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   59篇
  免费   6篇
耳鼻咽喉   3篇
儿科学   1篇
妇产科学   2篇
基础医学   14篇
口腔科学   1篇
临床医学   6篇
内科学   8篇
神经病学   11篇
特种医学   3篇
综合类   3篇
预防医学   4篇
眼科学   2篇
药学   4篇
中国医学   3篇
  2022年   2篇
  2021年   3篇
  2018年   1篇
  2017年   1篇
  2016年   4篇
  2015年   1篇
  2014年   1篇
  2013年   3篇
  2012年   5篇
  2011年   3篇
  2010年   3篇
  2009年   5篇
  2008年   3篇
  2007年   2篇
  2006年   1篇
  2005年   4篇
  2004年   1篇
  2003年   7篇
  2001年   1篇
  1999年   2篇
  1998年   1篇
  1997年   4篇
  1996年   2篇
  1993年   1篇
  1987年   1篇
  1984年   1篇
  1981年   1篇
  1978年   1篇
排序方式: 共有65条查询结果,搜索用时 156 毫秒
51.
山东省乙型肝炎疫苗免疫效果考核的初步分析   总被引:3,自引:2,他引:1  
为了考核中国肝炎防治基金会乙型肝炎(乙肝)疫苗扶贫项目实施情况,在山东省济阳、莒南县采用逐级分层抽样的方法,抽取2000年出生的儿童560名及其母亲557名,进行一般情况调查,并用胶体金试纸条法检测其末梢血中的乙肝病毒表面抗原(HBsAg).结果显示2个县儿童乙肝疫苗接种率和全程接种率均为100.00%,第1针乙肝疫苗及时接种率为99.11%,母亲HBsAg阳性率为4.67%,儿童HBsAg阳性率为0.18%,围产期阻断率为90.38%,乙肝疫苗综合保护率为96.15%.表明乙肝疫苗的母婴阻断效果好,HBsAg胶体金试纸条是基层检测HBsAg比较理想的检测方法.  相似文献   
52.
53.
李武  杜炜杰 《浙江医学》2011,33(9):1265-1268
目的 本研究旨在评价人绒毛膜促性腺激素(β-hCG)、孕酮(P)、CA125结合子宫内膜厚度(EST)测定对早期不明位置妊娠(PUL)的预测价值.方法 收集被诊断为PUL的114例早期停经患者,分别于就诊当天抽血检测β-hCG、P及CA125水平,并经阴道超声(TVS)检测EST,48h后再次抽血检测β-hCG,以诊断准确率、敏感性和特异性来评价各种指标组合预测PUL结局的有效性.结果 114例患者中,84例确诊为异位妊娠(EP),14例为宫内妊娠(IUP),10例为先兆流产(IUPM),6例为难免流产.β-hCG预测PUL结局的诊断准确率最高(86.8%),β-hCG+P+CA125+EST(三者符合)次之(84.2%).在诊断EP方面,β-hCG的灵敏度最高(90.5%),β-hCG+P+CA125+EST(三者符合)次之(82.1%),β-hCG+P+CA125+EST(三者符合)特异度最高(86.7%).结论 β-hCG 、P、CA125及EST 4个指标结合使用具有较好的敏感性和特异性,可作为今后预测PUL结局的简便方法.  相似文献   
54.
目的:研究天然维生素E特征与高效液相指纹图谱及其应用。方法:HPLC-荧光,紫外检测C-RIB处据处理及指纹图谱鉴别。结果:共检测我省市售几十种品牌植物油以及新开发的营养,保健食品,回归方程与相关系数分别为:α-E,Y=4.64X 2.55,r=0.9998,r-E,Y=3.2X 1.15,r=0.9993,δ-E:Y=2.21X 1.21,r=0.9991,方法回收率92.7%-96.2%,RSD2.17%-2.75%^[1],结论:维生素E高效液相指纹图谱分析是植物油鉴定鉴别,品质评价,卫生检测的快速准确的效手段。  相似文献   
55.
Our previous research found that NSvc4, the movement protein of rice stripe virus (RSV), could localize to the actin filaments, endoplasmic reticulum, plasmodesmata, and chloroplast, but the roles of NSvc4 played in the chloroplast were opaque. Here, we confirm the accumulation of NSvc4 in the chloroplasts and the N-terminal 1–73 amino acids of NSvc4 are sufficient to localize to chloroplasts. We provide evidence to show that chloroplast-localized NSvc4 can impair the chloroplast-mediated immunity. Expressing NSvc4 in Nicotiana benthamiana leaves results in the decreased expression of defense-related genes NbPR1, NbPR2, and NbWRKY12 and the inhibition of chloroplast-derived ROS production. In addition, generation of an infectious clone of potato virus X (PVX) carrying NSvc4 facilitates PVX infection in N. benthamiana plants. Moreover, we identify two chloroplast-related host factors, named NbGAPDH-A and NbPsbQ1, both of which can interact with NSvc4. Knockdown of NbGAPDH-A or NbPsbQ1 can both promote RSV infection. Our results decipher a detailed function of NSvc4 in the chloroplast.  相似文献   
56.
