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61.
The ras and myc oncoproteins cooperate to transform the established murine fibroblast cell line C3H10T1/2. To determine the impact of overexpression of the myc oncoprotein on the phenotype of C3H10T1/2 cells, two C3H10Tl/2-myc clonal cell lines, SVc-myc 11A and myc neo 13A, were isolated and characterized. Although both C3H10Tl/2-myc cell lines are morphologically indistinguishable from wild-type C3H10T1/2 cells and possess growth properties similar to those of C3H10T1/2 cells, each displays a predisposition to transformation following transfection with the activated form of the human H-ras gene. In C3H10T1/2 cells overexpressing the v-myc or H-ras oncogenes, the levels of mRNA encoding max, the recently identified oligomerization partner of myc, remain unchanged, suggesting that the endogenous level of max in C3H10T1/2 cells is sufficient for a high frequency of transformation by ras and myc. Based on these studies, the C3H10Tl/2-myc clonal cell lines we describe are suitable model systems for examining the molecular role of the myc protein in transformation and for characterizing additional factors that synergize with myc in multistep transformation. 相似文献
62.
The refined crystal structures of chicken, yeast and trypanosomal triosephosphate isomerase (TIM) have been compared. TIM is known to exist in an "open" (unliganded) and "closed" (liganded) conformation. For chicken TIM only the refined open structure is available, whereas for yeast TIM and trypanosomal TIM refined structures of both the open and the closed structure have been used for this study. Comparison of these structures shows that the open structures of chicken TIM, yeast TIM and trypanosomal TIM are essentially identical. Also it is shown that the closed structures of yeast TIM and trypanosomal TIM are essentially identical. The conformational difference between the open and closed structures concerns a major shift (7 A) in loop-6. Minor shifts are observed in the two adjacent loops, loop-5 (1 A) and loop-7 (1 A). The pairwise comparison of the three different TIM barrels shows that the 105C alpha atoms of the core superimpose within 0.9 A. The sequences of these three TIMs have a pairwise sequence identity of approximately 50%. The residues that line the active site are 100% conserved. The residues interacting with each other across the dimer interface show extensive variability, but the direct hydrogen bonds between the two subunits are well conserved. The orientation of the two monomers with respect to each other is almost identical in the three different TIM structures. There are 56 (22%) conserved residues out of approximately 250 residues in 13 sequences. The functions of most of these conserved residues can be understood from the available open and closed structures of the three different TIMs. Some of these residues are quite far from the active site. For example, at a distance of 19 A from the active site there is a conserved saltbridge interaction between residues at the C-terminal ends of alpha-helix-6 and alpha-helix-7. This anchoring contrasts with the large conformational flexibility of loop-6 and loop-7 near the N termini of these helices. The flexibility of loop-6 is facilitated by a conserved large empty cavity near the N terminus of alpha-helix-6, which exists only in the open conformation. 相似文献
63.
