全文获取类型
收费全文 | 20456篇 |
免费 | 1476篇 |
国内免费 | 10篇 |
出版年
2023年 | 175篇 |
2022年 | 271篇 |
2021年 | 701篇 |
2020年 | 494篇 |
2019年 | 632篇 |
2018年 | 747篇 |
2017年 | 644篇 |
2016年 | 886篇 |
2015年 | 1196篇 |
2014年 | 1302篇 |
2013年 | 1502篇 |
2012年 | 1641篇 |
2011年 | 1531篇 |
2010年 | 922篇 |
2009年 | 823篇 |
2008年 | 1009篇 |
2007年 | 989篇 |
2006年 | 887篇 |
2005年 | 776篇 |
2004年 | 725篇 |
2003年 | 628篇 |
2002年 | 536篇 |
2001年 | 329篇 |
2000年 | 290篇 |
1999年 | 251篇 |
1998年 | 120篇 |
1997年 | 106篇 |
1996年 | 89篇 |
1995年 | 86篇 |
1994年 | 102篇 |
1993年 | 87篇 |
1992年 | 131篇 |
1991年 | 107篇 |
1990年 | 78篇 |
1989年 | 95篇 |
1988年 | 81篇 |
1987年 | 94篇 |
1986年 | 77篇 |
1985年 | 70篇 |
1984年 | 73篇 |
1983年 | 54篇 |
1982年 | 48篇 |
1981年 | 45篇 |
1980年 | 35篇 |
1979年 | 56篇 |
1978年 | 42篇 |
1976年 | 39篇 |
1975年 | 41篇 |
1974年 | 32篇 |
1973年 | 49篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
101.
The effects of hyperthermia (42 degrees C) on 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU)-mediated DNA interstrand crosslink formation were investigated in 9L rat brain tumor cells using the technique of alkaline elution. When cells were treated with 60 microM BCNU for 1 hr at 37 degrees C and incubated for 6 hr in drug-free medium at 42 degrees C, there was a 50% increase in crosslinking; and when cells were treated at 42 degrees C and incubated at 37 degrees C, there was a 45% increase in crosslinking compared with the results for cells treated and incubated at 37 degrees C. When cells were treated and incubated at 42 degrees C, there was a 129% increase in DNA crosslinking. The same relative order of results was found for cell survival. These results suggest that hyperthermia can increase DNA interstrand crosslink formation and the consequent cell death through two independent mechanisms: an increase in the amount of initial alkylation because of the increased rate of hydrolysis of BCNU at higher temperatures, and the effect of heat on DNA structure that leads to an increase in the number of crosslinks formed. 相似文献
102.
Danielle J. Donnelly William E. Vidaver Kwai Y. Lee 《Plant Cell, Tissue and Organ Culture》1985,4(1):43-50
The leaf, petiole, stem and root anatomy of an aseptically cultured red raspberry clone (Rubus idaeus L.) was studied before and 5 weeks after transfer to soil under controlled environmental conditions. Tissues persistent from culture showed little or no change with time in soil; they grew minimally and slight secondary wall deposition occurred. New organs formed in successive weeks after transplantation showed a graded increase in potential size and development. Some features, such as collenchyma formation, rapidly returned to control levels; this was seen in new leaves expanding in the first week after transplantation. Other features, such as sclerenchyma formation, did not occur in leaves expanding during the first 2 weeks after transplantation, even when these were a month or more in age. Some sclerenchyma was seen in leaves expanding in the third week after transplantation, increasing in later-formed leaves. Increasing the light intensity of transplant accelerated the return to control-type organ size and appearance. During acclimatization transitional forms of leaves, petioles, stems and roots develop that ranged anatomically from culture-to control-type. This trend is analagous to the normal developmental sequence of organ formation as it affects the potential for development of successily formed organs. 相似文献
103.
104.
105.
Danielle G. Marty 《Biotechnology letters》1985,7(12):900-904
Summary Study of CMC fermentation by a marine syntrophic association of an anaerobic cellulose-degrader, a carbohydrate-fermenter, and a methanogen. Altered fermentation pattern in general agreement with the concept of interspecies hydrogen transfer was obtained only with pregrowth of methanogen followed by inoculation of the two fermentative bacteria. 相似文献
106.
