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61.
This study aimed to monitor the present and future developments of the resistance of Tetranychus urticae Koch to fenpyroximate and pyridaben, using the relationship of the LC50 and slope of the concentration-mortality line in a probit model, for the provision of reliable resistance management tactics. Tetranychus urticae populations were collected from 16 commercial greenhouses, where various crops were cultivated, as well as from 10 apple orchards throughout Korea. The resistance to fenpyroximate and pyridaben of each population was estimated by calculating the median lethal concentration (LC50), resistance ratio (RR) and slope of the concentration-mortality regression. Most of the greenhouse populations exhibited moderate levels of resistance, whereas the apple orchard populations showed only low levels, indicating that T. urticae populations in greenhouses were more strongly selected than those in apple orchards. Four population groups were established based on either the habitats (greenhouse and apple orchard) or acaricides (fenpyroximate and pyridaben). To test the hypothesis, “the slope is greatest at low and high levels of resistance,” the slopes were regressed as a function of the LC50, and fitted to a polynomial regression. The polynomial regression model explained this relationship well for the four population groups (p < 0.05), indicating that the development of resistance toward fenpyroximate or pyridaben was consistent with the gradient. A laboratory selection study agreed with the results from both acaricide field populations. These results suggest that the gradient was a good indicator of the susceptibility of T. urticae to genetic variations, which was related to the LC50. The application of these findings is also discussed in relation to the resistance management of T. urticae. 相似文献
62.
On variance estimation in nonparametric regression 总被引:8,自引:0,他引:8
63.
Survival analyses in twin studies and matched pair experiments 总被引:1,自引:0,他引:1
64.
Neurotoxicity has become an important area in the study of the risk to children of noncarcinogens. Many of the tests used to evaluate neurotoxic effects in neurotoxic studies are psychometric tests to assess cognitive, motor, and perceptual performance in individuals in order to determine the presence of psychological problems, impaired educational achievement, or neurological abnormalities. The underlying assumption of these procedures are that a test performance deficit is indicative of a neurological disability, and that such disability derives from the prenatal exposure to an offending substance. The usual analytic paradigm for discerning environmental impacts is to analyze the scores of a particular subtest in a battery taken separately as the dependent variable with regression analysis, which adjusts for cultural background, educational level, and socioeconomic status. The impact of this analysis is to determine the correlation of each of the psychometric test results to exposure. We show a statistical method to simultaneously analyze the multiple outcomes of many tests using General Estimating Equations (GEE) to determine if a correlation exists between the global measure of all these tests and exposure adjusted for covariates of interest and the correlation among the dependent psychometric variables. We show the application of this method to the results of children whose mothers were exposed to mercury during pregnancy. 相似文献
65.
Neural networks have received much attention in recent years mostly by non-statisticians. The purpose of this paper is to incorporate neural networks in a non-linear regression model and obtain maximum likelihood estimates of the network parameters using a standard Newton-Raphson algorithm. We use maximum likelihood estimators instead of the usual back-propagation technique and compare the neural network predictions with predictions of quadratic regression models and with non-parametric nearest neighbor predictions. These comparisons are made using data generated from a variety of functions. Because of the number of parameters involved, neural network models can easily over-fit the data, hence validation of results is crucial. 相似文献
66.
67.
Summary It has become increasingly common in epidemiological studies to pool specimens across subjects to achieve accurate quantitation of biomarkers and certain environmental chemicals. In this article, we consider the problem of fitting a binary regression model when an important exposure is subject to pooling. We take a regression calibration approach and derive several methods, including plug‐in methods that use a pooled measurement and other covariate information to predict the exposure level of an individual subject, and normality‐based methods that make further adjustments by assuming normality of calibration errors. Within each class we propose two ways to perform the calibration (covariate augmentation and imputation). These methods are shown in simulation experiments to effectively reduce the bias associated with the naive method that simply substitutes a pooled measurement for all individual measurements in the pool. In particular, the normality‐based imputation method performs reasonably well in a variety of settings, even under skewed distributions of calibration errors. The methods are illustrated using data from the Collaborative Perinatal Project. 相似文献
68.
Wei Chen Debashis Ghosh Trivellore E. Raghunathan Daniel J. Sargent 《Biometrics》2009,65(4):1030-1040
Summary Colorectal cancer is the second leading cause of cancer related deaths in the United States, with more than 130,000 new cases of colorectal cancer diagnosed each year. Clinical studies have shown that genetic alterations lead to different responses to the same treatment, despite the morphologic similarities of tumors. A molecular test prior to treatment could help in determining an optimal treatment for a patient with regard to both toxicity and efficacy. This article introduces a statistical method appropriate for predicting and comparing multiple endpoints given different treatment options and molecular profiles of an individual. A latent variable‐based multivariate regression model with structured variance covariance matrix is considered here. The latent variables account for the correlated nature of multiple endpoints and accommodate the fact that some clinical endpoints are categorical variables and others are censored variables. The mixture normal hierarchical structure admits a natural variable selection rule. Inference was conducted using the posterior distribution sampling Markov chain Monte Carlo method. We analyzed the finite‐sample properties of the proposed method using simulation studies. The application to the advanced colorectal cancer study revealed associations between multiple endpoints and particular biomarkers, demonstrating the potential of individualizing treatment based on genetic profiles. 相似文献
69.
70.
Summary. In this proof-of-concept study, we attempt to determine whether the cause-mutation relationship defined by randomness is protein
dependent by predicting mutations in H5N1 neuraminidases from influenza A virus, because we have recently conducted several
concept-initiated studies on the prediction of mutations in hemagglutinins from influenza A virus. In our concept-initiated
studies, we defined the randomness as a cause for mutation, upon which we built a cause-mutation relationship, which is then
switched into the classification problem because the occurrence and non-occurrence of mutations can be classified as unity
and zero. Thereafter, we used the logistic regression and neural network to solve this classification problem to predict the
mutation positions in hemagglutinins, and then used the amino acid mutating probability to predict the would-be-mutated amino
acids. As the previous results were promising, we extend this approach to other proteins, such as H5N1 neuraminidase in this
study, and further address various issues raised during the development of this approach. The result of this study confirms
that we can use this cause-mutation relationship to predict the mutations in H5N1 neuraminidases.
Authors’ address: Guang Wu, Computational Mutation Project, DreamSciTech Consulting 301, Building 12, Nanyou A-zone, Jiannan
Road, Shenzhen, Guangdong Province CN-518054, China 相似文献