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排序方式: 共有4512条查询结果,搜索用时 671 毫秒
41.
J. Strid J. Hourihane† I. Kimber‡ R. Callard S. Strobel§ 《Clinical and experimental allergy》2005,35(6):757-766
BACKGROUND: Food allergies are an important cause of life-threatening hypersensitivity reactions. Oral tolerance can be considered the default immune response to dietary antigens, with immune deviation resulting in allergic sensitization. However, primary sensitization to food allergens may not solely be through the gastrointestinal mucosa, as strong T-helper type 2 (Th2)-biased immunity can result from exposure to protein allergens on barrier-disrupted skin. OBJECTIVE: The purpose of this study was to examine whether exposure to allergens through the skin may interfere with the normal development of oral tolerance and promote allergic sensitization to food proteins. METHODS: Female BALB/c mice were exposed epicutaneously to peanut protein and induction of systemic oral tolerance through high dose feeds of peanut protein was subsequently assessed. Other mice were rendered tolerant prior to epicutaneous peanut exposure. Sensitivity to peanut was determined by assessing delayed-type hypersensitivity, proliferative, cytokine and antibody responses. RESULTS: Epicutaneous exposure to peanut protein induced potent Th2-type immunity with high levels of IL-4 and serum IgE. Primary skin exposure prevented the subsequent induction of oral tolerance to peanut in an antigen-specific manner. Upon oral challenge, mice became further sensitized and developed strong peanut-specific IL-4 and IgE responses. Furthermore, animals with existing tolerance to peanut were partly sensitized following epicutaneous exposure. CONCLUSION: Epicutaneous exposure to peanut protein can prevent induction of oral tolerance, and may even modify existing tolerance to peanut. Epidermal exposure to protein allergens selectively drives Th2-type responses, and as such may promote sensitization to food proteins upon gastrointestinal exposure. 相似文献
42.
43.
Z. Peng Q. Liu Q. Wang E. Rector Y. Ma R. Warrington 《Clinical and experimental allergy》2007,37(7):1040-1048
BACKGROUND: Immunotherapy with anti-IgE antibodies for treatment of allergy is promising but a short half-life and extremely high cost limit its application. OBJECTIVE: We sought to develop IgE vaccines that induce longer-lasting auto-antibodies to neutralize self-IgE as an alternative therapy. METHODS: The vaccine was made by conjugating three synthetic peptides corresponding to human IgE receptor-binding sites to a carrier, hepatitis B surface antigen. To test the immunogenicity of the vaccine, rats were immunized with the vaccine or hepatitis B surface antigen as control. Serum IgG titres to human IgE and the IgE of other species were measured. The inhibition by rat antisera of the binding of human IgE to its receptor was assessed by ELISA, flow cytometry analysis, and passive cutaneous anaphylaxis (PCA), and its ability to recognize receptor-bound IgE was examined. The in vivo effect of the vaccine was evaluated in trichosanthin-sensitized mice and rats. In the preventative study, vaccination started before sensitization commenced, while in the treatment study, vaccination started after sensitization. Sensitized mice and rats receiving injections of the carrier served as controls. Trichosanthin-specific IgE was measured using PCA. RESULTS: Sera from vaccine-immunized rats contained high titre antibodies that reacted with soluble and plate-bound but not with receptor-bound human IgE; they also reacted with mouse, rat, and dog IgE. Furthermore, the sera inhibited the binding of human IgE to its receptor in a dose-dependent manner. In preventative and treatment studies, serum trichosanthin-specific IgE levels were significantly reduced in vaccinated groups compared with controls. CONCLUSION: Antibodies against self-IgE can be induced by IgE peptide-based vaccines, which are effective in preventing the increase of IgE and in down-regulating IgE in sensitized animals. 相似文献
44.
