全文获取类型
收费全文 | 10941篇 |
免费 | 593篇 |
国内免费 | 52篇 |
专业分类
耳鼻咽喉 | 105篇 |
儿科学 | 224篇 |
妇产科学 | 137篇 |
基础医学 | 1791篇 |
口腔科学 | 125篇 |
临床医学 | 996篇 |
内科学 | 2535篇 |
皮肤病学 | 304篇 |
神经病学 | 1276篇 |
特种医学 | 622篇 |
外科学 | 1660篇 |
综合类 | 77篇 |
一般理论 | 2篇 |
预防医学 | 382篇 |
眼科学 | 173篇 |
药学 | 594篇 |
中国医学 | 7篇 |
肿瘤学 | 576篇 |
出版年
2023年 | 68篇 |
2022年 | 115篇 |
2021年 | 212篇 |
2020年 | 132篇 |
2019年 | 187篇 |
2018年 | 210篇 |
2017年 | 208篇 |
2016年 | 272篇 |
2015年 | 288篇 |
2014年 | 324篇 |
2013年 | 394篇 |
2012年 | 657篇 |
2011年 | 740篇 |
2010年 | 454篇 |
2009年 | 438篇 |
2008年 | 669篇 |
2007年 | 683篇 |
2006年 | 611篇 |
2005年 | 679篇 |
2004年 | 653篇 |
2003年 | 612篇 |
2002年 | 622篇 |
2001年 | 128篇 |
2000年 | 142篇 |
1999年 | 175篇 |
1998年 | 158篇 |
1997年 | 134篇 |
1996年 | 112篇 |
1995年 | 95篇 |
1994年 | 67篇 |
1993年 | 77篇 |
1992年 | 85篇 |
1991年 | 69篇 |
1990年 | 51篇 |
1989年 | 51篇 |
1988年 | 59篇 |
1987年 | 43篇 |
1986年 | 44篇 |
1985年 | 54篇 |
1984年 | 39篇 |
1983年 | 39篇 |
1982年 | 30篇 |
1981年 | 25篇 |
1979年 | 22篇 |
1978年 | 23篇 |
1977年 | 24篇 |
1976年 | 19篇 |
1974年 | 20篇 |
1971年 | 25篇 |
1931年 | 18篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
31.
Daniel F. Legler Marcel Loetscher Simon A. Jones Clemens A. Dahinden Michel Arock Bernhard Moser 《European journal of immunology》1996,26(4):753-758
The proteolytic cleavage product of complement component 3, (C3a), like C4a and C5a, is a potent anaphylatoxin and induces the production of inflammatory mediators in phagocytes. Notably, mast cells respond to C3a with the release of vasoactive substances, including histamine. We have examined the function and receptor binding of C3a in a human leukemic mast cell line, HMC-1. Similar to chemoattractant agonists in leukocytes, C3a induced rapid cytosolic free calcium concentration increases in HMC-1 cells. EGTA did not diminish this response, indicating that mobilizable Ca2+ was from intracellular stores. Receptors for C3a in HMC-1 cells couple in part to Bordetella pertussis toxin-sensitive G-proteins and, therefore, appear to belong to the family of serpentine receptors that require G-proteins for signal transduction. HMC-1 cells express two types of C3a receptors, C3aR1 and C3aR2, that were shown to bind 125I-C3a with high-(Kd1 = 2.1–4.8 nM) or low-affinity (Kd2 = 30–150 nM), and both receptors are expressed at high level: 3 × 105–6 × 105 C3aR1/cell and 5 × 105–2.3 × 106 C3aR2/cell. Results from cross-linking experiments with 125I-C3a fully agree with the presence of two different classes of C3a receptors in HMC-1 cells. Two membrane proteins with apparent molecular masses of 54–61 kDa (p57) and 86–107 kDa (p97) could be covalently modified with 125I-C3a, and this cross-linking was inhibited with an excess of unlabeled C3a. Many of the known agonists for leukocytes including 13 chemokines (IL-8, NAP-2, GROα, ENA-78, IP10, PF4, MCP-1, 2 and 3, RANTES, MIP-1α, MIP-1β and 1309), three neuropeptides (neuropeptide Y, somatostatin and calcitonin), as well as C5a, did not activate HMC-1 cells, indicating that C3a is one of a few protein ligands for which this cell line expresses specific receptors. The apparent selectivity for C3a and the abundant expression of C3a receptors make the HMC-1 cell line an excellent choice for the cloning of the receptor genes. 相似文献
32.
Ch. Breier A. Dzien H. -J. Lisch H. Braunsteiner 《Journal of molecular medicine (Berlin, Germany)》1984,62(12):593-594
Summary Diseases associated with acidotic blood-pH, such as chronic renal disease, diabetes mellitus or chronic alcoholism, show a marked impairment of lipoprotein lipase. Therefore we influenced blood-pH in 3 healthy subjects by infusions to get alkalotic, neutral and acidotic blood-pH on three days in series. On each day blood-pH from capillary blood and post-heparin lipoprotein lipase from fasting plasma was determined. In comparison to neutral blood-pH in vivo, alkalosis did not influence lipoprotein lipase. In contrast, during artificial acidosis, lipoprotein lipase was impaired significantly (p<0.01). Therefore, it seems, that acidosis inhibits lipoprotein lipase in vivo. 相似文献
33.
