首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   1350篇
  免费   100篇
  2024年   3篇
  2023年   12篇
  2022年   11篇
  2021年   66篇
  2020年   31篇
  2019年   41篇
  2018年   55篇
  2017年   41篇
  2016年   60篇
  2015年   90篇
  2014年   85篇
  2013年   92篇
  2012年   138篇
  2011年   124篇
  2010年   59篇
  2009年   67篇
  2008年   77篇
  2007年   72篇
  2006年   60篇
  2005年   68篇
  2004年   62篇
  2003年   32篇
  2002年   38篇
  2001年   11篇
  2000年   3篇
  1999年   7篇
  1998年   5篇
  1997年   5篇
  1996年   7篇
  1995年   2篇
  1994年   9篇
  1993年   2篇
  1992年   3篇
  1991年   1篇
  1990年   2篇
  1989年   1篇
  1984年   1篇
  1983年   2篇
  1981年   1篇
  1971年   1篇
  1969年   1篇
  1968年   1篇
  1967年   1篇
排序方式: 共有1450条查询结果,搜索用时 328 毫秒
1.
We report here the construction and analysis of insertional mutations in each of the three genes of the gltBDF operon and the nucleotide sequence of the region downstream from gltD. Two open reading frames were identified, the first of which corresponds to gltF. The gltB and gltD genes code for the large and small subunits, respectively, of the enzyme glutamate synthase (GOGAT). gltF codes for a protein, with a molecular mass of 26,350 Da, which is required for Ntr induction. Histidase synthesis was determined as a measure of Ntr function. First, insertions in gltB, gltD or gltF all prevent Ntr induction. Second, complementation analysis indicates that high-level expression of both the gltD and gltF genes is required for the induction of the Ntr enzymes under nitrogen-limiting conditions, indicating that the phenotype of the gltB insertion probably results from polarity on gltD and gltF. Third, glutamate-dependent repression of the glt operon appears to be mediated by the product of the gltF gene. Thus, the gltBDF operon of Escherichia coli is involved in induction of the so-called Ntr enzymes in response to nitrogen deprivation, as well as in glutamate biosynthesis.  相似文献   
2.
3.
4.
We present evidence thatRhizobium etli has two glutaminases differentiated by their thermostability and electrophoretic mobility. The thermostable glutaminase (B) is constitutive, in contrast with the thermolabile glutaminase (A), which is positively regulated by glutamine and negatively regulated by ammonium and by the carbon source. In distinction to glutaminase A, glutaminase B plays a minor role in the utilization of glutamine as a carbon source, but it may play a role in maintaining the balance of glutamine and glutamate. By complementation of theRhizobium etli LM16 mutant that lacks glutaminase A, we have cloned the gene that codes for this enzyme.  相似文献   
5.
Etiolated Vicia faba seedlings were exposed to continuous red light to investigate whether changes in extracellular peroxidase activity were correlated in time and localization with changes in extension growth and/or lignin content in the subapical region of the epicotyl. Continuous red light: (a) increased extracellular peroxidase activity after a lag of ca 0.5 h, followed by a maximum peak after 2.5 h due to slightly acidic isoforms (pI = 6–6.5, according to isoelectrofocusing gels), a minimum after 4 h and a second maximum after 8 h due to acidic isoforms (pI=4–5), (b) increased lignin content and epicotyl resistance to bending after a lag of ca 4 h, i.e. simultaneously with changes in acidic extracellular peroxidase activity, and (c) reduced extension growth to a stable rate after a lag of ca 1 h, not coinciding with the kinetics of any of the extracellular peroxidase isoforms. These effects of continuous red light were at least partially mediated by phytochrome. Tissue printing and anatomical studies revealed red light effects on extracellular peroxidase activity and lignin content mainly in the outer cortical parenchyma. The results are consistent with the involvement of phyto-chrome-mediated effects on extracellular peroxidases (acidic isoforms) in the transduction chain leading to lignin responses to red light.  相似文献   
6.
Journal of Plant Growth Regulation - Auxin is a hormone that delays ripening in part by reducing anthocyanin content and impairing color development. Auxin content declines during the ripening...  相似文献   
7.
Sagitta otoliths are usually formed of calcium carbonate polymorphs as aragonite. The objective of this study was to verify which carbonate polymorph is predominant in the sagitta otolith of Menticirrhus americanus and check whether this pattern remains in otoliths with morphological alterations. Otoliths of M. americanus were obtained from five sites on the southeast‐south coast of Brazil (São Sebastião (SS) 23°45′S–45°24′O, n = 29; Cananéia‐Iguape Estuarine Complex (CI) 25°02′S–47°54′O, n = 30; Paranaguá Estuarine Complex (PEC) 25°28′S–48°20′O, n = 35; Itapoá (IT) 26°07′S–48°36′O, n = 31; Laguna (LA) 28°28′S–48°46′O, n = 13). The characterization of carbonate polymorphs of otoliths was performed through Raman spectroscopy, a photonic and non‐destructive technique that analyzes molecular vibrations induced by laser. We analyzed 138 pairs of M. americanus otoliths, of which eight otoliths from different pairs presented morphological alterations (SS n = 1, CEP n = 5, IT n = 1, LA n = 1). The Raman spectra show that normal otoliths, that is, without morphological alterations, presented only aragonite in their structure. Among the otoliths that presented morphological alterations, the Raman spectra allowed to identify in six otoliths the deposition of aragonite and in only two otoliths the deposition of vaterite (one specimen of the PEC and one of SS).  相似文献   
8.
9.
群落的多样性取决于物种相互共存的能力,以及克服环境胁迫的能力,从而可能扮演一个环境过滤器的角色。生态位分化导致了比种间竞争更强的种内竞争,促进了物种共存。由于胁迫影响相互作用,生态位分化的强度可能沿胁迫作用的梯度发生变化。在有胁迫的栖息地,如沙漠和高山地区,植物的生长形式更加多样化,这表明在环境胁迫下植物具有更强的生态位分化。我们验证了生态位差异和环境过滤作用随着环境胁迫的增加而增强的假设。在墨西哥南部的半干旱草原上,我们沿着水分胁迫梯度在田间种植了6种一年生植物。植物进行三种种植处理:单独种植(没有相互作用),与同种植物为邻(种内相互作用)或与异种植物为邻(种间相互作用)。我们分析了种内与种间竞争的比值是如何沿水分胁迫梯度变化的,以评估水分如何决定生态位分化的强度。我们还测定了水分胁迫是否代表了一种环境过滤作用。我们发现了种内竞争比种间竞争更强,尤其是在水分胁迫更大的情况下。因此,我们的结果表明,除了一个物种外,所有物种至少在部分水分胁迫梯度下存在生态位分化。一些物种受到胁迫的阻碍,而另一些物种可能因为胁迫消除了土壤病原体而受到它的青睐。虽然高强度的生态位分化在环境胁迫下出现的频率略高,但由于我们的物种样本很小,而且这种通用的模式也存在例外,因此需要进一步的研究来确定这是否是自然界普遍存在的现象。  相似文献   
10.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号