Characteristics of thermoluminescence glow curves were compared in three types of Euglena cells: (i) strictly autotrophic, Cramer and Myers cells; (ii) photoheterotrophic cells sampled from an exponentially growing culture containing lactate as substrate repressing the photosynthetic activity; (iii) semiautotrophic cells, sampled when the lactate being totally exhausted, the photosynthesis was enhanced.In autotrophic and semiautotrophic cells, composite curves were observed after series of two or more actinic flashes fired at –10°C, which can be deconvoluted into a large band peaking in the range 12–22°C and a smaller one near 40°C, This second band presents the characteristics of a typical B band (due to S2/3QB
- recombination), whereas the first one resembled the band, shifted by -15–20°C, which is observed in herbicide resistant plants. The amplitude of this major band, which was in all cases very low after one flash, exhibited oscillations of period four but rapidly damping, with maxima after two and six flashes. In contrast, photoheterotrophic Euglena displayed single, non-oscillating curves with maxima in the range 5–10°C.In autotrophic and semiautotrophic cells, oxidizing pretreatments by either a preillumination with one or more (up to twenty-five) flashes, or a far-red preillumination in the presence of methylviologen, followed by a short dark period, induced thermoluminescence bands almost single and shifted by +3–5°C, or +12°C, respectively. In autotrophic cells, far-red light plus methyl viologen treatment induced a band peaking at 31°C, as in isolated thylakoids from Euglena or higher plants, while it had barely any effect in photoheterotrophic cells.Due to metabolic activities in dark-adapted cells, a reduction of redox groups at the donor and acceptor sides of PS II dark-adapted cells is supposed to occur. Two different explanations can be proposed to explain such a shift in the position of the main band in dark-adapted autotrophic control. The first explanation would be that in these reducing conditions a decreasing value of the equilibrium constant for the reaction: SnQA
-QBSnQAQB
-, would determine the shift of the main TL band towards low temperatures, as observed in herbicide resistant material. The second explanation would be that the main band would correspond to peak III already observed in vivo and assigned to S2/3QB
2- recombinations.Abbreviations CM
Cramer and Myers
- D1
a 32 kDa protein component of the PS II reaction center, psbA.gene product
- D2
a 34 kDa protein component of the PS II reaction center, psbD gene product
- FR
lar-red illumination
- Lexpo and Lstat
cells from lactate culture samples at exponential and stationary phase of growth
- MV
methylviologen
- pBQ
parabenzoquinone
- PQ
plastoquinone
- PS II
photosystem II
- QA
primary quinone electron acceptor
- QB
secondary quinone electron acceptor
- TL
thermoluminescence 相似文献
64.
Phyto- and bacterioplankton biomass and activity were simultaneously measured during the course of one year in the shallow Créteil Lake (France).Phytoplankton was dominated, during the whole year, by small-sized organisms (10 to 25 µm). Bacteria were in a majority small coccoids (<0.3 µm). Phyto -and bacterioplankton abundances averaged respectively 3.3 × 106 cells l–1 and 6 × 109 cells l–1.The phasing of the activity and biomass periods suggest a close coupling between phyto- and bacterioplankton. There were two distinct periods of high activity and biomass. Maximal values were observed in summer but an early increase occurred also in winter. Low or undetectable phytoplankton excretion rates, when heterotrophic activity was maximum, indicated a bacterial uptake of up to 100% of the released algal products during the incubation period. Heterotrophic uptake measurements with both glucose and amino acids revealed a seasonal change of the substrates in the lake, glucose uptake being associated more with the maximum activity of the algae, while the amino acids uptake was relatively higher during their decline.The maximal photosynthetic rate averaged 21.5 mgC m–3 h–1 and mean Vmax values were 0.056 and 0.050 mgC m–3 h–1 respectively for glucose and amino acids uptake. 相似文献
65.
Diagnostic value of crush artifact in cytologic specimens. Occurrence in small cell carcinoma of the lung 总被引:1,自引:0,他引:1
R D Davenport 《Acta cytologica》1990,34(4):502-504
The occurrence of nuclear crush artifact (NCA) in cytologic specimens of small cell undifferentiated carcinoma (SCUC) and other carcinomas of the lung, lymphoma and benign lymphoid proliferations was studied to determine its diagnostic usefulness. NCA was found to be a common and morphologically distinct feature in SCUC, depending on how the specimen was prepared; it was present in aspirates, washings, brushings and sputum, but not in pleural or cerebrospinal fluids. It was absent in other types of cancer and could be distinguished from other similar-appearing artifacts. These results demonstrate that NCA is a diagnostically useful feature in pulmonary SCUC. 相似文献
66.
67.
