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     The performance of different tasks and event-related potential (ERP) by using three different memory loads of visual informative selection task were analyzed in 259 healthy young subjects divided into four-age(9. 8±0. 7, 12.0±0.7, 14.1±0. 8 and 17.1±0. 8) groups.
     本研究采用了3种不同记忆负荷视觉信息选择的作业,对4个年龄组(9.8±0.7、12.0±0.7、14.1±0.8和17.1±0.8),共259名正常青少年各作业时的工效,以及事件相关电位(ERP)进行了分析。
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     IHC-72 also shortened action potential duration at 50%, 100% repolarization(APD50, APD100).
     IHC-72还能缩短SAP复极50%、100%的时程(APD50、APD100),相对延长其有效不应期(ERP)
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     Particularly, the impact to Enterprise Application Integration, including Enterprise Resource Planning, is distinguished which will be described in this paper later.
     其中对企业资源计划(Enterprise Resource Planning,简称ERP)为核心的企业应用集成(Enterprise Application Integration,简称EAI)领域的冲击尤为明显,后文将对此展开详细论述。
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     The ERP Solution Based on Internet/Intranet
     基于Internet/Intranet企业资源计划(ERP)系统方案
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     The Enterprise Resources Planning (ERP) Application Mode Research Based on the Electronic Commerce
     基于电子商务的企业资源计划(ERP)应用模式研究
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     Study on ERP
     浅谈ERP
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     ERP for medium-sized enterprises
     中产阶级ERP
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  erp
The whole system is set up on the base of engineering database technology, integrating Product Data Management (PDM), Enterprise Resource Planning (ERP) etc.
      
The following analogs of the N-terminal ACTH fragments were used: rMEHFPGP, where r is glucuronic acid, KEHFPGP, GEHFPGP, EHFPGP, HFPGP, and ERP.
      
The dependence of differences of ERP to thesame anddifferent images on the stimulated visual field was revealed for the 320-500-ms interval (N400 and late positive complex) in the occipital regions.
      
The analysis of the event-related potentials (ERP) from different cortical areas revealed a specific role of the frontal and temporo-parieto-occipital cortical areas in the classification of additional sensory information.
      
Event-related potentials (ERP) in response to complex target stimuli, which consisted of a central recognizable picture and a lateral masked image (analyzed at the unconscious level) were recorded in adult subjects and seven-year-old children.
      
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Isolated frog retinas were kept for 10 minutes at various temperatures, then cooled to the ambient temperature (about 15℃) and ERP was elicited with flash stimulation. The results showed that R_2 amplitudes underwent different changes with retinas treated at different temperatures. It was not until above 40°C that the R_2 amplitude began to show enhancement. R_2 increased when the temperature was raised to above 40℃ and remained so till the temperature rose above 50℃. The augmentation of R_2 amplitudes...

Isolated frog retinas were kept for 10 minutes at various temperatures, then cooled to the ambient temperature (about 15℃) and ERP was elicited with flash stimulation. The results showed that R_2 amplitudes underwent different changes with retinas treated at different temperatures. It was not until above 40°C that the R_2 amplitude began to show enhancement. R_2 increased when the temperature was raised to above 40℃ and remained so till the temperature rose above 50℃. The augmentation of R_2 amplitudes was particulary marked at 47~48℃, the R_2 amplitude rising to 2.57 times that for retinas without treatment. But when the temperature was raised above 50℃, the R_2 amplitude decreased and went below the average for the control group. At 58℃, R_2 was almost abolished.In addition, these changes of R_2 amplitude also depended on the duration of heating, the shorter the duration of heating, the higher the temperature necessary for the same changes of R_2 amplitude. Therefore, with shorter heating times the R_2 amplitude was enhanced, decreased and abolished respectively at relative higher temperatures. The relationship between changes observed in R_2 amplitude of ERP and changes of order and fluidity of the liquid (?)rystals of the lamellar membranes of the visual cell was also briefly discussed.

经不同温度(从30°至58℃)处理的离体蛙视网膜,冷却后在室温(15℃左右)的情况下引导ERP,R_2振幅随处理温度不同而有不同的变化,处理温度不超过40℃,对R_2几乎没有影响,其振幅与对照组相近。用40℃以上至50℃以下的温度处理后,R_2显著加大,尤其是47~48℃处理后,R_2达最大值,为对照组的2.57倍。用50℃及更高温度处理后,R_2又急剧下降,且低于对照值。经58℃处理后,R_2基本消失。此外,这种变化还与处理时间长短有关,若缩短加温时间,则分别需要在更高一些的温度处理,R_2振幅才依次增大、减小和消失。本文对上述变化,从温度影响视细胞外段膜结构液晶态的流动性和有序性的角度,进行了初步的讨论。

1. At low environmental temperatures (<5°C), we have recorded the ERP of isolated frog retinas. The results obtained may be summarized as follows. With unheated retinas or those that had been heated for 10 minutes at 40℃, it was found that the R_1 amplitude was slightly increased and R_2 was markedly decreased, as compared with the values recorded at the ambient temperature (about 15℃). However, if the retinas were heated for 10 minutes at 47℃, and then ERP was recorded at a low ambient temperature...

