全文获取类型
收费全文 | 3798篇 |
免费 | 340篇 |
国内免费 | 329篇 |
专业分类
4467篇 |
出版年
2024年 | 7篇 |
2023年 | 45篇 |
2022年 | 111篇 |
2021年 | 203篇 |
2020年 | 131篇 |
2019年 | 165篇 |
2018年 | 157篇 |
2017年 | 125篇 |
2016年 | 184篇 |
2015年 | 225篇 |
2014年 | 248篇 |
2013年 | 281篇 |
2012年 | 319篇 |
2011年 | 289篇 |
2010年 | 185篇 |
2009年 | 165篇 |
2008年 | 205篇 |
2007年 | 154篇 |
2006年 | 167篇 |
2005年 | 145篇 |
2004年 | 136篇 |
2003年 | 107篇 |
2002年 | 115篇 |
2001年 | 97篇 |
2000年 | 85篇 |
1999年 | 79篇 |
1998年 | 46篇 |
1997年 | 44篇 |
1996年 | 38篇 |
1995年 | 34篇 |
1994年 | 28篇 |
1993年 | 21篇 |
1992年 | 19篇 |
1991年 | 23篇 |
1990年 | 11篇 |
1989年 | 6篇 |
1988年 | 10篇 |
1987年 | 14篇 |
1986年 | 8篇 |
1985年 | 8篇 |
1984年 | 8篇 |
1983年 | 4篇 |
1982年 | 2篇 |
1981年 | 5篇 |
1980年 | 1篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1977年 | 1篇 |
1974年 | 1篇 |
1971年 | 1篇 |
排序方式: 共有4467条查询结果,搜索用时 10 毫秒
71.
72.
薏苡胚发育及贮藏营养物质积累的研究 总被引:4,自引:0,他引:4
薏苡(Coix lacrym a-jobi)胚发育分下列各期:棒形胚前的原胚期、棒形胚期、胚芽鞘期、1叶期、2 叶期、3叶期、4 叶期、5 叶期及6叶期成熟胚。3 叶期胚具1 条不定根(种子根),4 叶期具2 条,5 叶期及成熟胚期具3 条。不定根与胚根排成1 纵行。营养物质最先在盾片细胞中积累。开花后9 天的1 叶期胚,在盾片、胚芽鞘及胚轴细胞中积累了淀粉,以后遍及成熟胚的各部分。淀粉粒含量与器官发生及生长顺序成正相关,但发育后期,盾片细胞内的淀粉粒含量下降。开花后10 天,盾片细胞中形成含晶体的蛋白质体,晶体含蛋白质及植酸钙镁。以后,这种蛋白质体增多、增大。同时,又形成不含晶体的蛋白质体。一定时期,含晶体的蛋白质体消失,不含晶体的蛋白质体增多,直到胚成熟。开花后13 天,胚芽鞘上部细胞形成蛋白质体。以后遍及成熟胚的各部分,器官发生越早,所含蛋白质体越多、越大。开花后10 天,盾片细胞中产生了脂体,成熟胚的盾片细胞,含有大量的脂体。还观察了胚发育各期与颖果及盾片长度的对应关系 相似文献
73.
经典分子生物学的中心法则描述了遗传信息的传递方向.中心法则认为RNA只有通过翻译产生蛋白质才在生命活动中发挥功能.但是随着分子生物学的发展,很多RNA其本身就可以承担生命学功能.而且RNA的形式也不仅仅只有线性这一种.本文总结了RNA转录后命运的4种形式:不翻译、部分翻译、从头翻译和过度翻译.RNA命运的多样性使得对于翻译的理解比经典的中心法则规定的内容将更加丰富、复杂.充分了解RNA转录后的命运,对以后研究RNA的功能提出了更高的要求,也为我们真正而全面地了解RNA的功能提供了可能. 相似文献
74.
以牛血球为材料,经溶血等处理和丙酮沉淀,获得牛血球超氧化物歧化酶粗品。此粗酶可以通过DEAE-Sepharose和CM-Sepharose快速柱层析,获得超氧化物歧化酶纯品。纯化的酶比活可达13500u/mg,经PAGE、SDS-PAGE和快速蛋白液相色谱(FPLC)检测,结果表明,纯化酶是均一的Sephadex G-100凝胶过滤测得该酶分子量为31,800,SDS-PAGE测得亚基分子量为15 相似文献
75.
