全文获取类型
收费全文 | 5586篇 |
免费 | 508篇 |
国内免费 | 1篇 |
专业分类
6095篇 |
出版年
2023年 | 28篇 |
2022年 | 76篇 |
2021年 | 135篇 |
2020年 | 83篇 |
2019年 | 113篇 |
2018年 | 119篇 |
2017年 | 104篇 |
2016年 | 172篇 |
2015年 | 315篇 |
2014年 | 330篇 |
2013年 | 411篇 |
2012年 | 494篇 |
2011年 | 480篇 |
2010年 | 283篇 |
2009年 | 252篇 |
2008年 | 355篇 |
2007年 | 326篇 |
2006年 | 297篇 |
2005年 | 327篇 |
2004年 | 301篇 |
2003年 | 256篇 |
2002年 | 218篇 |
2001年 | 50篇 |
2000年 | 34篇 |
1999年 | 45篇 |
1998年 | 48篇 |
1997年 | 29篇 |
1996年 | 32篇 |
1995年 | 21篇 |
1994年 | 39篇 |
1993年 | 21篇 |
1992年 | 26篇 |
1991年 | 24篇 |
1990年 | 16篇 |
1989年 | 17篇 |
1988年 | 10篇 |
1987年 | 16篇 |
1986年 | 18篇 |
1985年 | 10篇 |
1984年 | 21篇 |
1983年 | 7篇 |
1982年 | 10篇 |
1980年 | 11篇 |
1979年 | 10篇 |
1978年 | 9篇 |
1977年 | 25篇 |
1976年 | 12篇 |
1974年 | 6篇 |
1972年 | 8篇 |
1971年 | 7篇 |
排序方式: 共有6095条查询结果,搜索用时 15 毫秒
41.
Thomas C Bishop DJ Lambert K Mercier J Brooks GA 《American journal of physiology. Regulatory, integrative and comparative physiology》2012,302(1):R1-14
Two lactate/proton cotransporter isoforms (monocarboxylate transporters, MCT1 and MCT4) are present in the plasma (sarcolemmal) membranes of skeletal muscle. Both isoforms are symports and are involved in both muscle pH and lactate regulation. Accordingly, sarcolemmal MCT isoform expression may play an important role in exercise performance. Acute exercise alters human MCT content, within the first 24 h from the onset of exercise. The regulation of MCT protein expression is complex after acute exercise, since there is not a simple concordance between changes in mRNA abundance and protein levels. In general, exercise produces greater increases in MCT1 than in MCT4 content. Chronic exercise also affects MCT1 and MCT4 content, regardless of the initial fitness of subjects. On the basis of cross-sectional studies, intensity would appear to be the most important factor regulating exercise-induced changes in MCT content. Regulation of skeletal muscle MCT1 and MCT4 content by a variety of stimuli inducing an elevation of lactate level (exercise, hypoxia, nutrition, metabolic perturbations) has been demonstrated. Dissociation between the regulation of MCT content and lactate transport activity has been reported in a number of studies, and changes in MCT content are more common in response to contractile activity, whereas changes in lactate transport capacity typically occur in response to changes in metabolic pathways. Muscle MCT expression is involved in, but is not the sole determinant of, muscle H(+) and lactate anion exchange during physical activity. 相似文献
42.
