全文获取类型
收费全文 | 11318篇 |
免费 | 948篇 |
国内免费 | 801篇 |
出版年
2024年 | 7篇 |
2023年 | 186篇 |
2022年 | 173篇 |
2021年 | 619篇 |
2020年 | 402篇 |
2019年 | 517篇 |
2018年 | 546篇 |
2017年 | 352篇 |
2016年 | 516篇 |
2015年 | 721篇 |
2014年 | 804篇 |
2013年 | 934篇 |
2012年 | 1096篇 |
2011年 | 951篇 |
2010年 | 601篇 |
2009年 | 519篇 |
2008年 | 558篇 |
2007年 | 509篇 |
2006年 | 458篇 |
2005年 | 378篇 |
2004年 | 319篇 |
2003年 | 236篇 |
2002年 | 189篇 |
2001年 | 205篇 |
2000年 | 175篇 |
1999年 | 180篇 |
1998年 | 103篇 |
1997年 | 124篇 |
1996年 | 106篇 |
1995年 | 88篇 |
1994年 | 91篇 |
1993年 | 50篇 |
1992年 | 76篇 |
1991年 | 55篇 |
1990年 | 44篇 |
1989年 | 46篇 |
1988年 | 38篇 |
1987年 | 27篇 |
1986年 | 19篇 |
1985年 | 22篇 |
1984年 | 12篇 |
1983年 | 9篇 |
1982年 | 2篇 |
1981年 | 2篇 |
1980年 | 1篇 |
1979年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
971.
Palm F Onozato ML Luo Z Wilcox CS 《American journal of physiology. Heart and circulatory physiology》2007,293(6):H3227-H3245
Asymmetric (N(G),N(G))-dimethylarginine (ADMA) inhibits nitric oxide (NO) synthases (NOS). ADMA is a risk factor for endothelial dysfunction, cardiovascular mortality, and progression of chronic kidney disease. Two isoforms of dimethylarginine dimethylaminohydrolase (DDAH) metabolize ADMA. DDAH-1 is the predominant isoform in the proximal tubules of the kidney and in the liver. These organs extract ADMA from the circulation. DDAH-2 is the predominant isoform in the vasculature, where it is found in endothelial cells adjacent to the cell membrane and in intracellular vesicles and in vascular smooth muscle cells among the myofibrils and the nuclear envelope. In vivo gene silencing of DDAH-1 in the rat and DDAH +/- mice both have increased circulating ADMA, whereas gene silencing of DDAH-2 reduces vascular NO generation and endothelium-derived relaxation factor responses. DDAH-2 also is expressed in the kidney in the macula densa and distal nephron. Angiotensin type 1 receptor activation in kidneys reduces the expression of DDAH-1 but increases the expression of DDAH-2. This rapidly evolving evidence of isoform-specific distribution and regulation of DDAH expression in the kidney and blood vessels provides potential mechanisms for nephron site-specific regulation of NO production. In this review, the recent advances in the regulation and function of DDAH enzymes, their roles in the regulation of NO generation, and their possible contribution to endothelial dysfunction in patients with cardiovascular and kidney diseases are discussed. 相似文献
972.
Mechanisms of acrolein-induced myocardial dysfunction: implications for environmental and endogenous aldehyde exposure 总被引:1,自引:0,他引:1
Luo J Hill BG Gu Y Cai J Srivastava S Bhatnagar A Prabhu SD 《American journal of physiology. Heart and circulatory physiology》2007,293(6):H3673-H3684
Aldehydes are ubiquitous pollutants generated during the combustion of organic materials and are present in air, water, and food. Several aldehydes are also endogenous products of lipid peroxidation and by-products of drug metabolism. Despite well-documented high reactivity of unsaturated aldehydes, little is known regarding their cardiovascular effects and their role in cardiac pathology. Accordingly, we examined the myocardial effects of the model unsaturated aldehyde acrolein. In closed-chest mice, intravenous acrolein (0.5 mg/kg) induced rapid but reversible left ventricular dilatation and dysfunction. In mouse myocytes, micromolar acrolein acutely depressed myofilament Ca(2+) responsiveness without altering catecholamine sensitivity, similar to the phenotype of stunned myocardium. Immunoblotting revealed increased acrolein-protein adducts and protein-carbonyls in both acrolein-exposed myocardium (1.8-fold increase, P < 0.002) and myocytes (6.4-fold increase, P < 0.02). Both the contractile dysfunction and adduct formation were markedly attenuated by pretreatment with the thiol donor N-acetylcysteine (5 mM). Two-dimensional gel electrophoresis and mass-assisted laser desorption/ionization time-of-flight mass spectrometry analysis revealed two groups of adducted proteins, sarcomeric/cytoskeletal proteins (cardiac alpha-actin, desmin, myosin light polypeptide 3) and energy metabolism proteins (mitochondrial creatine kinase-2, ATP synthase), indicating site-specific protein modification that was confirmed by immunohistochemical colocalization. We conclude that direct exposure to acrolein induces selective myofilament impairment, which may be, in part, related to the modification of proteins involved in myocardial contraction and energy metabolism. Myocardial dysfunction induced by acrolein and related aldehydes may be symptomatic of toxicological states associated with ambient or occupational exposures or drug toxicity. Moreover, aldehydes such as acrolein may mediate cardiac dysfunction in pathologies characterized by high-oxidative stress. 相似文献
973.
