首页 | 本学科首页   官方微博 | 高级检索  
文章检索
  按 检索   检索词:      
出版年份:   被引次数:   他引次数: 提示:输入*表示无穷大
  收费全文   26236篇
  免费   1385篇
  国内免费   930篇
耳鼻咽喉   155篇
儿科学   521篇
妇产科学   337篇
基础医学   3934篇
口腔科学   540篇
临床医学   1766篇
内科学   4034篇
皮肤病学   395篇
神经病学   2914篇
特种医学   490篇
外国民族医学   3篇
外科学   1611篇
综合类   3471篇
预防医学   1052篇
眼科学   235篇
药学   4755篇
  3篇
中国医学   1013篇
肿瘤学   1322篇
  2023年   152篇
  2022年   336篇
  2021年   432篇
  2020年   440篇
  2019年   874篇
  2018年   766篇
  2017年   620篇
  2016年   534篇
  2015年   570篇
  2014年   1042篇
  2013年   1347篇
  2012年   1137篇
  2011年   1316篇
  2010年   1261篇
  2009年   1232篇
  2008年   1299篇
  2007年   1220篇
  2006年   1124篇
  2005年   919篇
  2004年   964篇
  2003年   933篇
  2002年   743篇
  2001年   729篇
  2000年   614篇
  1999年   621篇
  1998年   511篇
  1997年   438篇
  1996年   384篇
  1995年   298篇
  1994年   274篇
  1993年   226篇
  1992年   172篇
  1991年   171篇
  1990年   136篇
  1989年   151篇
  1988年   100篇
  1986年   107篇
  1985年   460篇
  1984年   622篇
  1983年   489篇
  1982年   459篇
  1981年   443篇
  1980年   351篇
  1979年   321篇
  1978年   227篇
  1977年   173篇
  1976年   193篇
  1975年   188篇
  1974年   152篇
  1973年   143篇
排序方式: 共有10000条查询结果,搜索用时 515 毫秒
71.
目的:探讨感觉神经肽P物质(SP)对离体培养的肉芽组织成纤维细胞的促增殖作用及其对表皮生长因子(EGF)基因表达的调控作用。方法:采用MTT法测定SP对肉芽组织成纤维细胞的促增殖作用;采用逆转录-聚合酶链反应(RT-PCR)方法检测SP对成纤维细胞EGF基因表达的调控作用,观察时间及剂量-效应关系。结果:10^-9~10^-5mol/L的SP在体外对肉芽组织成纤维细胞均具有明显的促增殖作用(P<0.01),且具有明显的剂量依赖性(γ=0.594,P<0.01),EGF抗体只能部分抑制这一作用(与对照组比较,P<0.01;与10^-7mol/L SP组比较,P<0.05)。10^-7mol/L SP可诱导成纤维细胞EGF mRNA的表达,在作用后6h与对照组比较,差异有非常显著性意义(P<0.01);SP在10^-8~10^-6mol/L范围内可以显著促进成纤维细胞EGF mRNA表达,在10^-7mol/L达到峰值,当浓度>10^-7mol/L时,其促EGF mRNA表达的效应强度随浓度升高而有所降低,至10^-5mol/L时与对照组比较,差异无显著性意义。结论:SP对肉芽组织成纤维细胞具有明显的促增殖作用,这种作用与其诱导成纤维细胞EGF表达有关。  相似文献   
72.
P38MAPK抑制剂对缺血/再灌注大鼠肾脏功能损伤的保护作用   总被引:1,自引:0,他引:1  
目的:观察P38MAPK抑制剂对缺血/再灌注大鼠肾脏功能损伤的保护作用。方法:夹闭肾动脉制遣大鼠肾脏缺血/再灌注损伤动物模型,静脉注射P38MAPK抑制剂阻断P38MAPK信号转导通路,测量其对肾功能及细胞因子含量的影响。结果:肾脏和血浆中TNF—α和IL-β含量随缺血/再灌注时间的延长而升高,肾功能损伤也随缺血/再灌注时间的延长而加重。应用P38MAPK抑制剂可显著降低TNF-α和IL-β含量,对缺血/再灌注所致的肾功能损伤具有明显改善作用。结论:P38MAPK抑制剂可通过抑制致炎因子的产生而减轻缺血/再灌注所致的大鼠肾脏功能损伤。  相似文献   
73.