Maunoury F Berveiller D Lelarge C Pontailler JY Vanbostal L Damesin C 《Oecologia》2007,151(2):268-279
The stable C isotope composition (δ13C) of CO2 respired by trunks was examined in a mature temperate deciduous oak forest (Quercus petraea). Month-to-month, day-to-day and diurnal, measurements were made to determine the range of variations at different temporal
scales. Trunk growth and respiration rates were assessed. Phloem tissue was sampled and was analysed for total organic matter
and soluble sugar 13C composition. The CO2 respired by trunk was always enriched in 13C relative to the total organic matter, sometimes by as much as 5‰. The δ13C of respired CO2 exhibited a large seasonal variation (3.3‰), with a relative maximum at the beginning of the growth period. The lowest values
occurred in summer when the respiration rates were maximal. After the cessation of radial trunk growth, the respired CO2 δ13C values showed a progressive increase, which was linked to a parallel increase in soluble sugar content in the phloem tissue
(R = 0.95; P < 0.01). At the same time, the respiration rates declined. This limited use of the substrate pool might allow the discrimination
during respiration to be more strongly expressed. The late-season increase in CO2 δ13C might also be linked to a shift from recently assimilated C to reserves. At the seasonal scale, CO2 δ13C was negatively correlated with air temperature (R = −0.80; P < 0.01). The diurnal variation sometimes reached 3‰, but the range and the pattern depended on the period within the growing
season. Contrary to expectations, diurnal variations were maximal in winter and spring when the leaves were missing or not
totally functional. By contrast to the seasonal scale, these diurnal variations were not related to air temperature or sugar
content. Our study shows that seasonal and diurnal variations of respired 13C exhibited a similar large range but were probably explained by different mechanisms. 相似文献
43.
Claire Farrell Christopher Szota Nicholas S. G. Williams Stefan K. Arndt 《Plant and Soil》2013,372(1-2):177-193
Background and aims
Green roofs are often installed to reduce urban stormwater runoff. To optimally achieve this, green roof plants need to use water when available, but reduce transpiration when limited to ensure survival. Succulent species commonly planted on green roofs do not achieve this. Water availability on green roofs is analogous to natural shallow-soil habitats including rock outcrops. We aimed to determine whether granite outcrop species could improve green roof performance by evaluating water use strategies under contrasting water availability.Methods
Physiological and morphological responses of 12 granite outcrop species with different life-forms (monocots, herbs and shrubs) and a common green roof succulent were compared in well watered (WW) and water deficit (WD) treatments.Key results
Granite outcrop species showed a variety of water-use strategies. Unlike the green roof succulent all of the granite outcrop species showed plasticity in water use. Monocot and herb species showed high water use under WW but also high water status under WD. This was achieved by large reductions in transpiration under WD. Maintenance of water status was also related to high root mass fraction.Conclusions
By developing a conceptual model using physiological traits we were able to select species suitable for green roofs. The ideal species for green roofs were high water users which were also drought tolerant. 相似文献44.
Background
Protein HMGB1, an abundant nuclear non-histone protein that interacts with DNA and has an architectural function in chromatin, was strikingly shown some years ago to also possess an extracellular function as an alarmin and a mediator of inflammation. This extracellular function has since been actively studied, both from a fundamental point of view and in relation to the involvement of HMGB1 in inflammatory diseases. A prerequisite for such studies is the ability to detect HMGB1 in blood or other biological fluids and to accurately measure its concentration.Methodology/Principal Findings
In addition to classical techniques (western blot, ELISA) that make use of specific anti-HMGB1 antibodies, we present here a new, extremely sensitive technique that is based on the fact that hemicatenated DNA loops (hcDNA) bind HMGB1 with extremely high affinity, higher than the affinity of specific antibodies, similar in that respect to DNA aptamers. DNA-protein complexes formed between HMGB1 and radiolabeled hcDNA are analyzed by electrophoresis on nondenaturing polyacrylamide gels using the band-shift assay method. In addition, using a simple and fast protocol to purify HMGB1 on the basis of its solubility in perchloric acid allowed us to increase the sensitivity by suppressing any nonspecific background. The technique can reliably detect HMGB1 at a concentration of 1 pg per microliter in complex fluids such as serum, and at much lower concentrations in less complex samples. It compares favorably with ELISA in terms of sensitivity and background, and is less prone to interference from masking proteins in serum.Conclusion
The new technique, which illustrates the potential of DNA nanoobjects and aptamers to form high-affinity complexes with selected proteins, should provide a valuable tool to further investigate the extracellular functions of HMGB1 and its involvement in inflammatory pathologies. 相似文献45.
46.
