全文获取类型
收费全文 | 8262篇 |
免费 | 654篇 |
国内免费 | 592篇 |
专业分类
9508篇 |
出版年
2024年 | 16篇 |
2023年 | 104篇 |
2022年 | 266篇 |
2021年 | 434篇 |
2020年 | 306篇 |
2019年 | 346篇 |
2018年 | 370篇 |
2017年 | 251篇 |
2016年 | 356篇 |
2015年 | 503篇 |
2014年 | 570篇 |
2013年 | 599篇 |
2012年 | 759篇 |
2011年 | 633篇 |
2010年 | 384篇 |
2009年 | 369篇 |
2008年 | 408篇 |
2007年 | 378篇 |
2006年 | 347篇 |
2005年 | 276篇 |
2004年 | 237篇 |
2003年 | 202篇 |
2002年 | 175篇 |
2001年 | 142篇 |
2000年 | 114篇 |
1999年 | 133篇 |
1998年 | 79篇 |
1997年 | 89篇 |
1996年 | 80篇 |
1995年 | 74篇 |
1994年 | 85篇 |
1993年 | 60篇 |
1992年 | 73篇 |
1991年 | 69篇 |
1990年 | 60篇 |
1989年 | 33篇 |
1988年 | 36篇 |
1987年 | 25篇 |
1986年 | 19篇 |
1985年 | 23篇 |
1984年 | 9篇 |
1983年 | 11篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1978年 | 1篇 |
排序方式: 共有9508条查询结果,搜索用时 0 毫秒
11.
The carboxy-terminal 41 amino acids of herpes simplex virus type 1 glycoprotein B are not essential for production of infectious virus particles. 总被引:6,自引:6,他引:0
下载免费PDF全文
![点击此处可从《Journal of virology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Glycoprotein B (gB) is a virally encoded protein that is found in the envelope of herpes simplex virus type 1 and membranes of cells infected with herpes simplex virus type 1. It is essential for the production of infectious virus particles. An amber mutation was introduced into the gB gene by oligonucleotide-directed mutagenesis at the codon for amino acid 863 of the protein. Virus carrying this mutation should synthesize gB molecules lacking the last 41 amino acids of the cytoplasmic domain. Immunoprecipitation of infected cell extracts demonstrated the synthesis of appropriately truncated gB molecules. Characterization of the mutant virus indicated that the loss of the carboxy-terminal 41 amino acids has little effect on gB function. 相似文献
12.
从“湖北光敏感核不育水稻”的未受精子房和花药培养出单倍体植株 总被引:10,自引:0,他引:10
采用10种诱导培养基,培养湖北光敏感核不育水稻农垦58品种的未受精子房和花药。共培养未受精子房2790个,获得胚囊愈伤组织17块,最高诱导频率达3.33%,其中2块分化出绿苗。培养花药16740个,获得花药愈伤组织15块,最高诱导频率为0.92%,其中3块分化出苗,2丛白苗,1株绿苗。胚囊植株和花粉植株经根尖染色体检查为单倍体,2n=x=12。实验证明,液体培养、2,4-D0.2-0.5 mg/1、低温预处理对诱导胚囊愈伤组织及花粉愈伤组织的形成具良好效果。 相似文献
13.
Hydrolysis of phosphatidylcholine is stimulated by Ras proteins during mitogenic signal transduction.
下载免费PDF全文
![点击此处可从《Molecular and cellular biology》网站下载免费的PDF全文](/ch/ext_images/free.gif)
H Cai P Erhardt J Szeberényi M T Diaz-Meco T Johansen J Moscat G M Cooper 《Molecular and cellular biology》1992,12(12):5329-5335
We have used a dominant inhibitory ras mutant (Ha-ras Asn-17) to investigate the relationship of Ras proteins to hydrolysis of phosphatidylcholine (PC) in the transduction of mitogenic signals. Expression of Ha-Ras Asn-17 inhibited NIH 3T3 cell proliferation induced by polypeptide growth factors or phorbol esters. In contrast, the mitogenic activity of PC-specific phospholipase C (PC-PLC) was not inhibited by Ha-Ras Asn-17 expression. Similarly, cotransfection with a cloned PC-PLC gene bypassed the block to NIH 3T3 cell proliferation resulting from expression of the inhibitory ras mutant. Hydrolysis of PC can therefore induce cell proliferation in the absence of normal Ras activity, suggesting that PC-derived second messengers may act downstream of Ras in mitogenic signal transduction. This was substantiated by the finding that Ha-Ras Asn-17 expression inhibited growth factor-stimulated hydrolysis of PC. Taken together, these results indicate that PC hydrolysis is a target of Ras during the transduction of growth factor-initiated mitogenic signals. 相似文献
14.