本文介绍了点阵打印机图像打印的一般原理,并应用循环链表结构,生成任意等宽的黑白条纹组,通过打印机直接打印,用于眼科视力检查,不仅精确度高,而且省时省力。  相似文献   
57.
58.
Liang D  Qu Z  Ma X  Hull R 《Virus genes》2005,31(2):211-221
The genome of the Tenuivirus, Rice stripe virus (RSV) comprises four RNAs, the smallest three of which each contain two open reading frames (ORFs) arranged in an ambisense manner. The expression of the ORFs from RNAs 2–4 in plants and the insect vector, Laodelphax striatellus, was studied using antisera raised against the gene products. In Western blotting of the proteins from infected plants, the molecular masses of p2, p3, pc3 (nucleocapsid protein, N) and p4 (major non-structural protein, NCP) were as expected; that of pc4 appeared larger than expected. Antisera to the N- and C-terminal parts of the complementary ORF on RNA 2, analogous to that encoding glycoproteins on genomes of bunyaviruses and tospoviruses, revealed banding patterns suggestive of processing of the product; the possible processing is discussed. Four types of inclusion bodies were identified by immunofluorescent and immunogold microscopy of thin sections of infected leaves. Most electron-dense amorphous semi-electron-opaque inclusion bodies (dASO) contained only p4 while some contained at least p2, pc2-N, p3, pc3 as well as p4. A ring-like structure containing at least pc2-N, p4 and pc4 was also identified in infected plant cells. Fibrillar amorphous semi-electron-opaque inclusion bodies (fASO) contained only p4. Filamentous electron-opaque inclusion bodies (FEO), which consist of pc2-N.and p4, were found both in infected plant cells and in the mid-gut lumen and mid-gut epithelial cells of L. striatellus. This suggests an interaction between p4 and pc2-N and a function of pc2-N distinct from that of its-homologue in Bunyaviridae. Our results confirm the in vivo ambisense coding strategy of Tenuivirus RNA 2 and provide further evidence that RSV does not produce enveloped virions in infected rice plants.  相似文献   
59.
Plant viruses transmitted by hemipteran vectors commonly cause losses to crop production. Rice stripe virus (RSV) and rice black streaked dwarf virus (RBSDV) are transmitted to rice plants by the same vector, the small brown planthopper (SBPH), Laodelphax striatellus Fallén, in a persistent propagative manner. However, rarely do the respective diseases they cause occur simultaneously in a field. Here, we determined the acquisition efficiency of RSV and RBSDV when acquired in succession or simultaneously by SBPH. When RBSDV was acquired first, RSV acquisition efficiency was significantly lower than when only acquiring RSV. However, RBSDV acquisition efficiency from insects that acquired RSV first was not significantly different between the insects only acquiring RBSDV. Immunofluorescence assays showed that the acquisition of RBSDV first might inhibit RSV entry into midgut epithelial cells, but RSV did not affect RBSDV entry. SBPHs were more likely to acquire RBSDV when they were feeding on plants coinfected with the two viruses. When RBSDV was acquired before RSV, RBSDV titer was significantly higher and RSV titer first declined, then increased compared to when only acquiring RBSDV or RSV. Only 5% of the SBPHs acquired both viruses when feeding on plants coinfected with RSV and RBSDV. These results provide a better understanding of the interaction between two persistent viruses when present in the same vector insect and explain why RSV and RBSDV occur in intermittent epidemics.  相似文献   
60.
Objective. Transcranial images are affected by a “stripe artifact” (also known as a “streak artifact”): two dark stripes stem radially from the apex to the base of the scan. The stripes limit the effective field of view even on patients with good temporal windows. This study investigated the angle dependency of ultrasound transmission through the skull to elucidate this artifact. Methods. In vivo transcranial images were obtained to illustrate the artifact. In vitro hydrophone measurements were performed in water to evaluate transcranial wavefronts at different incidence angles of the ultrasound beam. Both a thin acrylic plate, as a simple bone model, and a human temporal bone sample were used. Results. The imaging wavefront splits into two after crossing the solid layer (acrylic model or skull sample) at an oblique angle. An early‐arrival wavefront originates from the direct longitudinal wave transmission through water‐bone interfaces, while a late‐arrival wavefront results from longitudinal‐to‐transverse mode conversion at the water‐bone interface, propagation of the transverse wave through the skull, and transverse‐to‐longitudinal conversion at the bone‐water interface. At normal incidence, only the direct wavefront (without mode conversion) is observed. As the incidence angle increases, the additional “mode conversion” wavefront appears. The amplitude of the transcranial wavefront decreases and reaches a minimum at an incidence angle of about 27°. Beyond that critical angle, only the mode conversion wavefront is transmitted. Conclusions. The stripes are a consequence of the angle‐dependent ultrasound transmission and mode conversion at fluid‐solid interfaces such as between the skull and the surrounding fluidlike soft tissues.  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