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1.

Background

Developmental biology has made great strides in recent years towards the quantification of cellular properties during development. This requires tissues to be imaged and segmented to generate computerised versions that can be easily analysed. In this context, one of the principal technical challenges remains the faithful detection of cellular contours, principally due to variations in image intensity throughout the tissue. Watershed segmentation methods are especially vulnerable to these variations, generating multiple errors due notably to the incorrect detection of the outer surface of the tissue.

Results

We use the level set method (LSM) to improve the accuracy of the watershed segmentation in different ways. First, we detect the outer surface of the tissue, reducing the impact of low and variable contrast at the surface during imaging. Second, we demonstrate a new edge function for a level set, based on second order derivatives of the image, to segment individual cells. Finally, we also show that the LSM can be used to segment nuclei within the tissue.

Conclusion

The watershed segmentation of the outer cell layer is demonstrably improved when coupled with the LSM-based surface detection step. The tool can also be used to improve watershed segmentation at cell-scale, as well as to segment nuclei within a tissue. The improved segmentation increases the quality of analysis, and the surface detected by our algorithm may be used to calculate local curvature or adapted for other uses, such as mathematical simulations.
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Postweaning multisystemic wasting syndrome (PMWS), a new disease in Hungary, was recognized in a swine herd located in Southeast Hungary, during the early winter of 1999. The first clinical signs of paleness, anaemia, and leanness appeared immediately after weaning, at the age of 40-50 days. Pustules were frequently observed on the skin of the trunk, and signs of necrotic dermatitis were also visible. A syndrome of poor growth and wasting was characteristic of the affected pigs. A porcine circovirus (PCV), the suspected causative agent, was detected by polymerase chain reaction (PCR). Sequencing data and restriction endonuclease (RE) analysis of the PCR products suggested that the virus belonged to the PCV-II group where all the causative agents of PMWS are also grouped.  相似文献   
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The western corn rootworm, Diabrotica virgifera virgifera LeConte, is the most important pest of maize in the Midwestern USA, and since its detection in 1992 in Europe, also in several countries of Central and Eastern Europe. Methods for managing this pest vary from region to region, depending upon: the different cultural practices in maize production, climatic conditions, soil types, pest behaviour, infestation level and socio-economic conditions. Factors including date of planting, amount of rotated or continuous maize, irrigation, date of rootworm hatching and differences in behaviour of the pest, necessitate developing different management strategies in different areas of the infested countries. Pest monitoring, damage evaluation, threshold development, use of insecticides, risk estimation and crop rotation are some of the starting points in the development of management strategies. Approaches and experiences in D. v. virgifera control and management in Italy, Hungary and the USA, based on the understanding of local agro-ecosystems and socio-economic conditions, are reported.  相似文献   
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A new pentacyclic triterpene, 11alpha-acetoxy-20,24-epoxy-25-hydroxy-dammar-3-one (1), has been isolated from the African tree Combretum nigricans, together with the known corresponding diol, 20,24-epoxy-11alpha, 25-dihydroxy-dammar-3-one (2). They are responsible, at least in part, for the cytotoxic activity of the methanolic extract of the plant.  相似文献   
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Synchrony between development of five corn hybrid varieties of various seasonal growing rates (FAO numbers), seasonal flight pattern of male cotton bollworm, Helicoverpa armigera Hb. (Lepidoptera: Noctuidae), as monitored by pheromone traps, and the subsequent appearance of newly hatched larvae on developing cobs were studied at Mezőhegyes, South-Hungary, in 2003 and 2004. The phenological stages of corn hybrids were evaluated using the Iowa State University Scale (R1–R5), the flight of male moths was monitored by large capacity, funnel type of pheromone traps and the appearance of freshly hatched larvae on developing cobs were counted by visual inspection. The synchrony between the flight peak of male moths and the peak apperance of L1 larvae on cobs was investigated by cross-correlation. In 2003 (average daily temperatures 20.7°C, average daily relative humidity 59.9% for the period of 4–18 July) “DK 391”, “DK 443” and “Maraton” hybrid varieties already reached silking stage (R1) by the time when pheromone traps indicated a peak, at 7 July (peak capture at 3-day intervals 755.5 males/traps). The number of L1 larvae peaked on developing cobs of these varieties also at 7 July (7.0, 4.0 and 3.8 larvae/50 cobs, respectively). The synchrony between the flight peak of male moths and the peak appearance of L1 larvae on cobs was proven (LAG = 0). A rather similar trend was observed in “Vilma” hybrid variety: it reached R1 stage at 7 July, and L1 larvae appeared only a few days later (11 July, 3.8 larvae/50 cobs) (LAG = −1). However, “Maxima” hybrid variety reached R1 stage 1 week later (14 July) than the time of peak captures. Here L1 larvae peaked as late as at 18 July (0.8 larvae/50 cobs), i.e., only after the cob had reached R1 stage (LAG = −3). A reverse order of dates of R1 stage and peak capture was observed in “Maxima” in 2004 (average daily temperatures; 22.5°C, average daily relative humidities 72.6% for the period of 15 July–6 August): it reached R1 stage at 19 July, while peak trap captures were recorded at 6 August (peak capture at 3-day intervals 20.5 males/traps). L1 larvae were found in the highest numbers on 2 August (1.5 larvae/50 cobs), practically in synchrony with peak caputres (LAG = 0). “Káma” reached R1 stage in 16 July, and L1 larvae peaked at 2 August (1.3 larvae/50 cobs) (LAG = 0). On the rest of the corn varieties larvae were found only in too numbers for performing statistical analysis. We conclude that in order to predict the appearance of L1 larvae, the phenological stage of the corn variety and the seasonal flight pattern of moths, as measured by large capacity pheromone traps, should be considered in combination. If the corn variety already reached R1 stage, L1 larvae appear on cobs as early as the time of peak flight of moths. However, no young larvae appear on cobs despite of high trap captures, until the corn reaches the R1 stage. These findings are discussed in the view of specifying optimal timing of a pesticide application.  相似文献   
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Background

The success of the microarray reproducibility is dependent upon the performance of standardized procedures. Since the introduction of microarray technology for the analysis of global gene expression, reproducibility of results among different laboratories has been a major problem. Two of the main contributors to this variability are the use of different microarray platforms and different laboratory practices. In this paper, we address the latter question in terms of how variation in one of the steps of a labelling procedure affects the cDNA product prior to microarray hybridization.

Results

We used a standard procedure to label cDNA for microarray hybridization and employed different types of column chromatography for cDNA purification. After purifying labelled cDNA, we used the Agilent 2100 Bioanalyzer and agarose gel electrophoresis to assess the quality of the labelled cDNA before its hybridization onto a microarray platform. There were major differences in the cDNA profile (i.e. cDNA fragment lengths and abundance) as a result of using four different columns for purification. In addition, different columns have different efficiencies to remove rRNA contamination. This study indicates that the appropriate column to use in this type of protocol has to be experimentally determined. Finally, we present new evidence establishing the importance of testing the method of purification used during an indirect labelling procedure. Our results confirm the importance of assessing the quality of the sample in the labelling procedure prior to hybridization onto a microarray platform.

Conclusion

Standardization of column purification systems to be used in labelling procedures will improve the reproducibility of microarray results among different laboratories. In addition, implementation of a quality control check point of the labelled samples prior to microarray hybridization will prevent hybridizing a poor quality sample to expensive micorarrays.  相似文献   
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