The effect of chemical deafferentation, vagotomy(VGX), and gangliosympathectomy (GSX) on the density offibers containing calcitonin gene-related peptide (CGRP)and substance P (Sub.P) in the rat gastric wall was studied. Chemical deafferentation bycapsaicin abolished the density of CGRP-immunoreactive(IR) fibers, not Sub.P-IR fibers. Ten days after VGX,the density of CGRP-IR or Sub.P-IR fibers in the mucosa was largely reduced, while no reductionof CGRP-IR and Sub.P-IR fibers was seen in submucosaland muscular layers. GSX significantly reduced thedensity of CGRP-IR fibers in the mucosa and caused a moderate decrease in the fibers in submucosaland muscular layers. Pretreatment with6-hydroxydopamine, a neurotoxin for noradrenergicnerves, did not affect the density of CGRP-IR fibers inthe gastric wall. The density of Sub.P-IR fibers in thegastric wall was not affected by GSX. These studiesindicate that the CGRP-IR and Sub.P-IR fibers in themucosa are susceptible to extrinsic nerve denervation compared with those in the submucosa and musclelayers, that a major portion of the CGRP-IR fibers inthe mucosa is of both vagal and spinal origin, and thata major portion of the Sub.P-IR fibers in the mucosa is of vagal origin. Furthermore, thepresent results support that CGRP-IR fibers, notSub.P-IR fibers, in the rat stomach arecapsaicin-sensitive.  相似文献   
74.
75.
选择经典的实验指标,对海风藤及其3种代用品山Ju,石楠藤有毛Ju的药理作用进行了比较研究,结果表明海风藤,山Ju和毛Ju在抗炎,镇痛和抗血小板聚集方面均有效,其中海风藤作用最强,其次为山Ju,毛Ju石楠藤没有明显的抗炎作用,其抗血小板聚集及止痛作用稍强于毛Ju。  相似文献   
76.
77.
We have developed an isolated spinal cord-skin preparation of the newborn rat. The spinal cord together with a piece of skin connected to the cord by the saphenous nerve was isolated from 1- to 4-day-old rats and separately superfused with artificial cerebrospinal fluid in two neighbouring chambers. Potentials were recorded extracellularly from the third lumbar ventral root. Application of capsaicin (0.5-2 μM) or KCl (60–350 mM) with brief pressure pulses to the perfusion bath of the skin evoked a depolarizing response of 20- to 40-s duration in the ventral root. The response was depressed by [Met5]enkcphalin (0.03–3 μM). morphine (0.1–2 μM) and a tachykinin antagonist, [D-Arg1,D-Trp7,9,Leu11] substance P (spantide), 1–10 μM), applied to the spinal cord by superfusion, whereas the response was augmented by centrally administered calcitonin gene-related peptide (0.1–0.2 μM) or bicuculline (0.5–1 μM).  相似文献   
78.
In addition to the well-known control circuits involved in the regulation and adaptation of testicular androgen biosynthesis, it is proposed that two new control strategies are involved in the maintenance of steady-state testosterone secretion rates by testicular Leydig cells. Cytochrome P450XVII (steroid-17 alpha-monooxygenase/steroid-17,20-lyase), one key enzyme in steroid hormone biosynthesis, responds to external human choriogonadotropin stimulation with an oxygen-dependent and substrate flux-dependent inactivation and decomposition, and increased substrate availability decreases the efficiency of androgen formation in favour of abortive intermediate leakage. These results are discussed as a paradigm of substrate-dependent modulation of cytochrome P450 activities.  相似文献   
79.
细胞色素P450调节剂对DNA加合物形成的影响   总被引:1,自引:0,他引:1  
人羊膜上皮细胞FL系分别接触a-萘黄酮(0.6mmol·L ̄(-1))β-萘黄酮(20pmol·L ̄(-1))24h后,再用苯并(a)芘[B(a)P,10umol·L ̄(-1)]处理24h,用32P后标记技术测定以B(a)-DNA加合物。结果发现,阳性对照组,a-萘黄酮预处理组及β-萘黄酮预处理组加合物的量分别为(加合物个数/10’个核苷酸):4.7±0.2(100%),1.8±0.9(38.3%),16.0±2.2(340.1%).该实验结果直接显示了纳胞色素P450调节剂对肿瘤发生影响的作用水平。亦为药物对致癌物代谢影响的研究提供了一种方法.  相似文献   
80.
Event-related potential (ERP), electroencephalographic (BEG), and behavioral data were collected from squirrel monkeys (Saimiri sciureus) in a 90−10 auditory oddball paradigm. Background or target tones were presented once every 2 s, and responses to the targets were rewarded. ERPs were recorded from epidural electrodes following systemic administration of clonidine (0.1 mg/kg) or a saline placebo. EEG power spectra and behavioral performance were assessed simultaneously as indices of behavioral state. Clonidine significantly decreased the area and increased the latency of a P300-like potential. The amplitudes and areas of the earlier P1, N1, and P2 components and a later slow wave-like potential were not reduced, nor were their latencies altered. Clonidine produced increased EEG power in the alpha range (7.5–12 Hz) and decreased power in the upper beta range (20–40 Hz) but did not affect performance in the oddball task. Because two major effects of clonidine are to substantially reduce activity in the noradrenergic nucleus locus coeruleus (LC) and to reduce norepinephrine (NE) release from axons, the present results support the hypothesis that the LC and its efferent projection system are important in modulating the activity of P300-like potentials.  相似文献   
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号