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   336篇
  免费   18篇
  国内免费   16篇
儿科学   3篇
妇产科学   2篇
基础医学   51篇
口腔科学   17篇
临床医学   20篇
内科学   28篇
神经病学   7篇
特种医学   19篇
外科学   9篇
综合类   26篇
预防医学   19篇
眼科学   1篇
药学   136篇
中国医学   23篇
肿瘤学   9篇
  2023年   4篇
  2022年   9篇
  2021年   10篇
  2020年   10篇
  2019年   4篇
  2018年   5篇
  2017年   14篇
  2016年   11篇
  2015年   12篇
  2014年   24篇
  2013年   22篇
  2012年   16篇
  2011年   34篇
  2010年   17篇
  2009年   21篇
  2008年   18篇
  2007年   28篇
  2006年   14篇
  2005年   18篇
  2004年   5篇
  2003年   12篇
  2002年   1篇
  2001年   7篇
  2000年   7篇
  1999年   8篇
  1998年   5篇
  1997年   4篇
  1996年   4篇
  1995年   1篇
  1994年   4篇
  1992年   1篇
  1991年   1篇
  1990年   4篇
  1989年   2篇
  1987年   2篇
  1986年   1篇
  1985年   1篇
  1984年   3篇
  1983年   1篇
  1981年   1篇
  1980年   1篇
  1979年   1篇
  1978年   1篇
  1977年   1篇
排序方式: 共有370条查询结果,搜索用时 265 毫秒
1.
This study deals with a series of operations to isolate the micro-cellulose from the palm tree spathe sheath by using a modified chemical method to take into account the low cost and the completion speed and its characterization using X-ray diffraction technique (XRD), infrared spectroscopy (FTIR) and scanning electron microscope coupled with element analyzer (SEM/EDX). The results showed that the extraction method succeeded in obtaining very pure microscopic fibers with a width of 2–10 μm with a crystallinity index equal to 79.21%, containing the two cellulose features Iβ and II, that, the conversion ratio of the first to the second was estimated at 32, 87%.  相似文献   
2.
O-羧甲基N-半乳糖化壳聚糖衍生物的设计、合成和表征   总被引:7,自引:0,他引:7  
目的:合成和表征O-羧甲基-N-半乳糖化壳聚糖衍生物作为潜在的肝靶向基因载体。方法:以天然聚合物壳聚糖为原料,首先制备得O-羧甲基壳聚糖,然后在其2-NH2上和乳糖酸反应,制得O-羧甲基-N-乳糖酰化壳聚糖;或与乳糖反应,用KB}14还原,制得O-羧甲基-N-乳糖胺化壳聚糖。结果与结论:分别用VF-IR、^1H NMR、^13C NMR和元素分析对其进行了表征。用粉末X-衍射、DSC、TG对其物理性质进行了分析。制得的O-羧甲基-N-乳糖酰化壳聚糖O-羧甲基-N-乳糖胺化壳聚糖有望作为潜在的肝靶向基因载体。  相似文献   
3.
肠激酶特点及其基因工程的研究进展   总被引:3,自引:0,他引:3  
肠激酶是从哺乳动物体内提取的一种丝氨酸蛋白酶,广泛应用于基因T程领域切割融合蛋白。文章对肠激酶的特点及其基因工程研究进展进行了综述。  相似文献   
4.
Magnetic resonance imaging of soft tissue tumors   总被引:4,自引:0,他引:4  
This article outlines the ability of MR imaging in staging, grading, tissue characterization, and posttherapeutic surveillance of soft tissue tumors. Well-known staging parameters, such as extent, relationship with adjacent structures, and detection of intralesional necrosis, are used in the MR protocol for locoregional staging. Bone scintigraphy and high-resolution CT scan of the lungs are best methods for ruling out metastatic spread. A variety of (solitary or combinations of) grading parameters are described in the radiological literature. The role of MR imaging is to afford recognition of these lesions that need further aggressive work-up, excluding all others. Despite controversial reports, the definite role of MR imaging in grading of soft tissue tumors seems to become established. As for grading, a lot of individual imaging characteristics used for tissue characterization have low sensitivity, but combinations of parameters (age, site, signal intensities) are more useful and often allow to predict a specific diagnosis or to narrow down the list of differential diagnoses. Local recurrences of soft tissue tumors are frequent and can be detected accurately by an easy-to-use MR algorithm.  相似文献   
5.
