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961.
S. Butz R. Benz T. Wacker W. Welte A. Lustig R. Plapp J. Weckesser 《Archives of microbiology》1993,159(4):301-307
Oligomeric porin of the phototrophic bacterium Rhodopseudomonas blastica DSM 2131 was obtained from cell envelopes by differential temperature extraction in the presence of detergent and salt. The isolated porin exhibited strong porin activity after reconstitution into lipid bilayer membranes. The effective channel diameter for the trimer was estimated as 1.5 nm from single channel conductance measurements in the presence of 1 M KCl. Moderate cation-selectivity was observed. Oligomeric porin migrated as a single band (apparent molecular weight 81 kDa) on sodium dodecyl sulfate polyacrylamide gelelectrophoresis when solubilized below 70 °C. The oligomers were converted into monomers on heating to 70 °C or above forming two bands with apparent molecular weight of 36 kDa and 35 kDa. The oligomer was not sensitive to EDTA. Its molecular weight was determined to be 119.3 kDa by analytical ultracentrifugation. The isoelectric point was 5.7. Circular dichroism data indicated a high content of -sheet structure. Gasphase sequencing of the N-terminal residues revealed the sequence: NH2-Glu-Ile-Ser-Leu-Asn-Gly-Tyr-Gly-Arg-Phe. Crystals with a maximal side length of 300 m and diffracting to 0.32 nm resolution were obtained with the porin oligomer in the presence of C8E4 and 1,2,3-heptanetriol by using the vapor phase equilibration technique.Abbreviations C8E4
n-octyl tetraoxyethylene
- Mr
apparent molecular weight
- Octyl-POE
n-octyl polyoxyethylene
- LDAO
N,N-dimethyl dodecyl aminoxide
- LPS
lipopolysaccharide
- PAGE
polyacrylamide gel-electrophoresis
- PEG
polyethylene glycol 相似文献
962.
G. K. Haines G. D. Ghadge S. Becker M. Kies H. Pelzer B. Thimmappaya J. A. Radosevich 《Virchows Archiv. B, Cell pathology including molecular pathology》1993,63(1):289-295
p68 is an inducible protein kinase which is believed to be an important factor in the regulation of both viral and cellular
protein synthesis. We have produced a monoclonal antibody (TJ4C4) which specifically detects p68, and which can be used to
detect this antigen in formalin-fixed, paraffin-embedded tissues. Because p68 plays an important role in cellular protein
synthesis, we hypothesized that it may correlate with normal and neoplastic cellular differentiation. One hundred and seventy-seven
head and neck squamous cell carcinoma specimens, representing 82 patients, were studied. The relative amount, frequency, and
distribution of p68 expression were determined by microscopic evaluation of ABC immunoperoxidase-stained specimens. A spectrum
of immunoreactivity was detected in 156 of 177 tumors, as well as within the normal squamous epithelium. Normal, actively
proliferating cells, such as the basal layer of squamous epithelium, expressed comparatively little p68. Increased p68 expression
was noted to parallel the morphologic features of cellular differentiation. In neoplastic tissue, p68 expression also increased
with the degree of cellular differentiation. These data demonstrate that the expression of p68 parallels the degree of cellular
differentiation in squamous cell carcinoma of the head and neck region, as well as within normal squamous mucosa. Therefore,
p68 may provide an objective biologic measure of cellular differentiation which does not depend on morphologic features. 相似文献
963.
Toshitsugu Nakamura Masao Hotchi 《Virchows Archiv. B, Cell pathology including molecular pathology》1993,63(1):11-16
DNA strand breaks (nicks) in non-parenchymal cells (NPCs) in CCl4-induced acute or chronic liver injury in rats were detected using an in situ nick translation method; their dynamic changes
were analysed in relation to the proliferation pattern of hepatocytes and NPCs, as revealed by bromodeoxyuridine (BrdU)-up-take.
In acute injury, hepatocyte proliferation started before centrilobular necrosis had occurred, whereas BrdU-labeled sinusoidal
NPCs markedly increased only after centrilobular necrosis was apparent. DNA breakages in NPCs paralleled the proliferation
pattern of these cells, suggesting that nicks are physiological, and reflect proliferation and activated gene expression.
