全文获取类型
收费全文 | 16578篇 |
免费 | 1250篇 |
国内免费 | 1197篇 |
专业分类
19025篇 |
出版年
2024年 | 42篇 |
2023年 | 238篇 |
2022年 | 574篇 |
2021年 | 950篇 |
2020年 | 571篇 |
2019年 | 761篇 |
2018年 | 758篇 |
2017年 | 557篇 |
2016年 | 786篇 |
2015年 | 1041篇 |
2014年 | 1291篇 |
2013年 | 1415篇 |
2012年 | 1510篇 |
2011年 | 1370篇 |
2010年 | 829篇 |
2009年 | 744篇 |
2008年 | 848篇 |
2007年 | 705篇 |
2006年 | 566篇 |
2005年 | 505篇 |
2004年 | 421篇 |
2003年 | 365篇 |
2002年 | 269篇 |
2001年 | 251篇 |
2000年 | 223篇 |
1999年 | 231篇 |
1998年 | 158篇 |
1997年 | 135篇 |
1996年 | 121篇 |
1995年 | 110篇 |
1994年 | 104篇 |
1993年 | 87篇 |
1992年 | 102篇 |
1991年 | 101篇 |
1990年 | 53篇 |
1989年 | 56篇 |
1988年 | 41篇 |
1987年 | 32篇 |
1986年 | 22篇 |
1985年 | 27篇 |
1984年 | 23篇 |
1983年 | 15篇 |
1982年 | 7篇 |
1981年 | 4篇 |
1980年 | 3篇 |
1979年 | 3篇 |
排序方式: 共有10000条查询结果,搜索用时 8 毫秒
31.
Sphingolipids comprise approximately 25% of the stratum corneum lipids and are considered critical constituents of the epidermal permeability barrier. Whether sphingoid base structures are synthesized in the epidermis or whether they are derived from circulating or dermal sources is not known. We report here the initial characterization of serine-palmitoyl transferase (EC 2.3.1.50; SPT), the rate-limiting enzyme in the synthesis of sphingolipids, from cultured human neonatal keratinocytes. Subcellular fractionation studies demonstrated that 79% of the total cellular SPT activity was associated with the microsomes. The specific activity of keratinocyte SPT was 270 +/- 20 pmol/min per mg of microsomal protein, a level significantly higher than activities reported in other tissues. Keratinocyte SPT showed an apparent Km for L-serine of 0.40 (+/- 0.04 mM, with an alkaline pH optimum (8.2 +/- 0.4). Keratinocyte SPT utilizes palmitoyl-CoA preferentially over other saturated or unsaturated acyl-CoA substrates; increasing acyl-CoA chain lengths above C16 by one or two carbons was less detrimental to activity than similar decrements in chain length. Finally, the mechanism-based inhibitors L-cycloserine and beta-chloro-L-alanine, demonstrated potent inhibition of keratinocyte SPT activity, with 50% inhibitory concentrations of approximately 3.0 and 25 microM, respectively. In summary, we have found that cultured human neonatal keratinocytes contain unusually high levels of serine-palmitoyl transferase activity, and that the substrate specificity of keratinocyte SPT may determine the base composition of epidermal sphingolipids. 相似文献
32.
Changes of (Na+-K+)-ATPase activity, cAMP and fibronectin (FN) content and cell surface microvilli were studied cytochemically, immunocytochemically and scanning electron microscopically on human stomach Glandular carcinoma (SGC-7901) cells treated with NaBT(2.5 mM). It was found that NaBT not only inhibited cell growth but also remarkably decreased the activity of cell surface (Na+-K+)-ATPase of SGC-7901 cells. Note worthy was that, in comparison with the untreated tumor cells, the increase of the intensity of intracellular cAMP and FN immunofluorescence in NaBT-treated tumor cells was striking. Moreover, in contrast to untreated tumor cells, the cell surface of NaBT-treated tumor cells showed more smooth and fewer microvilli under SEM. That NaBT may induce differentiation of SGC-7901 cells through inhibition of (Na+-K+)-ATPase activity and modulation of cellular cAMP and FN content was discussed. 相似文献
33.
