全文获取类型
收费全文 | 105548篇 |
免费 | 9959篇 |
国内免费 | 6595篇 |
专业分类
耳鼻咽喉 | 1116篇 |
儿科学 | 1211篇 |
妇产科学 | 891篇 |
基础医学 | 11346篇 |
口腔科学 | 1858篇 |
临床医学 | 12002篇 |
内科学 | 13839篇 |
皮肤病学 | 1167篇 |
神经病学 | 4574篇 |
特种医学 | 4663篇 |
外国民族医学 | 24篇 |
外科学 | 12949篇 |
综合类 | 20294篇 |
现状与发展 | 26篇 |
一般理论 | 18篇 |
预防医学 | 7875篇 |
眼科学 | 2570篇 |
药学 | 10768篇 |
111篇 | |
中国医学 | 6471篇 |
肿瘤学 | 8329篇 |
出版年
2024年 | 249篇 |
2023年 | 1258篇 |
2022年 | 2852篇 |
2021年 | 4730篇 |
2020年 | 3621篇 |
2019年 | 3065篇 |
2018年 | 3228篇 |
2017年 | 3183篇 |
2016年 | 3080篇 |
2015年 | 4757篇 |
2014年 | 6060篇 |
2013年 | 6304篇 |
2012年 | 9041篇 |
2011年 | 9481篇 |
2010年 | 7050篇 |
2009年 | 6012篇 |
2008年 | 6866篇 |
2007年 | 6645篇 |
2006年 | 6326篇 |
2005年 | 5345篇 |
2004年 | 4059篇 |
2003年 | 3835篇 |
2002年 | 3318篇 |
2001年 | 2537篇 |
2000年 | 1897篇 |
1999年 | 1495篇 |
1998年 | 901篇 |
1997年 | 870篇 |
1996年 | 653篇 |
1995年 | 538篇 |
1994年 | 499篇 |
1993年 | 292篇 |
1992年 | 336篇 |
1991年 | 295篇 |
1990年 | 220篇 |
1989年 | 253篇 |
1988年 | 185篇 |
1987年 | 179篇 |
1986年 | 100篇 |
1985年 | 106篇 |
1984年 | 59篇 |
1983年 | 47篇 |
1982年 | 42篇 |
1981年 | 34篇 |
1980年 | 27篇 |
1979年 | 39篇 |
1978年 | 22篇 |
1975年 | 17篇 |
1974年 | 18篇 |
1973年 | 12篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
161.
Yong Li A. John Vartanian Francis J. White Chang-Jiang Xue M. E. Wolf 《Psychopharmacology》1997,134(3):266-276
We examined the effect of 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(f)quinoxaline (NBQX), an antagonist of the α-amino-3-hydroxy-5-methyl-4-isoxazole
propionate (AMPA) subtype of glutamate receptor, on the development and expression of behavioral sensitization to amphetamine
and cocaine in rats. A single injection of NBQX (12.5 mg/kg) administered 30 min prior to cocaine during the induction phase
(days 1–5) prevented the development of cocaine sensitization, assessed by responsiveness to cocaine challenge on day 8. This
NBQX regimen did not affect development of amphetamine sensitization. Two pretreatment injections of NBQX, one 20 min before
and one 70 min after amphetamine on each day of the induction phase (days 1–6), did not affect sensitization of stereotypy
but prevented sensitization of post-stereotypy ambulatory hyperactivity (both assessed by responsiveness to amphetamine challenge
on day 8). The effect of NBQX on ambulatory sensitization was dose-dependent (attenuation with 12.5 mg/kg, complete prevention
with 25 mg/kg). In contrast to its effects on development, NBQX (25 mg/kg) did not prevent expression of sensitization to
cocaine or amphetamine. NBQX itself exerted no significant effects on locomotor activity in either drug-naive rats or rats
that had received either NBQX or amphetamine repeatedly. These findings support a requirement for AMPA receptor stimulation
in the development of locomotor sensitization to cocaine and amphetamine, but suggest a different mechanism for sensitization
of amphetamine stereotypy.
