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71.
《Vaccine》2022,40(16):2388-2398
Universal coverage of routine childhood vaccines remains a challenge in many low- and middle-income countries (LMICs). In India, vaccination campaigns have increased full immunization coverage among 12–23 month old children from an estimated 62% in 2015–2016 to 76% in 2019–2020. Long-term improvements in coverage will likely require systemic changes to both the supply and demand sides of immunization programs. However, the effect of health system inputs on child vaccination outcomes remains poorly quantified in India. We examined the association between the quality of public health facilities and child vaccination outcomes in rural India using data from the nationally representative Integrated Child Health and Immunization Survey (2015–2016) which covered 1,346 public primary health sub-centers and 44,571 households. We constructed two indices of sub-center quality using multiple correspondence analysis: one related to the general health infrastructure quality and the other measuring vaccine service delivery. Using probit regression, we analyzed the relationship between vaccination outcomes in children under 2 years of age and sub-center quality, controlling for household socioeconomic characteristics. Additionally, we conducted Fairlie decomposition analysis by wealth group — bottom wealth quintile relative to the top four wealth quintiles— to examine factors contributing to gaps in immunization between rich and poor households. Infrastructure quality index was positively associated with completion of seven vaccination outcomes: full immunization, DPT-1 (first dose of diphtheria, pertussis, and tetanus), DPT-2, DPT-3, Bacillus Calmette–Guérin (BCG), hepatitis B (birth dose), and on-time vaccination (OTV). Vaccine service delivery index was positively associated with completion of measles vaccination. The distribution of infrastructure quality contributed to increased gaps in full immunization and OTV between rich and poor households, while greater proximity to vaccination site for poorer households reduced these gaps. Improved quality of health facilities, particularly facilities used by low-income households, may improve vaccination outcomes. 相似文献
72.
Miyake A Akagi T Enose Y Ueno M Kawamura M Horiuchi R Hiraishi K Adachi M Serizawa T Narayan O Akashi M Baba M Hayami M 《Journal of medical virology》2004,73(3):368-377
We have previously reported that concanavalin A-immobilized polystyrene nanospheres (Con A-NS) could efficiently capture HIV-1 particles and that intranasal immunization with inactivated HIV-1-capturing nanospheres (HIV-NS) induced vaginal anti-HIV-1 IgA antibody response in mice. In this study, to evaluate the protective effect of immunization, each three macaques was intranasally immunized with Con A-NS or inactivated simian/human immunodeficiency virus KU-2-capturing nanospheres (SHIV-NS) and then intravaginally challenged with a pathogenic virus, SHIV KU-2. After a series of six immunizations, vaginal anti-HIV-1 gp120 IgA and IgG antibodies were detected in all SHIV-NS-immunized macaques. After intravaginal challenge, one of the three macaques in each of the Con A-NS- and SHIV-NS-immunized groups was infected. Plasma viral RNA load of infected macaque in SHIV-NS-immunized macaques was substantially less than that in unimmunized control macaque and reached below the detectable level. However, it could not be determined whether intranasal immunization with SHIV-NS is effective in giving complete protection against intravaginal challenge. To explore the effect of the SHIV-NS vaccine, the remaining non-infected macaques were rechallenged intravenously with SHIV KU-2. After intravenous challenge, all macaques became infected. However, SHIV-NS-immunized macaques had lower viral RNA loads and higher CD4(+) T cell counts than unimmunized control macaques. Plasma anti-HIV-1 gp120 IgA and IgG antibodies were induced more rapidly in the SHIV-NS-immunized macaques than in the controls. The rapid antibody responses having neutralizing activity might contribute to the clearance of the challenge virus. Thus, SHIV-NS-immunized macaques exhibited partial protection to vaginal and systemic challenges with SHIV KU-2. 相似文献
73.
肿瘤在体内的排斥/控制主要依赖于肿瘤抗原特异性T淋巴细胞.T淋巴细胞通过TCR与肿瘤细胞表面表达的HLA-抗原肽复合物的相互作用来识别其靶分子.与特异性HLA-抗原肽复合物有价值的相互作用诱导了淋巴细胞克隆的扩增以及一系列的免疫反应.目前,从理论上已经提出了以整个肿瘤细胞,或纯化的肿瘤抗原作为疫苗(包括整个蛋白质分子和抗原肽及纯化的DNA分子)来提高免疫系统对肿瘤的识别和排斥.本文从免疫系统对肿瘤细胞的识别、疫苗诱导的体内抗肿瘤免疫的假设机制、疫苗接种所诱导的抗肿瘤反应以及临床结果几个方面,对当前肿瘤疫苗的研究现状作一简要综述,并对肿瘤疫苗研究中尚待解决的问题作了简单的归纳. 相似文献
74.
75.
