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31.
青霉素酶电极的研制   总被引:3,自引:0,他引:3  
探讨了青霉素酶电极的制备方法,以青霉素酶为敏感膜偶合玻璃电极制成青霉素酶电极,在0.15 ̄1.5m mol/L青霉素钠浓度范围内,该电极的动力学响应与青霉素钠浓度的对数呈良好的线性关系,相关系数为0.9988,对电极性能的影响因素如介质条件,温度、膜厚度等进行了考察,并试验了电极的有效活性期。测得平均回收率为99.0%。  相似文献   
32.
We used molecular modeling to examine the binding of 1, 2-dioctanoyl-sn-glycero-3-phosphocholine (a lecithin), 1-octanoyl-sn-glycero-3-phosphocholine (a lysolecithin) and their tetrahedral intermediates in the catalytic site of phospholipase A2 (PLA2). We performed energy minimization on each complex, computed the binding energy, determined the relative binding energy among the complexes and calculated the difference in inter- and intramolecular energies of the components in the complexes. We found that the calculated orientation of the sn-1 ester bond of lysolecithin in the active site is similar to that of the sn-2 ester bond in lecithin, thus permitting PLA2 to hydrolyze lysolecithin using the same mechanism as it uses to hydrolyze lecithin. On the other hand, the binding of lecithin is energetically more favorable by 4.5 kcal/mol than the binding of lysolecithin to the enzyme, and the binding of the lecithin tetrahedral intermediate is also energetically more favorable by 19.7 kcal/mol than the binding of the lysolecithin tetrahedral intermediate to the enzyme, which explains why lecithin is a better substrate than lysolecithin in the catalytic site. These results indicate that the activation energy for the hydrolysis of lysolecithin is higher than that for lecithin, consistent with the observed slower rate for the hydrolysis of lysolecithin.  相似文献   
33.
The electrodeposition of Ag on Pt(100)-(1 × 1) in perchlorate electrolyte was studied by means of time-resolved in situ scanning tunnelling microscopy (STM) and cyclic voltammetry. One monolayer of Ag is deposited underpotentially (upd) ca. 500 mV positive of the Ag+/Ag equilibrium potential. Several millivolts positive of the equilibrium potential, a second well defined upd layer forms. Its growth was observed to proceed via island formation and coalescence. This process occurs in two separate stages that manifest themselves in voltammetric peaks as well as in the STM images.  相似文献   
34.
The cellular and regional distribution of glutathione (GSH) and GSH-related enzyme systems involved in cellular defense against reactive oxygen species and electrophilic xenobiotics in the nervous system has been extensively studied. However, little is known about the subcellular distribution of GSH systems in brain tissue and cultured neural cells. The present study investigates the distribution of mitochondrial and cytosolic GSH and GSH-related enzymes in cultured cerebellar astrocytes and granule cells, and compares them with levels in the adult rat cerebellum. Cytosolic GSH levels and cytosolic activities of glutathione reductase (GR), glutathione peroxidase (GPx) and glutathione-S-transferase (GST) in astrocytes were 57, 153, 245, and 92% higher than those found in granule cells, respectively. In contrast, granule cells contained significantly higher mitochondrial GSH levels than astrocytes. Granule cells also demonstrated comparable mitochondria/cytosolic concentrations of GSH and GR, GPX and GST activities to those observed in the cerebellar tissue, whereas ratios in astrocytes were markedly lower. Although in vitro treatments with 100 μM ethacrynic acid depleted both cytosolic and mitochondrial GSH in cultured astrocytes and granule cells in a time-dependent fashion, cellular GSH in granule cells was more resistant to the GSH-depleting agent than astrocytes. These results suggest that although GSH and GSH-related enzymes are abundant in cytosolic compartments of astrocytes, mitochondrial pools are relatively small. Since brain mitochondria are sites of significant hydrogen peroxide generation, the mitochondrial localization of GSH and its associated enzymes in neural cells provide important defenses against toxic oxygen species in the nervous system. Differences in subcellular distribution of GSH systems in individual neural cell types may provide a basis for selective cellular and/or subcellular expression of neurotoxicity.  相似文献   
35.
一种新的五步蛇蛇毒类凝血酶Cdna的克隆和序列分析   总被引:2,自引:0,他引:2  
目的:克隆出五步蛇的类凝血酶cDNA,为研究其结构和功能的关系。并为下一步基因表达开发抗血栓药物提供依据和基础。方法:从五步蛇蛇腺中提取了总RNA,通过反转录合成第一链cDNA,经PCR扩增出五步蛇毒腺中类凝血酶TLE1的cDNA片段,并将其连接到质粒载体扩增,然后进行DNA测序。结果:成功克隆出一种新的五步蛇类凝血酶的cDNA片段。此片段全长794bp,包括编码部分的全长为777bp。推导其编码的蛋白质序列为258个氨基酸,其中包括18个氨基酸的信号肽,6个氨基权的前肽和234个氨基酸的成熟氨基酸顺序。TLE1成熟肽与其它蛇毒类凝血酶相比,蛋白质一级结构具有较高的同源性。结论:从五步蛇中成功克隆出一 种新的类凝血酶cDNA,并确定了它的DNA顺序。  相似文献   
36.