15.
Iris Maldener Wolfgang Lockau Yuping Cai C. Peter Wolk 《Molecular & general genetics : MGG》1991,225(1):113-120
Summary It has been suggested that a calcium-dependent intracellular protease of the cyanobacterium, Anabaena sp., participates in the differentiation of heterocysts, cells that are specialized for fixation of N2. Clones of the structural gene (designated prcA) for this protease from Anabaena variabilis strain ATCC 29413 and Anabaena sp. strain PCC 7120 were identified via their expression in Escherichia coli. The prcA gene from A. variabilis was sequenced. The genes of both strains, mutated by insertion of a drug resistance cassette, were returned to these same strains of Anabaena on suicide plasmids. The method of sacB-mediated positive selection for double recombinants was used to achieve replacement of the wild-type prcA genes by the mutated forms. The resulting mutants, which lacked Ca2+-dependent protease activity, were not impaired in heterocyst formation and grew on N2 as sole nitrogen source. 相似文献
16.
Chlorinated methanes are important environmental pollutants, which can be metabolized by bacteria. The biotransformation of chlorinated methanes by bacteria has been shown to be due either to gratuitous metabolism (cometabolism) or their use as a source of carbon and energy. The reactions which result in carbon-halogen bond cleavage include substitutive, reductive, oxygenative, and gem-elimination mechanisms. Certain methylotrophic bacteria can use dichloromethane as a source of carbon and energy. Dichloromethane dehalogenase catalyzes the first substitutive reaction in this metabolism. The enzyme shows a 1010-fold rate enhancement over the reaction of the bisulfide anion with dichloromethane in water. Pseudomonas putida G786 synthesizes cytochrome P-450CAM which catalyzes the gratuitous reduction of chlorinated methanes. These studies with purified enzymes are beginning to reveal more detailed mechanistic features of bacterial chlorinated methane metabolism.Abbreviations DNA
deoxyribonucleic acid
- kcat
catalytic first order rate constant for an enzyme catalyzed reaction
- KM
Michaelis constant for an enzyme catalyzed reaction
- MNDO
modified neglect of diatomic overlap
- PIMA
pattern induced multialignment
- DCMD
dichloromethane dehalogenase 相似文献
17.
18.
19.
<正> 为了在TSr(Bgl Ⅱ-1)核苷酸顺序中寻找有无类似α—顺序的冷点区顺序,我们在微型电子计算机上编制了查找相似序列顺序(WSS程序)。本程序的特点是运行速度快,无重复扫描,可自行选择欲查找的相似百分比和百分比精度,它不仅适用于寻找内切酶的酶切点,而且可以在相当长度的已测序DNA顺序中快速准确地检出碱基位置和数量发生随机变异的DNA相似片段,并直接计算、打印出相似百分比值。 相似文献
20.
<正> 本文报道以pAT153质粒为载体克隆的adr亚型乙型肝炎病毒(HBV)全基因的限制性内切酶图谱。重组质粒已命名为pHBV-NCl。重组质粒的提取和酶解采用常规方法。限制性内切酶为Bio-Labs公司产品。用Sepharcry S-1000纯化得到的质粒,经电泳鉴定都是完整的超螺旋DNA。经过鉴定其BamHⅠ、XhoⅠ、XbaⅠ、SstⅡ、SphⅠ、BglⅠ、BglⅡ、BstEⅡ、AceⅠ、AvaⅠ、HincⅡ、HpaⅠ等12种酶的21个切口已被定位。其中XhoⅠ、XbaⅠ、SstⅡ、 相似文献