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   407篇
  免费   26篇
  国内免费   18篇
  2023年   10篇
  2022年   9篇
  2021年   18篇
  2020年   29篇
  2019年   14篇
  2018年   16篇
  2017年   17篇
  2016年   8篇
  2015年   15篇
  2014年   9篇
  2013年   35篇
  2012年   19篇
  2011年   14篇
  2010年   7篇
  2009年   18篇
  2008年   17篇
  2007年   14篇
  2006年   11篇
  2005年   11篇
  2004年   9篇
  2003年   12篇
  2002年   10篇
  2001年   8篇
  2000年   12篇
  1999年   7篇
  1998年   5篇
  1997年   8篇
  1996年   4篇
  1994年   4篇
  1993年   5篇
  1992年   4篇
  1991年   6篇
  1990年   4篇
  1989年   2篇
  1988年   1篇
  1987年   3篇
  1986年   1篇
  1985年   7篇
  1984年   2篇
  1983年   2篇
  1982年   5篇
  1981年   6篇
  1980年   6篇
  1979年   2篇
  1978年   1篇
  1977年   5篇
  1976年   2篇
  1975年   4篇
  1974年   7篇
  1973年   4篇
排序方式: 共有451条查询结果,搜索用时 15 毫秒
1.
2.
Approximately half of the subclones examined from one clone of the wild carrot cell culture WC63-1-9-1 accumulated dihydroquercetin in the culture medium. The amount of dihydroquercetin accumulated in the medium varied with the subclone used, the size of the inoculum, the medium used and the time of sampling.Dedicated to Dr. Friedrich Constabel on the occasion of his 60th birthday  相似文献   
3.
Flower pigmentation patterns were scored in 185 senseChalcone synthase (Chs) transgenotes and 85 antisenseChs transgenotes; upon first flowering, 139 (75%) of sense transgenotes were found to be phenotypically altered, as were 70 (82%) of the antisense transgenotes. The observed patterns document the range of phenotypic variations that occur, as well as confirm and extend the finding that senseChs constructs produce several types of morphologybased based flower pigmentation patterns that antisenseChs constructs do not. Long-term monitoring for epigenetic variations in one population of 44 senseChs transgenotes showed that 43 (98%) were capable of producing a cosuppression phenotype. The primary determinant of sense-specific patterns of cosuppression ofChs was found to be the repetitiveness and organization pattern of the transgene, not position effects by, or readthrough from, flanking plant DNA sequences. The degree of cosuppression observed in progeny of transgenotes carrying multiple, dispersed copies as compared to that observed with a single copy of the transgene suggests that sense cosuppression ofChs is subject to a transgene dosage effect.  相似文献   
4.
5.
In petals of Silene dioica, gene P controls the 3′-hydroxylation of the anthocyanin B-ring and the hydroxylation pattern of the hydroxycinnamoyl acyl group bound to the 4″'-hydroxyl group of rhamnose of anthocyanidin 3-rhamnosyl(1→6)glucoside-5-glucoside. In this paper, experiments are presented which show that gene P is involved in the hydroxylation of p-coumaroyl-CoA to caffeoyl-CoA, which is then used both as a precursor in anthocyanin biosynthesis and as a substrate for the final acylation.  相似文献   
6.
Abstract. A brief high temperature treatment (45 C) promoted anthocyanin synthesis in 2-d-old dark-grown red cabbage seedlings. The increased effectiveness of a temperature/red light treatment as opposed to the reverse sequence suggests that an elevated temperature 'induces' some component which facilitates the phytochrome response.  相似文献   
7.
8.
The promotion of anthocyanin synthesis in red-cabbage seedlings by 5 min exposure to R light is inhibited by subsequent application of CaCl2. The stimulation of dark synthesis of anthocyanin by n-PrOH and by kinetin is also reduced by Ca2+ and by cholesterol, both of which are well known to stabilize cell membranes. By contrast, EDTA, which chelates Ca2+, promotes dark synthesis of anthocyanin. Assay of native Ca2+ extractable from seedlings immersed in EDTA demonstrates that R light exposure promotes a highly significant increase in extractable Ca2+. It is suggested that the molecular configuration of the phytochrome molecule affects the ability of a membrane to bind Ca2+ and that this in turn affects the permeability to substrates which are required for anthocyanin biosynthesis.  相似文献   
9.
10.
为进一步理解细风轮花青素合成途径,本研究利用华大基因BGISEQ-500平台对细风轮中的根、茎、叶、花4个组织进行了转录组测序,从头组装后得到128 856个Unigene。KEGG通路表明有40个Unigene编码了细风轮的花青素生物合成途径中6个关键酶。我们对其中的关键酶DFR(二氢黄酮醇还原酶)进行同源比对和空间结构模拟,结果显示DFR序列和结构均具有良好的保守性,且具有高度保守的NAD+结合位点,其二级结构主要由α螺旋和β折叠组成,在空间上α螺旋包裹着β折叠,形成“夹心饼干”样结构。  相似文献   
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