Molecular cloning of cDNA coding for human preprourokinase 总被引:2,自引:0,他引:2
A cDNA library was constructed in pBR322 from 18S to 20S mRNA that was extracted from human kidney cells, fractionated on oligo(dT)-cellulose column and sucrose-density gradient, and confirmed for urokinase production in Xenopus laevis oocytes. The Escherichia coli RR1 transformants were hybridized to synthetic oligonucleotide probe prepared according to the known amino acid sequence, Glu 73 to Glu 77 of human urinary urokinase chain B. The entire cloned cDNA covers a 2250-bp region, wherein the 1293-bp sequence codes for preprourokinase consisting of 431 amino acids, with the first 20 residues being a signal peptide. The 5'-untranslated region is at least 80 bp long and the 3'-untranslated region is longer than 850 bp. 相似文献
107.
F. J. Silva 《Genetica》1984,63(2):147-152
The3H-uridine labelling patterns in J and U polytene chromosomes ofDrosophila subobscura were determined. The analysis was carried out in two developmental stages and in two strains proceeding from the same geographical origin whose genotypes were: Jst/Jst; U1+2/U1+2 and J1/J1; U1+2+8/U1+2+8 respectively. It was observed that the labelling pattern coincided very approximately with the puffing pattern in the same stages and chromosomal arrangements. Comparison of the3H-Uridine incorporation patterns between chromosomal arrangements showed light quantitative differences. These results are discussed in relation to the inversion effect. 相似文献
108.
K B Alves C M Brandi J C Souza-Pinto J A Guimar?es 《The International journal of biochemistry》1984,16(12):1295-1300
An aminopeptidase from human urine (HUA) able to hydrolyze L-aminoacyl-2-naphthylamides, L-Leu-p-nitroanilide and to convert both MLBK and LBK to BK has been further purified and characterized. The preparation now obtained showed a 3-fold higher specific activity than the previously described one and a single active protein band in 7% polyacrylamide gel electrophoresis accounting for 86% of total protein. Kinetic constants for this kinin-converting enzyme were determined using L-aminoacyl-2-naphthylamides, L-Leu-p-nitroanilide and LBK. The Km values for different naphthylamides were in the 10(-5) M range while that for L-Leu-p-nitroanilide was 3.6 X 10(-4) M. With LBK as substrate the aminopeptidase activity showed the highest catalytic efficiency in spite of a Km in the mM range. The enzyme was poorly inhibited by -SH and -S-S- group reagents. Some L-aminoacids, as well as mono- and diamines, indomethacin, puromycin and bestatin were equipotent competitive inhibitors of both arylamidase and aminopeptidase activities. Results obtained in this paper are compatible with our conclusion that human urine, unlike other enzyme sources, contains only one aminopeptidase, and that this enzyme displays both arylamidase and kinin-converting activities. The enzyme's action may be important in the metabolism of kinins, yielding peptides which could interact with both B-1 and B-2 kinin receptors in the kidney. 相似文献
109.
Rita Delgado J. J. R. Fraústo Da Silva M. Cndida T. A. Vaz 《Inorganica chimica acta》1984,90(3):185-190
Enthalpy changes for the complexation of alkaline-earth and transition metals with three cyclic tetra-aza-tetracetic acids (cDOTA, cTRITA and cTETA) were obtained by continuous titration calorimetry. From these values and free energy data, the entropy changes for the same reactions were derived. The results show that these complexes are stabilised by both favourable enthalpy and entropy changes, except those of Mg2+ and those of Sr2+ and Ba2+ with cTETA. Generally, the entropy changes for the reactions of the alkaline-earth metals are higher than for the reactions of the non cyclic polyaminocarboxylic acids, but for the reactions of the transition metals the entropy changes are comparable for the cyclic and non cyclic ligands. These results are discussed in terms of a model of ‘cage’ coordination of the metals.The enthalpy changes decrease with the increase in size of the tetra-aza ring (except in the case of Cu2+) but no specific cavity size effect is noticeable. Consideration of the temperature-dependent and temperature-independent contributions to ΔH supports the idea that the number of coordinated nitrogen atoms and carboxylate groups vary along the series. 相似文献
110.
Karla J. Matteson Bon-chu Chung Walter L. Miller 《Biochemical and biophysical research communications》1984,120(1):264-270
P450scc is the rate-limiting hormonally regulated enzyme that cleaves the cholesterol side chain. Translation of bovine adrenocortical mRNA and immunoprecipitation with rabbit anti-bovine P450scc indicates P450scc mRNA represents 1% of the total. DNA complementary to bovine adrenocortical mRNA was cloned in the site of pBR322 by dC·dG tailing and high-efficiency transformation. A clone containing sequences complementary to P450scc mRNA was identified by hybrid-selected translation only when plasmid DNA was first purified by CsCl gradient centrifugation. As is often the case with hybrid-selected translation, the clone identified contains a small insert. 相似文献