目的:探讨大鼠三叉神经节不同直径神经元ATP-激活电流的特征。方法:应用全细胞膜片钳技术进行实验。结果:①92.3%(60/65)的细胞对ATP敏感,有反应的细胞可记录到三种型式的ATP-激活电流:快速激活快速失活型(Fast type,F型)、快速激活缓慢失活型(Intermediate type,I型)和缓慢激活缓慢失活型(Slowtype,S型)。三种电流均具有浓度依赖性。②小直径的细胞多表现为F型特征,大直径的细胞多表现为S型特征,而中等大小的细胞多表现为I型特征。③动力学特征:三种类型的ATP激活电流上升相从10%到90%的时间:F型:(33.6±4.5)ms;Ⅰ型:(62.2±9.9)ms;S型:(302.1±62)ms。去敏感相从10%到90%的时间:F型:(399.4±58.2)ms;S型:>500ms。④I-V曲线:三种电流均表现为内向整流的特性,而且翻转电位均为0~5mV。⑤量-效关系:Ⅰ型的量-效曲线居中间,F型的下移,S型的上移,三种类型电流量-效曲线的EC50非常接近。结论:三种型式的ATP-激活电流可能是由不同亚单位组合的P2X受体各亚型所介导,这些亚型分布于不同大小的三叉神经节神经元,从而传导不同的信息。 相似文献
974.
阿米洛利抑制NHE-1减轻低氧性肺动脉平滑肌细胞增殖 总被引:1,自引:0,他引:1
目的:研究Na^+/H^+交换抑制剂阿米洛利对低氧刺激的大鼠肺动脉平滑肌细胞(PASMCs)增殖的影响,以及Na^+/H^+交挟体-l(NHE-1)活性和表达的变化.方法:常氧(21%O2)或低氧(2%O2)条件下培养PASMCs,并分别给予浓度为1.653、3.125、6.25、12.5、25和50μmol/L.等不同浓度的阿米洛利,培养24h,采用MTT比色实验和免疫组化检测PCNA阳性细胞率的方法反映细胞增殖情况,同时采用激光共聚焦检测细胞内pH以反映Na^+/H^+交换体-1活性,RT—PCR法检测Na^+/H^+交换体-1mRNA的表达量.结果:低氧培养的PASMCs细胞内pH升高,NHE—1mRNA的表达增多,而阿米洛利可以降低细胞内pH,减少NHE—1mRNA的表达量。同时低氧较常氧培养MTT光吸收值较常氧培养明显升高。PCNA阳性细胞率明显增高,而给予阿米洛利时上述两个指标随药物浓度增加而逐渐下降。结论:低氧可以激活PASMCs细胞膜上的E—1,增加其mRNA水平表达量,使细胞内碱化,促进细胞增殖,而Na^+/H^+交换抑制剂阿米洛利可以抑制其活性,减少mRNA水平的表达,导致细胞内酸化,从而抑制细胞增殖,并且此抑制作用在3.125~50μmol/L.浓度范围内呈现明显的浓度依赖性。 相似文献
975.
AcSDKP对PDGF诱导的大鼠心脏成纤维细胞增殖和胶原合成的调节作用 总被引:2,自引:0,他引:2
目的:探讨N-乙酰基-丝氨酰-天门冬酰-赖氨酰-脯氨酰(AcSDKP)对血小板源性生长因子(PDGF)诱导的大鼠心脏成纤维细胞增殖和胶原合成的调节作用。方法:建立新生大鼠心脏成纤维细胞系;采用四甲基偶氮唑(MTT)法和^3H-TdR掺入法检测心脏成纤维细胞的增殖;采用^3H-脯氨酸掺入法检测心脏成纤维细胞胶原的合成。结果:PD3F在1~20ng/ml浓度范围内对心脏成纤维细胞增殖和胶原合成均有促进作用。且随着PDGF浓度的增加,其促细胞增殖和胶原合成作用增强,并在10ng/ml浓度时PDGF的促增殖和胶原合成效应最强。在10^-10~10^-8mol/L浓度范围内,AcSDKP对PDGF介导的心脏成纤维细胞增殖和胶原合成均有抑制作用,并且在10叫mol/L时,AcSDKP抑制心脏成纤维细胞增殖和胶原合成作用最强。结论:AcSDKP对PDGF介导的心脏成纤维增殖和胶原合成均有明显抑制作用,这可能与其抗心脏纤维化的作用相关。 相似文献
976.
977.
rPA(K)是经过缺失/定点突变技术所获得的t-PA突变体。本实验以IPTG诱导,实现了rPA(K)在原核系统中的表达。实验证明目的产物的表达形式为包涵体,且当以IPTG诱导3h时,表达量最高,为41%。此后对该表达产物进行了初步纯化,即通过对不同超声破碎次数,包涵体洗涤液(脲,Triton X-100,乙醇)的不同浓度对纯化的影响因素进行了摸索。结果表明,超声2次,2M脲,0.5%Triton X-100,20%乙醇对目的蛋白纯化的效果最好,从而为进一步的纯化和复性奠定基础。 相似文献
978.
979.
980.
Perni RB Chandorkar G Cottrell KM Gates CA Lin C Lin K Luong YP Maxwell JP Murcko MA Pitlik J Rao G Schairer WC Van Drie J Wei Y 《Bioorganic & medicinal chemistry letters》2007,17(12):3406-3411
Reversible tetrapeptide-based compounds have been shown to effectively inhibit the hepatitis C virus NS3.4A protease. Inhibition of viral replicon RNA production in Huh-7 cells has also been demonstrated. We show herein that the inclusion of hydrogen bond donors on the P4 capping group of tetrapeptide-based inhibitors result in increased binding potency to the NS3.4A protease. The capping groups also impart significant effects on the pharmacokinetic profile of these inhibitors. 相似文献