海藻、甘草及其相伍用对小鼠肝药酶的影响   总被引:5,自引:0,他引:5  
目的:研究海藻、甘草单煎液及其不同比例合煎,单煎后混合液以及单体A、B;C、D、E对小鼠肝药酶的影响。方法:取小鼠随机分组,分别ig给药,qd,连续4d后禁食20h,处死取肝脏,称重后制成匀浆,紫外分光光度计于450nm,490nm波长下测其光密度值,计算肝匀浆中细胞色素P-450的含量。结果:甘草、甘草与海藻合煎液及单体A,B,C,D,E均能显著提高小鼠肝匀浆中细胞色素P-450的含量,而海藻,甘草与海藻单煎后混合液未能提高小鼠肝心浆中的细胞色素P-450的含量。结论:甘草,甘草与海藻合煎液及单体,A,B,C,D,E均能显著提高小鼠肝匀浆中细胞色素P-450的含量,对肝药酶有诱导作用。  相似文献   
37.
1. Since plasma renin activity is increased in cyclosporin A (CsA)-induced hypertension in the rat, the role of the vascular renin-angiotensin system (RAS) in CsA-induced hypertension was investigated in rat mesenteric resistance vessels. 2. Female Wistar rats received CsA (10 mg/kg per day, s.c.) or vehicle for 30 days. CsA treatment increased tail-cuff systolic blood pressure (CsA treated 135 ± 3 mmHg vs control 125 ± 1 mmHg, P<0.0001). 3. Mesenteric resistance arteries (200–300 μm) were isolated and mounted in a microvessel myograph. Concentration-response curves to tetradecapeptide renin substrate (10-11-10?6 mol/L), angiotensin I (10-l1-10?6 mol/L) and angiotensin II (10-12-10?6 mol/L) showed no differences between CsA-treated and control groups. 4. Mesenteric vascular angiotensin-converting enzyme (ACE) characteristics were determined by radioligand binding. There were no differences in the content or affinity of ACE between CsA-treated and control rats. 5. These results suggest that the mesenteric vascular RAS does not play a major role in CsA-induced hypertension in the rat.  相似文献   
38.
目的 制备甘草蛋白免疫磁性微球,并建立快速、精确的免疫磁性捕获ELISA法检测甘草蛋白。方法 采用种子聚合法合成聚苯乙烯磁性微球,并以兔抗甘草蛋白IgG抗体致敏,制备特异性捕获甘草特征蛋白的免疫磁性微球。以生物素标记抗体为示踪抗体,结合辣根过氧化物酶标亲和素建立ELISA检测系统,用于甘草药材和含甘草中成药中甘草蛋白的分析。结果 利用该方法对甘草药材和中成药中甘草蛋白抗原检测,检测灵敏度达到10ng/mL。结论 免疫磁性捕获ELISA检测技术方便、快速、准确,为生药的品种鉴定及中成药的质量控制提供一种新方法。  相似文献   
39.
Abstract:  Angiotensin-converting enzyme inhibitor (ACEI) has become recognized as agents that have renoprotective effects in the treatment of progressive renal diseases including post-transplant kidneys. Previously we demonstrated the safety and effectiveness of ACEI treatment on the hypertensive proteinuric post-transplant patients ( N  = 10) who had been followed up for 12 months. However, not all patients show good response in urinary protein reduction. We aimed to analyse the histopathological factor(s) affecting the responsiveness of proteinuria to ACEI treatment. Fourteen post-transplant patients with proteinuria who were treated with ACEI and underwent allograft biopsy were analysed. Eight patients showed 50% or more reduction in proteinuria (responder). The other 6 patients showed less (< 50%) reduction in proteinuria (non-responder). There was no difference in clinical characteristics (BP, renal function, donor age, recipient body mass index), dietary sodium or protein intake, and diuretic use between the two groups. As a histopathological characteristic, glomerular size in responder group was significantly larger than that in non-responder group. This suggests that the large glomerular size at least partly contributes to the responsiveness in urinary protein reduction to ACEI treatment in kidney allograft recipients with proteinuria.  相似文献   
40.
Primary cultures enriched in neurons dissociated from embryonic rat cerebra were used to demonstrate that platelet activating factor and the structurally related ether glycerolipid, dodecylglycerol, are readily taken up in small amounts by neurons and that they stimulate the differentiation of neurons. The stimulation of neuronal differentiation was observed as a precocious development of axon-like extensions which correlated with a concentration-dependent increase in neuronal-specific enzyme activities. This stimulation of morphological and neurochemical factors by either platelet activating factor or dodecylglycerol was almost completely abolished by triazolam, a known inhibitor of platelet activating factor function. Neither platelet activating factor nor dodecylglycerol at the concentrations used to achieve stimulation of neuronal differentiation compromised the plasma membrane, as indicated by the lack of leakage of cytoplasmic lactic acid dehydrogenase.  相似文献   
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