本文研究了连香树科(Cercidiphyllaceae)叶的宏观结构,首次报道连香树齿腺体显微结构及晶体类型,并对叶柄维管束的变化作了进一步研究。通过与近缘科的比较,我们认为连香树科的系统演化处于孤立地位,和金缕梅科有较近的亲缘关系,与木兰科较为疏远。 相似文献
34.
35.
随着化石燃料消耗量不断增加,由此产生的主要大气污染物之一SO_2的浓度和影响范围也日趋增大。SO_2对植物,特别是对农作物的影响已受到普遍重视。本研究选择我国北方种植面积大、分布广的大豆为供试作物,在野外开顶式熏气装置中进行低浓度SO_2长期暴露试验,观察SO_2对大豆生长发育及产量的影响,以期为制订农田大气环境质量标准提供有一定参考价值的生态学基准。 相似文献
36.
Separate functional domains of the herpes simplex virus type 1 protease: evidence for cleavage inside capsids. 总被引:5,自引:5,他引:0 下载免费PDF全文
B J Robertson P J McCann rd L Matusick-Kumar W W Newcomb J C Brown R J Colonno M Gao 《Journal of virology》1996,70(7):4317-4328
The herpes simplex virus type 1 (HSV-1) protease (Pra) and related proteins are involved in the assembly of viral capsids and virion maturation. Pra is a serine protease, and the active-site residue has been mapped to amino acid (aa) 129 (Ser). This 635-aa protease, encoded by the UL26 gene, is autoproteolytically processed at two sites, the release (R) site between amino acid residues 247 and 248 and the maturation (M) site between residues 610 and 611. When the protease cleaves itself at both sites, it releases Nb, the catalytic domain (N0), and the C-terminal 25 aa. ICP35, a substrate of the HSV-1 protease, is the product of the UL26.5 gene. As it is translated from a Met codon within the UL26 gene, ICP35 cd are identical to the C-terminal 329-aa sequence of the protease and are trans cleaved at an identical C-terminal site to generate ICP35 e,f and a 25-aa peptide. Only fully processed Pra (N0 and Nb) and ICP35 (ICP35 e,f) are present in B capsids, which are believed to be precursors of mature virions. Using an R-site mutant A247S virus, we have recently shown that this mutant protease retains enzymatic activity but fails to support viral growth, suggesting that the release of N0 is required for viral replication. Here we report that another mutant protease, with an amino acid substitution (Ser to Cys) at the active site, can complement the A247S mutant but not a protease deletion mutant. Cell lines expressing the active-site mutant protease were isolated and shown to complement the A247S mutant at the levels of capsid assembly, DNA packaging, and viral growth. Therefore, the complementation between the R-site mutant and the active-site mutant reconstituted wild-type Pra function. One feature of this intragenic complementation is that following sedimentation of infected-cell lysates on sucrose gradients, both N-terminally unprocessed and processed proteases were isolated from the fractions where normal B capsids sediment, suggesting that proteolytic processing occurs inside capsids. Our results demonstrate that the HSV-1 protease has distinct functional domains and some of these functions can complement in trans. 相似文献
37.
38.
大豆子叶内酸性磷酸酶活性的超微结构定位 总被引:6,自引:0,他引:6
开花后35~50 d 期间和萌发早期(播种后4~8 d)的大豆(Glycinem ax L.)种子中,酸性磷酸酶主要分布在子叶细胞中的蛋白体内;在内质网内也检测到酸性磷酸酶活性。此外,在萌发早期的部分子叶细胞的质膜外侧及其细胞壁基质中可见密集的酸性磷酸酶活性;而且在近质膜的胞质中常见到一些富含磷酸铅沉淀的胞质小泡,似与质膜融合 相似文献
39.
40.