Optimization of operating and design parameters is needed for the greater application to achieve higher quality, performance, and minimum cost. The paper mainly concentrates on, the optimization of process parameters influencing the deflouridation of water by Analysis of mean (ANOM) approach. The current work mainly aims at the utilization of the Taguchi approach to optimize influencing operating parameters for maximizing the removal of fluoride under batch experimental studies by using biosorbent developed from Saccharum spontaneum, weed plant. The optimum conditions were found at pH 7, sorbate content 5 mg/L, period of contact 120 min, sorbent dosage 10 g/L, and temperature 30 °C. The percent part of various process parameters is obtained in the successive sequence pH 56.21% > initial concentration of adsorbate 33.94% > biosorbent dose 5.49% > contact time 3.35% > temperature 1.01%. The equilibrium study indicates fluoride sorption on Saccharum spontaneum adsorbent fulfill the Langmuir model with parameters ‘a' and ‘b' determined as 1.617 mg/g and 0.473 L/mg. The kinetic study with sorption data suggested the Pseudo-second order kinetic model as best fitting with kinetic rate k2 0.218 g/mg min. The thermodynamic analysis suggested a spontaneous and endothermic nature (ΔH = 16.268 kJ/mol). Characterization of adsorbent was done using BET, SEM, and also by the determination of textual properties. Regeneration of the biosorbent is done for three cycles and is used for fluoride removal.  相似文献   
6.
7.
A simple, precise, accurate stability-indicating gradient reversed-phase high-performance liquid chromatographic (RP–HPLC) method was developed for the quantitative determination of zotepine (ZTP) in bulk and pharmaceutical dosage forms in the presence of its degradation products (DPs). The method was developed using Phenomenex C18 column (250 mm×4.6 mm i.d., 5 µm) with a mobile phase containing a gradient mixture of solvents, A (0.05% trifluoroacetic acid (TFA), pH=3.0) and B (acetonitrile). The eluted compounds were monitored at 254 nm; the run time was within 20.0 min, in which ZTP and its DPs were well separated, with a resolution of >1.5. The stress testing of ZTP was carried out under acidic, alkaline, neutral hydrolysis, oxidative, photolytic and thermal stress conditions. ZTP was found to degrade significantly in acidic, photolytic, thermal and oxidative stress conditions and remain stable in basic and neutral conditions. The developed method was validated with respect to specificity, linearity, limit of detection, limit of quantification, accuracy, precision and robustness as per ICH guidelines. This method was also suitable for the assay determination of ZTP in pharmaceutical dosage forms. The DPs were characterized by LC–MS/MS and their fragmentation pathways were proposed.  相似文献   
8.
Lopinavir is an antiretroviral drug used for the inhibition of HIV protease. Four related substances of lopinavir were observed during the manufacturing process of lopinavir in the laboratory and they were identified. The present work describes the origin, synthesis, characterization, and control of these related substances.  相似文献   
9.
The beta-receptors were isolated from rat cardiac myocytes and characterized. Isolated myocytes were prepared from adult rat hearts and characterized for viability. Membrane proteins were solubilized from myocytes with 1% Triton X-102. The solubilized membrane proteins were fractionated by DEAE-Sephacel ion exchange column chromatography. Two major protein peaks were obtained. The second protein peak sample was found to contain beta-receptors to which 125I-15-(4'-azido-3'-iodobenzyl)-carazolol (125I-ABC) was specifically bound. This sample was labeled covalently with 125I-ABC by UV irradiation. The radiolabeled sample was applied to a Sepharose CL-6B gel column. Two radiolabeled protein peaks, one with a molecular weight of approximately 570,000 and the other with a molecular weight of approximately 95,000 were found. When the 570,000-dalton complex was subjected to sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) under reducing conditions, it was dissociated into a component with a molecular weight of 66,000. The 95,000-dalton complex was dissociated into a 58,000-dalton component upon SDS-PAGE under reducing conditions. An excess amount of isoproterenol and propranolol decreased photolabeling of the beta-receptors with 125I-ABC by 60% and 40%, respectively.  相似文献   
10.
目的 研究不同剂量NaOH条件对制备BiOIO3/g-C3N4复合纳米光催化剂的结构形貌及其可吸收光谱的影响,为研制适用于口腔修复纳米光催化功能性材料提供依据.方法 水热法制备BiOIO3/g-C3N4,通过XRD(X射线衍射仪)、SEM(扫描电镜图)和UV-vis(紫外-可见光吸收光谱)对其形貌、结构、分子组成和理化特性等进行表征.结果 在5mol/L的NaOH溶液条件下制备出BiOIO3/g-C3N4(BC-5),其(010)峰和(040)峰的强度最弱,(121)峰的强度最强,形貌呈方形块状,出现圆角形状,尺寸在100~200 nm范围,厚度约为60 nm.其富含异质结构,禁带宽度降低,吸收光谱红移,光吸收边界有明显拓宽.结论 g-C3N4掺杂形成了Z型异质结构,提高了电子-空穴分离效率,提升了可见光响应性能.该结果为新型牙科修复功能性光催化材料的选择提供了一定的理论依据.  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