全文获取类型
收费全文 | 41986篇 |
免费 | 3903篇 |
国内免费 | 5841篇 |
专业分类
51730篇 |
出版年
2024年 | 143篇 |
2023年 | 578篇 |
2022年 | 1355篇 |
2021年 | 2176篇 |
2020年 | 1574篇 |
2019年 | 1996篇 |
2018年 | 1835篇 |
2017年 | 1426篇 |
2016年 | 1914篇 |
2015年 | 2794篇 |
2014年 | 3387篇 |
2013年 | 3503篇 |
2012年 | 4175篇 |
2011年 | 3755篇 |
2010年 | 2407篇 |
2009年 | 2152篇 |
2008年 | 2447篇 |
2007年 | 2205篇 |
2006年 | 1933篇 |
2005年 | 1594篇 |
2004年 | 1353篇 |
2003年 | 1228篇 |
2002年 | 1100篇 |
2001年 | 728篇 |
2000年 | 627篇 |
1999年 | 567篇 |
1998年 | 395篇 |
1997年 | 346篇 |
1996年 | 307篇 |
1995年 | 254篇 |
1994年 | 237篇 |
1993年 | 171篇 |
1992年 | 183篇 |
1991年 | 142篇 |
1990年 | 104篇 |
1989年 | 94篇 |
1988年 | 87篇 |
1987年 | 60篇 |
1986年 | 62篇 |
1985年 | 73篇 |
1984年 | 52篇 |
1983年 | 36篇 |
1982年 | 35篇 |
1981年 | 26篇 |
1980年 | 10篇 |
1979年 | 20篇 |
1978年 | 9篇 |
1974年 | 8篇 |
1973年 | 11篇 |
1971年 | 8篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
RGDS肽对大鼠主动脉球囊内膜剥脱后血管壁增殖的影响 总被引:1,自引:0,他引:1
在大鼠主动脉球囊内膜剥脱术后血管壁细胞过度增殖模型上,用合成的血小板膜纤维蛋白原受体(glycoproteinⅡb/Ⅲacomplex,GPⅡb/Ⅲa)拮抗剂RGDS(Arg-Gly-Asp-Ser,50μmol·kg-1·d-1)治疗可有效地抑制损伤血管壁的细胞计数增加和内膜增厚以及血管平滑肌细胞增殖,显著降低其血管组织3H-TdR和3H-Leu的参入增加程度。实验结果提示RGDS肽作为血管成型术的辅佐剂,对于防治血管再狭窄可能具有潜在的临床应用前景。 相似文献
102.
腹腔注射链脲佐霉素(65mg/kg)诱发Wistar大鼠糖尿病。糖尿病发病4周后,向饲料中加尼群地平(30mg·kg-1·d-1)。结果表明,糖尿病4周时大鼠心室舒张功能首先受损,8周后心室舒张和收缩功能均明显受累。尼群地平处理对糖尿病大鼠的心肌收缩性有一定的改善作用。提示尼群地平对大鼠糖尿病性心肌病有一定有益作用。 相似文献
103.
用电生理细胞内记录的方法记录了10个以上小叶神经元对闪光、运动光斑及运动光栅刺激的电生理反应特点,结果表明:(1)小叶神经元对闪光刺激具有特征性反应,细胞对给光和撤光刺激都会表现出不同程度的去极化和超极化,反应的波形不随闪光时间的改变而改变,两次去极化之间的时间间隔与闪光刺激的时间长度成线性关系;(2)小叶神经元对运动光斑的运动速度非常敏感,而对光斑的运动方向的改变却不敏感,尽管有的细胞存在一个能使反应的变化更快的优势方向,但并没有明显的运动方向选择性;(3)小叶神经元对运动光栅的响应频率受光栅的空间频率和运动速度的双重调制,与光栅的运动方向无关。 相似文献
104.
自然免耕下的稻田生态系统 总被引:15,自引:0,他引:15
自然免耕是一种新型的稻田耕作法,通过人为改变地表微地形,建立了一个适合水旱作物复种轮作,鱼、萍、鸭周年共生的稻田生态系统.自然免耕促进了土壤内、外环境的物质、能量和信息交换,水、热、气、肥谐调.并通过环境网络效应,强化了环境与生物区系间的缓冲-调节力.提高了土壤自调能力和土壤有序度. 相似文献
105.
Arabidopsis COP8, COP10, and COP11 genes are involved in repression of photomorphogenic development in darkness. 总被引:16,自引:6,他引:10 下载免费PDF全文
Wild-type Arabidopsis seedlings are capable of following two developmental programs: photomorphogenesis in the light and skotomorphogenesis in darkness. Screening of Arabidopsis mutants for constitutive photomorphogenic development in darkness resulted in the identification of three new loci designated COP8, COP10, and COP11. Detailed examination of the temporal morphological and cellular differentiation patterns of wild-type and mutant seedlings revealed that in darkness, seedlings homozygous for recessive mutations in COP8, COP10, and COP11 failed to suppress the photomorphogenic developmental pathway and were unable to initiate skotomorphogenesis. As a consequence, the mutant seedlings grown in the dark had short hypocotyls and open and expanded cotyledons, with characteristic photomorphogenic cellular differentiation patterns and elevated levels of light-inducible gene expression. In addition, plastids of dark-grown mutants were defective in etioplast differentiation. Similar to cop1 and cop9, and in contrast to det1 (deetiolated), these new mutants lacked dark-adaptive change of light-regulated gene expression and retained normal phytochrome control of seed germination. Epistatic analyses with the long hypocotyl hy1, hy2, hy3, hy4, and hy5 mutations suggested that these three loci, similar to COP1 and COP9, act downstream of both phytochromes and a blue light receptor, and probably HY5 as well. Further, cop8-1, cop10-1, and cop11-1 mutants accumulated higher levels of COP1, a feature similar to the cop9-1 mutant. These results suggested that COP8, COP10, and COP11, together with COP1, COP9, and DET1, function to suppress the photomorphogenic developmental program and to promote skotomorphogenesis in darkness. The identical phenotypes resulting from mutations in COP8, COP9, COP10, and COP11 imply that their encoded products function in close proximity, possibly with some of them as a complex, in the same signal transduction pathway. 相似文献
106.