[目的]探讨干扰素-γ(IFN-γ)对支气管哮喘(哮喘)小鼠气道炎症及肺T淋巴细胞和血浆中IgE的影响。[方法]C57BL/6小鼠随机分为正常对照组(A组,10只)、哮喘模型组(B组,10只)、IFN-γ注射组(C组,10只)。采用卵蛋白(OVA)和氢氧化铝致敏、雾化建立哮喘模型,B组、C组分别在致敏同时第1、3、5、9、15、17、20 d,1次/d腹腔注射生理盐水(0.1 m1)和IFN-γ(1 500U)。第22 d收取肺泡灌洗液(BALF)并取其肺T淋巴细胞体外培养及血浆中IgE。分析小鼠BALF和肺部淋巴细胞产生的细胞因子IL-4、IL-5及血浆中IgE水平的变化。[结果]A组无症状,B组哮喘鼠症状重,C组哮喘鼠症状轻。在BALF中嗜酸性粒细胞百分比(EOS%)计数A组0,B组20.1±7.0,C组0.7±0.2。哮喘模型组肺T淋巴细胞中IL-4、IL-5,血浆中IgE显著高于正常对照组(P<0.01),治疗组肺T淋巴细胞中IL-4、IL-5,血浆中IgE显著低于哮喘模型组(P<0.01)。[结论]IFN-γ可以抑制哮喘小鼠气道炎症,其机制之一可能与是抑制肺T淋巴细胞产生的IL-4、IL-5,降低血清中总IgE水平有关。 相似文献
45.
Tsuneo Namba Hongxi Xu Shigetoshi Kadota Masao Hattori Tooru Takahashi Yasuhiko Kojima 《Phytotherapy research : PTR》1993,7(3):227-230
The inhibitory effects of glycoproteins separated from a hot water extract of corn silk (U-CSE) on the formation of IgE antibodies after primarily and secondarily challenged responses with dinitrophenyl (DNP)-ovalbumin (OVA) antigen in mice were investigated using the passive cutaneous anaphylaxis (PCA) test. When U-CSE was given intranasally or intraperitoneally the day before primary immunization, IgE antibody production was strongly inhibited. Furthermore, it was found that new formation of IgE antibodies was readily inhibited by U-CSE administration in mice with high levels of IgE after primary immunization. It was also found that U-CSE markedly suppressed IgE antibody formation in secondarily challenged responses with the antigen. U-CSE may be clinically applicable to type I allergic diseases. 相似文献
46.
Feather mites are potentially an important source of allergens for pigeon and budgerigar keepers 总被引:1,自引:0,他引:1
M. J. COLLOFF† T. G. MERRETT‡ J. MERRETT† C. McSHARRY † G. BOYD§ 《Clinical and experimental allergy》1997,27(1):60-67
Background Previous studies on allergy to feathers have not adddressed whether orgatiisms living on feathers (mites. lice, moulds) are a source of allergens. Objective To investigate whether feather mites produced allergens of clinical relevance to bird keepers. Methods We examined serum IgE responses of 96 pigeon breeders to an extract of feather mites from pigeons (predominantly Diplaegidia columbae). using Western blotting, specific IgE assay using AlaSTAT EIA and RAST inhibition. Results Feather mites are a major source of soluble proteins derived from feathers, accounting for up to 10% of the total weight of the feather. Forty-three sera had a negative score (0) for anti-feather mite IgE. 27 were weakly positive (1–2) and 26 had strongly positive scores (3–4). Fewer pigeon breeders with scores ± 3 were asymptomatic than those with negative scores (12 versus 40%). more had late onset symptoms (with or without early onset symptoms; 77% versus 44%) and had IgE antibody against house dust mite (89% versus 23%). Western blotting of eight sera against the extract of Diplaegidia columbae revealed 20 IgE-binding components ranging from 22 to 200 kDa. A high diversity of components was recognized by each serum: arithmetic mean 7 (range 2 14). RAST inhibition indicated feather mites had species-specific epitopes as well as ones that cross-reacted with Dermatophagoides pteronyssinus. Conclusion Strongly-positive AlaSTAT scores to pigeon leather mite were associated with allergic symptoms of late onset in pigeon breeders. We conclude that feather mites are a major source of clinically-relevant allergens for pigeon breeders. 相似文献
47.
人FcεRⅠα亚基细胞外区的原核表达及其和IgE结合的机制 总被引:2,自引:0,他引:2
应用两种不同的表达系统对FcεRⅠα亚基的细胞外区进行克隆和表达,表达产物经纯化后用免疫斑点杂交法检测其与IgE结合的能力,探索IgE与其高亲和力受体FcεRⅠα亚基的细胞外区结合的机制。结果两种体系均成功表达出FcεRⅠα亚基的细胞外区,pBAD/gⅢA表达的FcεRⅠα亚基的细胞外区能与IgE结合,而PQE30表达的FcεRⅠα亚基的细胞外区不能与IgE结合。提示FcεRⅠα亚基的细胞外区已足够和。IgE结合,无需β、γ亚基的存在,其所具有的一定的空间构型和二硫键的形成在与IgE结合时是必需的,而糖基化位点在与IgE的结合时是非必需的。 相似文献
48.
