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Objective: To establish the model of inbred strain rat heart heterotopic transplantation.

目的:建立近交系大鼠同种异位腹腔心脏移植动物模型。

METHODS: Models of segmental heterotopic small intestine transplantation were established using three sleevelet vascular anastomosis.

采用三袖套血管吻合法建立大鼠节段性异位小肠移植模型。

METHODS: Heterotopic heart transplantations of male SD rats were performed by using Onos method with modifications of preparation of recipient, donor cardiectomy and vascular anastomosis.

对传统Ono术式的受体准备、供心切取和吻合方法等环节进行改进,采用此改良方法建立SD大鼠的腹部异位心脏移植模型。

METHODS: Heterotopic heart transplantations of male SD rats were performed by using Ono s method with modifications of preparation of recipient, donor cardiectomy and vascular anastomosis.

对传统Ono术式的受体准备、供心切取和吻合方法等环节进行改进,采用此改良方法建立SD大鼠的腹部异位心脏移植模型。

Objective To investigate the condition about cell differentiation and distribution in the super-thin epidermal graft, confirming the existence of phenomenon of cell ectopy during wound repair.

目的:了解超薄表皮片移植中干细胞的分化和分布的状况,初步探讨创面修复过程中细胞异位现象的存在。

Objective: To establish an improved heterotopic cardiac transplantation model in rats.

目的:建立一种更加方便、稳定的大鼠异位心脏移植模型。

Objective:To develop a abdominal heterotopic heart transplantation model in rats by using improved methods.

目的:探讨大鼠腹腔异位心脏移植模型的改进方法。

RESULTS: Of the 105 cases receiving heterotopic abdominal cardiac xenotransplantation, complete success was achieved in 95 cases.

结果:共实施105例异位腹部异种心脏移植模型,95例成功。

Aim: To improve the technique of abdominal heterotopic heart transplantation in rats.

目的:探讨大鼠腹腔异位心脏移植Ono术式的改进。

Objective To explore the role of donor specific blood transfusion and FK506 on heterotopic cardiac transplantation in rats.

目的 探讨FK506和供体特异性输血在大鼠异位心脏移植中的作用。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。