全文获取类型
收费全文 | 15190篇 |
免费 | 1167篇 |
国内免费 | 1117篇 |
专业分类
17474篇 |
出版年
2024年 | 34篇 |
2023年 | 177篇 |
2022年 | 464篇 |
2021年 | 835篇 |
2020年 | 498篇 |
2019年 | 606篇 |
2018年 | 639篇 |
2017年 | 530篇 |
2016年 | 627篇 |
2015年 | 902篇 |
2014年 | 1083篇 |
2013年 | 1210篇 |
2012年 | 1420篇 |
2011年 | 1263篇 |
2010年 | 779篇 |
2009年 | 707篇 |
2008年 | 757篇 |
2007年 | 630篇 |
2006年 | 610篇 |
2005年 | 489篇 |
2004年 | 433篇 |
2003年 | 333篇 |
2002年 | 347篇 |
2001年 | 312篇 |
2000年 | 254篇 |
1999年 | 250篇 |
1998年 | 169篇 |
1997年 | 131篇 |
1996年 | 139篇 |
1995年 | 129篇 |
1994年 | 140篇 |
1993年 | 95篇 |
1992年 | 97篇 |
1991年 | 70篇 |
1990年 | 66篇 |
1989年 | 58篇 |
1988年 | 56篇 |
1987年 | 31篇 |
1986年 | 33篇 |
1985年 | 19篇 |
1984年 | 23篇 |
1983年 | 12篇 |
1982年 | 8篇 |
1981年 | 2篇 |
1980年 | 3篇 |
1979年 | 1篇 |
1976年 | 1篇 |
1975年 | 1篇 |
1933年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
Replacement of the arginine-138 of adenylate kinase (AK) by lysine or methionine resulted in a decrease in kcat by a factor of 10(4), increases in Km by a factor of 10-20, and relatively little changes in dissociation constants. Proton nuclear magnetic resonance (NMR) studies were then undertaken to obtain structural information for quantitative interpretation of the kinetic data. Since the lysine mutant (R138K) represents a conservative mutation with surprisingly large effects on kinetics, structural studies were focused on the wild type (WT) and R138K. The results and conclusions are summarized as follows: (i) The aromatic spin systems of WT and R138K were assigned from total correlated spectroscopy (TOCSY). Comparison of the chemical shifts of aromatic protons, one-dimensional spectra, TOCSY, and nuclear Overhauser enhanced spectroscopy (NOESY) indicated that the conformation of R138K was almost unperturbed relative to that of WT. Thus Arg-138 is not important for the tertiary structure. (ii) Proton NMR titrations with AMP and MgATP suggested that substrate binding affinities and substrate-induced conformational changes are nearly identical between WT and R138K. Thus arginine-138 should not be involved in stabilizing the first substrate in the binary complex. (iii) Notable differences were observed between the proton NMR spectra of the WT and R138K complexes with the reaction mixture, which agrees with the perturbation in the Km values of R138K. The differences were analyzed in detail by using a "static reaction mixture'--p1, p5-bis(5'-adenosyl)pentaphosphate (MgAP5A). The aromatic spin systems of WT + MgAP5A and R138K + MgAP5A were partially assigned from various two-dimensional spectra.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
102.
103.
We have used amphibian gastrulation as a model system to study the action of the extracellular matrix (ECM) glycoprotein tenascin on mesodermal cell migration. Tenascin function was assayed in vitro during spreading of isolated cells from the dorsal marginal zone (DMZ) and during cell migration from DMZ explants. Plastic coated with bovine fibronectin or gastrula ECM was used as a substratum. In both cases, tenascin added to the medium inhibited spreading and migration of mesodermal cells. In addition, a substratum coated with a mixture of fibronectin and tenascin was found to prevent mesodermal cell migration. Tenascin was also microinjected into the blastocoel cavity of living embryos at the late blastula stage. This led to a complete arrest of gastrulation in more than 80% of the cases. Scanning electron microscopy of fractures from arrested gastrulae showed that mesodermal cell migration was blocked. Similar injection experiments carried out at the middle gastrula stage demonstrated that tenascin is able to inhibit cell migration after cells have already contacted the ECM. Mesodermal cell migration in the presence of tenascin could be restored in vitro and in vivo by the monoclonal antibody mAb Tn68 which is known to mask a cell binding site of the molecule. Finally, tenascin microinjected into the blastocoel of blastula or gastrula stage embryos bound within 15 min to the ECM fibrils at all the stages studied. Our results show that exogenous tenascin can be incorporated into embryonic ECM and interferes in vivo with the interactions of cells with a fibronectin-rich matrix. 相似文献
104.
