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   9428篇
  免费   874篇
  国内免费   1226篇
  2024年   25篇
  2023年   100篇
  2022年   272篇
  2021年   367篇
  2020年   306篇
  2019年   376篇
  2018年   329篇
  2017年   264篇
  2016年   338篇
  2015年   550篇
  2014年   649篇
  2013年   697篇
  2012年   908篇
  2011年   829篇
  2010年   547篇
  2009年   529篇
  2008年   575篇
  2007年   508篇
  2006年   440篇
  2005年   418篇
  2004年   327篇
  2003年   302篇
  2002年   296篇
  2001年   169篇
  2000年   166篇
  1999年   118篇
  1998年   116篇
  1997年   69篇
  1996年   76篇
  1995年   79篇
  1994年   67篇
  1993年   54篇
  1992年   62篇
  1991年   48篇
  1990年   51篇
  1989年   43篇
  1988年   47篇
  1987年   39篇
  1986年   31篇
  1985年   36篇
  1984年   31篇
  1983年   26篇
  1982年   26篇
  1981年   18篇
  1980年   14篇
  1979年   18篇
  1977年   16篇
  1974年   16篇
  1972年   16篇
  1971年   14篇
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
981.
Bemporad D  Sands ZA  Wee CL  Grottesi A  Sansom MS 《Biochemistry》2006,45(39):11844-11855
VSTx1 is a tarantula venom toxin which binds to the archaebacterial voltage-gated potassium channel KvAP. VSTx1 is thought to access the voltage sensor domain of the channel via the lipid bilayer phase. In order to understand its mode of action and implications for the mechanism of channel activation, it is important to characterize the interactions of VSTx1 with lipid bilayers. Molecular dynamics (MD) simulations (for a total simulation time in excess of 0.2 micros) have been used to explore VSTx1 localization and interactions with zwitterionic (POPC) and with anionic (POPE/POPG) lipid bilayers. In particular, three series of MD simulations have been used to explore the net drift of VSTx1 relative to the center of a bilayer, starting from different locations of the toxin. The preferred location of the toxin is at the membrane/water interface. Although there are differences between POPC and POPE/POPG bilayers, in both cases the toxin forms favorable interactions at the interface, maximizing H-bonding to lipid headgroups and to water molecules while retaining interactions with the hydrophobic core of the bilayer. A 30 ns unrestrained simulation reveals dynamic partitioning of VSTx1 into the interface of a POPC bilayer. The preferential location of VSTx1 at the interface is discussed in the context of Kv channel gating models and provides support for a mode of action in which the toxin interacts with the Kv voltage sensor "paddle" formed by the S3 and S4 helices.  相似文献   
982.
983.
Liu S  Yang Z  Liu Z  Kong L 《Analytical biochemistry》2006,353(1):108-116
Gold nanoparticles with a 12-nm diameter were used as probes for the determination of proteins by resonance Rayleigh-scattering techniques. In weak acidic solution, large amounts of citrate anions will self-assemble on the surface of positively charged gold nanoparticles to form supermolecular compounds with negative charges. Below the isoelectric point, proteins with positive charges such as human serum albumin (HSA), bovine serum albumin (BSA), and ovalbumin (Ova) can bind gold nanoparticles to form larger volume products (the diameter of the binding product of gold nanoparticles with HSA is 23 nm.) through electrostatic force, hydrogen bonds, and hydrophobic effects, which can result in a red shift of the maximum absorption wavelength, the remarkable enhancement of the resonance Rayleigh-scattering intensity (RRS), and the appearance of the RRS spectra. At the same time, the second-order-scattering (SOS) and frequency-doubling-scattering (FDS) intensities are also enhanced. The binding products of gold nanoparticles with different proteins have similar spectral characteristics and the maximum wavelengths are located near 303 nm for RRS, 540 nm for SOS, and 390 for FDS, respectively. The scattering enhancement (DeltaI) is directly proportional to the concentration of proteins. Among them, the RRS method has the highest sensitivity and the detection limits are 0.38 ng/ml for HSA, 0.45 ng/ml for BSA, and 0.56 ng/ml for Ova, separately. The methods have good selectivity. A new RRS method for the determination of trace proteins using a gold nanoparticle probe has been developed. Because gold nanoparticle probes do not need to be modified chemically in advance, the method is very simple and fast.  相似文献   
984.
985.
本文对思茅新木蛾Neospastis simaona Wang幼虫的取食行为、取食偏好性以及明暗条件对其取食量的影响进行了观察研究,为该昆虫的防治提供了理论依据.研究结果表明:思茅新木蛾幼虫随着龄期的增加,取食次数增多,取食总时间增加,但一次取食时间无明显变化;思茅新木蛾幼虫对木荷(Schima superba)有强烈嗜食性,4龄幼虫喜食木荷幼叶,5、6龄幼虫对木荷幼叶、成熟叶无明显偏好性;明暗条件对思茅新木蛾4至6龄幼虫的取食量没有显著影响(P>0.05).  相似文献   
986.