电针肾俞、膈俞、百会穴对拟血管性痴呆学习记忆障碍小鼠水迷宫实验的影响 总被引:9,自引:1,他引:8
目的 观察电针肾俞、膈俞、百会穴对拟血管性痴呆小鼠学习记忆障碍的影响。方法 复制脑缺血再灌注拟血管性痴呆小鼠模型 ,并电针肾俞、膈俞、百会穴 ,分别于术后 7天、15天、30天 ,与药物喜德镇对照 ,采用水迷宫法 ,记录游全程时间、错误次数。结果 造模导致了小鼠学习与记忆能力下降 ,表现为游全程时间延长 ,错误次数增加 ,且随着观察时间的延长 ,这种改变逐渐加重。电针和喜德镇均可使模型小鼠的游全程时间缩短 ,错误次数减少 ,但电针组于 7天和 30天时 ,成绩显著优于药物组。结论 电针肾俞、膈俞、百会穴对模型小鼠学习与记忆能力下降有改善和提高作用 相似文献
76.
Ivet A. Yordanova Luis E. Elizalde-Velázquez Susanne Hartmann 《European journal of immunology》2023,53(5):2250237
Parasitic nematodes infect more than 1 billion people in the global south. The development of effective antihelminthic vaccines is a crucial tool for their future elimination. Protective immune responses to nematodes depend on Gata3+ Th2 cells, which can also be induced by nematode-released products. Whether these nematode products induce antigen-specific long-lived memory T cells and thereby confer protection against a challenge infection is not known yet. Hence, we set out to characterize the formation of memory Th2 cells induced by immunization with Heligmosomoides polygyrus excretory-secretory (HES) products, infection-induced versus immunization-induced recall responses to a challenge infection, and whether HES-induced memory T cells show protective properties following adoptive transfer. Our results show that 8 weeks postimmunization, HES induces long-lived functional memory Th2 cells at the site of immunization in the peritoneal cavity. Following a H. polygyrus challenge infection, HES-immunized mice display MHC-II-dependent antigen-specific Th2 cytokine responses in the gut-draining lymph nodes, comparable to those induced by a prior natural infection. Moreover, adoptive transfer of sorted memory CD4+ T cells from HES-immunized donors reduces female worm fecundity following a challenge H. polygyrus infection in recipient mice, highlighting a protective role for immunization-induced memory T cells. 相似文献
77.
人乳头瘤病毒16型(湖北株)E7基因在体内和体外的表达 总被引:2,自引:1,他引:1
构建人乳头瘤病毒16型(HPV16)E7湖北株(HB)基因真核表达质粒,探讨其在哺乳动物体外,体内表达状况,为本地区HPV相关肿瘤的基因治疗提供依据。方法采用分子克隆技术,构建HPV16E7-HB重组表达质粒,磷酸钙-DNA沉淀技术及基因免疫技术将外源目的基因(HPV16E7-HB)导入NIH3T3细胞及大、小鼠体内PCR,RT-PCR,免疫荧光染色技术对外源目的基因及其产物(mR-NA,蛋白质。 相似文献
78.
采用IFAT法检测特异IgG荧光抗体,用MCPENT法检测中和抗体滴度,追踪流行病学防病效果。结果表明,该疫苗的安全性较好,总反应率为319%,中强反应182%,反应以局部一过性疼痛多见,无异常反应。疫苗3针全程免疫后2周、加强前、加强后2周、1年和2年,3年中和抗体阳转率分别为3140%、933%、8750%、5385%、3810%和3500%。荧光抗体阳转率分别为8491%、2250%、8500%、1579%、1020%和905%。疫苗的流行病学防病效果好,3针全程免疫后(19954)至今(1999.3)接种者无人发病,对照组发病8例,保护率为10000%,观察到试区疫情较四周非试区低,疫苗复盖率达50%以上,似可有效控制疫情。发现有1例接种者在经过一个流行高峰期后荧光抗体较前呈4周以上增高,但无临床表现。未发现接种人群中有免疫(感染)增强问题。 相似文献
79.
Mice fed 0 serotype-specific strains of P. aeruginosa for two weeks, had increased titers of IgM but not IgG antibodies to the strains fed. Immunized mice, burned and infected with P. aeruginosa, showed significant 0 serotype-specific enhanced survival. Survival of mice fed several 0 serotype-specific strains simultaneously increased when these mice were burned and infected with P. aeruginosa homologous to those fed except when a high exotoxin A producing strain was used. Mice fed purified exotoxin A showed an increased LD50 when injected with graded toxin doses. Feeding both 0 serotype-specific P. aeruginosa plus exotocin A increased survival even with burn and infection using the high toxin producing strain. We conclude that feeding P. aeruginosa antigens provides successful immunization which avoids the effects of parental adminstration. 相似文献
80.
Infections by hepatotropic viruses belong to the most common complications of chemotherapy in children suffering from neoplastic
diseases. The rate of hepatitis B virus (HBV) or hepatitis C virus (HCV) infection and the effectiveness of passive immunization
against HBV were studied in 285 children; 148/285 with lymphoproliferative diseases and 137/285 with solid tumours. HBV infection
was observed in 10.2% children receiving hepatitis B immune globulin as compared to 36.8% without passive immunization against
HBV. Anti-HCV antibodies were similar in both groups amounting 38.7% and 32.6% respectively.
Conclusion The results show that hepatitis B immune globulin administration is effective and that HCV might become the main cause of
hepatitis among immunosuppressed patients in the future.
Received: 13 December 1994 / Accepted: 18 October 1996 相似文献