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71.
Zingraff J.; Caillat-Vigneron N.; Urena P.; Gagne E.-R.; Bererhi L.; Moretti J.-L.; Bardin T.; Drueke T. B. 《Nephrology, dialysis, transplantation》1995,10(2):223-229
Dialysis amyloidosis is one of the most incapacitating complicationsof long-term dialysis treatment. Quantitative assessment ofamyloid deposition using radiolabelled tracers has been recentlyproposed but convincing evidence of its validity in uraemicpatients remains to be provided. We studied the plasma kineticsof i.v. administered 125I-labelled serum amyloid P component(125I-SAP) in 20 chronic haemodialysis patients compared withthose of nine healthy volunteers and three non-dialysed patientswith systemic amyloidosis. Plasma clearance of the tracer wasabnormal in 17 of 20 dialysis patients in whom plasma radioactivitydeclined in a bi-exponential mode, in contrast to the single-exponentialslope observed in all healthy controls. 125I-SAP plasma half-lifeof the second component, probably reflecting metabolic clearance,was significantly prolonged in these dialysis patients comparedwith the healthy controls (35.3 versus 24.6 h, P<0.001).Among the long-term haemodialysis patients the calculated extravasculardistribution of 125I-SAP was significantly greater in thosewith severe arthropathy than in asymptomatic patients. Thesefindings demonstrate for the first time that SAP clearance isdisturbed in haemodialysis patients due to both failing renalelimination and retention in extravascular sites. The extravasculardiffusion is greatly enhanced in patients with clinical evidenceof amyloidosis. Therefore the study of plasma 125I-SAP kineticspromises to be a valuable tool to quantitate the extent of amyloidosis. 相似文献
72.
In spite of significant efforts in academic and commercial laboratories, major breakthroughs in oral peptide and protein formulation have not been achieved. The major barriers to developing oral formulations for peptides and proteins include poor intrinsic permeability, lumenal and cellular enzymatic degradation, rapid clearance, and chemical and conformational stability. Pharmaceutical approaches to address these barriers, which have been successful with traditional, small, organic drug molecules, have not readily translated into effective peptide and protein formulations. The success achieved by Sandoz with cyclosporin formulations remains one clear example of what can be achieved, although it is likely that effective oral formulations for peptides and proteins will remain highly compound specific. Although the challenges are significant, the potential therapeutic benefit remains high, particularly with the increasing identification of potential peptide and protein drug candidates emerging from the biotechnology arena. Successful formulations will most likely require a systematic and careful merger of formulation and design delivery systems which maximize the potential for absorption across the epithelial cell layer. 相似文献
73.
本文定义了一类“近乎双线性”系统。可用以近似一类奇异摄动双线性系统,而且可以描述某些实际工业对象。并发现其控制器的设计较方便。文中还给出了一种简单的反馈控制器的设计方法。又对一类多输入双线性系统,提出一种设计反馈控制器的改进方案,根据Lyapunov定理得到一非线性反馈控制律。以上设计方法分别对某合成氨反应器作了应用研究,仿真结果表明了方法的有效性。 相似文献
74.
Tryptamine (TA) occurs in trace levels in the brain, but its role in the central nervous system is not clear. However, there is evidence that TA may be a neuromodulator since it binds to specific binding sites in the brain. TA was measured as a diheptafluorobutyryl derivative in rat whole brain by capillary gas chromatography—mass spectrometry using negative chemical ionization (NCI) and single ion monitoring (SIM). d4-TA was used as the internal standard. The ions m/z 532 and m/z 536 were monitored to identify TA and d4-TA, respectively and to calculate the concentration of TA in rat whole brain which was found to be 0.19 ± 0.08 ng g−1 (n = 8). The results confirm the earlier TA concentrations measured by GC—MS using positive electron impact ionization. However, NCI improved the signal/noise ratio of the method increasing its sensitivity for TA. 相似文献
75.
