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91.
Øivind Øines Thomas Schram 《Acta parasitologica / Witold Stefański Institute of Parasitology, Warszawa, Poland》2008,53(1):93-105
Two mitochondrial and one nuclear genetic marker were used to study the phylogenetic position of the two reported CO1-genotypes
of Caligus elongatus in a group of closely related caligid parasites. Molecular analysis of the two mitochondrial genes (CO1 and 16S), indicate
genetic distances of the two C. elongatus genotypes in the lower range of distances previously reported between other crustacean species, but higher than comparable
reported within-species differences. Analyses of nuclear 18S sequences indicate no detectable differentiation between these
genotypes, but may be due to expected differences in the resolution of these genetic markers. Investigation of two of three
selected morphological characters reveals phenotypes supporting the division based on the molecular division. The species
status on the two C. elongatus genotypes cannot be drawn conclusively, although the molecular and morphological data presented here suggests the presence
of sibling species. 相似文献
92.
Saiki O Uda H Nishimoto N Miwa T Mima T Ogawara T Azuma N Katada Y Sawaki J Tsutsui H Matsui K Maeda A Nakanishi K 《Clinical immunology (Orlando, Fla.)》2004,112(1):120-125
Adult Still's disease (ASD) is a chronic multisystemic disease. Extraordinarily high serum levels of IL-18 in ASD patients have been described, whereas the mechanism remains to be clarified. This study aimed to evaluate proinflammatory cytokines and to consider their pathological roles. In patients with rheumatic diseases (n = 151), blood samples were taken at the active phase and the serum levels of IL-18 and other proinflammatory cytokines were measured by ELISA. The extra-high levels of IL-18 were confirmed selectively in ASD patients (n = 10). In the active phase of ASD patients, the levels of IL-6 were elevated accordingly, but IL-1beta and TNF-alpha were undetectable. As to Th1-Th2 cytokines, the levels of IL-4 and IL-13, but not INF-gamma, IL-12, or IL-2, were elevated in all ASD patients examined. Moreover, the serum levels of IL-18 showed a good correlation with those of IL-4, suggesting that ASD reflects a Th2 rather than a Th1 cytokine profile. 相似文献
93.
Demonstration of the presence of IL-16, IL-17 and IL-18 at the murine fetomaternal interface during murine pregnancy 总被引:6,自引:0,他引:6
Ostojic S Dubanchet S Chaouat G Abdelkarim M Truyens C Capron F 《American journal of reproductive immunology (New York, N.Y. : 1989)》2003,49(2):101-112
PROBLEM: To determine if interleukin-16 (IL-16), IL-17, and IL-18 are present at the murine fetomaternal interface during pregnancy as a first step towards investigating their roles in fetomaternal relationship. METHODS: Expression of IL-16, IL-17, and IL-18, was assessed by immunohistochemistry (IHC) in the BALB/c x BALB/k (H2d x H2k), and the CBA/J x BALB/c non-abortion prone, and CBA/J x DBA/2 abortion prone matings. Enzyme-linked immunosorbent assay (ELISA) were performed for the two latter cytokines to compare local production in the abortion prone CBA/J x DBA/2 versus the non-abortion prone CBA/J x BALB/c matings. RESULTS: Expression of IL-17 was borderline. The anti-IL-16 staining specifically localized in the uterine stroma and glandular epithelium and was rather low in the placenta. IL-18 staining started in the peri-implantation uterus in the basal proliferative stroma, and was also traced, although weaker, in the glandular epithelium. In the immediate post-implantation period, a weak stromal staining persisted but there was a strong labeling of the ectoplacental cone. Interestingly, when the ectoplacental cone differentiates into placenta having a major histocompatibility complex (MHC) class I + spongiotrophoblast and a (MHC class I-) labyrinth, a very strong transient labeling of uterine natural killer (u-NK) cells was found. Later in gestation, IL-18 was also produced by giant cell and spongiotrophoblast. Finally, we compared by ELISA the production of IL-17/-18 in CBA/J x DBA/2 and CBA/J x BALB/c matings. We detected significantly more IL-18 in the non-abortion prone combination decidua or placenta. CONCLUSION: The three cytokines IL-16, IL-17, and IL-18 were detected at the fetomaternal interface with a tissue specific, stage-dependent distribution. The predominance of IL-18 secretion in the non-resorption prone matings lead us to question the general validity of the classical T-helper (Th)1/2 paradigm. 相似文献
94.