Neurochemical Studies of the Mesolimbic Dopaminergic Pathway: Somatodendritic Mechanisms and GABAergic Neurones in the Rat Ventral Tegmentum 总被引:6,自引:4,他引:2
Abstract: The rat ventral tegmentum (containing dendrites and somata of mesolimbic neurones) contained 1.3 μg/g of dopamine, which was reduced to 40% of the control level by reserpine. Slices of ventral tegmentum were able to accumulate and release (elevated potassium or protoveratrine A) exogenous [3 H]dopamine. In parallel studies the uptake mechanism in ventral tegmentum was shown to be virtually identical to the nerve terminal uptake of [3 H]dopamine by slices of nucleus accumbens. The release of [3 H]dopamine was indistinguishable from that observed in substantia nigra, where there is substantial evidence for dendritic mechanisms. Basal adenylate cyclase activity was present, but dopamine-stimulated activity was not detected. A high GABA concentration (7.7 μmol/g) was present in ventral tegmentum, in conjunction with an uptake and a release mechanism for [3 H]GABA. GABA and muscimol elicited a small, reproducible efflux of [3 H]dopamine, but an interaction between dopamine and [3 H]GABA efflux was not observed. The results are in accord with transmitter roles for dopamine and GABA in the somatoden-dritic area of mesolimbic dopaminergic neurons. 相似文献
68.
Patrice C. Dubreuil Daniel Z. Birnbaum Danielle H. Caillol Francois A. Lemonnier 《Immunogenetics》1982,16(5):407-424
The inhibitory capacity of 17 monoclonal antibodies (m.Ab.) specific for the products of the I-A
k
subregion was evaluated in proliferative responses of B10.BR T-lymphocytes to GAT, Keyhole limpet hemocyanin, and ovalbumin. Considered in isolation, each m.Ab. mediated inhibitory effects of comparable magnitude on these three different proliferative responses. On the other hand, clear differences were observed when the magnitude of the inhibitory effects was compared from one m.Ab. to another. The m.Ab. were consequently classified as strong or moderate-to-weak inhibitors of T-cell proliferative responses. Evidence was simultaneously gained indicating the following: (a) the determinants recognized by different m.Ab. were expressed on the same molecules; (b) the differences in affinity of the m.Ab. for I-Ak positive cells did not explain their differences in inhibitory capacities; (c) conversely, the inhibitory capacity of each m.Ab. followed its ability to inhibit the cell surface fixation of Ia.17-specific 10-2.16 m.Ab.; (d) the strong inhibitory capacity of some m.Ab. was not related to a special ability to modulate cell surface Ia molecules. These results suggest that antigen recognition by T lymphocytes is preferentially restricted by a functional site of the I-Ak molecules related to the Ia.17 and Ia.1 specificities.Abbreviations EDTA
Ethylenediamine-tetraacetic acid disodium salt
- EHAA
Eagle's Hanks' amino acids medium
- FCS
fetal calf serum
- in polypeptide
G is glutamate, A, alanine, T, tyrosine
- HEPES
N-2-hydroxy-piperazine-N-2-ethane sulfonic acid
- kd
dissociation rate constant
- KLH
Keyhole limpet hemocyanin
- LPS
lipopolysaccharide
- m.Ab.
monoclonal antibodies
- NP-40
nonidet P-40
- PBS
phosphate buffered saline
- PBS-BSA
PBS supplemented with 1% bovine serum albumin
- PBS-BSA-NP-40
PBS-BSA supplemented with 0.5% NP-40
- RT
room temperature
- SEM
standard error of the mean
- s.c.
spleen cells 相似文献
69.
Monotritylation of O-acetyl derivatives of D-xylopyranose and D-xylofuranose with trityl chloride in acetonitrile-pyridine gave the tri-O-acetyl derivatives of 1-,2-, 3-, and 5-O-trityl-D-xylofuranose and of 1-, 2-, 3-, and 4-O-trityl-D-xylopyranose which were required for the identification of the various monotrityl derivatives obtained in the tritylation at 50° of D-xylose with trityl chloride in pyridine or hexamethylphosphoric triamide-silver acetate. 相似文献
70.
Résumé Un milieu de culture permettant d'isoler et de dénombrer les colonies deBeauveria tenella parmi d'autres champignons du sol a été mis au point en vue de faciliter l'étude du comportement d'un germe entomopathogène
artificiellement introduit pour lutter contre les pullulations des larves du Hanneton commun.
Summary A culture medium composed of 8 vegetable juices, glucose, yeast extract, dried oxgall and antibiotics (actidione, streptomycine, tetracycline) allows the isolation ofBeauveria tenella blastospores or conidiospores artificialy introduced in soil when the concentration of this inoculum varies between 100 and 40,000 spores per gram.相似文献