太子参内生细菌RPB-32的分类鉴定及其代谢物对小鼠肠道微生物群落的影响 总被引:1,自引:0,他引:1
【背景】肠道微生物在宿主肠道微环境稳态中起着至关重要的作用。众多因子,如抗生素、饮食和年龄等会干扰这种微平衡,引起菌群平衡发生改变,进而影响到机体健康状况。太子参具有心肌保护、增加免疫、抗氧化、抗糖尿病、抗应激、抗疲劳等药理活性,而太子参内生菌代谢物对肠道微生物的调控作用以及可能对机体健康的影响目前还未见报道。【目的】研究太子参内生菌RPB-32分类地位及其代谢提取物对小鼠肠道微生物的调节作用,以探讨其对机体健康的影响。【方法】对RPB-32进行传统方法和分子鉴定。将120只KM小鼠随机分为溶剂对照组(3%乙醇)及石油醚提取物、正丁醇提取物和乙酸乙酯提取物低、中、高剂量组(n=12)。小鼠灌胃处理14 d后采集粪便,通过选择性培养基培养及宏基因组测序[溶剂对照(S.F.1为3%乙醇溶液)、乙酸乙酯提取物高剂量组(S.F.2)]检测灌胃前后小鼠肠道微生物的变化。【结果】常规传统方法与分子鉴定结果表明RPB-32为芽孢杆菌(Bacillus sp.)。与空白对照组相比,给予内生菌代谢提取物的乙酸乙酯中剂量组、乙酸乙酯高剂量组、正丁醇低剂量组、正丁醇中剂量组及正丁醇高剂量组乳酸菌数量明显增加... 相似文献
105.
106.
107.
Bo Li YuZhen Ge WeiWei Yan Bin Gong Kun Cao Rui Zhao Chao Li YeWei Zhang YiHeng Jiang Shi Zuo 《Cell proliferation》2022,55(9)
As a member of the deoxyribonuclease 1 family, DNASE1L3 plays a significant role both inside and outside the cell. However, the role of DNASE1L3 in hepatocellular carcinoma (HCC) and its molecular basis remains to be further investigated. In this study, we report that DNASE1L3 is downregulated in clinical HCC samples and evaluate the relationship between its expression and HCC clinical features. In vivo and in vitro experiments showed that DNASE1L3 negatively regulates the proliferation, invasion and metastasis of HCC cells. Mechanistic studies showed that DNASE1L3 recruits components of the cytoplasmic β‐catenin destruction complex (GSK‐3β and Axin), promotes the ubiquitination degradation of β‐catenin, and inhibits its nuclear transfer, thus, decreasing c‐Myc, P21 and P27 level. Ultimately, cell cycle and EMT signals are restrained. In general, this study provides new insight into the mechanism for HCC and suggests that DNASE1L3 can become a considerable target for HCC.Decreased expression of DNASE1L3 is associated with poor prognosis in patients with HCC DNASE1L3 inhibits the proliferation and cell cycle of HCC cells in vitro and promotes the invasion and metastasis of HCC cells DNASE1L3 inhibits the tumorigenicity and metastasis of HCC cells in vivo DNASE1L3 interacts with β‐catenin and promotes its binding to the β‐catenin destroying complex DNASE1L3 interacts with P21 and stabilizes P21 by mediating the deubiquitin activity 相似文献
108.
109.
Ruye Ma Dandan Yu Yu Peng Hongfei Yi Yingcong Wang Taofang Cheng Bingqing Shi Guang Yang Weiming Lai Xiaosong Wu Ye Lu Jumei Shi 《Acta biochimica et biophysica Sinica》2021,(6):775-783
Resveratrol,a natural compound extracted from the skins of grapes,berries,or other fruits,has been shown to have anti-tumor effects against multiple myeloma(MM)... 相似文献
110.
Ze-Hua Wang Yue-Nan Zhou Xi-Qian Ye Xiao-Tong Wu Pei Yang Min Shi Jian-Hua Huang Xue-Xin Chen 《Insect Science》2021,28(6):1567-1581
Polydnaviruses (PDVs) are obligatory symbionts of parasitoid wasps and play an important role in suppressing host immune defenses. Although PDV genes that inhibit host melanization are known in Microplitis bracovirus, the functional homologs in Cotesia bracoviruses remain unknown. Here, we find that Cotesia vestalis bracovirus (CvBV) can inhibit hemolymph melanization of its host, Plutella xylostella larvae, during the early stages of parasitization, and that overexpression of highly expressed CvBV genes reduced host phenoloxidase activity. Furthermore, CvBV-7-1 in particular reduced host phenoloxidase activity within 12 h, and the injection of anti-CvBV-7-1 antibody increased the melanization of parasitized host larvae. Further analyses showed that CvBV-7-1 and three homologs from other Cotesia bracoviruses possessed a C-terminal leucine/isoleucine-rich region and had a similar function in inhibiting melanization. Therefore, a new family of bracovirus genes was proposed and named as C -terminal L eucine/isoleucine-rich P rotein (CLP). Ectopic expression of CvBV-7-1 in Drosophila hemocytes increased susceptibility to bacterial repression of melanization and reduced the melanotic encapsulation of parasitized D. melanogaster by the parasitoid Leptopilina boulardi. The formation rate of wasp pupae and the eclosion rate of C. vestalis were affected when the function of CvBV-7-1 was blocked. Our findings suggest that CLP genes from Cotesia bracoviruses encoded proteins that contain a C-terminal leucine/isoleucine-rich region and function as melanization inhibitors during the early stage of parasitization, which is important for successful parasitization. 相似文献