全文获取类型
收费全文 | 3313篇 |
免费 | 143篇 |
国内免费 | 352篇 |
专业分类
系统科学 | 30篇 |
丛书文集 | 82篇 |
教育与普及 | 42篇 |
理论与方法论 | 11篇 |
现状及发展 | 207篇 |
研究方法 | 1篇 |
综合类 | 3428篇 |
自然研究 | 7篇 |
出版年
2024年 | 2篇 |
2023年 | 11篇 |
2022年 | 50篇 |
2021年 | 34篇 |
2020年 | 44篇 |
2019年 | 36篇 |
2018年 | 40篇 |
2017年 | 60篇 |
2016年 | 46篇 |
2015年 | 87篇 |
2014年 | 112篇 |
2013年 | 95篇 |
2012年 | 158篇 |
2011年 | 145篇 |
2010年 | 132篇 |
2009年 | 187篇 |
2008年 | 200篇 |
2007年 | 249篇 |
2006年 | 267篇 |
2005年 | 236篇 |
2004年 | 249篇 |
2003年 | 230篇 |
2002年 | 239篇 |
2001年 | 176篇 |
2000年 | 154篇 |
1999年 | 114篇 |
1998年 | 100篇 |
1997年 | 58篇 |
1996年 | 65篇 |
1995年 | 46篇 |
1994年 | 51篇 |
1993年 | 24篇 |
1992年 | 27篇 |
1991年 | 24篇 |
1990年 | 26篇 |
1989年 | 11篇 |
1988年 | 7篇 |
1987年 | 3篇 |
1986年 | 7篇 |
1985年 | 5篇 |
1955年 | 1篇 |
排序方式: 共有3808条查询结果,搜索用时 15 毫秒
141.
A. Shukla P. Chaurasia S. R. Bhaumik 《Cellular and molecular life sciences : CMLS》2009,66(8):1419-1433
Methylation of lysine residues of histones is associated with functionally distinct regions of chromatin, and, therefore,
is an important epigenetic mark. Over the past few years, several enzymes that catalyze this covalent modification on different
lysine residues of histones have been discovered. Intriguingly, histone lysine methylation has also been shown to be cross-regulated
by histone ubiquitination or the enzymes that catalyze this modification. These covalent modifications and their cross-talks
play important roles in regulation of gene expression, heterochromatin formation, genome stability, and cancer. Thus, there
has been a very rapid progress within past several years towards elucidating the molecular basis of histone lysine methylation
and ubiquitination, and their aberrations in human diseases. Here, we discuss these covalent modifications with their cross-regulation
and roles in controlling gene expression and stability.
Received 24 September 2008; received after revision 21 November 2008; accepted 28 November 2008 相似文献
142.
C. Schubert 《Cellular and molecular life sciences : CMLS》2009,66(7):1178-1197
The Williams-Beuren syndrome is a genomic disorder (prevalence: 1/7,500 to 1/20,000), caused by a hemizygous contiguous gene
deletion on chromosome 7q11.23. Typical symptoms comprise supravalvular aortic stenosis, mental retardation, overfriendliness
and visuospatial impairment. The common deletion sizes range of 1.5–1.8 mega base pairs (Mb), encompassing app. 28 genes.
For a few genes, a genotype-phenotype correlation has been established. The best-explored gene within this region is the elastin
gene; its haploinsufficiency causes arterial stenosis. The region of the Williams-Beuren syndrome consists of a single copy
gene region (~1.2 Mb) flanked by repetitive sequences – Low Copy Repeats (LCR). The deletions arise as a consequence of misalignment
of these repetitive sequences during meiosis and a following unequal crossing over due to high similarity of LCRs. This review
presents an overview of the Williams-Beuren syndrome region considering the genomic assembly, chromosomal rearrangements and
their mechanisms (i.e. deletions, duplications, inversions) and evolutionary and historical aspects.
Received 11 July 2008; received after revision 15 October 2008; accepted 16 October 2008 相似文献
143.
本文提出一种基于音乐基因的乐谱存储模型S-MusicXML.将乐谱的存储和处理的基本单位由音阶提升到基因,有利于通过数据挖掘技术对音乐内涵的挖掘和存储.定义了旋律基因等概念,并通过实验进一步分析了挖掘音乐基因比挖掘音乐频繁模式更有优势. 相似文献
144.
