全文获取类型
收费全文 | 36742篇 |
免费 | 2821篇 |
国内免费 | 2827篇 |
出版年
2024年 | 68篇 |
2023年 | 491篇 |
2022年 | 1066篇 |
2021年 | 1847篇 |
2020年 | 1321篇 |
2019年 | 1652篇 |
2018年 | 1596篇 |
2017年 | 1193篇 |
2016年 | 1644篇 |
2015年 | 2312篇 |
2014年 | 2691篇 |
2013年 | 2970篇 |
2012年 | 3431篇 |
2011年 | 3190篇 |
2010年 | 1883篇 |
2009年 | 1601篇 |
2008年 | 1795篇 |
2007年 | 1654篇 |
2006年 | 1427篇 |
2005年 | 1236篇 |
2004年 | 1007篇 |
2003年 | 823篇 |
2002年 | 747篇 |
2001年 | 499篇 |
2000年 | 496篇 |
1999年 | 456篇 |
1998年 | 294篇 |
1997年 | 272篇 |
1996年 | 296篇 |
1995年 | 254篇 |
1994年 | 224篇 |
1993年 | 167篇 |
1992年 | 233篇 |
1991年 | 203篇 |
1990年 | 180篇 |
1989年 | 146篇 |
1988年 | 132篇 |
1987年 | 127篇 |
1986年 | 97篇 |
1985年 | 118篇 |
1984年 | 65篇 |
1983年 | 67篇 |
1982年 | 40篇 |
1981年 | 30篇 |
1980年 | 28篇 |
1979年 | 45篇 |
1978年 | 32篇 |
1976年 | 24篇 |
1975年 | 37篇 |
1974年 | 24篇 |
排序方式: 共有10000条查询结果,搜索用时 62 毫秒
191.
192.
武汉东湖水生植被及其恢复途径探讨 总被引:4,自引:0,他引:4
1992~1993年对武汉东湖三个主要湖区(郭郑湖、汤林湖和牛巢湖)水生植被的调查表明,该湖区共有水生植物32种,优势种为大茨藻、狐尾藻、苦草和菱。金鱼藻呈不断扩大的趋势。植被类型可分为11个群丛,植被面积约为0.65km ̄2,总生物量为1236.39t(湿重),植被带状分布仅见于汤林湖北部和其他部分湖汊。汤林湖和牛巢湖水生植被正处于自然恢复演替阶段。 相似文献
193.
酸水解蚕蛹制备复合氨基酸的研究 总被引:7,自引:0,他引:7
采用硫酸水解法,以蚕蛹制取复合氨基酸产品,得到氨基酸态氮分别为9.05%和13.45%的食用复合氨基粉和精制复合氨基酸粉。食用复合氨基酸粉含有18种氨基酸,其中必需氨基酸含量为39.2%。食用复合氨基酸粉的制备方法经工厂小批量生产证实,其工艺简单易行,适合于中小企业采用,该产品的质量优良,生产成本低廉,具有市场竞争力。 相似文献
194.
多异瓢虫生物学的研究 总被引:3,自引:0,他引:3
多异瓢虫在山东省德州地区一年发生4代,部分个体5代,以成虫在杂草丛内、残枝落叶及土块下越冬。在自然变温下,卵、幼虫、预蛹、蛹、成虫产卵前期和全世代的发育始点和有效积温分别为18.8±0.52℃和15.0日度、16.97±0.03℃和73.3日度、15.97±0.01℃和10.23日度、15.47±0.05℃和23.05日度、17.6±0.04℃和34.1日度、18.2±0.10℃和170.3日度。据Holing圆盘方程测定,1─4龄幼虫和产卵前期成虫日最大捕食棉蚜量依次力6.7头、36.4头、77.5头、81.3头和68.0头。 相似文献
195.
通过DNA体外重组技术,以pET-3b为表达载体,构建了重组表达质粒pET-6R(B)和PET-6R(B)4,分别编码28kD的hIL-6R配基结合区片段及其53kD的二联体蛋白,并为酶切分析和DNA序列分析所证实。SDS-PAGE分析表明,含有重组表达质粒的菌株可分别表达出28kD的蛋白rIL6R-28和53kD的rIL6R-53。重组蛋白分别占菌体总蛋白的45%和29%左右。重组蛋白主要以包涵体形式存在,Western印迹表明重组蛋白具有IL-6R的抗原性。 相似文献
196.
Enrique Galindo Guadalupe Salcedo Ma. Eugenia Ramírez 《Applied microbiology and biotechnology》1994,40(5):634-637
Xanthomonas campestris NRRL B-1459 and a variant E2, when preserved on agar slopes (transferred monthly) over 11 months did not deteriorate in their ability to produce xanthan in quantity and quality, as determined by culture in 500-ml baffled flasks. Variations between 8 and 14% (with respect to the average) in the final xanthan concentration were observed for the E2 and B-1459 strains, respectively. A wide range of final viscosities was obtained; these were consistent with the changes in gum concentration. Differences were more likely associated with differences in fermentation kinetics rather than being inherent to the strains. The rheological quality of both polysacharides was relatively constant throughout the time of culture maintenance. Preservation of these bacteria on agar slopes was an adequate method, in contrast to previous reports. In the period studied, strain E2 produced higher gum titres and slightly lower gum quality compared to strain B-1459.