K. Kuribayashi T. Kodama H. Okamura M. Sugita T. Matsuyama 《Clinical and experimental allergy》2002,32(4):641-649
BACKGROUND: Correcting Th1/Th2 imbalance with administration of IL-12 before and during antigen challenge holds therapeutic promise in asthma. However, the effects of IL-12 on the established asthmatic responses have not fully been examined. OBJECTIVE: We investigated whether IL-12 administered after antigen challenge could diminish airway hyper-reactivity (AHR) and eosinophilia in mice actively sensitized to ovalbumin. We also have investigated the ability of administered IL-12 to induce IL-18 receptor (IL-18R) expression that may lead possible synergic action of IL-12 with endogenous IL-18. METHODS: C57BL/6 mice immunized to ovalbumin (OVA) by intraperitoneal (i.p.) injection, were challenged three times with an aerosol of OVA every second day for 8 days. Recombinant IL-12 (500 ng) was intravenously administered on a single occasion 1 h after the final challenge of mice. Mice were analysed for effects of IL-12 on AHR, inflammatory cell infiltration and cytokine levels in lung tissue as well as serum immunoglobulin (Ig) E levels. Immunohistochemistry for IL-18R was performed using rat monoclonal antibody specific for murine IL-18Ralpha (IL-1 receptor related protein; IL-1Rrp). RESULTS: An intravenous IL-12 administration diminished AHR, pulmonary eosinophilia and T lymphocyte infiltration, serum IgE, IL-4 and IL-13 in lung tissue. Expression of IL-18R was induced in the mononuclear cells in the lung of mice exposed to OVA. IL-12 administration enhanced the IL-18R expression compared with the control. CONCLUSION: These data indicate that IL-12 can attenuate established antigen-induced AHR and inflammation. In this mechanism it would be interpreted as follows: IL-12 administration in OVA-challenged mice decreased IL-4 production and IgE production thereafter through direct effect on inhibiting the activation of established Th2 cells response and also combined effect with up-regulation of IL-18R expression by inflammatory cells in the lung. 相似文献
95.
96.
Christine R. Bryke Valerie Lindgren Julie S. Fryburg Teresa L. Yang-Feng 《American journal of medical genetics. Part A》1990,36(2):247-250
A previously unreported isodicentric chromosome 18 was discovered in an abnormal infant boy whose mosaic karyotype was 46, XY/46,XY,–18, + idic(18)(q12.2). His constellation of congenital anomalies was typical of the 18q-syndrome. The clinical and cytogentic characteristics of this patient are reported, and the literature concerning isochromosomes of 18 is reviewed. 相似文献
97.
目的 研究重组白细胞介素18(rIL-18)对肺炎链球菌肺炎小鼠Th1/ Th2免疫应答的影响.方法 鼻腔接种肺炎链球菌建立小鼠肺炎链球菌肺炎模型,将Balb/c小鼠24只随机分为3组,分别为对照组,肺炎组和肺炎rIL-18干预组(n=8 ),RT-PCR法检测各组小鼠肺组织中IFN-γ、IL-4 mRNA 的表达,同时支气管肺泡灌洗液(BALB)进行活菌计数,有核细胞分类计数.结果 ①肺炎rIL-18干预组BA LF中性粒细胞和巨噬细胞计数显著高于肺炎组和对照组(P<0.001);②肺炎rIL-18 干预组BALF活菌计数显著低于肺炎组(P<0.001);③肺炎rIL-18干预组肺组织IFN- γ mRNA表达上调而IL-4 mRNA表达下调(P<0.001).结论 在小鼠肺炎链球菌肺炎早期给予rIL-18可诱导IFN-γ的合成,促进Th1免疫应答,使Th1/ Th2免疫平衡向Th1免疫偏移、促进宿主对肺炎链球菌的防御. 相似文献
98.