Berner Bret Wilson Donald R. Guy Richard H. Mazzenga Gerard C. Clarke Frank H. Maibach Howard I. 《Pharmaceutical research》1988,5(10):660-663
The relationship between pK
a and skin irritation in man is studied for a homologous series of benzoic acid derivatives, which permeate through human skin at comparable rates (15–88 µg/cm2/hr). Skin irritation and pK
a are correlated for pK
a 4. Laser Doppler velocimetric assessment of skin blood flow, color meter readings, erythema, edema, and the primary irritation index are all linearly correlated and related to pK
a, erythema at 24 hr appears to be the most sensitive parameter to variation in pK
a when pK
a 4. 相似文献
76.
目的 测量不同脊柱组织的电阻抗,基于支持向量机建立电阻抗数据的组织分类算法并验证算法的准确性,寻找不同组织电阻抗分类阈值。 方法 取离体脊柱组织,应用电化学分析仪采集10~100 kHz频率范围内皮质骨、松质骨、脊髓、肌肉、髓核的电阻抗。将两只猪采集的数据集分别作为训练集和测试集,应用主成分分析降维至二维数据,训练和验证基于支持向量机(SVM)建立的分类算法,应用集成学习的方法计算不同组织分类的电阻抗阈值。 结果 5种组织在10~100 kHz的测量频率内,电阻抗值差异有统计学意义(P<0.001)。应用主成分分析降维的数据集建立的支持向量机分类算法识别不同组织的准确率为100%。应用集成学习建立的多个分类器计算出了不同组织的电阻抗分类阈值。 结论 基于支持向量机可以实现脊柱术区组织电阻抗的准确识别,有望应用于临床协助医生提升组织识别准确率。 相似文献
77.
目的探讨装潢居室空气中挥发性化合物的遗传毒性.方法采用小鼠骨髓嗜多染性红细胞微核试验和小鼠精子畸形试验检测居室装潢后空气中挥发性化合物的遗传毒性.结果该化合物对小鼠呼吸系统有明显的刺激作用,与阴性对照组比较,高、中、低剂量组的微核率、精子畸形率均有显著差异性.结论居室装潢后室内空气中挥发性化合物具有遗传毒性作用. 相似文献
78.
CPP-SOM整合cDNA基因芯片平台的建立 总被引:2,自引:0,他引:2
目的 在转录组水平全面迅速地了解疾病发生和药物作用的分子机理 ,以及寻找潜在的治疗靶标。方法 通过建立基因芯片平台 ,用全反式维甲酸诱导急性早幼粒细胞白血病来源的 NB4细胞分化作为模型 ,并应用自主开发的自组织图结合成分平面展示 (componentplane presentation integrated self-organizing map,CPP- SOM)的方法对数据进行初步分析。结果 建立的 c DNA芯片共有 12 6 30条克隆 ,其中已知基因 94 36条。应用该芯片进行实验 ,结果重复性好、准确性高。CPP- SOM不仅可以将功能相关的基因进行聚类 ,而且可以动态性地从全基因组水平观察药物作用过程中基因的表达变化。结论 我们建立的芯片平台是稳定、可靠的技术平台 ,CPP- SOM是一种新型有效的芯片数据的处理方法。 相似文献
79.
Lankin VZ Sherenesheva NI Konovalova GG Tikhaze AK 《Bulletin of experimental biology and medicine》2000,130(7):694-696
The effects of pretreatment with β-carotene-containing preparation carinat on the development of renal tumors in rats receiving
single intravenous injection of chemical carcinogen 3-(1-α-L-arabinopyranosyl)-1-methyl-1-nitrosourea were studied. Fourteen
months after carcinogen administration, the degree of lipid oxidation in rat kidneys 2.5-fold surpassed that in animals receiving
carinat in a dose producingin vivo antioxidant effect. Carinat decreased the total number of induced tumors and the incidence of mesenchymal renal tumors and
suppressed the development of multiple tumors. The accumulation of lipoperoxides in the kidneys during carcinogenesis is associated
with activation of free radical processes and carcinogen-induced inhibition of lipoperoxide enzymatic degradation and probably
promotes renal malignancies due to co-carcinogenic action of these compounds. The data suggest that carinat-induced suppression
of tumor development attests to antioxidant effects of β-carotene.
Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 130, No. 7, pp. 95–97, July, 2000 相似文献