全文获取类型
收费全文 | 2146篇 |
免费 | 116篇 |
国内免费 | 3篇 |
出版年
2022年 | 20篇 |
2021年 | 38篇 |
2020年 | 16篇 |
2019年 | 17篇 |
2018年 | 24篇 |
2017年 | 31篇 |
2016年 | 34篇 |
2015年 | 60篇 |
2014年 | 65篇 |
2013年 | 116篇 |
2012年 | 111篇 |
2011年 | 125篇 |
2010年 | 73篇 |
2009年 | 78篇 |
2008年 | 97篇 |
2007年 | 114篇 |
2006年 | 115篇 |
2005年 | 117篇 |
2004年 | 126篇 |
2003年 | 104篇 |
2002年 | 101篇 |
2001年 | 64篇 |
2000年 | 46篇 |
1999年 | 45篇 |
1998年 | 20篇 |
1997年 | 23篇 |
1996年 | 28篇 |
1995年 | 19篇 |
1994年 | 19篇 |
1993年 | 13篇 |
1992年 | 27篇 |
1991年 | 30篇 |
1990年 | 36篇 |
1989年 | 22篇 |
1988年 | 35篇 |
1987年 | 24篇 |
1986年 | 21篇 |
1985年 | 27篇 |
1984年 | 18篇 |
1983年 | 26篇 |
1982年 | 26篇 |
1981年 | 22篇 |
1980年 | 9篇 |
1979年 | 15篇 |
1978年 | 7篇 |
1977年 | 13篇 |
1976年 | 5篇 |
1975年 | 11篇 |
1972年 | 6篇 |
1966年 | 4篇 |
排序方式: 共有2265条查询结果,搜索用时 15 毫秒
1.
Involvement of the Binuclear Copper Site in the Proteolytic Activity of Polyphenol Oxidase 总被引:2,自引:0,他引:2
Plant polyphenol oxidase (PPO) is apt to degrade during andeven after purification. We developed a method to stabilizePPO by 0.3 M NaCl, 0.1% (w/v) Tween 20, and 50% (w/v) ethyleneglycol at pH 6.5. The protein slowly degraded by itself whenthe stabilizing reagents were removed. Ascorbate and/or H2O2accelerated the degradation. The ascorbate-induced degradationwas inhibited by catalase, suggesting that H2O2 is generatedthrough reduction of PPO by ascorbate. It is likely that dissolvedoxygen is converted to peroxide through two-electron reductionby the reaction center of PPO, binuclear Cu site, and a Fenton-typereaction occurred on it. This understanding was supported bythe finding that the H2O2-induced degradation was inhibitedby metal-chelators as well as by polyphenolic substrate of PPO.Considering the postulated mechanism of the self-degradationof PPO, we re-examined the degradation of the 23-kDa proteinof PSII by PPO [Kuwabara et al. (1997) Plant Cell Physiol. 38:179]. The obtained results suggested that the 23-kDa proteintriggers the active oxygen production by the binuclear Cu site,probably as reductant, and receives the radical species preferentiallyto the polypeptide moiety of PPO. (Received April 15, 1999; Accepted July 21, 1999) 相似文献
2.
Subnuclear localization and antitransforming activity of N-myc:beta-galactosidase fusion proteins. 总被引:3,自引:2,他引:1
N-myc expression is under stage- and tissue-specific regulation in mammalian development, but its function is totally unknown. We sought agents to block N-myc activity in order to infer from the effect the possible function of N-myc in the apparently complex processes. As candidates for such agents, we tested fusion genes encoding N-myc:beta-galactosidase fusion proteins for their effects on the formation of transformed foci of rat embryo primary fibroblasts as the result of transfection with N-myc and activated H-ras. One of the gene constructs very efficiently antagonized N-myc activity, as assessed by its effect on focus formation, but did not appreciably affect cell viability. The product of this gene was not only targeted to the nucleus but also accumulated in subnuclear loci which may represent the sites where normal N-myc proteins reside. The occurrence of antagonistic effect at a low stoichiometric ratio suggested that the fusion protein gene competed with the N-myc gene in a fashion analogous to a dominant negative mutation. 相似文献
3.
4.
Interposon mutagenesis of a region upstream of the petABC(fbcFBC) operon, encoding the ubiquinol: cytochrome c2 oxidoreductase (bc1 complex) of the photosynthetic bacterium Rhodobacter capsulatus revealed the presence of two genes, petP and petR. DNA nucleotide sequence determination of this region indicated that petP and petR are transcribed in the same direction as the petABC(fbcFBC) operon, and are translationally coupled. A silent insertion located in the interoperonal region separating petPR and the petABC(fbcFBC) genes indicated that these clusters have separate promoters. The deduced amino acid sequence of the putative petR gene product is homologous to various bacterial response regulators, especially to those of the OmpR subgroup. Moreover, it was found that PetR mutants are unable to grow on rich or minimal media by either photosynthesis or respiration, demonstrating that these gene products are essential for growth of R. capsulatus. 相似文献
5.