In chronic injury, liver cirrhosis developed after 9 weeks, but BrdU-labeling of hepatocytes was almost the same level as
that in untreated liver. The number of BrdU-labeled NPCs showed only a slight increase, while those with DNA breakages were
much more frequent in the cirrhotic stage, suggesting a significant role for NPCs in the fibrotic process. These results indicate
that DNA strand breaks in NPCs act as a marker for activation states such as proliferation, differentiation and/or activated
gene expression. 相似文献
964.
Shinya Arinaga Nobuya Karimine Masashi Adachi Hiroshi Inoue Shigeru Nanbara Tsukasa Asoh Hiroaki Ueo Tsuyoshi Akiyoshi 《Cancer immunology, immunotherapy : CII》1993,37(4):220-226
We previously found that the ability of peripheral blood mononuclear cells (PBM) of cancer patients to generate lymphokine-activated killer (LAK) cells became remarkably augmented after mitomycin C administration. On the basis of the clinical finding, we designed a treatment regimen comprised of 12 mg/m2 mitomycin C i. v. on day 1 and 700 U/m2 recombinant interleukin-2 (IL-2) i.v. every 12 h from day 4 through day 8. Of 25 patients with advanced carcinoma, 9 had a partial response and 3 had a minor response. Cytotoxic cell function, including natural killer activity, lymphokine-activated killer (LAK) activity, and the ability to generate LAK cells, and lymphocyte subsets in PBM was measured 1 day before and after either the first or second course of this therapy. The relationship between these parameters and the clinical antitumor response to this treatment was examined. Although the cytotoxic activities were significantly augmented after either the first or second treatment course, no positive correlation was observed between the changes in these cytotoxic activities and the clinical response to this therapy, when patients who either showed a partial response or whose disease remission was partial or minor were defined as responders. Further, phenotypic analysis showed a significant increase in CD2+, CD3+ CD4+ and CD4+Leu8– cells after the firs course, and CD25+ cells after either the first or second course of this treatment. The precentages of CD2+ and CD25+ cells were significantly elevated only in responders but not in nonresponders, suggesting the increase in these subsets was related to clinical response. 相似文献
965.
To place associations among body size, age at maturity, age, and reproductive traits of a long-lived organism in the context of current life history models based on the concept of norms of reaction, we examined data from a mark-recapture study of Blanding's turtles (Emydoidea blandingi) in southeastern Michigan during 24 of the years between 1953 and 1988. Females matured between 14 and 20 years of age. Both the smallest and largest adult females in the population were reproducing for the first time in their lives. This result suggests that a combination of differences in juvenile growth rates and ages at maturity, and not indeterminate growth, are the primary cause of variation in body size among adults. Body size variation among individuals was not related to age at sexual maturity. Females that had slower growth rates as juveniles matured later at similar mean body size compared to those with more rapid growth that matured at an earlier age. As a result, a linear model of age at sexual maturity with growth rates of primiparous females between hatching and maturity was significant and negative (R2 = 0.76). Frequency of reproduction of the largest and smallest females was not significantly different. Clutch size did not vary significantly with age among either primiparous or multiparous females. Clutch sizes of primiparous females and multiparous females were not significantly different. However, older females (>55 years minimum age) reproduced more frequently than did younger females (minimum age <36 y). 相似文献
966.
Ana Buchadas Martin Jung Mercedes Bustamante Álvaro Fernández-Llamazares Stephen T. Garnett Ana Sofía Nanni Natasha Ribeiro Patrick Meyfroidt Tobias Kuemmerle 《Global Change Biology》2023,29(17):4880-4897
Tropical and subtropical dry woodlands are rich in biodiversity and carbon. Yet, many of these woodlands are under high deforestation pressure and remain weakly protected. Here, we assessed how deforestation dynamics relate to areas of woodland protection and to conservation priorities across the world's tropical dry woodlands. Specifically, we characterized different types of deforestation frontier from 2000 to 2020 and compared them to protected areas (PAs), Indigenous Peoples' lands and conservation areas for biodiversity, carbon and water. We found that global conservation priorities were always overrepresented in tropical dry woodlands compared to the rest of the globe (between 4% and 96% more than expected, depending on the type of conservation priority). Moreover, about 41% of all dry woodlands were characterized as deforestation frontiers, and these frontiers have been falling disproportionately in areas with important regional (i.e. tropical dry woodland) conservation assets. While deforestation frontiers were identified within all tropical dry woodland classes of woodland protection, they were lower than the average within protected areas coinciding with Indigenous Peoples' lands (23%), and within other PAs (28%). However, within PAs, deforestation frontiers have also been disproportionately affecting regional conservation assets. Many emerging deforestation frontiers were identified outside but close to PAs, highlighting a growing threat that the conserved areas of dry woodland will become isolated. Understanding how deforestation frontiers coincide with major types of current woodland protection can help target context-specific conservation policies and interventions to tropical dry woodland conservation assets (e.g. PAs in which deforestation is rampant require stronger enforcement, inactive deforestation frontiers could benefit from restoration). Our analyses also identify recurring patterns that can be used to test the transferability of governance approaches and promote learning across social–ecological contexts. 相似文献
967.