Louis Faso Richard S. Trowbridge Wei Quan Xiu-Lan Yao Edmund C. Jenkins Alma Maciulis Thomas D. Bunch Henry M. Wisniewski 《In vitro cellular & developmental biology. Animal》1994,30(4):226-235
Summary A strain of cerebral endothelial cells was established from isolated cortical microvessels of caprine brain. These cells,
which are referred to as ECl cells, can be routinely subcultured to 32 passages without the loss of differentiated morphologic
and immunologic traits. The ability to routinely subculture ECl cells is an important asset, given that isolated cerebral
endothelial cells in mammals generally lose their differentiated traits after only 2 to 3 passages.
ECl cells were shown to contain Factor VIII-related antigen, which is a specific marker for cells of endothelial origin. ECl
cells morphologically demonstrated a scarcity of pinocytotic vesicles on their apical surfaces, a lack of trans-cytoplasmic
vesicles, and the ability to form in culture confluent monolayers with tight junctional complexes. Therefore, ECl cells possess
specific antigenic and ultrastructural features which classify them as being small vessel endothelial cells of the blood-brain
barrier type. Cytogenetic evaluation of ECl cells demonstrated a normal female goat 60,XX karyotype and confirmed the apparent
non-transformed nature of ECl cells due to the lack of chromosome abnormalities or rearrangements. Using scanning electron
microscopy, ECl cells were also shown to form confluent monolayers on mixed nitrocellulose filters, a feature that will enable
the development of an in vitro system to study trans-endothelial transport. Given that ECl cells are readily subcultured and
grow well on nitrocellulose filters, and that they resemble cerebral endothelium in vivo, it seems evident that ECl cells
can be used as a versatile model for the study of blood-brain barrier function, regulation, and pathology. 相似文献
107.
108.
Some of the early genes of Bacillus subtilis bacteriophage SPO1 were hypothesized to function in the shutoff of host biosyntheses. Two of these genes, e3 and e22, were cloned and sequenced. E22 showed no similarity to any known protein, while E3, a highly acidic protein, showed significant similarity only to other similarly acidic proteins. Each gene was immediately downstream of a very active early promoter. Each was expressed actively during the first few minutes of infection and was then rapidly shut off and its RNA rapidly degraded. An e3 nonsense mutation severely retarded the degradation of e3 RNA. Expression of a plasmid-borne e3 gene, in either B. subtilis or Escherichia coli, resulted in the inhibition of host DNA, RNA, and protein syntheses and prevented colony formation. However, the e3 nonsense mutation caused no measurable decrease in either burst size or host shutoff during infection and, in fact, caused an increased burst size at high multiplicities of infection. We suggest that e3 is one of several genes involved in host shutoff, that its function is dispensable both for host shutoff and for phage multiplication, and that its shutoff function is not entirely specific to host activities. 相似文献
109.
This article demonstrates the successful in situ real-time monitoring of the cell concentration of Perilla frutescens in a bioreactor by using a laser turbidimeter. It was found that turbidity measurements at 780 nm with the laser sensor were hardly affected by the red color of the anthocyanin produced by P. frutescens cells, nor by the aeration rate or agitation speed within the ranges investigated. There was an excellent linear relationship, with a correlation coefficient (r(2)) higher than 0.99, between the sensor's response and the cell concentration. The whole growth stage of the cells, i.e., lag, logarithmic, and stationary phases, in bioreactor cultivations, could be satisfactorily estimated on-line by means of the in situ turbidimeter. However, during the declining phase of the cells, an apparent deviation was observed between the on-line estimations and off-line measurements of cell concentrations by dry cell weight, while the wet cell weight could be estimated by the same turbidimeter system. We found that this deviation was caused by a decrease in the cell density due to an increase of the individual cell volume and a decrease of the cell dry weight during the declining phase. (c) 1993 John Wiley & Sons, Inc. 相似文献
110.
Through simple model analysis, the mass action kinetic model for lipolytic enzymes in biphasic aqueous-organic systems can be simplified using the quasi-steady state assumption (or the quasi-equilibrium state assumption) for the adsorbed enzyme E* or the enzyme-substrate complex E*S. Some parameter combinations leading to the above assumptions are derived confirmed by full numerical integration of the whole enzymatic process. The results may be classified into three categories: (1) the quasi-equilibrium state assumption for E*, (2) the quasi-steady state assumption for E*, and (3) the quasi-steady state assumption for E*S. Further simplification for both E* and E*S is also discussed. (c) 1993 Wiley & Sons, Inc. 相似文献