Acetylcholine receptor (AChR) purified from human skeletal muscle affinity-alkylated with bromoacetyl[methyl-3H]choline bromide ([3H]BAC) in mildly reducing conditions to yield a specifically radiolabeled polypeptide, Mr 44,000, the alpha-subunit. The binding of [125I]alpha-bungarotoxin to AChR was completely inhibited by affinity-alkylation, indicating that the human AChR's binding site for alpha-bungarotoxin is closely associated with the alpha-subunit's acetylcholine binding site. Structures in the vicinity of the alpha-bungarotoxin binding sites of AChRs from human muscle and Torpedo electric organ were compared by varying the conditions of alkylation. Under optimal conditions of reduction and alkylation, both human and Torpedo AChR incorporated BAC in equivalence to the number of alpha-bungarotoxin binding sites. However, with limited conditions of reduction but sufficient BAC to alkylate 100% of the alpha-bungarotoxin binding sites of human AChR, only 71% of the Torpedo AChR's binding sites were alkylated. In optimal conditions of reduction but with the minimal concentration of BAC that permitted 100% alkylation of the human AChR's alpha-bungarotoxin sites, only 74% of the Torpedo AChR's binding sites were alkylated. These data suggest that the neurotransmitter binding region of human muscle AChR is structurally dissimilar from that of Torpedo electric organ, having a higher binding affinity for BAC and an adjacent disulfide bond that is more readily accessible to reducing agents. 相似文献
6.
Using Toyopearl and cyclohexane: cyclohexanol solvent, fourCl-containing Chls were separated from 36Cl-labeled cells ofthe blue-green, Plectonema boryanum. In normally grown cells,all four Cl-containing chlorophylls amounted to less than 1/2,000of the total Chi and about 1/50 of P700, values much lower thanpreviously reportedcontents of Chi RC I, and varied from algato alga. The level of Cl-containing Chi was markedly enhancedwhen the cells were poisoned with methyl viologen. These resultssuggests that these Cl-containing Chls are not related to thereaction center of PS I. (Received June 23, 1987; Accepted September 17, 1987) 相似文献
7.
The effects of defoliation treatments on plant growth in sunflower (Helianthus annuus) were studied in the field. Four defoliation treatments, 0 (control), 37.4, 56.1 and 93.4% of the total leaf dry weight,
were applied to plants that had small third leaves. Decreased leaf weight/whole plant weight (F/W) ratios in defoliated plants
rapidly recovered to almost the same ratio as that observed in the control within 12 to 16 days after defoliation according
to the degree of defoliation. The mechanism involved in the recovery of the F/W ratio in defoliated plants mainly consisted
of three parameters: enhancement of (1) carbon distribution ratios in the leaves, (2) photosynthetic activity in the remaining
leaves, and (3) retranslocation of carbon from the stem and/or roots to leaves.
Inhibitive effects of defoliation on relative growth rate and net assimilation rate were seen at an early stage, but subsequently
both rates became larger in defoliated plants than in controls. Defoliated plants tended to show rapid development and expansion
of new leaves, and to show increased specific leaf area and protein synthesis in individual leaves. The sugar content of leaves
in defoliated plants was higher than that in controls, while the content in both stem and roots was lower. These responses
seem to be advantageous for development of the photosynthetic system. Heights of defoliated plants were clearly depressed
according to the degree of defoliation, and this was attributed largely to differences in the elongation rates of the internodes
resulting from defoliation. 相似文献
8.
9.
M Sobue J Takeuchi T Fukatsu T Nagasaka N Nakashima T Ogura T Katoh K Yoshida 《Stain technology》1989,64(1):43-47
Dermatan sulfate proteoglycan chains were detected in tissue sections treated with chondroitin B-lyase (0.01 units/ml) in 20 mM Tris-HCl (pH 8.0) for 1 hr, followed by staining with antibody 9A2 specific for unsaturated uronic acid coupled to N-acetylgalactosamine-4 sulfate. In contrast, after treatment with chondroitin B-lyase, no positive staining was observed with antibodies 3B3 and 1B5 which react to the unsaturated uronic acid coupled to N-acetylgalactosamine 6-sulfate and unsaturated uronic acid coupled to N-acetylgalactosamine, respectively. The distribution of dermatan sulfate thus revealed was confirmed by comparison with that found by monoclonal antibody 6B6 which reacts with small proteoglycans carrying dermatan sulfate side chains. The localization of positive staining in fibrous connective tissues was almost identical with these two procedures. 相似文献
10.
A mycolic acid-containing glycolipid, trehalose 2,3,6'-trimycolate, prepared from a non-pathogenic acid-fast bacterium Gordona aurantiaca, was shown to induce strong tumoricidal activity in peritoneal exudate cells by intravenous or intraperitoneal injection of liposome-encapsulated preparations. The mycolic acid derivative containing a high proportion of unsaturated fatty acids rendered macrophages cytotoxic against syngeneic mastocytoma cells in the absence of endotoxin, for over 14 days after the injection. The macrophages were ascertained to be at low intracellular levels of a lysosomal enzyme beta-galactosidase and an ectoenzyme alkaline phosphodiesterase, a specific pattern as previously described for "primed macrophages". However the culture supernatants of the peritoneal exudate cells were not cytotoxic. 相似文献