1. At low environmental temperatures (<5°C), we have recorded the ERP of isolated frog retinas. The results obtained may be summarized as follows. With unheated retinas or those that had been heated for 10 minutes at 40℃, it was found that the R_1 amplitude was slightly increased and R_2 was markedly decreased, as compared with the values recorded at the ambient temperature (about 15℃). However, if the retinas were heated for 10 minutes at 47℃, and then ERP was recorded at a low ambient temperature (<5℃), the R_2 amplitude remained comparatively greater than that of unheated retinas or that of retinas heated at 40℃.2. When the retina was treated with 5% glutaraldehyde phosphate buffer solution, the R_2 was completely abolished and R_1 alone remained, whether or not the retinas have been heated at 47℃. Only treatment with phosphate buffer solution (not containing glutaraldehyde) could both R_1 and R_2 be recorded.

1.在低温条件下,记录蛙离体视网膜的ERP,所得结果如下:未经加温处理过的及用400℃处理过的视网膜,在低于50℃的环境中记录到的ERP,与在室温(150℃)环境下记录到的ERP相比较,R_1略有增大,而R_2却明显减小。用47℃处理过的视网膜,在低于50℃的环境中记录,R_2的振幅值仍然较大,要比未经加温处理或经40℃处理者大4.5倍。2.用5%戊二醛磷酸缓冲溶液浸泡过的蛙视网膜,在室温条件下记录ERP时,不论是未经加温处理过的,还是事先用47℃处理过的蛙视网膜,都可使R_2消失,而只保留R_1。若用不含戊二醛的磷酸缓冲溶液浸泡蛙的视网膜,记录到的ERP,R_1和R_2都保留。

Isolated frog retinas were kept for 10 minutes at various temperatures, then cooled to the ambient temperature (about 16℃) and ERP was elicited with flash stimulation. The results showed that R_2 amplitudes underwent different changes with retinas treated at different temperatures. It was not until above 40℃ that the R_2 amplitude began to show enhancement. R_2 increased when the temperature was raised to above 40℃ and remained so till the temperature rose above 50℃. The augmentation of R_2 amplitudes...

Isolated frog retinas were kept for 10 minutes at various temperatures, then cooled to the ambient temperature (about 16℃) and ERP was elicited with flash stimulation. The results showed that R_2 amplitudes underwent different changes with retinas treated at different temperatures. It was not until above 40℃ that the R_2 amplitude began to show enhancement. R_2 increased when the temperature was raised to above 40℃ and remained so till the temperature rose above 50℃. The augmentation of R_2 amplitudes was partioulary marked at 47~48℃, the R_2 amplitude rising to 2.57 times that for retinas without treatment. But when the temperature was raised above 50℃, the R_2 amplitude decreased and went below the average for the control group. At 58℃, R_2 was almost abolished.In addition, these ohanges of R_2 amplitude also depended on the duration of heating, the shorter the duration of heating, the higher the temperature necessary for the same changes of R_2 amplitude. Therefore, with shorter heating times the R_2 amplitude was enhanced, decreased and abolished respectively at relative higher temperatures. The relationship between changes observed in R_2 amplitude of ERP and changes of order and fluidity of the liquid crystals of the lamellar membranes of the visual cell was also briefly discussed.

经不同温度(从30°至58℃)处理的离体蛙视网膜,冷却后在室温(15℃左右)的情况下引导ERP,R_2振幅随处理温度不同而有不同的变化,处理温度不超过40℃,对R_2几乎没有影响,其振幅与对照组相近。用40℃以上至50℃以下的温度处理后,R_2显著加大,尤其是47~48℃处理后,R_2达最大值,为对照组的2.57倍。用50℃及更高温度处理后,R_2又急剧下降,且低于对照值。经58℃处理后,R_2基本消失。此外,这种变化还与处理时间长短有关,若缩短加温时间,则分别需要在更高一些的温度处理,R_2振幅才依次增大、减小和消失。本文对上述变化,从温度影响视细胞外段膜结构液晶态的流动性和有序性的角度,进行了初步的讨论。

 
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