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61.
Bart M. Nicolaï Jan F. Van Impe Peter A. Vanrolleghem Joos Vandewalle 《Antonie van Leeuwenhoek》1992,62(4):273-283
The mathematical model for the penicillin G fed-batch fermentation proposed by Heijnen et al. (1979) is compared with the model of Bajpai & Reuß (1980). Although the general structure of these models is similar, the difference in metabolic assumptions and specific growth and production kinetics results in a completely different behaviour towards product optimization. A detailed analysis of both models reveals some physical and biochemical shortcomings. It is shown that it is impossible to make a reliable estimation of the model parameters, only using experimental data of simple constant glucose feed rate fermentations with low initial substrate amount. However, it is demonstrated that some model parameters might be key factors in concluding whether or not altering the substrate feeding strategy has an important influence on the final amount of product.It is illustrated that feeding strategy optimization studies can be a tool in designing experiments for parameter estimation purposes. 相似文献
62.
Edward J. B. Beeley P. A. Bennett L. G. I. Poland J. S. 《Biological trace element research》1990,(1):53-61
A microcomputer-controlled irradiation and measurement system and a microprocessor-controlled sample changer have been installed
at the SLOWPOKE-2 Facility at the Royal Military College of Canada (RMC). These systems can provide the gamut of instrumental
neutron activation analysis (INAA) techniques for the analyst. Custom software has been created for system control, data acquisition,
and off-line spectral analysis using programs that incorporate Gaussian peak-fitting methods of analysis. The design and use
of the equipment is discussed, and the performance is illustrated with results obtained from the analysis of marine sediment
and biological reference materials. 相似文献
63.
64.
Mark Phillippe Trevania Saunders Shrikar Bangalore 《In vitro cellular & developmental biology. Plant》1990,26(4):369-378
Summary The following studies were undertaken to develop a cultured uterine myocyte model which would allow further clarification
of the adrenergic signal transduction mechanisms utilized by these myocytes. After mechanical removal of the endometrium,
rabbit uterine myoctes were isolated by an overnight enzymatic disaggregation using collagenase and DNase I. The isolated
myocytes were maintained in culture in 75-cm2 flasks containing Waymouth's MB 751/1 medium-10% fetal bovine serum along with 10−8
M estradiol, penicillin, streptomycin, and Fungizone. The phase contrast and electron micrographic appearance of these cells
was consistent with that previously reported for smooth muscle myocytes in culture. Immunocytochemical studies utilizing monoclonal
anti-alpha-smooth muscle actin antibodies confirmed the presence of smooth muscle actin in these cultured myocytes. Western
blot studies similarly confirmed the presence of alpha-smooth muscle actin in rabbit myometrial tissue and the cultured myocytes,
both the primary and F1 generation. After prelabeling the myocytes with [3H]inositol, adrenergic stimulation experiments demonstrated alpha-1 receptor mediated stimulation of inositol phosphates.
Beta receptor stimulation experiments confirmed cAMP production in these cultured myocytes, and the ability of clonidine,
an alpha-2 agonist, to inhibit forskolin stimulated cAMP production confirmed the presence of functional alpha-2 adrenergic
receptors in these myocytes. In conclusion, these cultured rabbit uterine myocytes have provided an in vitro model which can
be utilized to further clarify the adrenergic receptor signal transduction mechanisms in genital tract smooth muscle.
This research was supported by grant HD-22063 from the National Institutes of Health, Bethesda, MD. 相似文献
65.
Grant St. Julian Rodney J. Bothast Larry H. Krull 《Journal of industrial microbiology & biotechnology》1990,5(6):391-394
Summary By succesive recycling of the thin stillage in mashing and fermenting fresh corn, the glycerol content in each fermentation increased by about 0.4% and accumulated to a high of 2.1% in the beer of the fifth recycle. Glycerol concentration declined after the fifth recycle. The original fermentation contained 0.8% glycerol.Presented in part at the Society for Industrial Microbiology Annual Meeting, August 7–12, 1988, Chicago, IL.The mention of firm names or trade products does not imply that they are endorsed or recommended by the U.S. Department of Agriculture over other firms or similar products not mentioned. 相似文献
66.
Tansley Review No. 86 Accumulation of phytoalexins: defence mechanism and stimulus response system 总被引:1,自引:1,他引:0
C.J. SMITH 《The New phytologist》1996,132(1):1-45
67.
Transformation of the extremely thermoacidophilic archaeon Sulfolobus solfataricus via a self-spreading vector 总被引:1,自引:0,他引:1
Abstract The comparative chromosomal locations of polymeric β-fructosidase SUC genes have been determined by Southern blot hybridization with the SUC2 probe in 91 different strains of Saccharomyces cerevisiae . Most of the strains exhibited a single SUC2 gene, but in some strains two or three SUC genes were found. All Suc− strains carried a silent suc20 sequence. The accumulation of SUC genes was observed in populations derived from sources containing sucrose and seems to be absent in strains from sources promoting the MEL gene. 相似文献
68.
