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11.
Shinsuke Hara H. Dorota Halicka Silvia Bruno Jianping Gong Frank Traganos Zbigniew Darzynkiewicz 《Experimental cell research》1996,223(2):372
Proteolysis is an early event of apoptosis which appears to be associated with activation of the endonuclease which is responsible for internucleosomal DNA cleavage. The present study was designed to reveal the possible role of proteolysis in other early events, such as chromatin condensation, nuclear breakdown, and destabilization ofin situDNA double-stranded structure. Apoptosis of human leukemic HL-60 cells and rat thymocytes was induced by different agents, including DNA topoisomerase inhibitors, an RNA antimetabolite, and the glucocorticosteroid, prednisolone. DNA degradation was evaluated by pulsed field and conventional gel electrophoresis and by the presence ofin situDNA strand breaks. DNA stability was estimated by the measure of its sensitivityin situto denaturation. Chromatin condensation, nuclear breakdown, and other morphological changes were monitored by interference contrast and UV microscopy following cell staining with the DNA-specific fluorochrome 4′,6-diamidino-2-phenylindole. Several irreversible or reversible serine protease inhibitors prevented internucleosomal DNA degradation, nuclear breakdown, and destabilization of DNA double-stranded structure. The effective inhibitors, however, did not prevent the onset of chromatin condensation, nor the loss of the fine structural framework, nor the initial step of DNA cleavage generating DNA fragments of ≥50 kb in size. The data indicate that in both cell systems the activity of proteases sensitive to the inhibitors tested is needed for internucleosomal DNA cleavage to occur. The data also suggest that these proteases may be involved in dissolution of the nuclear envelope. Because nuclear matrix proteins and histones stabilize DNAin situ,and the decrease in DNA stability which occurs during apoptosis is precluded by the inhibitors, it is likely that serine proteases may degrade DNA stabilizing proteins. The activity of these proteases, however, appears needed neither for DNA cleavage to ≥50-kb fragments nor for the onset of chromatin condensation which is associated with dissolution of the structural framework of the nucleus. 相似文献
12.
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
13.
Non-photochemical fluorescence quenching and the diadinoxanthin cycle in a marine diatom 总被引:7,自引:0,他引:7
Miguel Olaizola Julie La Roche Zbigniew Kolber Paul G. Falkowski 《Photosynthesis research》1994,41(2):357-370
The diadinoxanthin cycle (DD-cycle) in chromophyte algae involves the interconversion of two carotenoids, diadinoxanthin (DD) and diatoxanthin (DT). We investigated the kinetics of light-induced DD-cycling in the marine diatom Phaeodactylum tricornutum and its role in dissipating excess excitation energy in PS II. Within 15 min following an increase in irradiance, DT increased and was accompanied by a stoichiometric decrease in DD. This reaction was completely blocked by dithiothreitol (DTT). A second, time-dependent, increase in DT was detected 20 min after the light shift without a concomitant decrease in DD. DT accumulation from both processes was correlated with increases in non-photochemical quenching of chlorophyll fluorescence. Stern-Volmer analyses suggests that changes in non-photochemical quenching resulted from changes in thermal dissipation in the PS II antenna and in the reaction center. The increase in non-photochemical quenching was correlated with a small decrease in the effective absorption cross section of PS II. Model calculations suggest however that the changes in cross section are not sufficiently large to significantly reduce multiple excitation of the reaction center within the turnover time of steady-state photosynthetic electron transport at light saturation. In DTT poisoned cells, the change in non-photochemical quenching appears to result from energy dissipation in the reaction center and was associated with decreased photochemical efficiency. D1 protein degradation was slightly higher in samples poisoned with DTT than in control samples. These results suggest that while DD-cycling may dynamically alter the photosynthesis-irradiance response curve, it offers limited protection against photodamage of PS II reaction centers at irradiance levels sufficient to saturate steady-state photosynthesis.Abbreviations CAP
chloramphenicol
- D1
PS II reaction center protein
- DD
diadinoxanthin
- DD
cycle-diadinoxanthin cycle
- DT
diatoxanthin
- DTT
dithiothreitol
- FCP
fucoxanthin chlorophyll a-c protein
- Fm
maximum fluorescence yield in the dark-adapted state
- Fo
minimum fluorescence yield in the dark-adapted state
- Fm and Fo
maximum and minimum fluorescence yields respectively in some light adapted state
- Fv
maximum variable fluorescence yield in the dark-adapted state
- Ik
Irradiance at the intercept of the initial slope of the photosynthesis-irradiance curve and the maximum photosynthetic rate
- kD
first order rate constant for nonradiative de-excitation of excitions in the PS II antenna
- kd
first order rate constant for non-radiative de-excitation of excitons in the PS II reaction center
- kF
first order rate constant for fluorescence
- kT
first order rate constant for exciton transfer to the reaction center
- kt
first order rate constant for exciton transfer from the reaction center to the antenna
- Rubisco
ribulose bisphosphate carboxylase
- SVm
Stern-Volmer quenching coefficient of the maximum fluorescence yield
- SVo
Stern-Volmer quenching coefficient of the miniximum fluorescence yield
- PS II
apparent absorption cross-section of PS II
- arr
average interval between exciton arrival to the PS II reaction center (ms)
- rem
average interval between electron turnover during photosynthesis in the PS II reaction center (ms)
- d
the probability that an exciton is non-radiatively dissipated in the reaction center
- T
the probability that an exciton in the antenna is transferred to the reaction center
- t
the probability that an exciton is transferred back from the reaction center to the antenna 相似文献
14.