以粒细胞巨噬细胞集落刺激因子(GMCSF) 为筛选文库的靶分子, 通过高效筛选(High throughputscreening, HTS) 方法来筛选多种多肽噬菌体文库, 在一个以噬菌体主要蛋白质为载体的多肽噬菌体文库中筛选到了一些与GMCSF结合的多肽, 并通过了ELISA和微淘选(micropanning) 实验的证实。这些多肽先导化合物经过进一步的优化, 可能成为GMCSF细胞因子的拮抗剂 相似文献
76.
Ming‐Hui Qian Qiong‐Bo Hu Shun‐Xiang Ren Nasser S. Mandour Bao‐Li Qiu P. A. Stansly 《Insect Science》2012,19(3):403-411
Abstract Effects of sublethal piperonyl butoxide (PB) on parasitization of Bemisia tabaci (Gennadius ) (Hemiptera: Aleyrodidae) by Encarsia bimaculata Heraty et Polaszek (Hymenoptera: Aphelinidae) were evaluated both in cage and greenhouse experiments. When first, second and third instar B. tabaci nymphs were treated with PB, all but the first instar were significantly prolonged. Data indicated that sublethal PB could improve E. bimaculata parasitism rates without influencing parasitoid eclosion rates. Prolonged development increased rates of parasitism by E. bimaculata, from 17.6% to 24.7% in cages, presumably by increasing the duration of host exposure. Sublethal PB combined with E. bimaculata as an integrated approach to control B. tabaci was evaluated using life table parameters under greenhouse conditions. Indices of population trend (I) calculated from life tables were estimated at 4.6 for B. tabaci exposed to PB and parasitoids compared to 14.1 with parasitoids alone and 23.5 in untreated controls. The results showed that after PB was sprayed and parasitoids introduced, development of B. tabaci was delayed and the peak of each stage was postponed. The older nymphal stage had highest mortality, primarily due to mortality caused by parasitism by E. bimaculata. 相似文献
77.
78.
Alzheimer''s disease (AD) is associated with abnormal functioning of the default mode network (DMN). Functional connectivity (FC) changes to the DMN have been found in patients with amnestic mild cognitive impairment (aMCI), which is the prodromal stage of AD. However, whether or not aMCI also alters the effective connectivity (EC) of the DMN remains unknown. We employed a combined group independent component analysis (ICA) and Bayesian network (BN) learning approach to resting-state functional MRI (fMRI) data from 17 aMCI patients and 17 controls, in order to establish the EC pattern of DMN, and to evaluate changes occurring in aMCI. BN analysis demonstrated heterogeneous regional convergence degree across DMN regions, which were organized into two closely interacting subsystems. Compared to controls, the aMCI group showed altered directed connectivity weights between DMN regions in the fronto-parietal, temporo-frontal, and temporo-parietal pathways. The aMCI group also exhibited altered regional convergence degree in the right inferior parietal lobule. Moreover, we found EC changes in DMN regions in aMCI were correlated with regional FC levels, and the connectivity metrics were associated with patients'' cognitive performance. This study provides novel sights into our understanding of the functional architecture of the DMN and adds to a growing body of work demonstrating the importance of the DMN as a mechanism of aMCI. 相似文献
79.
Zhang J Bao S Furumai R Kucera KS Ali A Dean NM Wang XF 《Molecular and cellular biology》2005,25(22):9910-9919
In response to DNA damage or replication stress, the protein kinase ATR is activated and subsequently transduces genotoxic signals to cell cycle control and DNA repair machinery through phosphorylation of a number of downstream substrates. Very little is known about the molecular mechanism by which ATR is activated in response to genotoxic insults. In this report, we demonstrate that protein phosphatase 5 (PP5) is required for the ATR-mediated checkpoint activation. PP5 forms a complex with ATR in a genotoxic stress-inducible manner. Interference with the expression or the activity of PP5 leads to impairment of the ATR-mediated phosphorylation of hRad17 and Chk1 after UV or hydroxyurea treatment. Similar results are obtained in ATM-deficient cells, suggesting that the observed defect in checkpoint signaling is the consequence of impaired functional interaction between ATR and PP5. In cells exposed to UV irradiation, PP5 is required to elicit an appropriate S-phase checkpoint response. In addition, loss of PP5 leads to premature mitosis after hydroxyurea treatment. Interestingly, reduced PP5 activity exerts differential effects on the formation of intranuclear foci by ATR and replication protein A, implicating a functional role for PP5 in a specific stage of the checkpoint signaling pathway. Taken together, our results suggest that PP5 plays a critical role in the ATR-mediated checkpoint activation. 相似文献
80.