Ondrej Prasil Zbigniew Kolber Joseph A. Berry Paul G. Falkowski 《Photosynthesis research》1996,48(3):395-410
The oxygen flash yield (YO2) and photochemical yield of PS II (PS II) were simultaneously detected in intact Chlorella cells on a bare platinum oxygen rate electrode. The two yields were measured as a function of background irradiance in the steady-state and following a transition from light to darkness. During steady-state illumination at moderate irradiance levels, YO2 and PS II followed each other, suggesting a close coupling between the oxidation of water and QA reduction (Falkowski et al. (1988) Biochim. Biophys. Acta 933: 432–443). Following a light-to-dark transition, however, the relationship between QA reduction and the fraction of PS II reaction centers capable of evolving O2 became temporarily uncoupled. PS II recovered to the preillumination levels within 5–10 s, while the YO2 required up to 60 s to recover under aerobic conditions. The recovery of YO2 was independent of the redox state of QA, but was accompanied by a 30% increase in the functional absorption cross-section of PS II (PS II). The hysteresis between YO2 and the reduction of QA during the light-to-dark transition was dependent upon the reduction level of the plastoquinone pool and does not appear to be due to a direct radiative charge back-reaction, but rather is a consequence of a transient cyclic electron flow around PS II. The cycle is engaged in vivo only when the plastoquinone pool is reduced. Hence, the plastoquinone pool can act as a clutch that disconnects the oxygen evolution from photochemical charge separation in PS II.Abbreviations ADRY
acceleration of the deactivation reactions of the water-splitting enzyme (agents)
- Chl
chlorophyll
- cyt
cytochrome
- DCMU
3-(3,4-dichlorophenyl)-1,1-dimethylurea
- FO
minimum fluorescence yield in the dark-adapted state
- FI
minimum fluorescence yield under ambient irradiance or during transition from the light-adapted state
- FM
maximum fluorescence yield in the dark-adapted state
- FM
maximum fluorescence yield under ambient irradiance or during transition from light-adapted state
- FV, FV
variable fluorescence (FV=FM–FO ; FV=FM–FI)
- FRR
fast repetition rate (fluorometer)
- PS II
quantum yield of QA reduction (PS II=(FM – FO)/FM or PS II)=(FM= – FI=)/FM=)
- LHCII
Chl a/b light harvesting complexes of Photosystem II
- OEC
oxygen evolving complex of PS II
- P680
reaction center chlorophyll of PS II
- PQ
plastoquinone
- POH2
plastoquinol
- PS I
Photosystem I
- PS II
Photosystem II
- RC II
reaction centers of Photosystem II
- PS II
the effective absorption cross-section of PHotosystem II
- TL
thermoluminescence
- YO2
oxygen flash yield
The US Government right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. 相似文献
69.
The light-induced oxidation of the accessory donor tyrosine-D (YD) has been studied by measurements of the EPR Signal IIslow at room temperature in the autotrophically and photoheterotrophically cultivated alga Chlamydobotrys stellata. After illumination and dark adaptation, YD Signal IIslow was observed only in autotrophic algae, i.e. under conditions of a linear photosynthetic electron transfer from water to NADP+. The addition of artificial electron acceptors phenyl-p-benzoquinone (PPQ) or dichloro-p-benzoquinone (DCQ) to the autotrophic cells caused an almost negligible increase of this signal. When photosynthetic electron flow and oxygen evolution were diminished by removal of the carbon source CO2 and addition of acetate (photoheterotrophy), a pronounced YD Signal IIslow was seen only in presence of DCQ or PPQ. Several possibilities are discussed to explain the absence of YD Signal IIslow in photoheterotrophic Chl. stellata such as the existence of a cyclic PS II electron flow very effectively reducing P680 and thereby preventing the possibility of YD oxidation. Artificial electron acceptors withdraw electrons from this cycle thus keeping the primary quinone acceptor, QA, oxidized and thereby diminishing the reduction of P680
+ by cyclic PSII. This leads to the appearance of the YD Signal IIslow also in the photoheterotrophically grown algae.Abbreviations A-band-
thermoluminescence band associated with S2QA
- charge recombination
- DCQ-
2,5-dichlorobenzoquinone
- D2-
structure protein of Photosystem II
- EPR-
electron paramagnetic resonance
- OEC-
oxygen evolving complex
- PPQ-
phenyl-p-benzoquinone
- PS II-
Photosystem II
- P680-
reaction center of Photosystem II
- Q-band-
thermoluminescence band associated with S2QA
- charge recombination
- Si-
oxidation levels of the OEC
- YD-
tyrosine-D accessory donor to P680
- YZ-
tyrosine-Z electron donor to P680
Dedicated to Prof. Dr E. Schnepf/Heidelberg. 相似文献
70.
Alexander A. Bulychev Tijmen van Voorthuysen Wim J. Vredenberg 《Physiologia plantarum》1996,98(2):605-611
Electrochemical data obtained with TMPD+ -sensitive electrodes indicate that ammonium-uncoupled chloroplasts retain TMPD (N,N,N',N'-tetramethyl- p -phenylenediamine) mainly in the reduced form during illumination, whereas uncoupled DCMU-treated chloroplasts accumulate TMPD in the oxidized form (TMPD+ ). This observation indicates that the reduced plastoquinol is the preferred electron donor for photosystem I (PSI) and TMPD can only compete efficiently when plastoquinone reduction is blocked. After adding DCMU the formation of a transmembrane gradient for TMPD+ is reflected by a slow-down of the electrogenic electron transport and by the emerging of the overshoot of the membrane current in the light-off response. A light-dependent increase in photoelectric current generated by chloroplasts in the presence of NH4 Cl and TMPD is observed and considered to be caused by a reversible release of current limitation in the interfacial conductance barriers in the lumen. 相似文献