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   jun protein 的翻译结果: 查询用时:0.011秒
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jun protein
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  jun蛋白
     In order to probe into the molecular mechanism of injury in rat hippocampus by methylmercuric chloride (MMC), the effect of MMC on the expression of JUN protein in rat hippocampus was observed using immunocyto-chemical method (the control group was physiological saline of 0.9%, the concentrations of expose groups were 0.05, 0.5, 5mg/kg respectively, the sampling times were 20, 60, 240, 1440min).
     为了探讨氯化甲基汞(MMC)对大鼠海马损伤的分子机制,应用免疫组织化学方法观察了氯化甲基汞对大鼠海马JUN蛋白表达的影响(对照组为0.9%生理盐水、暴露组浓度分别为0.05,0.5,5mg/kg;取样时间分别为20,60,240,1440min).
短句来源
     Effect of intrathecal ω-conopeptide SO_3 on expression of Fos and Jun protein in spinal cord of rats undergoing neuropathic pain
     鞘内注射ω-芋螺毒素SO_3对神经痛大鼠脊髓Fos及Jun蛋白表达的影响
短句来源
     The expression of Jun protein in hippocampus of experimental groups decreased progressively with increasing time of reperfusion(6 h>24 h>72 h).
     各组海马区的Jun蛋白表达随着缺血再灌注时间的延长呈递减趋势(再灌注6 h>再灌注24 h>再灌注72 h)。
短句来源
     The expression of Jun protein in the groups of reperfusion 6 h ranked in the following order: model group >high GP dosage group >low GP dosage group.
     再灌注6 h各实验组的Jun蛋白表达结果是:模型组>GP低剂量给药组>GP高剂量给药组。
短句来源
     Results It was found that the expressions of c-fos ,c-jun mRNA and their proteins could be obviously increased after the stimulating effects of substance P. The expressions of c-fos and c-jun mRNA reached peak level at 1 postburn hour(PBH) and FOS protein at 2 PBH, JUN protein at 3 PBH.
     结果 P物质刺激后c fos、c junmRNA及其蛋白表达增加 ,其中c fos、c junmRNA在刺激后 1h达峰值 ,Fos蛋白在刺激后 2h达峰值 ,Jun蛋白在刺激后 3h达峰值。
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  “jun protein”译为未确定词的双语例句
     The expression of Bcl 2 was lowered, while Bax and c Jun protein were increased.
     Bcl 2减少 ,而Bax与c Jun增加。
短句来源
     To explore the effect of redepolarization(25 mmol/L K +) on c Jun protein in primarily cultured rat cerebellar granule neurons and its underlying mechanism.
     【目的】观察重新去极化 (redepolarization ,2 5mmol/LK+ )对原代培养的大鼠小脑颗粒神经元蛋白质c Jun的影响 ,对去极化挽救神经元过程中c Jun的作用及其调节机制进行初步探讨。
短句来源
     The transcription factor Jun protein was measured by western blot.
     5.Westem blot检测核转录因子Jun的蛋白表达;
短句来源
     The C jun protein decreased at 4 h, but there was still significant difference (P< 0.05 ) and r= 0.626 (P< 0.05 ).
     4h组 ,C jun在炎症细胞内表达减弱 ,但其灰度值与对照组相比 ,差异仍有极显著性意义 (P <0 .0 1) ,亦与鼻分泌量呈正相关 (r =0 .6 2 6 ,P <0 .0 5 ) ;
短句来源
     Ceramide upregulated c_Jun protein expression at 3h, remained elevated at 6h, whereas at 24h c_jun expression decreased.
     c_Jun/AP_1蛋白在神经酰胺处理后3小时开始明显增高 ,持续到12小时 ,24小时下降至基础水平 ;
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  相似匹配句对
     Jun S .
     Jun.
短句来源
     protein.
     protein。
短句来源
     c-Jun protein expression was examined by immunocytochemistry.
     免疫细胞化学检测核转录因子c-Jun蛋白表达情况;
短句来源
     The protein expression of c-Jun was detected by immunocytochemistry.
     免疫细胞化学检测核转录因子 c- Jun蛋白表达水平。
短句来源
     Protein Plastics
     关于蛋白质塑料的研究
短句来源
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  jun protein
There was also a significant increase in c-Jun protein levels and the proportion of c-Jun present in AP-1 DNA binding complexes in hippocampal nuclei after hyperoxia.
      
While NGF somewhat increased c-Fos and c-Jun protein levels transiently, it had a more robust and persistent stimulatory effect on Jun B protein levels.
      
In HL-60 cells treated with 50 μM 18:1/DHA-PE and 200 μM dbcAMP for 24 h, the expression level of c-jun mRNA and c-Jun protein were remarkably elevated compared to cells treated with dbcAMP alone.
      
Moreover, transfected cells expressing high levels of abnormal c-Jun protein exhibited a reduction in the bFGF protein levels compared to parental cells.
      
Immunofluorescence analyses confirmed an increase in Egr-1 and c-jun protein in transgenic cardiomyocytes.
      
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The Fos protein derived from c-fos proto-oncogene has been known to form a heterodimer with Jun protein, which functions as a third messenger to indece the expression of target gene. Immunohistochemical technique was used in the present study to detect and compare Fos and Jun expressed in adjacent sections of the rat superior colliculus (SC) following electroacupuncture (EA) stimulation (2Hz, 1 - 2 - 3 mA, 30min). It was shown that the expression of Fos and Jun in SC was scaty in normal...