The effect of linolenic acid (18:3) on release of the 43 kDa polypeptide and manganese from photosystem II ( PS II ) membranes depleted of extrinsic polypeptides was studied. In both control and NaCl-washed particles which were depleted of the extrinsic 23 and 16 kDa polypeptides, the 18:3 treatment caused a 20% release of the 33 and 43 kDa polypeptides. In CaCl2 , (or urea + NaCl)-washed particles, which were depleted of the 33 kDa polypeptide in addition to the 23 and 16 kDa polypeptides, the release of the 43 kDa polypeptide increased to 70%, whereas only 25% of the 47 kDa polypeptide was removed. These findings suggest (i) that the 33 and the 43 kDa polypeptides are neighbows in the photosynthetic membrane and (ii) that the 33 kDa polypeptide shields the 43 kDa polypeptide against the action of 18:3. Incubation of CaCl2 , or (urea + NaCI)-treated PSII particles in the presence or absence of 18:3 resulted in the loss of only 2 of the 4 Mn atoms present per reaction center. this indicates that the 2 Mn atoms more firmly associated with PSII are not affected by the removal of the extrinsic 16, 23 and 33 kDa polypeptides, and the intrinsic 43 kDa polypeptide. nor by the treatment with linolenic acid. 相似文献
15.
Zbigniew Darzynkiewicz 《Journal of cellular biochemistry》1995,58(2):151-159
There is a strong evidence that administration of antitumor drugs triggers apoptotic death of target cells. A characteristic feature of appotosis is active participation of the affected cell in its demise. Attempts have been made, therefore, to potentiate the cytotoxicity of a variety of agents by modulating the propensity of cells to respond by apoptosis. Several strategies to enhance apoptosis that involve modulation of the cell cycle or differentiation are discussed. Loss of control of the G1 checkpoint in tumor cells allows one to design treatments that arrest normal cells at the checkpoint and attempt to selectively kill tumor cells with S phase specific drugs. The possibility of a restoration of the apoptosis triggering function of the tumor suppressor gene p53 when the G1 checkpoint function is abolished is expected to increase tumor cells' sensitivity to S phase poisons. Because induction of apoptosis by many antitumor drugs is cell cycle phase specific, drug combinations that preferentially trigger apoptosis at different phases of the cycle, or recruitment of cells to the sensitive phase, offer another antitumor strategy. There is also evidence that apoptosis is potentiated when cell differentiation is triggered follwing DNA damage. This observation suggests that strategies which combine DNA damaging and differentiating drugs, under conditions where the latter are administered following DNA damage caused by the former, may be successful. 相似文献
16.
17.
Andrzej Myśliwski Jolanta Myśliwska Zbigniew Kmieć 《Histochemistry and cell biology》1977,52(1):91-96
Summary A comparsion of the Feulgen hydrolysis curves and the chromatin compactness of the liver cell nuclei of young and old rats was made. It was found that the rate of DNA depurination and chromatin compactness are higher in the liver cell nuclei of old rats, both in di-and tetraploidal cells. The effect of fixation upon the course of the hydrolysis curves is discussed.This investigation was supported by grant 474/VI Committee of Cell Pathology, Polish Academy of Sciences 相似文献
18.
Zbigniew Witkowski 《Oecologia》1978,37(1):85-92
Summary Among the parameters describing weevil communities two groups of parameters, which are positively correlated among themselves, were found. The first group includes: relative abundance, number of species, and participation of habitat generalists, the second: stability, mean body size, and participation of habitat specialists. The parameters belonging to opposite groups were negatively correlated.Among the parameters describing host plants of the weevils, no correlation was found between species number and relative abundance, while a negative correlation was found between total mass of host plants and their relative abundance.Weevil species diversity and the group of its correlates were positively correlated with analogical parameters of their host plants while weevil stability showed positive correlation with the total mass of host plants and the proportion of these plants in the total mass of vegetation.The reasons for negative correlation between stability and diversity of weevils and relations of these two parameters to selection strategy of these beetles are discussed. 相似文献
19.
Ewa Surmacz Paul Nugent Zbigniew Pietrzkowski Renato Baserga 《Experimental cell research》1992,199(2):275-278
The levels of cdc2 mRNA increase when quiescent cells are stimulated by growth factors. In BALB/c 3T3, both platelet-derived growth factor and insulin-like growth factor 1 (IGF-1) are required to increase cdc2 mRNA levels. In p6 cells, which constitutively overexpress the IGF-1 receptor, IGF-1 is sufficient. The importance of the IGF-1/IGF-1 receptor interaction in regulating the levels of cdc2 mRNA was further confirmed by showing that an antisense oligodeoxynucleotide to the IGF-1 receptor RNA inhibited the IGF-1-mediated increase. 相似文献
20.
Gizela Takácsová Július ubík Zbigniew Kotylak 《Molecular & general genetics : MGG》1980,179(1):141-146
Summary Genetic relations between mitochondrial mucidin-resistant locus muc3 and ubiquinol-cytochrome c reductase-deficient box loci have been studied by recombination and petite deletion analysis. It was found that the locus muc3 maps in the segment of mitochondrial DNA corresponding to the locus box2. The results suggest the participation of box2/muc3 locus in the sequences of the structural gene for cytochrome b. 相似文献