Asero R Weber B Mistrello G Amato S Madonini E Cromwell O 《The Journal of allergy and clinical immunology》2005,116(5):1036-1041
BACKGROUND: Short ragweed and giant ragweed pollen allergens are considered largely cross-reactive, and it is generally believed that 1 species is sufficient for skin testing and immunotherapy. However, in the area north of Milan (a zone widely invaded only by short ragweed), about 50% of patients submitted to injection specific immunotherapy with giant ragweed showed little or no clinical response, but showed an excellent outcome if they were shifted to short ragweed specific immunotherapy. OBJECTIVE: To investigate allergenic differences between short and giant ragweed. METHODS: IgE reactivity to short ragweed of sera from 16 patients allergic to ragweed was assessed by immunoblot before and after absorption with short and giant ragweed. Moreover, 41 ragweed-monosensitive patients underwent skin prick test with both ragweed species. RESULTS: In several cases, preabsorption of sera with giant ragweed extract was unable to inhibit IgE reactivity fully against both a 43-kd allergen and other allergens at different molecular weights in short ragweed. On skin prick test, short ragweed induced larger wheals than giant ragweed in the majority of patients, and 6 of 41 (15%) patients were strongly short ragweed-positive but giant ragweed-negative. The immunoblot with the serum from 1 of these subjects showed a strong IgE reactivity to short ragweed at about 43 kd in the absence of any reactivity to giant ragweed. CONCLUSION: Short and giant ragweed are not allergenically equivalent. Allergenic differences involve both the major allergens Amb a 1-2/Amb t 1-2 and some minor allergens. In patients allergic to ragweed, both diagnosis in vivo and immunotherapy should always be performed by using the ragweed species present in that specific geographic area. 相似文献
34.
Summary The PAR1/SNQ3 gene of S. cerevisiae, which increases resistance to iron chelators in multi-copy transformants, is identical to the YAP1 gene, a yeast activator protein isolated as a functional homologue of the human c-jun oncogene by binding specifically to the AP-1 consensus box. The observed H2O2-sensitivity of par1 mutants has been attributed to an increased sensitivity to reduced oxygen intermediates. Accordingly, par1 mutants did not survive an elevated oxygen pressure and were very sensitive to menadione and methylviologene, two chemicals enhancing the deleterious effects of oxygen. The specific activities of enzymes involved in oxygen detoxification, such as superoxide dismutase, glucose 6-phosphate dehydrogenase and glutathione reductase, were decreased in par1 mutants and increased after PAR1 over-expression. As in the case of oxygen detoxification enzymes, the cellular levels of glutathione were similarly affected. These observations indicate that PAR1/YAP1/SNQ3 is involved in the gene regulation of certain oxygen detoxification enzymes. The finding that H2O2 promotes DNA-binding of human c-jun is consistent with a similar function for PAR1/YAP1/SNQ3 and c-jun in cellular metabolism.Dedicated to Professor Dr. R. W. Kaplan on the occasion of his 80th birthday 相似文献
35.
36.
Illigens BM Yamada A Fedoseyeva EV Anosova N Boisgerault F Valujskikh A Heeger PS Sayegh MH Boehm B Benichou G 《Human immunology》2002,63(10):912-925
In this study, we measured direct and indirect T-cell alloresponses mediated by CD4(+) and CD8(+) T cells in three mouse transplantation models: skin, cornea, and retina. We show that the contribution of direct and indirect antigen recognition pathways to the alloresponse to fully allogeneic grafts varies depending upon the nature of the tissue/organ transplanted. The implications of this finding for understanding the cellular mechanisms by which rejection is mediated in different transplant models are discussed. 相似文献
37.
Summary: The flame retardant mechanisms of red phosphorus, magnesium hydroxide and red phosphorus combined with magnesium hydroxide were studied in high impact polystyrene by means of comprehensive decomposition studies and combustion tests. The study is intended to illuminate prerequisites and the potential of red phosphorus as a fire retardant for hydrocarbon polymers in the condensed phase and in the gas phase. Thermal and thermo‐oxidative decomposition, decomposition kinetics and the product gases evolved were characterized using thermogravimetry coupled with Fourier transform infrared spectroscopy and mass spectroscopy, respectively. Fire behaviour was investigated with a cone calorimeter using different external heat fluxes, whereas the flammability was determined by limited oxygen indices. The combustion residues were analysed using XPS. Red phosphorus reduced the heat release in HIPS due to radical trapping in the gas phase. Magnesium hydroxide influenced fire behaviour by heat sink mechanisms, release of water and the formation of a magnesia layer acting as a barrier. The combination of both flame retardants in HIPS nearly resulted in a superposition. A slight synergy in barrier characteristics was due to the formation of magnesium phosphate, whereas a slight anti‐synergism occurred in flammability and in the gas phase action. The latter effect is controlled by a decreased fuel rate due to the barrier layer rather than by an initiation of red phosphorus oxidation in the condensed phase.
38.
39.
40.