The Fos protein derived from c-fos proto-oncogene has been known to form a heterodimer with Jun protein, which functions as a third messenger to indece the expression of target gene. Immunohistochemical technique was used in the present study to detect and compare Fos and Jun expressed in adjacent sections of the rat superior colliculus (SC) following electroacupuncture (EA) stimulation (2Hz, 1 - 2 - 3 mA, 30min). It was shown that the expression of Fos and Jun in SC was scaty in normal animals. EA stimulatin induced a 10 fold inerease in Fos expression and 18 fold increase in Jun expression. The distribution patterns for the two proteins in SC were similar, with the heaviet labeling found in the superficial layer, moderate in the intermediate layer and the lightest in the deep layer. The number of Jun-like immunoreactive neurons doubled that of Fos - like immunoreactive neurons in all levels and subdivisions of SC. SC has been known to be functionally related to vision, although recent studies suggest it may also be involved in nociception. The functional significance of a dramatic expression of Fos and Jun in SC following EA stimulation remains to be elucidaled.

大量资料表明,即刻早期基因产物Fos蛋白与Jun蛋自的诱导表达可以做为神经元活动的标志物。本研究利用免疫组化技术观察并比较外周电针刺激(2Hz,1—2-3mA,30min)后,Fos、Jun样蛋白在大鼠上丘的表达。结果表明,正常大鼠上丘的Fos、Jun表达很低,而电针可使Fos表达增加10倍,Jun的表达增加18倍。Fos、Jun样免疫反应阳性神经元在上丘备层的分布基本相似,均以表层分布最为密集,中间层次之,深层最少。阳性神经元计数结果表明,Jun在上丘各层次及各断面的表达高出Fos约一倍。关于电针刺激上丘表层大量Fos、Jun表达功能意义有待进一步研究。

NIH3T3 cells' total RNA was extracted at various lengths of time after the cells were induced to re-enter the cell cycle from quesent stage by serum stimulation and at G_1,S,G_2 and M phases synchronized by double thymidine block and colcemid block. These samples were then analyzed by dot hybridization to determine the levels of c-fos and c-jun mRNA. Our results show that the peaks of c-fos and c-jun mRNA accumulation were found at 1 h after serum stimulation. Besides,it shows a second c-jun mRNA accumulation...

NIH3T3 cells' total RNA was extracted at various lengths of time after the cells were induced to re-enter the cell cycle from quesent stage by serum stimulation and at G_1,S,G_2 and M phases synchronized by double thymidine block and colcemid block. These samples were then analyzed by dot hybridization to determine the levels of c-fos and c-jun mRNA. Our results show that the peaks of c-fos and c-jun mRNA accumulation were found at 1 h after serum stimulation. Besides,it shows a second c-jun mRNA accumulation peak at 16h after serum stimulation. For the continuous growing cells,c-fos was found to be in low expression in every phases of cell cycle,whereas c-jun was found to have a high level of expression in S phase. These results suggest that in addition to the associated function of c-fos and c-jun in cells which are entering cell cycle ,c-jun protein may play a unique role in G1/S phase which does not need c-fos protein to cooperate with.

NIH3T3细胞经血清刺激由静止期进入G1期,提取该期不同时相细胞的总体RNA,并提取同步化于G1、S、G2和M期细胞的总体RNA,分别与c-fos(2.1kb)和c-jun(1.8kb)基因探针进行斑点杂交。结果显示2个癌基因除了在血清刺激后1h都出现mRNA聚集高峰外,c-jun还在血清刺激后16h时出现第2个聚集峰,生长期细胞在细胞周期各时相均只有c-fos基因的少量表达,而c-jun在S期的表达量明显高于其他各期。说明c-fos和c-jun除了在细胞进入生长周期时发挥基因调控功能外,c-jun还可能在晚G1/S期产生作用,这种作用不需c-fos蛋白的参与。

The Medial Hyperstriatum Ventrale (MHV) and Lobus Parolfactorius (LPO) have been known to be the crucial part in the memory formation process in chick, the former is more important in the stability of memory, the latter is necessary for the store of long-term memory in the chick. The Jun protein derived -from c-fos proto-oncogene has been known to form a heterodimer with Fos protein, which functions as a third messenger to induce the expression of target gene. Immunohistochemical technique was used...

The Medial Hyperstriatum Ventrale (MHV) and Lobus Parolfactorius (LPO) have been known to be the crucial part in the memory formation process in chick, the former is more important in the stability of memory, the latter is necessary for the store of long-term memory in the chick. The Jun protein derived -from c-fos proto-oncogene has been known to form a heterodimer with Fos protein, which functions as a third messenger to induce the expression of target gene. Immunohistochemical technique was used in the present study to detect and compare Jun expressed in HV and LPO of monovisual deprived chick following one-trial passive avoidance task. It was shown that the expression of Jun was scatty in the normal chick: monovisual deprived 2.5 hours, 4 hours or 24 hours induced Jun expression definitely increased in HV and LPO; monovisual deprived hours and 24 hours following one-trail passive avoidance task and memory retention test at 10 minutes and 70 minutes after learning . induced Jun expression continue to increase in HV and LPO; Jun expression in LPO was higher than that in HV.

利用免疫组化技术,观察并比较剥夺一侧视觉及单眼一次性味觉厌恶回避学习后Jun样蛋白在雏鸡HV和LPO的表达,结果表明正常雏鸡HV、LPOJun表达几乎没有,剥夺左眼和单眼视觉学习后均可使Jun样蛋白增高。根据阳性神经元记数结果表明:1.视剥夺2.5、4、24小时后可使Jun样蛋白的表达逐渐增高,而且它们之间的差异显著;2.剥夺左眼2小时和24小时后训练,并分别于10分钟、70分钟记忆保持测验后可看到Jun样蛋白表达继续增多;3。无论单纯视剥夺组还是单眼视觉学习组,各组LPOJun样蛋白的表达均明显高于HV的Jun样蛋白表达,它们之间差异显著。

 
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