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   289797篇
  免费   21528篇
  国内免费   11132篇
电工技术   15408篇
技术理论   31篇
综合类   17446篇
化学工业   50246篇
金属工艺   16903篇
机械仪表   18460篇
建筑科学   22911篇
矿业工程   9534篇
能源动力   7968篇
轻工业   16674篇
水利工程   4797篇
石油天然气   20287篇
武器工业   2235篇
无线电   31519篇
一般工业技术   34445篇
冶金工业   15273篇
原子能技术   2859篇
自动化技术   35461篇
  2024年   1221篇
  2023年   4690篇
  2022年   7934篇
  2021年   11492篇
  2020年   8550篇
  2019年   7292篇
  2018年   8178篇
  2017年   9234篇
  2016年   8036篇
  2015年   11186篇
  2014年   13785篇
  2013年   16476篇
  2012年   17783篇
  2011年   19416篇
  2010年   16772篇
  2009年   15930篇
  2008年   15457篇
  2007年   15100篇
  2006年   15981篇
  2005年   14158篇
  2004年   9051篇
  2003年   7910篇
  2002年   7309篇
  2001年   6491篇
  2000年   7101篇
  1999年   8501篇
  1998年   6847篇
  1997年   5826篇
  1996年   5454篇
  1995年   4507篇
  1994年   3760篇
  1993年   2629篇
  1992年   2137篇
  1991年   1601篇
  1990年   1174篇
  1989年   933篇
  1988年   759篇
  1987年   523篇
  1986年   389篇
  1985年   265篇
  1984年   183篇
  1983年   120篇
  1982年   130篇
  1981年   86篇
  1980年   70篇
  1979年   24篇
  1978年   2篇
  1966年   1篇
  1965年   2篇
  1951年   1篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
151.
卸荷裂隙在水利水电工程建设中的危害   总被引:3,自引:0,他引:3  
卸荷裂隙是对水工建筑物稳定最不利的软弱结构面之一。文中较系统地介绍了这种结构面的特点、分布规律、形成的力学机理、对工程的危害、勘查方法及处理措施。  相似文献   
152.
153.
154.
本文介绍了用αβ谱仪系统同时测量αβ谱、实现Rn/Th子体补偿、确定超铀α核素气溶胶体积活度及人工放射性气溶胶总β体积活度的技术途径。利用RaA、RaC′a峰的二段时间计数可确定空气中RaA、RaB、RaC的气溶胶体积活度,相应的,也能给出RaB、RaC对总β计数的贡献。根据一般环境条件下的平衡比,用ThC′的。计数修正Th子体对αβ测量的影响。 ̄[239]pu或/和 ̄[241]Am人工核素的α计数,可通过两段时间分别扣除RaA、RaC′拖尾的方法确定;β计数分别扣除Rn/Th子体β贡献即可确定。在本文规定的测量条件下,对室内天然Rn子体水平在15Bq/m ̄3以下,超铀α核素气溶胶体积活度的测量下限可达到0.1Bq/m ̄3;即使在75Bq/m ̄3环境下,人工核素总β的测量下限也可达lBq/m ̄3以下。  相似文献   
155.
本文着重介绍了构成《现代勘探决策理论系统》的5个主要计算机模块,即:生油岩热演化处理、求任意曲边形面积、数学模拟预测资源量、勘探经济评价分析及决策、辅助处理等模块。该系统曾在塔里木盆地和准噶尔盆地的油气资源评价和勘探决策中发挥了作用,受到了专家和用户的好评。  相似文献   
156.