Received: 14 January 1997 / Final version: 24 June 1997 相似文献
162.
古主“玉泉丸”改制成颗粒剂后,对处方中人参,黄芪,麦冬,乌梅,天花粉,葛根,甘草等七味中药的薄层色谱鉴别方法进行了探讨。 相似文献
163.
双头加压螺纹钉贴股骨距内固定治疗股骨颈骨折 总被引:8,自引:0,他引:8
在X光电视下采用双头加压螺纹钉贴股骨距内固定治疗新鲜股骨颈骨折42例,随访平均2.5年,其中16例随访3年以上,骨折愈合率95.2%,骨折不愈合并股骨头缺血性坏死率4.76%。认为加压螺纹钉贴股骨距内固定可使钉的受力由较大剪应力变为较大轴向力承受,减少骨折处的剪应力,并加压于骨折端能促进骨折愈合。具有操作简单、进钉准确、创伤小、固定牢靠、并发症少等优点。 相似文献
164.
小儿病毒性心肌炎181例,其中暴发性及心源性休克型8例。其主要特点是:心脏增大(43.4%),心律失常(93.9%),其中早搏最多见(59.9%);传导阻滞(15.5%)。作者认为应强调对Ⅱ°-Ⅱ型以上传导阻滞病情严重应给激素及临时起搏器抢救治疗;心电轴异常(35.7%),亦是心肌炎的重要心电图改变之一。 相似文献
165.
G. Wu S. F. Fan Z.-H. Lu R. W. Ledeen S. M. Crain 《Journal of neuroscience research》1995,42(4):493-503
Prolongation of the action potential duration of dorsal root ganglion (DRG) neurons by low (nM) concentrations of opioids occurs through activation of excitatory opioid receptors that are positively coupled via Gs regulatory protein to adenylate cyclase. Previous results suggested GM1 ganglioside to have an essential role in regulating this excitatory response, but not the inhibitory (APD-shortening) response to higher (μM) opioid concentrations. Furthermore, it was proposed that synthesis of GM1 is upregulated by prolonged activation of excitatory opioid receptor functions. To explore this possibility we have utilized cultures of hybrid F11 cells to carry out closely correlated electrophysiological and biochemical analyses of the effects of chronic opioid treatment on a homogeneous population of clonal cells which express many functions characteristic of DRG neurons. We show that chronic opioid exposure of F11 cells does, in fact, result in elevated levels of GM1 as well as cyclic adenosine monophosphate (AMP), concomitant with the onset of opioid excitatory supersensitivity as manifested by naloxone-evoked decreases in voltage-dependent membrane K+ currents. Such elevation of GM1 would be expected to enhance the efficacy of excitatory opioid receptor activation of the Gs/adenylate cyclase/cyclic AMP system, thereby providing a positive feedback mechanism that may account for the remarkable supersensitivity of chronic opioid-treated neurons to the excitatory effects of opioid agonists as well as antagonists. These in vitro findings may provide novel insights into the mechanisms underlying naloxone-precipitated withdrawal syndromes and opioid-induced hyperalgesia after chronic opiatf addiction in vivo. © 1995 Wiley-Liss, Inc. 相似文献
166.
肿瘤转移相关蛋白在甲状腺乳头状腺癌伴淋巴结转移组织中的原位表达研究 总被引:1,自引:0,他引:1
利用免疫组化ABC法,研究甲状腺乳头状腺癌,甲状腺腺瘤和正常甲状腺组织中的肿瘤转移相关基因蛋白CD44v6,EGFR,转移抑制基因nm23-H1和抑癌基因p53蛋白的原位表达。结果发现CD44v6和EGFR表达上调与肿瘤转移密切相关(P<0.05,P<0.01),而nm23-H1的表达与肿瘤转移抑制密切相关(P<0.01)。这提示肿瘤转移相关基因和转移抑制基因之间的表达失衡是甲状腺乳头状腺癌易发生转移的重要原因。 相似文献
167.
