974年 | 12篇 |
1973年 | 7篇 |
1972年 | 11篇 |
1971年 | 12篇 |
1970年 | 7篇 |
1969年 | 8篇 |
1967年 | 8篇 |
1851年 | 7篇 |
排序方式: 共有1322条查询结果,搜索用时 15 毫秒
1.
2.
3.
4.
5.
6.
7.
Synopsis A sensitive method is presented for measurement of changes in the permeability of mitchondria in cultured cells. Rat heart endothelioid cells were used to determine the penetration rate of nitroblue tetrazolium (NitroBT) or other reactants into mitochondriain situ. Nitroblue formazan, produced as a consequence of succinate dehydrogenase activity in the mitochondria, was eluted and measured with a spectrophotometer. Prior injury of cells with hypo-osmolar solutions increased the rate of formazan production. Several methods are described or suggested for the statistical analysis of the data. 相似文献
8.
9.
10.
Whereas the chemotactic peptide, N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMet-Leu-Phe), induced NADPH-oxidase-catalyzed superoxide (O2-) formation in human neutrophils, purine and pyrimidine nucleotides per se did not stimulate NADPH oxidase but enhanced O2- formation induced by submaximally and maximally stimulatory concentrations of fMet-Leu-Phe up to fivefold. On the other hand, FMet-Leu-Phe primed neutrophils to generate O2- upon exposure to nucleotides. At a concentration of 100 microM, purine nucleotides enhanced O2- formation in the effectiveness order adenosine 5'-O-[3-thio]triphosphate (ATP[gamma S]) greater than ITP greater than guanosine 5'-O-[3-thio]triphosphate (GTP[gamma S]) greater than ATP = adenosine 5'-O-[2-thio]triphosphate (Sp-diastereomer) = GTP = guanosine 5'-O-[2-thio]diphosphate (GDP[beta S] = ADP greater than adenosine 5'-[beta, gamma-imido]triphosphate = adenosine 5'-O-[2-thio]triphosphate] (Rp-diastereomer). Pyrimidine nucleotides stimulated fMet-Leu-Phe-induced O2- formation in the effectiveness order uridine 5'-O-[3-thio]triphosphate (UTP[gamma S]) = UTP greater than CTP. Uracil (UDP[beta S]) = uridine 5'-O[2-thio]triphosphate (Rp-diastereomer) (Rp)-UTP[beta S]) = UTP greater than CTP. Uracil nucleotides were similarly effective potentiators of O2- formation as the corresponding adenine nucleotides. GDP[beta S] and UDP[beta S] synergistically enhanced the stimulatory effects of ATP[gamma S], GTP[gamma S] and UTP[gamma S]. Purine and pyrimidine nucleotides did not induce degranulation in neutrophils but potentiated fMet-Leu-Phe-induced release of beta-glucuronidase with similar nucleotide specificities as for O2- formation. In contrast, nucleotides per se induced aggregation of neutrophils. Treatment with pertussis toxin prevented aggregation induced by both nucleotides and fMet-Leu-Phe. Our results suggest that purine and pyrimidine nucleotides act via nucleotide receptors, the nucleotide specificity of which is different from nucleotide receptors in other cell types. Neutrophil nucleotide receptors are coupled to guanine-nucleotide-binding proteins. As nucleotides are released from cells under physiological and pathological conditions, they may play roles as intercellular signal molecules in neutrophil activation. 相似文献