Correspondence to: E. Galindo 相似文献
197.
Characterization of cis-acting elements in light regulation of the nuclear gene encoding the A subunit of chloroplast isozymes of glyceraldehyde-3-phosphate dehydrogenase from Arabidopsis thaliana. 总被引:10,自引:0,他引:10
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)
We have characterized cis-acting elements involved in light regulation of the nuclear gene (GapA) encoding the A subunit of chloroplast glyceraldehyde-3-phosphate dehydrogenase (GAPDH) in Arabidopsis thaliana. Our results show that a 1.1-kb promoter fragment of the GapA gene is sufficient to confer light inducibility and organ specificity in transgenic Nicotiana tabacum (tobacco) plants, using the beta-glucuronidase gene of Escherichia coli as the reporter gene. Deletion analysis indicates that the -359 to -110 bp region of the GapA gene is necessary for light responsiveness. Within this region there are three copies of a decamer repeat (termed the Gap box) having the consensus sequence 5'-CAAATGAA(A/G)A-3', which has not been characterized in the promoter regions of other light-regulated genes. A deletion (to -247) producing loss of one copy of these elements from the GapA promoter reduces light induction by two- to threefold compared with a promoter deletion (to -359) with all three Gap boxes present, while deletion of all three Gap boxes (to -110) abolishes light induction completely. Gel mobility shift experiments using tobacco nuclei as the source of nuclear proteins show that GapA promoter fragments that contain these repeats bind strongly to a factor in the nuclear extract and that binding can be abolished by synthetic competitors consisting only of a monomer or dimer of the Gap box. Furthermore, a trimer, dimer, and monomer of the Gap box show binding activity and, like the authentic GapA promoter-derived probes, show binding activities that are correlated with Gap box copy number. These results strongly suggest that these repeats play important roles in light regulation of the GapA gene of A. thaliana. 相似文献
198.
Ma Victoria Amores Paloma Hortelano Leticia García-Salguero José A. Lupiáñez 《Molecular and cellular biochemistry》1994,137(2):117-125
We have studied the effects of the diuretics mersalyl, furosemide and ethacrynic acid on renal gluconeogenesis in isolated rat-kidney tubules and on the activities of the most important gluconeogenic and glycolytic enzymes in both fed and fasted rats. Mersalyl (15 mg.kg–1 animal weight) significantly decreased the rate of gluconeogenesis in well-fed rats (68%) as well as in 24 and 48-h fasted ones (33 and 37% respectively). This inhibition occurred when lactate, pyruvate, glycerol or fructose were used as substrates. Ethacrynic acid at a dose of 50 mg.kg–1 animal weight provoked a transient inhibition of renal glucose production by almost 20% but only in fed rats with lactate as substrate, whereas the same dose of furosemide did not affect this metabolic pathway.Parallel to these changes, mersalyl caused a significant inhibition in the maximum activity of the most important gluconeogenic enzymes, phosphoenolpyruvate carboxykinase, fructose 1,6-bisphosphatase and glucose 6-phosphatase, in both fed and fasted rats. Neither ethacrynic acid nor furosemide produced any variations in the activities of these enzymes. The activity of the glycolytic enzymes phosphofructokinase and pyruvate kinase was not modified by these diuretics. Nevertheless, the activity of the thiol-enzyme glyceraldehyde 3-phosphate dehydrogenase was severely inhibited by mersalyl and to a lesser extent by the other diuretics. This inhibition was higher in fasted than fed rats. Hence, we conclude that the inhibitory effect of mersalyl on renal gluconeogenesis is due, at least partly, to a decrease in the flux through the gluconeogenic enzymes. Blood glucose was not modified after diuretic treatment in fed animals whereas mersalyl decreased the levels of blood glucose in 24-h fasted rats. Thein vivo effects of diuretics on gluconeogenesis correlate well with the previously observedin vitro effects, although ethacrynic acid was less potent as an inhibitorin vivo, probably because of its rapid clearance.Abbreviations EDTA
ethylenediaminetetraacetic acid
- EGTA
ethyleneglycolbis (-aminoethylether) N,N,N,N-tetraacetic acid
- DTT
dithiothreitol
- HEPES
N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid
- TRIS
2-amino-2-hydroxymethyl-1,3-propanediol
Publication No. 166 from Drogas, Tóxicos Ambientales y Metabolismo Celular Research Group, Department of Biochemistry and Molecular Biology, University of Granada, Granada, Spain 相似文献
199.
200.