目的:研究电刺激和化学刺激兔蓝斑(LC)对动脉血压(AP)和肾交感神经传出活动(RSA)的影响.方法:电刺激LC,LC微量注射LGlu、盐酸吗啡、GABA、电解毁损LC,记录AP和RSA.结果:电刺激LC和LC注射LGlu均引起AP升高(分别为135±03vs195±08kPa和138±04vs175±08kPa)和RSA增加.LC注射吗啡、GABA对AP和RSA无明显影响.电解毁损LC后电刺激LC区、LC区注射LGlu对AP和RSA无明显影响.结论:兔LC兴奋引起AP升高和RSA增加,但LC不是AP和RSA的紧张性中枢. 相似文献
168.
本文旨在阐明MRI对急性颈椎间盘突出的诊断价值。19例均有明显的外伤史,X线片无骨折脱位者12例。其中C_(5~6),髓核突出7例,C_(5~6)、C_(1~5),突出5例。有小关节绞锁半脱位者7例,MRI均示损伤间隙有髓核突出。19例均为不全瘫。全部病例经前路椎间盘切除、植骨融合。平均随访15个月,植骨块平均于12周愈合。除1例骨块退出4~5mm外,余位置良好。脊髓功能均有明显恢复。结论:外伤是急性颈椎间盘突出的主要原因,而颈椎间盘突出又是SCIWORA综合征的主要原因。对小关节绞锁半脱位者应考虑同时有椎间盘突出的可能。手术治疗一般效果良好。 相似文献
169.
米非司酮配伍卡前列甲酯89例与米非司酮配伍米索前列醇110例终止早期妊娠的比较 总被引:4,自引:0,他引:4
目的:比较米非司酮配伍卡前列甲酯与米非司酮配伍米索前列醇终止早期妊娠的疗效。方法:妊娠≤49d孕妇199例,年龄26±5a,随机分A组89例,B组110例。2组均用米非司酮25mg,bid,3d,于d4,A组阴道后穹窿置卡前列甲酯栓1mg。B组米索前列醇po,600μg。结果:A和B组完全流产率各为83%和93.6%,经X2检验,P<0.05;胎囊排出时间,A组4±5h,B组3±6h,2组无显著差异。结论:米非司酮配伍米索前列醇的抗早孕效果优于配伍卡前列甲酯。 相似文献
170.
The objective of this study was to determine whether the development of tolerance to CP 55,940, a potent cannabinoid agonist, was due to changes in the receptor or second messenger system. ICR mice treated with CP 55,940 (2 mg/kg) twice a day for 6 and one-half days developed a high degree of tolerance to the pharmacological effects of CP 55,940. The ability of CP 55,940 to produce motor hypoactivity, hypothermia and immobility was reduced 163-, 97- and 19-fold, respectively. Evaluation of 3H-CP 55,940 binding to rat brain membranes indicated no difference in receptor affinity between the vehicle- and CP 55,940-treated animals. However, these binding studies revealed a 50% decrease in receptor number in the cerebellum of the CP 55,940-tolerant mice. Although cAMP is generally considered to be the second messenger for cannabinoid receptors, little difference was observed in the inhibitory effects of CP 55,940 on adenylyl cyclase activity in cerebellum between vehicle and drug-treated mice. However, there was an increase in receptor mRNA which suggests a compensation for receptor loss. There are several possible explanations for these results. There may be sufficient spare receptors such that CP 55,940-tolerant mice are capable of producing a maximal effect on the second messenger system. On the other hand, one could conclude that cannabinoid receptor down-regulation does not account for the development of tolerance to all of the effects of CP 55,940 in mice. 相似文献