全文获取类型
收费全文 | 11430篇 |
免费 | 912篇 |
国内免费 | 778篇 |
专业分类
13120篇 |
出版年
2024年 | 21篇 |
2023年 | 215篇 |
2022年 | 401篇 |
2021年 | 634篇 |
2020年 | 403篇 |
2019年 | 516篇 |
2018年 | 542篇 |
2017年 | 346篇 |
2016年 | 510篇 |
2015年 | 720篇 |
2014年 | 801篇 |
2013年 | 924篇 |
2012年 | 1077篇 |
2011年 | 942篇 |
2010年 | 576篇 |
2009年 | 499篇 |
2008年 | 535篇 |
2007年 | 494篇 |
2006年 | 431篇 |
2005年 | 361篇 |
2004年 | 302篇 |
2003年 | 226篇 |
2002年 | 189篇 |
2001年 | 202篇 |
2000年 | 170篇 |
1999年 | 175篇 |
1998年 | 102篇 |
1997年 | 123篇 |
1996年 | 105篇 |
1995年 | 87篇 |
1994年 | 91篇 |
1993年 | 48篇 |
1992年 | 74篇 |
1991年 | 55篇 |
1990年 | 44篇 |
1989年 | 46篇 |
1988年 | 38篇 |
1987年 | 27篇 |
1986年 | 19篇 |
1985年 | 22篇 |
1984年 | 12篇 |
1983年 | 9篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1979年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
51.
目的探讨MMP-9和PCNA在宫颈癌组织中的联合表达、相关性及其临床意义。方法采用组织芯片和免疫组化技术检测143例宫颈浸润癌(ICC)、20例癌旁正常宫颈上皮(NCE)中MMP-9和PCNA的表达,统计分析MMP-9、PCNA表达与病理分级、临床分期和淋巴结转移等临床病理因素的关系。结果 MMP-9、PCNA在宫颈癌组织中的阳性率分别为89.5%(128/143)和93.7%(134/143),较正常宫颈组织中的阳性率40.0%(8/20)和15.0%(3/20)显著增高(P=0.000)。MMP-9的表达与病理分级(r=0.342,P=0.000)、淋巴结转移(r=0.197,P=0.018)和间质浸润深度(r=0.203,P=0.015)呈正相关。PCNA表达与临床分期(r=0.228,P=0.006)、病理分级(r=0.330,P=0.000)呈正相关。MMP-9和PCNA在宫颈癌组织中的表达强度呈正相关(r=0.228,P=0.006),二者表达一致的比例高达87.41%(125/143)。结论MMP-9和PCNA在宫颈癌中的异常表达与肿瘤的分化、侵袭和发展密切相关,联合检测二者的表达对于进一步理解宫颈癌的生物学行为和判断预后有一定价值。 相似文献
52.
53.
曝氧后,棕色固氮菌(Azotobacter vinelandii)固氮酶钼铁蛋白的催化活性和圆二色信号都显著降低,而吸收光谱则显著增加。与钼、铁、硫化合物和二硫苏糖醇组成的重组溶液保温后,曝氢蛋白的圆二色信号和吸收光谱几乎完全恢复至天然状态的同时,乙炔还原活性也得到了显著的恢复,表明重组溶液可使曝氧蛋白中的 P-cluster和其它活性部位都得到了不同程度的修复。 相似文献
54.
Effector and memory CD8+ T cells can be generated in response to alloantigen independently of CD4+ T cell help 总被引:3,自引:0,他引:3
Jones ND Carvalho-Gaspar M Luo S Brook MO Martin L Wood KJ 《Journal of immunology (Baltimore, Md. : 1950)》2006,176(4):2316-2323
There is now considerable evidence suggesting that CD8(+) T cells are able to generate effector but not functional memory T cells following pathogenic infections in the absence of CD4(+) T cells. We show that following transplantation of allogeneic skin, in the absence of CD4(+) T cells, CD8(+) T cells become activated, proliferate, and expand exclusively in the draining lymph nodes and are able to infiltrate and reject skin allografts. CD44(+)CD8(+) T cells isolated 100 days after transplantation rapidly produce IFN-gamma following restimulation with alloantigen in vitro. In vivo CD44(+)CD8(+) T cells rejected donor-type skin allografts more rapidly than naive CD8(+) T cells demonstrating the ability of these putative memory T cells to mount an effective recall response in vivo. These data form the first direct demonstration that CD8(+) T cells are able to generate memory as well as effector cells in response to alloantigen during rejection in the complete absence of CD4(+) T cells. These data have important implications for the design of therapies to combat rejection and serve to reinforce the view that CD8(+) T cell responses to allografts require manipulation in addition to CD4(+) T cell responses to completely prevent the rejection of foreign organ transplants. 相似文献
55.