IL-5 production by allergen-stimulated T cells following grass pollen immunotherapy for seasonal allergic rhinitis 总被引:1,自引:0,他引:1 下载免费PDF全文
S TILL S WALKER R DICKASON D HUSTON F O''''BRIEN J LAMB A B KAY C CORRIGAN S DURHAM 《Clinical and experimental immunology》1997,110(1):114-121
We have previously identified the hevein preprotein as a common allergen for latex allergic healthcare workers. The B cell epitopes in the hevein protein that are recognized by IgE of latex-allergic individuals have not been identified. In this study, we examined the hevein preprotein using epitope mapping. Overlapping synthetic peptides of 10 amino acids (two aa overlap) were synthesized on a derivatized cellulose membrane using Fmoc chemistry. The peptide spots were probed with pooled sera from 10 latex-allergic patients, and the IgE-reactive peptides identified with anti-IgE MoAbs. We identified six B cell epitopes within the full length hevein preprotein which bound IgE from latex-allergic patients. Two were located in the N-terminal 5-kD hevein domain and four were observed in the 14-kD C-domain. A broad epitope was located between the N-terminal amino acids 13–24. This epitope had nearly complete homology to wheat germ agglutinin (WGA). Immunological cross-reactivity to WGA was confirmed by Western blot analysis with purified WGA, and this reactivity could be inhibited by latex proteins or WGA. Of the five remaining epitopes, four had homologies to other proteins in the pathogenesis-related family of plant proteins (PR-4). The data demonstrate that hevein has multiple IgE epitopes. The significant homology of these epitopes to a broad family of plant defence proteins further explains the increased prevalence of food allergies in latex-allergic individuals. 相似文献
49.
B. J. Hales I. A. Laing L. J. Pearce L. A. Hazell K. L. Mills K. Y. Chua R. B. Thornton P. Richmond A. W. Musk A. L. James P. N. LeSouëf W. R. Thomas 《Clinical and experimental allergy》2007,37(9):1357-1363
BACKGROUND: There is evidence that the specificity of the IgE binding in allergy tests can vary for different populations. OBJECTIVE: We aimed to examine the allergenic specificity of IgE binding in sera from house dust mite (HDM)-atopic subjects in a tropical Australian Aboriginal community. METHODS: Sera shown to contain IgE antibodies to an HDM extract of Dermatophagoides pteronyssinus were examined for IgE binding to a panel of nine purified HDM allergens from this mite species by quantitative microtitre assays. IgG antibody binding (IgG1 and IgG4) was also measured. RESULTS: The IgE-binding activity in the sera from the Aboriginal community was not directed to the expected major groups 1 and 2 HDM allergens but instead to the group 4 amylase allergen. There was also little IgE binding to the potentially cross-reactive tropomyosin (Der p 10) or arginine kinase (Der p 20) allergens. The IgG4 antibody was rarely detected and limited to the Der p 4 allergen. IgG1 antibody binding was frequently measured to all the allergens regardless of an individual's atopic status, whereas in urban communities it is restricted to the major allergens and to atopic subjects. CONCLUSION: The high IgE anti-HDM response of Australian Aboriginals predominantly bound Der p 4 and not the Der p 1 and 2 allergens, showing a distinctive allergy that could affect the disease outcome and diagnosis. 相似文献
50.
BACKGROUND: We have previously demonstrated that the proteolytic activity of Der p 1 selectively cleaves human CD25, the 55 kDa alpha subunit of the IL-2 receptor. As a result of cleavage of surface CD25, peripheral blood T cells produce less IFN-gamma and more IL-4, thereby leading to progressive polarization of the T cells towards a Th2 cytokine profile. Therefore, these observations underline the potential role of the proteolytic activity of Der p 1 in creating a microenvironment conducive for IgE synthesis. OBJECTIVE: To study the effect of T cells that have been conditioned by the proteolytic activity of Der p 1 on IgE synthesis by B cells. METHODS: We have examined this concept in experiments whereby T cells that have been exposed to either proteolytically active or inactive Der p 1 were cocultured with autologous B cells and IgE antibody synthesis was monitored. RESULTS: Here we demonstrate for the first time that coculturing T cells that have been in contact with proteolytically active Der p 1 with autologous B cells leads to augmentation of IgE antibody responses. CONCLUSIONS: The proteolytic activity of Der p 1 conditions human T cells, which then become empowered to trigger enhanced IgE synthesis by B cells. 相似文献