全文获取类型
收费全文 | 78869篇 |
免费 | 6539篇 |
国内免费 | 4888篇 |
专业分类
90296篇 |
出版年
2024年 | 139篇 |
2023年 | 901篇 |
2022年 | 2076篇 |
2021年 | 3603篇 |
2020年 | 2326篇 |
2019年 | 2839篇 |
2018年 | 2869篇 |
2017年 | 2030篇 |
2016年 | 2873篇 |
2015年 | 4586篇 |
2014年 | 5295篇 |
2013年 | 5967篇 |
2012年 | 6904篇 |
2011年 | 6356篇 |
2010年 | 3819篇 |
2009年 | 3374篇 |
2008年 | 4113篇 |
2007年 | 3653篇 |
2006年 | 3172篇 |
2005年 | 2680篇 |
2004年 | 2276篇 |
2003年 | 1976篇 |
2002年 | 1730篇 |
2001年 | 1559篇 |
2000年 | 1565篇 |
1999年 | 1449篇 |
1998年 | 849篇 |
1997年 | 797篇 |
1996年 | 809篇 |
1995年 | 736篇 |
1994年 | 687篇 |
1993年 | 530篇 |
1992年 | 818篇 |
1991年 | 657篇 |
1990年 | 601篇 |
1989年 | 531篇 |
1988年 | 421篇 |
1987年 | 362篇 |
1986年 | 336篇 |
1985年 | 299篇 |
1984年 | 221篇 |
1983年 | 199篇 |
1982年 | 112篇 |
1981年 | 118篇 |
1980年 | 86篇 |
1979年 | 147篇 |
1978年 | 84篇 |
1977年 | 95篇 |
1975年 | 111篇 |
1974年 | 116篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
131.
cⅠ857基因的体外定位同义突变陈南春,高辉,陈苏民,杨萍,刘新平(西安第四军医大学分子生物学研究所,西安710032)外源基因要在大肠杆菌中获得高表达,需要合适的SD序列和可调控的强启动子[1]。PL启动子在原核启动子中属强启动子,它受cⅠ基因产物... 相似文献
132.
133.
Lipidomic changes during different growth stages of Nitzschia closterium f. minutissima 总被引:3,自引:0,他引:3
Xiaoling Su Jilin Xu Xiaojun Yan Peng Zhao Juanjuan Chen Chengxu Zhou Fang Zhao Shuang Li 《Metabolomics : Official journal of the Metabolomic Society》2013,9(2):300-310
Ultra Performance Liquid Chromatography-Electrospray ionization-Quadrupole-Time of Flight Mass Spectrometry (UPLC-ESI-Q-TOF–MS) is a powerful lipidomic tool. In this study, we developed a UPLC/Q-TOF–MS based method to investigate the lipid metabolomic changes in different growth phases of Nitzschia closterium f. minutissima. The data classification and biomarker selection were carried out by using multivariate statistical analysis, including principal components analysis (PCA), projection to latent structures with discriminant analysis (PLS-DA), and orthogonal projection to latent structures with discriminant analysis (OPLS-DA). We discovered that the intercellular lipid metabolites were significantly different among exponential, early stationary and late stationary phases. Thirty-one lipid molecules were selected and identified as putative biomarkers, including free fatty acid, Harderoporphyrin, phosphatidylglycerol, 1,2-diacyglycerl-3-O-4′-(N,N-trimethy)-homoserine, triacylglycerol, cholesterol, sulfoquinovosyldiacylglycerol, lyso-sulfoquinovosyldiacylglycerol, monogalactosyldiacylglycerol, digalactosyldiacylglycerol and lyso-digalactosyldiacylglycerol. These lipids have been shown previously to function in energy storage, membrane stability and photosynthesis efficiency during the growth of diatoms. Further analysis on the putative biomarkers demonstrated that nitrate starvation played critical role in the transition from exponential phase to stationary phase in N. closterium. This study is the first one to explore the lipidomic changes of microalgae in different growth phases, which promotes better understanding of their physiology and ecology. 相似文献
134.
135.
136.
137.
138.
DNA methylation changes in photoperiod-thermo-sensitive male sterile rice PA64S under two different conditions 总被引:1,自引:0,他引:1
Epigenetic modification can occur at a high frequency in crop plants and might generate phenotypic variation without changes in DNA sequences. DNA methylation is an important epigenetic modification that may contribute to environmentally-induced phenotypic variations by regulating gene expression. Rice Photoperiod-Thermo-Sensitive Genic Male Sterile (PTGMS) lines can transform from sterility to fertility under lower temperatures and short-day (SD) conditions during anther development. So far, little is known about the DNA methylation variation of PTGMS throughout the genome in rice. In this study, we investigated DNA cytosine methylation alterations in the young panicles of PTGMS line PA64S under two different conditions using methylation sensitive amplified polymorphism (MSAP) method. Compared with the DNA methylation level of PA64S under lower temperatures and SD conditions (fertility), higher methylation was observed in PA64S (sterility). The sequences of 25 differentially amplified fragments were successfully obtained and annotated. Three methylated fragments, which are homologous to D2, NAD7 and psaA, were confirmed by bisulfite sequencing and their expression levels were also evaluated by qPCR. Real time quantitative PCR analysis revealed that five of the six selected methylated genes were downregulated in PA64S (sterility). These results suggested that DNA methylation may be involved in the sterility–fertility transition of PA64S under two different environmental conditions. 相似文献
139.
艾滋病是本世纪80年代初发现的一种烈性传染病,5年病死率为100%,致病因子为人免疫缺陷病毒,该病毒的蛋白酶在病毒复制和成熟中具有决定性的意义。由于目前国内外尚未获得艾滋病病毒蛋白酶的高效表达的重组子及活性检测系统,限制了它的研究与应用。本文利用PCR技术修饰了艾滋病病毒蛋白酶的基因,使其具有便于克隆及表达用的限制酶切位点及转录终止码,井在其C末端设置了一个可用于检验该酶活性的特殊序列。DNA序列分析揭示上述突变策略成功,将修饰后的艾滋病病毒蛋白酶基因克隆入大肠杆菌表达系统,并获得高效表达(>30%),Western-Bolt鉴定结果表明所表达的蛋白为艾滋病病毒所特有,并具有较好的生物活性。 相似文献
140.