胰岛素样生长因子结合蛋白相关蛋白1(IGFBP-rP1)是近年来恶性肿瘤的研究热点.本文主要综述IGFBP-rP1在恶性肿瘤中的抑癌基因作用机制及可能的临床实用价值.IGFBP-rP1在恶性肿瘤中的作用广泛涉及细胞的增殖、衰老、凋亡、分化、血管生成等多方面,研究指出IGFBP-rP1可缩短细胞增殖周期并影响非停泊性生长从而抑制增殖,降低致瘤能力;调节BRAF-MEKERK信号通路及pRB、HSP60等相关蛋白的表达从而影响衰老及凋亡;主要通过IGF依赖方式抑制血管生成;而且IGFBP-rP1表达下降跟肿瘤细胞分化程度降低有关.研究显示IGFBP-rP1有一定的临床实用价值,如其表达量跟恶性肿瘤的进展相关,低表达提示某些化疗药物抵抗,可提示预后.而在恶性肿瘤中特异性地上调IGFBP-rP1,可抑制肿瘤增殖及血管生成、诱导细胞衰老凋亡、提高肿瘤分化程度及化疗敏感性,具有治疗意义,但研究者们还在努力探究,争取早日找到一种临床有效的靶向IGFBP-rP1的基因治疗方法. 相似文献
145.
用GEP实现复杂函数的自动建模 总被引:6,自引:0,他引:6
GEP是一种新颖的遗传算法,在函数建模的应用中取得良好的结果.给出计算有效基因长度的伪代码,结合GRCM方法阅读基因,快速计算出染色体的适应值.在算法中增加了参数估计模块,用GEP得到较好模型后,用参数估计模块进行参数优化,试验显示这种混合的GEP方法比传统的最小二乘法、神经网络以及遗传程序设计等方法具有更好的性能. 相似文献
146.
147.
Dolezel D Zdechovanova L Sauman I Hodkova M 《Cellular and molecular life sciences : CMLS》2008,65(6):964-969
Current models state that insect peripheral oscillators are directly responsive to light, while mammalian peripheral clock
genes are coordinated by a master clock in the brain via intermediate factors, possibly hormonal. We show that the expression
levels of two circadian clock genes, period (per) and Par Domain Protein 1 (Pdp1) in the peripheral tissue of an insect model species, the linden bug Pyrrhocoris apterus, are inversely affected by contrasting photoperiods. The effect of photoperiod on per and Pdp1 mRNA levels was found to be mediated by the corpus allatum, an endocrine gland producing juvenile hormone. Our results
provide the first experimental evidence for the effect of an endocrine gland on circadian clock gene expression in insects.
Received 31 October 2007; received after revision 7 January 2008; accepted 9 January 2008
D. Dolezel, L. Zdechovanova: These authors contributed equally to this work. 相似文献
148.
Many notions regarding the function, structure and regulation of cholera toxin expression have remained essentially unaltered
in the last 15 years. At the same time, recent findings have generated additional perspectives. For example, the cholera toxin
genes are now known to be carried by a non-lytic bacteriophage, a previously unsuspected condition. Understanding of how the
expression of cholera toxin genes is controlled by the bacterium at the molecular level has advanced significantly and relationships
with cell-density-associated (quorum-sensing) responses have recently been discovered. Regarding the cell intoxication process,
the mode of entry and intracellular transport of cholera toxin are becoming clearer. In the immunological field, the strong
oral immunogenicity of the non-toxic B subunit of cholera toxin (CTB) has been exploited in the development of a now widely
licensed oral cholera vaccine. Additionally, CTB has been shown to induce tolerance against co-administered (linked) foreign
antigens in some autoimmune and allergic diseases.
Received 25 October 2007; accepted 12 December 2007 相似文献
149.
The use of anti-5-methylcytosine antibodies in affinity columns allowed the identification of methylated sequences in the
genome of Drosophila melanogaster adults. In view of the presence of transposable elements amongst the identified sequences, it has been suggested that DNA
methylation is involved in transposon control in the fly genome. On the contrary, a reanalysis of these data furnishes several
intriguing elements that could raise new questions about the role that DNA methylation plays in the fly genome. The aim of
the present paper is to discuss some features that emerge from the analysis of the identified methylated sequences.
Received 26 January 2006; received after revision 8 May 2006; accepted 2 June 2006 相似文献
150.
General pedigrees are very common in farm animals,and the recent availability of large panels of SNPs in domestic species has given new momentum to the search for the mutations underlying variation in quantitative traits.In this paper,we proposed a new transmission disequilibrium test approach,called the pedigree transmission disequilibrium test,which deals with general pedigrees and quantitative traits in farm animals.Compared with the existing pedigree disequilibrium test (PDT) and general linear model-based method QTDT,our approach performed better with higher power and lower type I error,especially in scenarios where the quantitative trait locus (QTL) effect was small.We also investigated the application of our approach in selective genotyping design.Our simulation studies indicated that it was plausible to implement a selective genotyping strategy in the proposed pedigree transmission disequilibrium test.We found that our approach performed equally well or better when only some proportion of the individuals in the two tails were genotyped compared with its performance when all the individuals in the pedigree were genotyped. 相似文献