全文获取类型
收费全文 | 4168篇 |
免费 | 250篇 |
国内免费 | 2篇 |
出版年
2022年 | 37篇 |
2021年 | 63篇 |
2020年 | 24篇 |
2019年 | 41篇 |
2018年 | 73篇 |
2017年 | 58篇 |
2016年 | 94篇 |
2015年 | 147篇 |
2014年 | 163篇 |
2013年 | 271篇 |
2012年 | 251篇 |
2011年 | 262篇 |
2010年 | 176篇 |
2009年 | 150篇 |
2008年 | 263篇 |
2007年 | 254篇 |
2006年 | 227篇 |
2005年 | 253篇 |
2004年 | 238篇 |
2003年 | 246篇 |
2002年 | 240篇 |
2001年 | 71篇 |
2000年 | 61篇 |
1999年 | 70篇 |
1998年 | 57篇 |
1997年 | 36篇 |
1996年 | 31篇 |
1995年 | 29篇 |
1994年 | 31篇 |
1993年 | 28篇 |
1992年 | 41篇 |
1991年 | 44篇 |
1990年 | 38篇 |
1989年 | 37篇 |
1988年 | 27篇 |
1987年 | 22篇 |
1986年 | 24篇 |
1985年 | 26篇 |
1984年 | 25篇 |
1983年 | 17篇 |
1982年 | 20篇 |
1981年 | 13篇 |
1980年 | 11篇 |
1979年 | 9篇 |
1977年 | 13篇 |
1976年 | 13篇 |
1975年 | 10篇 |
1974年 | 13篇 |
1973年 | 14篇 |
1971年 | 9篇 |
排序方式: 共有4420条查询结果,搜索用时 31 毫秒
61.
62.
Nucleotide sequence of a Sendai virus genome region covering the entire M gene and the 3'' proximal 1013 nucleotides of the F gene. 总被引:11,自引:4,他引:7
下载免费PDF全文
![点击此处可从《Nucleic acids research》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Y Hidaka T Kanda K Iwasaki A Nomoto T Shioda H Shibuta 《Nucleic acids research》1984,12(21):7965-7973
We determined the sequence of the 2,138 nucleotides in the Sendai virus genome just following the 3' proximal 3,686 nucleotides which we had previously reported (Nucleic Acids Res. 11, 7317-7330, 1983). This covers the entire third gene of 1,173 nucleotides and the 3' proximal 1,013 nucleotides of the fourth gene. Like the NP and P+C genes, both the third and fourth genes start from consensus sequence R1 (3'-UCCCAC(or UA)UUUC) at the 3' end and the third gene terminates with consensus sequence R2 (3'-AUUCUUUUU) at the 5' end. The third gene was identified as M, and the deduced 348 amino acids indicated that the M protein is rich in basic residues and has hydrophobic domains near the C-terminal. The fourth gene, although sequencing is not complete yet, was identified as F, since a large open reading frame found in the gene contains the characteristic sequence of 20 amino acids located at the N-terminal of the F1 protein. Analyses of the amino acid sequence suggested that the structure of the F gene product is NH2-signal peptide-F2-F1-COOH. 相似文献
63.
64.
Junichi Kitajima Tetsuya Komori Toshio Kawasaki Hans-rolf Schulten 《Phytochemistry》1982,21(1):187-192
From the aerial parts of Fritillaria thunbergii, three glycosidal Solanum alkaloids (basic steroid saponins) were isolated together with minor 相似文献
65.
Tada Mikiro; Shiroishi Masahide; Hasegawa Kiyozo; Suzuki Tetsuya; Iwai Kazuo 《Plant & cell physiology》1982,23(4):607-614
The effect of light on the production of ergosterol and phytoeneand on the composition of carotenoids in Rhodotorula minutawas studied to determine which part of the pathway of carotenoidsynthesis regulated by light. The ergosterol content in the cells was in the range of 3.43.6mg/g dry cells regardless of the presence or absence of illuminationand the light intensity. The phytoene production in the cellswas markedly stimulated by light and was dependent on the lightintensity according to the amount of carotenoid pigments produced.In addition, the ratio of phytoene to carotenoid was in therange of 0.360.44, regardless of the presence or absenceof illumination and the light intensity. The fact that the ratio of carotenoid fractionated on the basisof the functional group involved in each carotenoid to the totalamount of carotenoid was almost constant regardless of the lightintensity suggested that the composition of the carotenoidssynthesized in the cells is not affected by light. It was deduced from these results that light induced the productionof enzyme(s) required for phytoene biosynthesis in Rhodotorulaminuta. (Received November 7, 1981; Accepted March 19, 1982) 相似文献
66.
