全文获取类型
收费全文 | 19438篇 |
免费 | 2569篇 |
国内免费 | 9645篇 |
出版年
2024年 | 232篇 |
2023年 | 661篇 |
2022年 | 1087篇 |
2021年 | 1241篇 |
2020年 | 1087篇 |
2019年 | 1229篇 |
2018年 | 836篇 |
2017年 | 836篇 |
2016年 | 881篇 |
2015年 | 1344篇 |
2014年 | 1703篇 |
2013年 | 1579篇 |
2012年 | 2046篇 |
2011年 | 1983篇 |
2010年 | 1552篇 |
2009年 | 1682篇 |
2008年 | 1789篇 |
2007年 | 1665篇 |
2006年 | 1517篇 |
2005年 | 1284篇 |
2004年 | 950篇 |
2003年 | 861篇 |
2002年 | 769篇 |
2001年 | 647篇 |
2000年 | 561篇 |
1999年 | 415篇 |
1998年 | 212篇 |
1997年 | 159篇 |
1996年 | 123篇 |
1995年 | 94篇 |
1994年 | 91篇 |
1993年 | 89篇 |
1992年 | 68篇 |
1991年 | 63篇 |
1990年 | 40篇 |
1989年 | 26篇 |
1988年 | 30篇 |
1987年 | 21篇 |
1986年 | 26篇 |
1985年 | 40篇 |
1984年 | 17篇 |
1983年 | 9篇 |
1982年 | 33篇 |
1981年 | 7篇 |
1980年 | 5篇 |
1964年 | 5篇 |
1958年 | 5篇 |
1955年 | 4篇 |
1953年 | 4篇 |
1950年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 421 毫秒
141.
The Hyper-Gene Conversion Hpr5-1 Mutation of Saccharomyces Cerevisiae Is an Allele of the Srs2/Radh Gene 总被引:7,自引:2,他引:5
下载免费PDF全文
![点击此处可从《Genetics》网站下载免费的PDF全文](/ch/ext_images/free.gif)
The HPR5 gene has been defined by the mutation hpr5-1 that results in an increased rate of gene conversion. This mutation suppresses the UV sensitive phenotype of rad18 mutations in hpr5-1 rad18 double mutants by channeling the aborted repair events into a recombination repair pathway. The HPR5 gene has been cloned and is shown to be allelic to the SRS2/RADH gene, a putative DNA helicase. The HPR5 gene, which is nonessential, is tightly linked to the ARG3 locus chromosome X. The hpr5-1 allele contains missense mutation in the putative ATP binding domain. A comparison of the recombination properties of the hpr5-1 allele and the null allele suggests that recombination events in hpr5 defective strains can be generated by several mechanisms. We propose that the HPR5 gene functions in the RAD6 repair pathway. 相似文献
142.
青海犹伊螨属一新种(蜱螨亚纲:犹伊螨科) 总被引:2,自引:1,他引:1
本文绘图描述了根田鼠犹伊螨新种Eviphis oeconomus sp.nov.,并讨论了与喜马拉雅犹伊螨E.himalayaensis Ma et Piao,1981的鉴别特征。模式标本采自青海久治县的根田鼠Microtus oeconmus Pallas体上,存放在青海省地方病防治研究所。 相似文献
143.
本文报道了发现于我国的俗草蛉属Suarius 3新种:海南俗草蛉S.hainanus sp.nov.,钩俗草蛉S.hamulasus sp.nov.及楔唇俗草蛉S.sphenochilus sp.nov.新种模式标本保存于北京农业大学昆虫标本室。 相似文献
144.
脉翅目(Neuroptera)草蛉科(Chrysopidae)作为一类重要天敌资源,在我国各地非常丰富,大量的标本有待鉴定。本文主要记述2新属及其所属种类,模式标本均保存于北京农业大学昆虫标本室。 相似文献
145.
Huiling Hao Yunquan Jiang S. J. Zhang Peng Zhang Rong X. Zeng Marietta Y. W. T. Lee 《Chromosoma》1992,102(Z1):S121-S127
A continuing theme of our laboraory, has been the understanding of human DNA polymerases at the structural level. We have
purified DNA polymerases delta, epsilon and alpha from human placenta. Monoclonal antibodies to these polymerases were isolated
and used as tools to study their immunochemical relationships. These studies have shown that while DNA polymerases delta,
epsilon and alpha are discrete protiens, they must share common structural features by virtue of the ability of several of
our monoclonal antibodies to exhibit cross-reactivity. A second approach we have taken is the molecular cloning of human DNA
polymerase delta and epsilon. We have cloned the DNA polymerase delta cDNA, and this has allowed us to compare its primary
structure to those of human polymerase alpha and other members of this polymerase family. Multiple sequence alignments have
revealed that human DNA polymerase delta is also closely related to the herpes virus family of DNA polymerases. In situ hybridization
has shown that the human DNA polymerase delta gene is localized to chromosome 19 q13.3–q13.4. In order to further determine
the functional regions of the DNA polymerase δ structure we are currently expressing human pol δ inE. coli and baculovirus systems. Other work in our laboratory is directed toward examining the expression of DNA polymerase δ during
the cell cycle. 相似文献
146.
电刺激大鼠扣带前回(ACg),血压升高,心率加快,同时缰核(Hb)内20.7%的神经元兴奋,22.4%的神经元抑制,56.9%的神经元无反应。双侧Hb内微量注射盐酸利多卡因,可明显阻断电刺激ACg引起的心血管反应。结果表明,ACg对心血管活动的调节,一部分是通过改变Hb的活动来实现的,Hb是ACg调节心血管活动的下行性通路之一。 相似文献
147.
148.
Regenerative medicine is a burgeoning field that is important to combat challenging diseases and functional impairments. Compared with traditional cell therapies with evident shortcomings (e.g., cell suspension injection or tissue engineering with scaffolds), scaffold-free cell sheet technology enables transplanted cells to be grafted and fully maintain their viability on target sites. Clinical and experimental studies have advanced the application of cell sheet technology to numerous tissues and organs (e.g., liver, cornea and bone). However, previous reviews have failed to discuss vital aspects of this rapidly developing technology, and many new challenges are gradually emerging. This review aims to provide a comprehensive introduction to cell sheet technology from cell selection to the ultimate applications of cell sheets, and challenges and future visions are also described. 相似文献
149.
150.