[目的]利用扫描电子显微镜(scanning electron microscopy,SEM)观察屋尘螨Dermatophagoides pteronyssinus 颚体、躯体、外生殖器及足等的形态结构.[方法]从床尘、枕尘中采集屋尘螨,分离出雌雄成螨,在体视显微镜下清洗处理活螨后,用SEM观察其外部形态特征.[结果]SEM照片显示,屋尘螨整肢钳状,须肢扁平;体表具细密皮纹,似指纹状,纹间距小于2 μm.外生殖器位于腹面正中,雌螨为产卵孔,雄螨生殖孔具1对叶状生殖盖.肛 门呈纵行裂孔,雄螨具2个肛吸盘.雌螨足跗节末端各具爪垫1个,雄螨跗节Ⅳ具2个吸盘.[结论]本研究观察结果为尘螨鉴定提供了更多依据.  相似文献   
987.
As toxic pollutants commonly found in tobacco (Nicotiana tabacum L.) products, lead (Pb) and cadmium (Cd) can enter the human body via smoking and thus pose a potential health risk to smokers. We conducted a greenhouse experiment to study the effects of arbuscular mycorrhizal (AM) inoculation with Glomus intraradices BEG 141 and organic amendment with cattle manure, alone or in combination, on the growth, P nutrition, and heavy-metal uptake by tobacco plants grown in soil to which was added Pb-Cd at 0/0, 350/1, 500/10, and 1,000/100?mg?kg?1, respectively. In general, AM colonization and plant growth were greatly reduced by Pb-Cd contamination, whereas organic amendment alleviated Pb-Cd stress and showed some beneficial effects on AM symbiosis and some soil parameters. AM inoculation, alone or in combination with organic amendment, increased plant dry weights and improved P nutrition significantly at all Pb-Cd addition levels, and, in most cases, it decreased Pb and Cd concentrations in tobacco plants and DTPA-extractable concentrations in soil. AM inoculation increased total glomalin-related soil protein (GRSP) concentrations in soil to which Pb-Cd was added. The higher soil pH and GRSP contents and the lower DTPA-extractable Pb and Cd concentrations contributed by AM inoculation and/or organic amendment may be contributing factors that lead to higher growth promotion and lower metal toxicity and uptake by plants. Our findings suggest that AM inoculation in combination with organic manure may be a potential method for not only tobacco production but phytostabilization of Pb-Cd-contaminated soil.  相似文献   
988.
Once overlooked as an evolutionary vestige, the primary cilium has recently been the focus of intensive studies. Mounting data show that this organelle is a hub for various signaling pathways during vertebrate embryonic development and pattern formation. However, how cilia form and how cilia execute the sensory function still remain poorly understood. Cilia dysfunction is correlated with a wide spectrum of human diseases, now termed ciliopathies. Various small GTPases, including the members in Arf/Arl, Rab, and Ran subfamilies, have been implicated in cilia formation and/or function. Here we review and discuss the role of one particular group of small GTPase, Arf/Arl, in the context of cilia and ciliopathy.  相似文献   
989.
Elongation and elevation of palatal shelves, mainly caused by proliferation and extra-cellular matrix synthesis of palatal mesenchymal cells (PMCs), are essential for normal palatal development. Transforming growth factor beta (TGFB) pathway could induce proliferation inhibition and collagen synthesis in PMCs. Recent studies found that miRNA-17-92 (miR-17-92) cluster, including miR-17, miR-18a, miR-19a, miR-20a, miR-19b, and miR-92a, expressed in the 1st bronchial arch of mouse embryos during the period of palatal shelf elongation and elevation, and directly targeted TGFB pathway in cancer cell lines. Whether miR-17-92 cluster expresses and targets TGFB pathway in PMCs has not yet been studied. Using quantitative real-time RT-PCR, we found that miR-17-92 expressed in PMCs and decreased from embryonic day (E) 12 to E14 in palatal shelves. MTT assay and Western blot showed that miR-17-92 inhibited TGFB1 induced proliferation inhibition and collagen synthesis in PMCs by decreasing TGFBR2, SMAD2, and SMAD4 protein level. Further luciferase assay showed that miR-17 and miR-20a directly targeted 3′UTR of TGFBR2, and that miR-18a directly targeted 3′UTR of SMAD2 and SMAD4. We thus conclude that miR-17-92 cluster could inhibit TGFB pathway induced proliferation inhibition and collagen synthesis in PMCs by directly targeting TGFBR2, SMAD2, and SMAD4.  相似文献   
990.
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