Tachykinin immunoreactivity is found in a ventromedial spinal plexus in the lamprey. Neurons in this plexus project bilaterally and are thus in a position to modulate locomotor networks on both sides of the spinal cord. We have examined the effects of the tachykinin substance P on NMDA-evoked locomotor activity. Brief (10 min) application of tachykinin neuropeptides results in a prolonged concentration-dependent (>24 hr) modulation of locomotor activity, shown by the increased burst frequency and more regular burst activity. These effects are blocked by the tachykinin antagonist spantide II. There are at least two phases to the burst frequency modulation. An initial phase (approximately 2 hr) is associated with the protein kinase C-dependent potentiation of cellular responses to NMDA. The long-lasting phase (>2 hr) appears to be protein synthesis-dependent, with protein synthesis inhibitors causing the increased burst frequency to recover after washing for 2-3 hr. The modulation of the burst regularity is caused by a separate effect of tachykinins, because unlike the burst frequency modulation it does not require the modulation of NMDA receptors for its induction and is blocked by H8, an inhibitor of cAMP- and cGMP-dependent protein kinases. The effects of substance P were mimicked by the dopamine D2 receptor antagonist eticlopride. The effects of eticlopride were blocked by the tachykinin antagonist spantide II, suggesting that eticlopride may endogenously release tachykinins. Because locomotor activity in vitro corresponds to that during swimming in intact animals, we suggest that endogenously released tachykinins will result in prolonged modulation of locomotor behavior.  相似文献   
157.
AIM: To study the effect of the angiotensin-converting enzyme (ACE) inhibitors perindopril (Per) and enalaprilat (Ena) on the reactivity of the endothelium in normal rats. METHODS: Male rats were treated intragastrically with Per (2 mg.kg-1.d-1) or placebo (n = 18) for 6 wk. Aorta was isolated for experiment. Another set of isolated aortic rings with and without endothelium were incubated with Ena (0.1 mumol.L-1) for 30 min. Responses to acetylcholine, serotonin, phenylephrine, sodium nitroprusside (SN), and nitroglycerin (Nit) were observed. RESULTS: Endothelium-dependent relaxation to acetylcholine was augmented in aortic rings from rats treated with Per in comparison with control. The IC50 value (95% confidence limits) decreased from 3.8 (0.56-26.1) mumol.L-1 (control group) to 0.98 (0.28-3.41) mumol.L-1 (Per-treated group). The maximal relaxation was augmented from 62 +/- 9% to 78 +/- 10% (P < 0.01). However, the responses to the endothelium-independent vasodilators, SN and Nit, were similar. Serotonin- and phenylephrine-induced contractions were decreased, which were influenced by basal release of endothelium-derived relaxing factor (EDRF). EC50 values was 6.1 (2.6-14.4) nmol.L-1 vs 8.3 (3.6-18.8) nmol.L-1 in comparison with control group and Per-treated group. The maximal contraction was decreased from 2.42 +/- 0.29 g (control group) to 1.96 +/- 0.25 g (treated group) (P < 0.01). Similar results were found in incubation with Ena. CONCLUSION: Ena and Per enhanced the basic release of EDRF from vascular endothelium.  相似文献   
158.
We cloned the murine full-length cDNA encoding Ahch, the mouse homologue of DAX1 (DSS-AHC Region on Human X Chromosome, Gene1) which is the gene responsible for human X-linked adrenal hypoplasia congenita (AHC) and hypogonadotropic hypogonadism (HH). Sequence analysis revealed that the murine and human cDNAs have 65% aa identity and 75% aa similarity overall. The cysteine residues in the putative DNA binding domain, which may interact with Zn2+ ions to form zinc fingers, are 100% conserved between the two species, indicating that the novel zinc-finger structures in DAX1 may be functional. In addition, mouse interspecific backcrosses show that the Ahch gene is closely linked to the glycerol kinase locus, GyK, on the mouse X chromosome, indicating that the order of the loci is conserved in this syntenic region between mouse and human.  相似文献   
159.
160.
北京谱仪(BESⅡ)顶点探测器数据获取系统是北京谱仪数据获取系统的一部分,该子系统电子学采用快总线标准,本文描述了该系统的硬件结构和软件系统,软件包括快总线系统的微码软件和上层控制软件,该系统的死时间为1.5ns,对BESⅡ系统总死时间的贡献小于0.5ms。  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