• Method: SD rats 30, which were divided into the fast decompression group, HBO exposure group and normal control group.

    方法:SD大鼠30只,随机分为快速减压组、高压氧暴露组和正常对照组。

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  • Methods All 72 male SD rats were randomly divided into stress and control group.

    方法将72只SD雄性大鼠随机分为对照组和应激组。

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  • For experimental group, in vitro cultured skull osteoblast from the male infant SD rats was transplanted into the osteoporotic fractured area of SD female rats.

    实验组将SD雄性乳鼠颅骨体外培养的成骨细胞移植到SD雌性鼠骨质疏松性骨折部位。

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  • Second, this paper establishes a SD model for Guangxi Beibu Gulf port group logistics system using of empirical research method, survey research method, simulation method.

    第二,运用实证研究法、调查研究法、仿真模拟法建立了广西北部湾港口群物流系统SD模型。

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  • Totally 30 SD rats were assigned randomly into sham-operation group, model group and DCBI group with 10 rats in each group.

    取30只SD大鼠随机分为假手术组、模型组和小牛血去蛋白注射液组3组,每组10只。

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  • Methods The male SD rats were divided into normal group, model group and positive drug group, extract group and remainder group.

    方法雄性SD大鼠随机分为正常对照、模型、阳性药、提取物及提取剩余物组。

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  • MethodThe male SD rats were divided into hypoxia stress group and control group (with 8 animals in each group).

    方法雄性SD大鼠分为低氧应激组和正常对照组(每组各8只)。

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  • Methods The 30 male SD rats were randomly assigned to sham operated group, ischemia-reperfusion group and TPM treated group.

    方法将健康30只雄性SD大鼠随机分为假手术组、缺血再灌注组和TPM干预组。

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  • Methods: selected 88 healthy SD male rats, 8 were selected randomly as group a, which was normal group.

    方法:将健康的SD雄性大鼠88只随机分为正常对照组(A组,8只)和造模组。

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  • Methods:44 SD rats were divided into the normal group (13 rats) and the osteoporotic model group (31 rats).

    方法:SD大鼠44只,随机分为正常组(13只)和骨质疏松模型组(31只)。

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  • Methods 72 SD rats were divided into three groups randomly. (empty group, control group and trial group).

    方法SD大鼠72只,随机分为治疗组、对照组及空白组。

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  • METHODS: The male SD rats were randomly and equally divided into injury group and treatment group.

    将雄性SD大鼠随机数字表法分为球囊损伤组和治疗组。

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  • Methods The SD rats in normal group were fed with basic forage and in hyperlipemia model group with high fat forage.

    方法以喂基础饲料方法建立SD大鼠正常组,以喂高脂饲料方法建立高脂血症大鼠模型。

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  • SD rats were randomly assigned to five groups as follows: saline control group, D-galactose group, DHEA-treated normal group, vehicle control group and DHEA-treated senescent group.

    衰老模型实验:SD大鼠随机分为对照组、D-半乳糖组、正常用药组、溶媒对照组和药物治疗组。

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  • Methods 45 female SD rats at 3 months were randomly divided into control group (group 1), tendency group (group 2) and experiment group (group 3).

    方法:采用3月龄SD雌性大鼠45只,随机分为正常对照组(1组)、去势组(2组)和实验组(3组)。

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  • MATERIALS AND METHODS: SD rats were divided into 6 groups (18 animals per group).

    材料与方法:将SD孕鼠随机分为6组,每组18只。

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  • The SD of mitral and tricuspid annuli were more lower than control group (P<0.01), and E velocity of mitral flow is higher (P<0.01) .

    患者较正常对照组心脏二尖瓣环、三尖瓣环下移距离显著减小(P<0.01),二尖瓣E波最大流速显著增大(P<0.01);

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  • Methods: SD rats were divided into control group, chronic visceral pain group and model with ea group, 6 rats in each group.

    方法:SD大鼠随机分成正常对照组,慢性内脏痛模型组和模型加电针组,每组6只。

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  • Methods SD rats were divided into 6 groups: 10-days morphine dependent group and its control, 30-days morphine dependent group and its control, detoxification group and its control.

    方法将SD大鼠分为6组:吗啡依赖10天组,吗啡依赖10天对照组,吗啡依赖30天组,吗啡依赖30天对照组,脱毒组,脱毒对照组。

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  • Method: 14 SD rats were randomly divided into the THD treatment group, control group and model group.

    方法:将14只SD大鼠随机分为中药组(通降和胃方组)、正常对照组、模型组。

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  • MethodsHealthy SD rats 40, half male and half female, were randomly divided into normal group, sham-operated group, model group, electro-acupuncture group.

    方法取健康SD大鼠40只,雌雄各半,随机分为正常组、假手术组、模型组、电针组。

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  • Methods 40 healthy male SD rats were randomly divided into the high-fat diet group, the DM control group and the normal group.

    方法:40只健康雄性SD大鼠随机分为高脂组、糖尿病对照组、正常组。

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  • Methods 12 male SD rats were randomly divided into control group and endotoxin group.

    方法将12只雄性SD大鼠随机分为对照组和内毒素组。

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  • Methods: Forty SD rats were randomly divided into five groups: control group, model group and three DWN-treated groups.

    方法:40只SD大鼠随机分为正常对照组、模型组和胆胃宁低、中、高剂量组共5组。

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  • Methods SD rats were divided into model group and normal group. CAG model was established according to the related literatures.

    方法将SD大鼠随机分为正常对照组和造模组,参照文献制造CAG模型;

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  • Methods The SD rats were randomly divided into two groups: control group and diabetic group.

    方法将SD大鼠随机分为对照组和糖尿病组。

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  • Abstract: 60 SD rats were randomly divided into normal control group, model control group, Se-enriched Ganoderma lucidum treatment group.

    摘要:60只SD大鼠随机分为正常对照组、模型对照组、富硒灵芝治疗组。

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  • Methods 24, female, SD rats were divided into 3 groups: normal group, end-to-end group, end-to-side group.

    方法雌性SD大鼠,共24只,实验分3组,分别为正常对照组、端端缝合组和端侧缝合组。

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  • METHODS The SD rats were randomly divided into control group, model group, high-dose tetramethylpyrazine group, low-dose tetramethylpyrazine group and GSH group.

    方法SD大鼠,随机分为对照组、模型组、川芎嗪大剂量组、川芎嗪小剂量组、古拉定组。

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  • METHODS The SD rats were randomly divided into control group, model group, high-dose tetramethylpyrazine group, low-dose tetramethylpyrazine group and GSH group.

    方法SD大鼠,随机分为对照组、模型组、川芎嗪大剂量组、川芎嗪小剂量组、古拉定组。

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