半枝莲中二萜内酯和黄酮化合物的分离和鉴定 总被引:1,自引:0,他引:1
半枝莲(Scutellaria barbata D.Don)为唇形科黄芩属植物,全草入药,具有清热解毒,化瘀利尿,消肿止痛和抗癌等功效。国内学者报道从全草中分得红花素(carthamidin)、异红花素(isocarthamidin)、印黄芩甙(scutellarein)、β-谷甾醇(β-sitosterol)、硬脂酸(stearic acid)和生物碱。台湾学者从中分离得汉黄芩素(wogonin)、5-羟基-7,8-二甲氧基黄酮(5-hydroxy-7,8-dimethoxyflavone)、半枝莲素(Rivularin)。我们从全草的乙醇提取液中分得两个化合物,经鉴定为汉黄芩素、新穿心莲内酯,该内酯在本植物中属首次发现。 相似文献
968.
Darja Lavogina Naila Nasirova Tanel Sõrmus Taavo Tähtjärv Erki Enkvist Kaido Viht Tõiv Haljasorg Koit Herodes Jana Jaal Asko Uri 《Journal of peptide science》2023,29(3):e3456
The conjugates of an adenosine mimetic and oligo-l -arginine or oligo-d -arginine (ARCs) were initially designed in our research group as inhibitors and photoluminescent probes targeting basophilic protein kinases. Here, we explored a panel of ARCs and their fluorescent derivatives in biochemical assays with members of the protein arginine methyltransferase (PRMT) family, focusing specifically on PRMT1. In the binding/displacement assay with detection of fluorescence anisotropy, we found that ARCs and arginine-rich peptides could serve as high-affinity ligands for PRMT1, whereas the equilibrium dissociation constant values depended dramatically on the number of arginine residues within the compounds. The fluorescently labeled probe ARC-1081 was displaced from its complex with PRMT1 by both S-adenosyl-l -methionine (SAM) and S-adenosyl-l -homocysteine (SAH), indicating binding of the adenosine mimetic of ARCs to the SAM/SAH-binding site within PRMT1. The ARCs that had previously shown microsecond-lifetime photoluminescence in complex with protein kinases did not feature such property in complex with PRMT1, demonstrating the selectivity of the time-resolved readout format. When tested against a panel of PRMT family members in single-dose inhibition experiments, a micromolar concentration of ARC-902 was required for the inhibition of PRMT1 and PRMT7. Overall, our results suggest that the compounds containing multiple arginine residues (including the well-known cell-penetrating peptides) are likely to inhibit PRMT and thus interfere with the epigenetic modification status in complex biological systems, which should be taken into consideration during interpretation of the experimental data. 相似文献
969.
桑白蚧恩蚜小蜂Encarsia(=Prospaltella)berlesel(Howard)是寄生桑白蚧Pseudaulacaspls pentagona(Targioni-Tozzctti)的重要寄生蜂,许多国家进行了引进移植,对控制桑白蚧的为害取得明显的成效.本记述了桑白蚧恩蚜小蜂形态特征的鉴别。以及各国引进利用的概况.并讨论了利用寄生蜂防治桑白蚧的重要性. 相似文献
970.
花生种子吸胀2d后,子叶中肽链内切酶活性上升,贮藏蛋白质开始降解。高活力种子肽链内切酶活性在吸胀2d后迅速上升,至4d时达到高峰,而中等活力种子的肽链内切酶活性上升速度绶慢。高活力种子萌发时贮藏蛋白质降解速度高于中等活力种子。中等活力种子经PEG和PUT处理可提高种子活力,也促进了种子贮藏蛋白质降解能力的提高。 相似文献