全文获取类型
收费全文 | 5573篇 |
免费 | 263篇 |
国内免费 | 199篇 |
出版年
2024年 | 7篇 |
2023年 | 52篇 |
2022年 | 90篇 |
2021年 | 108篇 |
2020年 | 113篇 |
2019年 | 111篇 |
2018年 | 137篇 |
2017年 | 102篇 |
2016年 | 99篇 |
2015年 | 112篇 |
2014年 | 227篇 |
2013年 | 265篇 |
2012年 | 139篇 |
2011年 | 236篇 |
2010年 | 158篇 |
2009年 | 236篇 |
2008年 | 270篇 |
2007年 | 232篇 |
2006年 | 242篇 |
2005年 | 242篇 |
2004年 | 228篇 |
2003年 | 190篇 |
2002年 | 183篇 |
2001年 | 115篇 |
2000年 | 92篇 |
1999年 | 124篇 |
1998年 | 145篇 |
1997年 | 118篇 |
1996年 | 118篇 |
1995年 | 111篇 |
1994年 | 124篇 |
1993年 | 95篇 |
1992年 | 87篇 |
1991年 | 106篇 |
1990年 | 124篇 |
1989年 | 87篇 |
1988年 | 82篇 |
1987年 | 97篇 |
1986年 | 66篇 |
1985年 | 65篇 |
1984年 | 102篇 |
1983年 | 79篇 |
1982年 | 83篇 |
1981年 | 58篇 |
1980年 | 57篇 |
1979年 | 46篇 |
1978年 | 22篇 |
1977年 | 18篇 |
1976年 | 18篇 |
1974年 | 6篇 |
排序方式: 共有6035条查询结果,搜索用时 515 毫秒
71.
Thylakoids isolated from peas (Pisum sativum cv. Kelvedon Wonder) and phosphorylated by incubation with ATP have been compared with non-phosphorylated thylakoids in their sensitivity to photoinhibition by exposure to illumination in vitro. Assays of the kinetics of fluorescence induction at 20° C and the fluorescence emission spectra at-196° C indicate a proportionally larger decrease in fluorescence as a result of photoinhibitory treatment of non-phosphorylated compared with phosphorylated thylakoids. It is concluded that protein phosphorylation can afford partial protection to thylakoids exposed to photoinhibitory conditions.Abbreviations and symbols DCMU
3-(3,4-dichlorophenyl)-1,1-dimethylurea
-
F
0
Level of chlorophyll fluorescence when photosystem 2 traps are open
-
F
m
Level of chlorphyll fluorescence when photosystem 2 traps are closed
- P
Maximum level of fluorescence reached in the absence of DCMU
- PSI (II)
photosystem I(II) 相似文献
72.
Photoacoustic and fluorescence measurements of the chilling response and their relationship to carbon dioxide uptake in tomato plants 总被引:5,自引:0,他引:5
The response of tomato plants to various chilling treatments was studied using two approaches for the measurement of photosynthetic activity. One involved the use of a portable fluorometer for the measurement of in-vivo chlorophyll fluorescence, while the other employed a newly introduced photoacoustic system which allowed changes in oxygen evolution to be followed in a leaf disc. A strong correlation was found between results obtained by each system and those obtained by a conventional open gas-exchange system for the determination of CO2 uptake. Both systems of measurements could readily distinguish between the effects of chilling in the dark (at 3° C for 18 h) and chilling at high photon flux density (2000 mol m-2 s-1 for 5h at 5° C). Chilling in the dark had practically no effect on the quantum yield of oxygen evolution, chlorophyll fluorescence or CO2 uptake, while chilling at excessively high photon flux density resulted in a sharp reduction (50–70%) in the quantum yields obtained. The results support the view that photosystem II cannot be the primary site of damage by chilling in the dark, although it is significantly affected by chilling at high light intensity.Abbreviations DCMU
3-(3,4-dichlorophenyl)-1,1-dimethylurea
- PA
photoacoustic
- PFD
photon flux density
- PSII
photosystem II 相似文献
73.
