2) skin tissue engineering
皮肤组织工程
1.
Aim To use the epiderm as the seeding cell in the skin tissue engineering, and choose the optimized conditions for the isolation and growth of human epidermal cells in culture.
目的 确定表皮细胞分离培养的最佳条件 ,为进一步将其作为皮肤组织工程种子细胞奠定基础。
2.
Many researches show that MSCs acts very well as seeding cells in skin tissue engineering to repair skin defect in animal models by autotransplantation or allotransplantation into immunodeficiency animals.
从国内外的报道中可以推测MSCs有可能作为皮肤组织工程的种子细胞,参与烧伤创面的愈合。
3) tissue engineered skin
组织工程皮肤
1.
However, the tissue engineered skin have not the physiological function of normal skin because they are absent of skin appendiges, such as hair follicle, sweat gland and sebaceous gland.
组织工程皮肤自发展20多年来取得了很大的进展,目前已有数种组织工程皮肤应用于临床,为大面积烧伤以及和各种原因引起的皮肤大面积溃烂患者带来了福音。
2.
Seeding cells isolated from skin biopsy and natural or synthetic materials are used to construct tissue engineered skin.
组织工程皮肤是目前治疗难治性溃疡、大面积烧伤等皮肤缺损性疾病最有效的方法之一。
4) tissue-engineered skin
组织工程皮肤
1.
Construction of tissue-engineered skin with BMSCs and tissue-engineered acellular dermal matrix;
骨髓间充质干细胞复合组织工程化脱细胞真皮基质构建组织工程皮肤
2.
Experimental research of histological difference between tissue-engineered skin and normal human skin
组织工程皮肤与正常皮肤组织学差异的实验研究
3.
Effect of Rumo Shengji San on Skin Defect After Repair with Tissue-engineered Skin
乳没生肌散对组织工程皮肤修复皮肤缺损的研究
5) tissue engineering skin
组织工程皮肤
1.
Percutaneous penetration of ketoprofen and ketoprofen isopropyl ester through a tissue engineering skin reconstructed with HaCaT cells;
酮洛芬及其异丙酯对HaCaT细胞构建的组织工程皮肤的渗透作用
2.
The progress of study on the biology behavior of epidermal stem cell as the seed cell of tissue engineering skin;
组织工程皮肤的种子细胞——表皮干细胞的生物学行为研究进展
3.
Method of detecting tissue engineering skin viability;
复方壳多糖组织工程皮肤活力测定的研究
6) Tissue engineering skin
组织工程化皮肤
1.
The use of tissue engineering skin in study of percutaneous drug absorption;
组织工程化皮肤在药物经皮吸收研究中的应用
补充资料：皮肤睾丸(卵睾)组织和中期羊水细胞培养
皮肤睾丸(卵睾)组织和中期羊水细胞培养
诊法。染色体检测的细胞培养技术之一。取小块皮肤或性腺，用无菌之含双抗的Ha～nks液清洗数遍后，在无菌条件下将标本剪成05～1mm3小块种入25ml小培养瓶内，倒置，加15～2ml培养液(RPMI1640或TC199等配制的培基，37℃，CO2孵箱内静置培养，24小时后翻瓶，使培养物全部浸泡于培养液内，一周不必翻动。此后每3～5天或视培养基pH值下降即液体转黄时换培养液一次，使培养液保持一定pH值，清澈透亮。一般7～10天培养物即开始生长。待细胞长满后可传代，部分细胞可液氮内保存备用；部分细胞以胰酶消化后加秋水仙素，制作染色体标本及显带分析。羊水细胞培养后染色体标本制备与上类同。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条