支气管哮喘患者粘附分子和细胞因子的变化及其意义 总被引:2,自引:0,他引:2
目的:探讨支气管哮喘患者外周血白细胞粘附分子β2整合素(β2-integrin熏CD18)、血清可溶性细胞间粘附分子-1(sICAM-1,CD54)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的变化及其意义。方法:采用流式细胞仪技术检测外周血白细胞CD18和血清sICAM-1的表达;采用酶连接免疫吸附方法(ELISA)检测血清IL-6和IL-8水平。结果:(1)与正常对照组相比,支气管哮喘患者外周血白细胞CD18和血清sICAM-1表达显著增加穴P<0.05雪;(2)与正常对照组相比,支气管哮喘患者血清IL-6和IL-8水平显著增加穴P<0.05雪;(3)支气管哮喘患者外周血白细胞CD18和血清sICAM-1表达呈显著正相关(r=0.791熏P<0.05)。结论:支气管哮喘患者外周血白细胞CD18和血清sICAM-1表达以及IL-6和IL-8水平增加,可能是支气管哮喘重要的发病机制之一。 相似文献
99.
人白细胞介素18(hIL-18)的纯化及生物学活性的鉴定 总被引:1,自引:1,他引:1
目的:在大肠杆菌中高效表达重组人IL-18(rhIL-18)蛋白,制备具有高纯度、高活性的rhIL-18。方法:用IFTG诱导重组蛋白表达载体pKK223-3/hIL-18进行蛋白表达;菌体经超声破碎分离包含体,并对包含体进行洗涤、变性和复性处理,用DEAE-Sepharose CL-6B阴离子交换柱纯化复性的rhIL-18;以人外周血单核淋巴细胞,通过T细胞增殖实验、^125I-UdR标记的细胞毒实验、ELISA方法检测细胞因子的产生量等方法,测定rhIL-18的生物学活性。结果:在大肠杆菌中成功地诱导、表达了rhIL-18,SDS-PAGE凝胶电泳分离显示在分子量大约18.3kD处有一诱导蛋白带,Western blot证明表达产物与抗IL-18单克隆抗体有特异性免疫反应;表达产物经纯化后纯度达94%;表达的rhIL-18蛋白具有促进T细胞增殖、增强NK细胞细胞毒作用及诱导外周血单核淋巴细胞合成IFN-γ的能力,基本上具有天然IL-18相同的生物学活性。结论:为rhIL-18的获得及为进一步研究其生物学功能提供了一定的条件,并为将rhIL-18用于肿瘤的免疫生物治疗奠定了基础。 相似文献
100.
Zahariev A Bergouignan A Caloin M Normand S Gauquelin-Koch G Gharib C Blanc S 《European journal of applied physiology》2005,95(4):344-350
Because body composition is altered during head-down bed rest (HDBR), body mass can not be used as an index of energy balance.
Consequently diet allowances should not be based on body mass evolution but on fat mass changes. Though criticized, skinfold
thickness (ST) is the costless, easiest and fastest method to use for such an objective. The aim of this study was to compare
the percentage of body fat (%BF) estimated by ST with the isotope dilution of H218O. We compiled data from three HDBR campaigns, one on women (n=8) in November 1998 and two on the same men (n=8) in December 1997 (without countermeasure) and January 1998 (with thigh-cuffs countermeasure), according to a crossover
design. Body composition was assessed before and after 6 days of HDBR. %BF was derived from the biceps, triceps, sub-scapular
and sup-iliac ST according to Durnin and Wormersly (1974). Fat-free mass was measured on the same day by H218O dilution and fat mass was calculated by the difference with body mass and expressed as a percentage. Based on precision
tests, the minimum measurable change by ST was 1.1%BF for single measurement point. Both intercepts (F
4,30=0.89, P=0.45) and slopes (F
4,30=0.74; P=0.57) of the ST versus dilution relationships were not affected by the periods (December vs January), experimental conditions
(control vs HDBR vs HDBR + thigh cuffs) or sex allowing the derivation of a common relationship %BFst=0.94 × %BFdil (F
1,47=97.9, P<0.0001; non-significant intercept excluded) with a bias between methods of −1.7±2.0 %BF (95% CI: −5.8, 2.4 %BF). ST can be
used to measure %BF during HDBR provided great care is placed on training and changes are higher than 1.1 %BF. If the method
can be applied for in-flight energy balance monitoring given the high observed energy deficit, a tight monitoring of the individual
nutritional status as needed during simulation appears, however, dubious based on this solely method. 相似文献