The effects of light and several photosynthetic inhibitors on the rate of sulfite metabolism in cells obtained from Cucumis sativus L. cotyledons was studied. The cells were treated with 200 M Na2SO3 and the disappearance of sulfite was monitored using either dithiobisnitrobenzoic acid or fuchsin. The rate of sulfite disappearance in light was double the dark rate. Disalicylidene propanediamine at 1 mM increased this light-enhanced metabolism approx. 50%; neither 1 M 3,4-dichlorophenyl-N,N-dimethylurea nor 0.1 mM cyanazine, which completely inhibited CO2-dependent oxygen evolution, affected the rate of sulfite metabolism. Addition of 200 M Na2SO3 to the cells partially inhibited 14CO2 fixation. The rate of sulfite consumption by the cells did not affect this inhibition. We conclude that light-dependent sulfite metabolism is cucumber cells may utilize reduced ferredoxin generated as a result of photosynthetic electron transport. An injurious interaction between CO2 fixation and sulfite appears to occur independently of the sulfite-metabolism process.Abbreviations DCMU
3,4-dichlorophenyl-N,N-dimethylurea
- DSPD
disalicylidene propanediamine
- DTNB
5,5-dithiobis-(2-nitrobenzoic acid) 相似文献
74.
CNBr cleavage of unreduced proenzyme Clr yielded fragment CP2b, isolated by gel filtration and highpressure gel permeation chromatography. This fragment (˜ Mτ 55000) comprised at least 4 disulphidelinked peptides, which were separated by gel filtration after reduction and alkylation. Peptide CP2bRA4, overlapping the A- and B-chain regions in proenzyme Clr was digested by V8 staphylococcal protease, and the digest separated by reversed-phase HPLC. N-terminal sequence analysis of peptide CP2bRA4SP9 established that Clr activation involves the cleavage of a single Arg-Ile bond, located in the sequence: Gln-Arg-Gln-Arg-Ile-Ile-Gly-Gly 相似文献
75.
The light energy requirements for photoactivation of two chloroplast enzymes: fructose-1,6-bisphosphatase and NADP-malate dehydrogenase were studied in a reconstituted chloroplast system. This system comprised isolated pea thylakoids, ferredoxin (Fd), ferredoxin-thioredoxin reductase (FTR) thioredoxinm and f (Tdm, Tdf) and the photoactivatable enzyme. Light-saturation curves of the photoactivation process were established with once washed thylakoids which did not require the addition of Td for light activation. They exhibited a plateau at 10 W·m–2 under nitrogen and 50 W·m–2 under air, while NADP photoreduction was saturated at 240 W·m–2. Cyclic and pseudocyclic phosphorylations saturated at identical levels as enzyme photoactivations. All these observations suggested that the shift of the light saturation plateau towards higher values under air was due to competing oxygen-dependent reactions. With twice washed thylakoids, which required Td for enzyme light-activation, photophosphorylation was stimulated under N2 by the addition of the components of the photoactivation system. Its rate increased with increasing Td concentrations, just as did the enzyme photoactivation rate, while varying the target enzyme concentration had only a weak effect. Considering that Td concentrations were in a large excess over target enzyme concentrations, it may be assumed that the observed ATP synthesis was essentially dependent on the rate of Td reduction.Under air, Fd-dependent pseudo-cyclic photophosphorylation was not stimulated by the addition of the other enzyme photoactivation components, suggesting that an important site of action of O2 was located at the level of Fd.Abbreviations Fd
ferredoxin
- FBPase
fructose-1,6-bisphosphatase
- FTR
ferredoxin-thioredoxin reductase
- LEM
light effect mediator
- NADP-MDH
NADP-malate dehydrogenase
- Td
thioredoxin 相似文献
76.
The cyanobacterium Oscillatoria agardhii was grown in continuous culture under various light conditions in order to study the interactions of light on phosphorus-limited growth. Under severe P-limiting (light-saturating) conditions, a low chlorophyll a and C-phycocyanin content was found. In addition, the light-harvesting capacity, reflected in the values of P
max (maximum light-saturated oxygen production rate) and (photosynthetic affinity), were low compared to light-limited cultures.Reduction of the light climate, either by reduction of the length of the photoperiod or light-intensity, resulted in an increase in light-harvesting capacity (higher pigment content, P
m and ) during growth under P-limiting conditions. Light-induced changes in P
max and could be related to the relative growth rate, being the actual growth rate as a fraction of the growth rate which would be observed under light-limiting conditions.Under P-limiting conditions, reduction of the light-climate caused a reduction in dry weight of the culture. This decrease was mainly due to a decrease in carbohydrate content of the cells. Under all conditions tested, carbohydrates were found to accumulate during the light-period and to be consumed during the dark-period.Evaluation of carbohydrate consumption in the dark yielded a specific maintenance rate constant of 0.001 h-1. This observation leads to the conclusion that the specific maintenance rate constant is independent on the character of the growth rate limiting nutrient for O. agardhii. 相似文献
77.
