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   462篇
  免费   9篇
  国内免费   4篇
管理学   62篇
民族学   3篇
人口学   1篇
丛书文集   31篇
理论方法论   10篇
综合类   284篇
社会学   5篇
统计学   79篇
  2023年   2篇
  2022年   5篇
  2021年   4篇
  2020年   8篇
  2019年   9篇
  2018年   7篇
  2017年   12篇
  2016年   15篇
  2015年   16篇
  2014年   19篇
  2013年   37篇
  2012年   20篇
  2011年   27篇
  2010年   15篇
  2009年   16篇
  2008年   20篇
  2007年   31篇
  2006年   28篇
  2005年   25篇
  2004年   20篇
  2003年   21篇
  2002年   29篇
  2001年   21篇
  2000年   13篇
  1999年   13篇
  1998年   3篇
  1997年   4篇
  1996年   7篇
  1995年   7篇
  1994年   8篇
  1993年   1篇
  1992年   5篇
  1991年   1篇
  1990年   2篇
  1988年   1篇
  1987年   2篇
  1985年   1篇
排序方式: 共有475条查询结果,搜索用时 31 毫秒
1.
Longitudinal studies are the gold standard of empirical work and stress research whenever experiments are not plausible. Frequently, scales are used to assess risk factors and their consequences, and cross-lagged effects are estimated to determine possible risks. Methods to translate cross-lagged effects into risk ratios to facilitate risk assessment do not yet exist, which creates a divide between psychological and epidemiological work stress research. The aim of the present paper is to demonstrate how cross-lagged effects can be used to assess the risk ratio of different levels of psychosocial safety climate (PSC) in organisations, an important psychosocial risk for the development of depression. We used available longitudinal evidence from the Australian Workplace Barometer (N?=?1905) to estimate cross-lagged effects of PSC on depression. We applied continuous time modelling to obtain time-scalable cross effects. These were further investigated in a 4-year Monte Carlo simulation, which translated them into 4-year incident rates. Incident rates were determined by relying on clinically relevant 2-year periods of depression. We suggest a critical value of PSC?=?26 (corresponding to ?1.4 SD), which is indicative of more than 100% increased incidents of persistent depressive disorder in 4-year periods compared to average levels of PSC across 4 years.  相似文献   
2.
谈新时期图书馆员的继续教育   总被引:1,自引:0,他引:1  
从分析太原理工大学图书馆人员现状入手 ,结合国内外图书馆员继续教育发展状况 ,提出图书馆开展继续教育的具体措施 :进行在职教育和在职培训  相似文献   
3.
Bayesian analysis of discrete time warranty data   总被引:1,自引:0,他引:1  
Summary.  The analysis of warranty claim data, and their use for prediction, has been a topic of active research in recent years. Field data comprising numbers of units returned under guarantee are examined, covering both situations in which the ages of the failed units are known and in which they are not. The latter case poses particular computational problems for likelihood-based methods because of the large number of feasible failure patterns that must be included as contributions to the likelihood function. For prediction of future warranty exposure, which is of central concern to the manufacturer, the Bayesian approach is adopted. For this, Markov chain Monte Carlo methodology is developed.  相似文献   
4.
职业地位取得的社会性别差异   总被引:6,自引:0,他引:6  
本文从描述被调查夫妇之间职业流动的性别差异出发,分别勾画出他们的地位实现模型。首先验证了不论性别,教育地位都是决定职业地位实现的首要变量;但也正是在教育地位的实现和向上流动(再求学)中,伴随婚姻生育等生命事件的发生,无形的结构性制度因素(意识形态层面的性别制度、性别规范和性别文化)正如后现代主义试图解构的那样依然支配着性别角色的社会化和继续社会化,使扮演双重角色的妻子或无意识地或有意识地遭遇了丈夫不为之所累的两难困境,并最终阻碍了女性的教育地位、既而是职业地位的实现。本文最后提出了三点建议和几个尚待解决的问题。  相似文献   
5.
本文利用极限定义及归结原则等方法,给出了几个一致连续的充要条件,得到了判定函数一致连续的有效方法。  相似文献   
6.
刑法理论通说基于我国刑法第89条追诉时效的规定,认为我国刑法中承认连续犯的观点,是对连续犯的一种曲解。对我国刑法中是否承认连续犯的考察,须从连续犯的理论入手,并考察实体法和程序法的相关规定,而我国现行刑事立法中目前还不具备连续犯的立法土壤。因我国刑法对同种数罪不实行并罚,连续犯与同种数罪的区分并无司法实践上的意义。  相似文献   
7.
在考虑了操作机的关节极限、自碰撞和静态障碍物的情况下,从给定的初始位形出发,发现一条到末端效应器目标位置和姿态的相连可到达路径。方法给出了机器人操作机点到点逆运动学问题求解算法,利用碰撞算法实现了冗余度机器人运动规划,仿真验证了该方法的有效性,并表明了该方法具有较大的实用价值。  相似文献   
8.
讨论了带连续时延神经网络的Hopf分岔现象。对于强核和弱核的情况,利用平均时延作为分岔参数,证明了模型经历了Hopf分岔过程。在带弱核的神经网络模型中,得到了分岔周期解稳定性准则。给出了一些数值例子,通过计算机仿真验证了所得结论的正确性。  相似文献   
9.
通过论述知识经济时代、经济全球化时代高校财会人员应不断地更新知识,接受继续教育的必要性和迫切性,分析当前高校财会人员继续教育中存在的主要问题,提出了加强高校财务人员继续教育问题的对策.  相似文献   
10.
Modeling for Risk Assessment of Neurotoxic Effects   总被引:2,自引:0,他引:2  
The regulation of noncancer toxicants, including neurotoxicants, has usually been based upon a reference dose (allowable daily intake). A reference dose is obtained by dividing a no-observed-effect level by uncertainty (safety) factors to account for intraspecies and interspecies sensitivities to a chemical. It is assumed that the risk at the reference dose is negligible, but no attempt generally is made to estimate the risk at the reference dose. A procedure is outlined that provides estimates of risk as a function of dose. The first step is to establish a mathematical relationship between a biological effect and the dose of a chemical. Knowledge of biological mechanisms and/or pharmacokinetics can assist in the choice of plausible mathematical models. The mathematical model provides estimates of average responses as a function of dose. Secondly, estimates of risk require selection of a distribution of individual responses about the average response given by the mathematical model. In the case of a normal or lognormal distribution, only an estimate of the standard deviation is needed. The third step is to define an adverse level for a response so that the probability (risk) of exceeding that level can be estimated as a function of dose. Because a firm response level often cannot be established at which adverse biological effects occur, it may be necessary to at least establish an abnormal response level that only a small proportion of individuals would exceed in an unexposed group. That is, if a normal range of responses can be established, then the probability (risk) of abnormal responses can be estimated. In order to illustrate this process, measures of the neurotransmitter serotonin and its metabolite 5-hydroxyindoleacetic acid in specific areas of the brain of rats and monkeys are analyzed after exposure to the neurotoxicant methylene-dioxymethamphetamine. These risk estimates are compared with risk estimates from the quantal approach in which animals are classified as either abnormal or not depending upon abnormal serotonin levels.  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