Lifang Guo Xingchao Geng Li Liu Yufa Miao Zhi Lin Min Yu Yan Fu Lihong Liu Bo Li Yongzhang Luo 《Journal of biochemical and molecular toxicology》2019,33(3)
Endostar, a potent endogenous antiangiogenic factor, is wildly used in clinics. However, it was easily degraded by enzymes and rapidly cleared by the kidneys. To overcome these shortcomings, PEGylated recombinant human endostatin was developed. In this study, the purity of M2ES was evaluated by silver stain and reversed‐phase high‐performance liquid chromatography. Ultraviolet spectrum was used to examine the structural of M2ES and endostar. The bioactivity and antitumor efficacy of M2ES were evaluated using an in vitro endothelial cell migration model and athymic nude mouse xenograft model of a heterogeneous lung adenocarcinoma, respectively. A preclinical study was performed to evaluate the acute toxicity and safety pharmacology in rhesus monkeys. The purity of M2ES was more than 98%; PEG modification has no effect on endostatin structure. Compared with the control group, M2ES dramatically retards endothelial cell migration and tumor growth. After intravenous (IV) infusions of M2ES at a dose level of three and 75 mg/kg in rhesus monkeys, there was no observable serious adverse event in both acute toxicity and safety pharmacology study. On the basis of the quality and bioactivity study data of M2ES and the absence of serious side effect in rhesus monkeys, M2ES was authorized to initiate a phase I clinical trial. 相似文献
56.
57.
Junna Wang Chong Li Xinbin Duan Daqing Chen Shunxin Feng Huihuang Luo Qidong Peng Wengen Liao 《Freshwater Biology》2014,59(7):1343-1360
- 相似文献
58.
山姜属(Alpinia L.)植物的花柱具卷曲运动的能力,该属植物的野生种群有两种表型的个体,其花柱运动方向相反。该文通过观察马来良姜(Alpinia mutica Roxb.)花柱的显微和超微结构来研究花柱卷曲运动的结构基础。结果表明两种表型的花柱解剖结构相同。花柱仅形态学上端区域(约占花柱总长度的25%)有卷曲运动能力,其它区域不能运动。运动区近轴侧分布着几层直径较大、形状不规则、相对较短且细胞壁较薄的细胞,远轴侧的细胞直径较小、狭长;非运动区近轴和远轴侧的细胞都呈狭长形。花柱运动区域近轴侧和远轴侧细胞结构和细胞层数的不对称可能是导致花柱卷曲运动的结构原因。 相似文献
59.
目的:探讨迷走神经复合体(Dorsal vagal complex,DVC)内orexin-A对顺铂所致胃功能紊乱的影响及可能机制。方法:随机选取30只大鼠并将其分为3组(n=10):对照组(NS组);24 h顺铂治疗组;48 h顺铂治疗组。24 h顺铂治疗组和48 h顺铂治疗组大鼠分别在腹腔注射顺铂后24 h和48 h处死大鼠,对照组大鼠腹腔注射生理盐水(Normal saline,NS)。采用定量实时PCR检测各组大鼠下丘脑orexin-A mRNA的表达,ELISA测量大鼠脑脊液中P物质水平;DVC内微量注射orexin-A和ghrelin受体拮抗剂后,检测大鼠食物和高岭土的摄入量。结果:顺铂可显著减少大鼠下丘脑orexin-A mRNA表达,增加其脑脊液内P物质的浓度。外源性orexin-A可改善顺铂引起的厌食症和异食癖。orexin-A以上的效应可被DVC内预先注射ghrelin受体拮抗剂部分逆转。结论:orexin-A可能通过ghrelin神经肽系统改善顺铂在化疗过程中诱导的胃功能紊乱。 相似文献
60.
Jinshan Yang Xiang Luo Xiaojiang Huang Qin Ning Minjie Xie Wei Wang 《Journal of neurochemistry》2014,131(3):383-394
Increasing evidence indicates that the Eph receptors and their ephrin ligands are involved in the regulation of interactions between neurons and astrocytes. Moreover, astrocytic ephrin‐A3 reverse signaling mediated by EphA4 receptors is necessary for controlling the abundance of glial glutamate transporters. However, the role of ephrin‐A3 reverse signaling in astrocytic function and neuronal death under ischemic conditions remains unclear. In the present study, we found that the EphA4 receptor and its ephrin‐A3 ligand, which were distributed in neurons and astrocytes, respectively, in the hippocampus showed a coincident up‐regulation of protein expression in the early stage of ischemia. Application of clustered EphA4 decreased the expressions of astrocytic glutamate transporters together with astrocytic glutamate uptake capacity through activating ephrin‐A3 reverse signaling. In consequence, neuronal loss was aggravated in the CA1 region of the hippocampus accompanied by impaired hippocampus‐dependent spatial memory when clustered EphA4 treatment was administered prior to transient global ischemia. These findings indicate that EphA4‐mediated ephrin‐A3 reverse signaling is a crucial mechanism for astrocytes to control glial glutamate transporters and prevent glutamate excitotoxicity under pathological conditions.