78.
Proton translocation during the reduction of NO
3
-
, NO
2
-
, N2O and O2, with endogenous substrates, in washed cells of Rhodopseudomonas sphaeroides f. denitrificans was investigated by an oxidant pulse method. On adding NO
2
-
to washed cells, anaerobically in the dark, an alkalinization occurred in the reaction mixture followed by acidification. When NO
3
-
, N2O or O2 was added to cells in the dark or with these compounds and NO
2
-
in light an acidification only was observed. Proton translocation was inhibited by carbonyl cyanide-m-chlorophenyl hydrazone.Valinomycin treated cells produced acid in response to the addition of either NO
3
-
, NO
2
-
, N2O or O2. The proton extrusion stoichiometry (
ratios) in illuminated cells were as follows: NO
3
-
0.5N2, 4.82; NO
2
-
0.5N2, 5.43; N2ON2, 6.20; and O2H2O, 6.43. In the dark the comparable values were 3.99, 4.10, 4.17 and 3.95. Thus, illuminated cells produced higher
values than those in the dark, indicating a close link between photosynthesis and denitrification in the generation of proton gradients across the bacterial cell membranes.When reduced benzyl viologen was the electron donor in the presence of 1 mM N-ethylmaleimide and 0.5 mM 2-n-heptyl-4-hydroxyquinoline-N-oxide in the dark, the addition of either NO
3
-
, NO
2
-
or N2O to washed cells resulted in a rapid alkalinization of the reaction mixture. The stoichiometries for proton consumption,
ratios without a permeant ion were NO
3
-
NO
2
-
,-1.95; NO
2
-
0.5 N2O,-3.03 and N2ON2,-2.02. The data indicate that these reductions occur on the periplasmic side of the cytoplasmic membrane.Abbreviations BVH
reduced benzyl viologen
- CCCP
carbonyl cyanide m-chlorophenyl hydrazone
- DIECA
N, N-diethyl-dithiocarbamate
- HOQNO
2-n-heptyl-4-hydroxyquinoline-N-oxide
- NEM
N-ethylmaleimide 相似文献
79.
The metabolism of N-methyl substituted 7H-dibenzo[c,g]carbazole (N-Me DBC) was investigated in vitro using liver microsomes from 3-methylcholanthrene (MC)-, benzo[c]carbazole (BC) and Arochlor-pretreated mice and rats. N-Me DBC is a potent sarcomatogen devoid of hepatotoxicity and liver carcinogenic activity. The ethyl acetate-extractable metabolites were separated by high performance liquid chromatography (HPLC) and most of them were identified by proton magnetic resonance (PMR), mass spectrometry (MS) and comparison with synthetically prepared specimens. Mouse and rat microsomes gave rise to the same metabolites. The major metabolites were 5-OH-N-Me DBC (50%), N-hydroxymethyl (HMe) DBC (25-30%) and 3-OH-N-Me DBC (10%). Addition of 1,1,1-trichloropropene-2,3-oxide (TCPO) to the standard incubation medium permitted the identification of two dihydrodiols among the minor metabolites. No metabolite of DBC was observed after incubation of N-Me DBC, or its major metabolite N-HMe DBC, with either mouse or rat microsomes, but the possibility of a slight demethylation cannot be totally excluded. The lack of biotransformation at the nitrogen atom site may explain the lack of hepatotoxicity and liver carcinogenic activity of N-Me DBC. The modulation of metabolism by epoxide hydrolase, cytosol and glutathione was also investigated. The results are discussed in the light of data previously obtained with hepatotoxic and hepatocarcinogenic DBC. 相似文献
80.
Electrophoretic analysis of polyphenoloxidase isoenzymes from a variety of angiosperms and from mushroom revealed that the enzymes remain active in the presence of 0.1 % sodium dodecylsulfate. Electrophoresis in the presence of sodium dodecylsulfate allows the detection of latent enzyme forms of polyphenoloxidase, and can also convert slower migrating enzyme forms to faster migrating forms. Electrophoresis in the absence of sodium dodecylsulfate followed by incubation in the presence of sodium dodecylsulfate can also be used to detect latent forms of polyphenoloxidase. Together, these approaches provide a method for screening latent enzymes and give some insight into the mechanism of activation by sodium dodecylsulfate. 相似文献