查询词典 sd.

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. Then 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只，正常对照组和正常银杏叶治疗组各6只，其余48只采用烧烙法，烙闭大鼠左眼2条浅层巩膜静脉，制作大鼠持续性高眼压模型，从中选出眼压稳定在实验要求水平的大鼠30只，随机分为生理盐水组，治疗A组（每日EGb 50mg/kg）、治疗B 组（每日EGb 100mg/kg）、治疗C 组（每日EGb 150mg/kg）、治疗D 组（每日EGb 200mg/kg），治疗时间为1mo，处死大鼠后做视网膜全层铺片，对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. The n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只，正常对照组和正常银杏叶治疗组各6只，其余48只采用烧烙法，烙闭大鼠左眼2条浅层巩膜静脉，制作大鼠持续性高眼压模型，从中选出眼压稳定在实验要求水平的大鼠30只，随机分为生理盐水组，治疗A组（每日EGb 50mg/kg）、治疗B 组（每日EGb 100mg/kg）、治疗C 组（每日EGb 150mg/kg）、治疗D 组（每日EGb 200mg/kg），治疗时间为1mo，处死大鼠后做视网膜全层铺片，对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只，正常对照组和正常银杏叶组各6只，其余48只采用烧烙法，烙闭大鼠左眼2条浅层巩膜静脉，制作大鼠持续性高眼压模型，从中选出眼压稳定在实验要求水平的大鼠30只，随机分为生理盐水组，治疗A组（每日EGb 50mg/kg）、治疗B 组（每日EGb 100mg/kg）、治疗C 组（每日EGb 150mg/kg）、治疗D 组（每日EGb 200mg/kg），治疗时间为1mo，处死大鼠后做视网膜全层铺片，对RGCL神经元做特异性染色后行神经元计数来评估神经元的情况。

Animals were in normal control group,6animals were in normal treated group (tPNS200mg/kg) The others were cauterized three episcleral vessels and were divided as experimental groups: groupA (50mg/kg), groupB(100mg/kg), groupC(150mg/kg), groupD (200mg/kg)and group treated by normal saline.Rat were sacrificed on schedule.

健康SD大鼠42只，其中6只为正常对照组，6只为正常用药组(三七总皂苷200mg/kg)，其余30只采Akira法，烙闭大鼠右眼上巩膜静脉，制作大鼠持续性高眼压模型，随机分为生理盐水组，量效关系组分别予tPNS 50mg/kg，100mg/kg，150mg/kg，200mg/kg进行治疗一个月。

Amylovora and as a new target applied for molecular detection of Erwinia amylovora.

本研究首次从梨火疫病菌中克隆sd／A基因并作为新靶标应用于该。。。。。。

Objective To investigate estrogen and andro gen on the regulation of gene expression of insulin-like growth factorⅠmRNA in prostatic tissues. Methods IGF-ⅠmRNA was quantitat ively ass essed in BPH and SD rat prostatic tissues using dot blot hybridization technique .

目的 探讨雌、雄激素对列腺中胰岛素样生长因子Ⅰ基因表达的影响方法采用斑点杂交结合图像分析技术，观察药物去势和未药物去势BPH患者前列腺组织以及正常组、去势组、外源性雄激素组、雌激素组鼠前列腺组织中IGF-ⅠmRNA表达情况。

Methods IGF-ⅠmRNA was quantitat ively ass essed in BPH and SD rat prostatic tissues using dot blot hybridization technique .

采用斑点杂交结合图像分析技术，观察药物去势和未药物去势BPH患者前列腺组织以及正常组、去势组、外源性雄激素组、雌激素组大鼠前列腺组织中IGF

Methods IGF-ⅠmRNA was quantitat ively ass essed in BPH and SD rat prostatic tissues using dot blot hybridization technique .

采用斑点杂交结合图像分析技术，观察药物去势和未药物去势BPH患者前列腺组织以及正常组、去势组、外源性雄激素组、雌激素组大鼠前列腺组织中IGF-ⅠmRNA表达情况。

Methods IGF-ⅠmRNA was quantitat ively ass essed in BPH and SD rat prostatic tissues using dot blot hybridization technique .

采用斑点杂交结合图像分析技术，观察药物去势和未药物去势BPH前列腺组织以及正常组、去势组、外源性雄激素组、雌激素组大鼠前列腺组织中IGF-ⅠmRNA表达情况。

Experiment 1, Establishment and evaluation of animal model about athletic estrous cycle dysfunction: Female SD rats were assigned randomly to training and control groups.

因此，本研究所建立的运动性动情周期紊乱动物模型符合过度训练的诊断标准，模型的准确性较高。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。