全文获取类型
收费全文 | 7513篇 |
免费 | 406篇 |
国内免费 | 6篇 |
出版年
2022年 | 19篇 |
2021年 | 65篇 |
2020年 | 43篇 |
2019年 | 63篇 |
2018年 | 107篇 |
2017年 | 72篇 |
2016年 | 142篇 |
2015年 | 212篇 |
2014年 | 251篇 |
2013年 | 650篇 |
2012年 | 429篇 |
2011年 | 450篇 |
2010年 | 267篇 |
2009年 | 259篇 |
2008年 | 454篇 |
2007年 | 470篇 |
2006年 | 423篇 |
2005年 | 470篇 |
2004年 | 447篇 |
2003年 | 472篇 |
2002年 | 388篇 |
2001年 | 126篇 |
2000年 | 110篇 |
1999年 | 116篇 |
1998年 | 95篇 |
1997年 | 85篇 |
1996年 | 75篇 |
1995年 | 68篇 |
1994年 | 61篇 |
1993年 | 73篇 |
1992年 | 95篇 |
1991年 | 75篇 |
1990年 | 71篇 |
1989年 | 70篇 |
1988年 | 57篇 |
1987年 | 37篇 |
1986年 | 42篇 |
1985年 | 58篇 |
1984年 | 38篇 |
1983年 | 37篇 |
1982年 | 42篇 |
1981年 | 62篇 |
1980年 | 34篇 |
1979年 | 33篇 |
1978年 | 20篇 |
1977年 | 25篇 |
1976年 | 20篇 |
1975年 | 30篇 |
1974年 | 15篇 |
1973年 | 23篇 |
排序方式: 共有7925条查询结果,搜索用时 15 毫秒
1.
Kenji Tsuji Shinji KitamuraHirofumi Makino 《Biochemical and biophysical research communications》2014
The kidneys are exposed to hypoxic conditions during development. Hypoxia-inducible factor (HIF), an important mediator of the response to hypoxia, is believed to have an important role in development. However, the relationship between HIF and branching morphogenesis has not been elucidated clearly. 相似文献
2.
Takumi Higaki Natsumaro Kutsuna Kae Akita Hisako Takigawa-Imamura Kenji Yoshimura Takashi Miura 《PLoS computational biology》2016,12(4)
Plant leaf epidermal cells exhibit a jigsaw puzzle–like pattern that is generated by interdigitation of the cell wall during leaf development. The contribution of two ROP GTPases, ROP2 and ROP6, to the cytoskeletal dynamics that regulate epidermal cell wall interdigitation has already been examined; however, how interactions between these molecules result in pattern formation remains to be elucidated. Here, we propose a simple interface equation model that incorporates both the cell wall remodeling activity of ROP GTPases and the diffusible signaling molecules by which they are regulated. This model successfully reproduces pattern formation observed in vivo, and explains the counterintuitive experimental results of decreased cellulose production and increased thickness. Our model also reproduces the dynamics of three-way cell wall junctions. Therefore, this model provides a possible mechanism for cell wall interdigitation formation in vivo. 相似文献
3.
4.
5.
Qi-Wen Fan Kenji Kadomatsu Kenji Uchimura Takashi Muramatsu 《Development, growth & differentiation》1998,40(3):277-286
Embigin and basigin are highly glycosylated transmembrane glycoproteins with two immunoglobulin domains and form a subgroup in the immunoglobulin superfamily. Previous studies have demonstrated the functional significance of these molecules. In the present study, in situ hybridization analysis of their expression was performed during mouse embryogenesis. Embigin was strongly expressed in the endoderm during early postimplantation embryogenesis, and in the somite stage in the gut and visceral endoderm. Embryonic ectoderm and its derivative tissues weakly to moderately expressed this molecule. From day 10 to 15 of gestation, no embigin signal was detected. Basigin was more broadly expressed. During the organogenesis period, basigin was expressed in various epithelial tissues, brain ventricles, the spinal cord and dorsal root ganglion. The modes of expression of these two proteins throughout the egg cylinder stage correlated with the expression of the carbohydrate markers that they carry; embigin with Dolichos biflorus agglutinin binding sites and basigin with Lex antigen and more closely with fucosyltransferase IV, which forms the antigenic epitope. These findings imply that proteins with specific carbohydrate epitopes play roles in early postimplantation embryogenesis. 相似文献
6.
7.
Monoclonal antibodies against chick embryonic beta-galactoside-binding lectin were obtained. One of the monoclonal antibodies was ineffective in Western blotting and seemed to be unable to bind the SDS-denatured lectin. When the native lectin was dotted on a nitrocellulose filter and subjected to denaturation by treatment with SDS, urea or heat, binding of this antibody no longer occurred, though other monoclonal antibodies bound normally. This antibody seems to have been raised against an epitope which is destroyed upon denaturation. 相似文献
8.
Cell walls were isolated by sonic disruption of log-phase cells of Clostridium botulinum type A strain 190L and purified by treatment with sodium dodecyl sulfate (SDS) followed by digestion with proteases. Electron microscopy revealed that the cell walls thus obtained were free of both cytoplasmic membrane and cytoplasmic fragments. The purified cell wall contained 8.7% total nitrogen, 15.0% total hexosamines, 22.4% reducing groups, 8.3% carbohydrate, and 3.1% glucose. The content of total phosphorus was very low (0.02%), and therefore it was expected that teichoic acid might be absent in the cell wall. The wall peptidoglycan contained glutamic acid, alanine, diaminopimelic acid, glucosamine and muramic acid in the molar ratios of 1.00:1.85:0:85:1.06:0.67. A low amount of galactosamine was also present, but no other amino acids were found in significant quantities. The SDS-treated cell walls were not attacked by lysozyme, but after extraction with hot formamide they were completely dissolved by the enzyme and released reducing groups. The lysozyme digest was separated into two constituents, the saccharide moiety and the peptide moiety on Sephadex G-50. 相似文献
9.
10.
K Nakajima H Kato J Oda Y Yamada T Hashimoto 《The Journal of biological chemistry》1999,274(23):16563-16568
Two tropinone reductases (TRs) constitute a key branch point in the biosynthetic pathway of tropane alkaloids, which are mainly produced in several solanaceous plants. The two TRs share 64% identical amino acid residues and reduce the 3-carbonyl group of a common substrate, tropinone, but they produce distinct alcohol products with different stereospecific configurations. Previous x-ray crystallographic analysis has revealed their highly conserved overall folding, and the modeling of tropinone within the putative substrate-binding sites has suggested that the different stereospecificities may be determined solely by the different binding orientations of tropinone to the enzymes. In this study, we have constructed various mutant TRs, in which putative substrate-binding residues from one TR were substituted with those found in the corresponding positions of the other TR. Substitution of five amino acid residues resulted in an almost complete reversal of stereospecificity, indicating that the different stereospecificities are indeed determined by the binding orientation of tropinone. Detailed kinetic analysis of the mutant enzymes has shown that TR stereospecificity is determined by varying the contributions from electrostatic and hydrophobic interactions and that the present TR structures represent highly evolved forms, in which strict stereospecificities and rapid turnover are accomplished together. 相似文献