Holzapfel E Eisner G Alami M Barrett CM Buchanan G Lüke I Betton JM Robinson C Palmer T Moser M Müller M 《Biochemistry》2007,46(10):2892-2898
Translocation of twin-arginine precursor proteins across the cytoplasmic membrane of Escherichia coli requires the three membrane proteins TatA, TatB, and TatC. TatC and TatB were shown to be involved in precursor binding. We have analyzed in vitro a number of single alanine substitutions in tatC that were previously shown to compromise in vivo the function of the Tat translocase. All tatC mutants that were defective in precursor translocation into cytoplasmic membrane vesicles concomitantly interfered with precursor binding not only to TatC but also to TatB. Hence structural changes of TatC that affect precursor targeting simultaneously abolish engagement of the twin-arginine signal sequence with TatB and block the formation of a functional Tat translocase. Since these phenotypes were observed for tatC mutations spread over the first half of TatC, this entire part of the molecule must globally be involved in precursor binding. 相似文献
47.
Claire E. Reynolds-Peterson Na Zhao Jie Xu Taryn M. Serman Jielin Xu 《Autophagy》2017,13(8):1262-1279
Heparan sulfate-modified proteoglycans (HSPGs) are important regulators of signaling and molecular recognition at the cell surface and in the extracellular space. Disruption of HSPG core proteins, HS-synthesis, or HS-degradation can have profound effects on growth, patterning, and cell survival. The Drosophila neuromuscular junction provides a tractable model for understanding the activities of HSPGs at a synapse that displays developmental and activity-dependent plasticity. Muscle cell-specific knockdown of HS biosynthesis disrupted the organization of a specialized postsynaptic membrane, the subsynaptic reticulum (SSR), and affected the number and morphology of mitochondria. We provide evidence that these changes result from a dysregulation of macroautophagy (hereafter referred to as autophagy). Cellular and molecular markers of autophagy are all consistent with an increase in the levels of autophagy in the absence of normal HS-chain biosynthesis and modification. HS production is also required for normal levels of autophagy in the fat body, the central energy storage and nutritional sensing organ in Drosophila. Genetic mosaic analysis indicates that HS-dependent regulation of autophagy occurs non-cell autonomously, consistent with HSPGs influencing this cellular process via signaling in the extracellular space. These findings demonstrate that HS biosynthesis has important regulatory effects on autophagy and that autophagy is critical for normal assembly of postsynaptic membrane specializations. 相似文献
48.
In order to cause disease in plants, many fungal pathogens develop a specialized structure called an appressorium. We have recently shown that the rice blast fungus Magnaporthe grisea undergoes a regulated form of programmed cell death during appressorium development involving autophagy. Significantly, this form of cell death is a prerequisite for plant infection and fungal pathogenesis and part of a growing body of evidence implicating autophagy as a key process in fungal developmental biology. 相似文献
49.
50.
Lydia N. Raines Matthew M. Hsieh Tina Nassehi Claire M. Drysdale John F. Tisdale Naoya Uchida 《Cytotherapy》2019,21(12):1206-1215
Background aimsAllogeneic hematopoietic stem cell transplantation is curative for sickle cell disease, and the use of matched related donors, non-myeloablative conditioning and sirolimus immunosuppression results in stable mixed chimerism without graft-versus-host disease (GVHD). However, the time to terminate sirolimus while maintaining mixed chimerism is unclear.MethodsIn this study, we developed a two-way mixed lymphocyte reaction (MLR) to evaluate ex vivo immunoreaction in mixed chimeric patients.ResultsIn co-culture of peripheral blood mononuclear cells (PBMCs) from two healthy controls (without irradiation), we detected proliferation at various ratios of PBMC mixtures (1:9 to 9:1) as well as various concentrations of sirolimus, suggesting that two-way MLR is applicable to patients (having >10% chimerism) undergoing sirolimus treatment. In two-way MLR using PBMCs (including donor and recipient cells) from mixed chimeric patients (n = 28), greater ex vivo proliferation was observed <6 months compared with >6 months post-transplant and healthy control PBMC monoculture. Robust ex vivo proliferation was observed in a patient with acute GVHD, and persistent ex vivo proliferation (until 2 years) was observed in a patient with decreasing donor chimerism.ConclusionsIn summary, we demonstrated that in two-way MLR, ex vivo immunoreaction decreases to low levels ~6 months post-transplant. These findings suggest a rationale to continue immunosuppression for 6 months. 相似文献