Terpenoid and acetylenic components not reported previously in Artemisia capillaris have been identified, including p-cymene, 5-phenyl-1, 3-diyne, dehydrofalcarinone and dehydrofalcarinol. The distribution of volatile components in different parts of the plant is described. 相似文献
67.
68.
Masakiyo Iwai Hiroshi Kanno Masashi Hashino Jinichi Suzuki Takumi Yanaihara Tetsuya Nakayama 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》1981,225(2)
A simple, rapid and highly specific method by selected ion monitoring (SIM), using 9α,11α-[2H2]estrone, [2,4-2H2]estradiol-17β and 2,4-[2H2]estriol as internal standards, was developed for the determination of serum estrogens during pregnancy. Serum samples were submitted to a simple extraction procedure and were analysed after formation of the trifluoroacetic anhydride derivative. The inter-assay coefficients of variation for estrone, estradiol-17β and estriol were 3.73%, 3.42% and 3.49%, respectively. The results obtained by SIM were compared with analysis performed using radioimmunoassay. 相似文献
69.
Interaction of subunits of polypeptide chain elongation factor I from pig liver. Formation of EF-1alpha.EF-1betagamma and EF-1beta complexes 总被引:2,自引:0,他引:2
In the preceding papers, we showed that one of the two complementar factors of polypeptide chain elongation factor 1 (EF-1) from pig liver, EF-1alpha, functionally corresponds to bacterial EF-Tu (Nagata, S., Iwasaki, K., and Kaziro, Y. (1976) Arch. Biochem. Biophys. 172, 168), while the other, EF-1betagamma, as well as one of its subunits, EF-1beta, corresponds to bacterial EF-Ts (Motoyoshi, K. and Iwasaki, K. (1977) J. Biochem. 82, 703). Therefore, the interaction between EF-1alpha and EF-1 betagamma or EF-1beta was was examined and the following results were obtained. i) EF-1betagamma catalytically promoted the exchange of [14C]GDP bound to EF-1alpha with exogenous [3H]GDP. ii). In the absence of the exogenous guanine nucleotide, EF-1betagamma as well as EF-1beta could displace GDP bound to EF-1alpha to form an EF-1alpha.EF-1betagamma as well as an EF-1alpha.EF-1beta complex. iii) The occurrence of EF-1alpha.EF-1betagamma and EF-1alpha.EF-1beta complexes was demonstrated by gel filtration on Sephadex G-150. These results strongly indicate that the mechanism of the action of EF-1betagamma or EF-1beta in converting EF-1alpha.GDP into EF-1alpha.GTP is analogous to bacterial EF-Ts, and the reaction is accomplished by the following reactions; EF-1alpha.GDP + EF-1betagamma (or EF-1beta) in equilibrium EF-1alpha.EF-1betagamma (or EF-1beta) + GDP; EF-1alpha.EF-1beta (or EF-1beta) + GTP IN EQUILIBRIUM EF-1alpha.GTP + EF-1betagamma (or EF-1beta). 相似文献
70.
Kozo Yamamoto Tetsuya Tosa Kiyokazu Yamashita Ichiro Chibata 《Biotechnology and bioengineering》1977,19(8):1101-1114
The kinetics of the reversible fumarase reaction of immobilized Brevibacterium ammoniagenes cells and the decay behavior of enzyme activity were investigated in a plug flow system. The time course of the reaction in the immobilized cell column was well explained by the time-conversion equation including the apparent kinetic constants of the immobilized cell enzyme. The decay rate of fumarase activity was faster in the upper sections of the column (inlet side of the substrate solution) compared with the lower sections when 1M sodium fumarate (pH 7.0) was continuously passed through the column at 37°C. It was shown that the decay rate of the fumarase activity in the immobilized cell column depends on the flow rate of the substrate solution. The effect of flow rate on the decay rate of enzyme activity was considered to be related to the rate of contamination of enzyme with poisonous substances derived from the substrate solution or to the rate of leakage of enzyme stabilizers and/or enzyme itself from the immobilized cells. 相似文献