2) skin precursor tissue
皮肤前体组织
1.
Xenotransplantation model of fetal pig skin precursor tissue;
胎猪皮肤前体组织异种移植模型的研究
3) skin-tissue
皮肤组织
1.
Calculation of thermal effect in skin-tissue induced by laser;
激光辐照皮肤组织的热效应解析计算研究
2.
This paper based on the interaction theory mechanism of laser-biotissue,the 2-D heat transfer model of laser-irradiated invitro human skin-tissue was established.
基于激光与生物组织相互作用的机理,建立了强激光辐照离体人皮肤组织的二维传热模型。
3.
It is found that the thermal damage of skin-tissue irradiated by pulses laser takes place firstly at the center of surface,and the temperature decreases in the z and radial direction.
具有一定强度的激光辐照皮肤组织时可造成组织的破坏。
4) skin tissue
皮肤组织
1.
Feasibility and stability of purification RNA from paraffin-embedded skin tissue and performance of PCR;
石蜡包埋皮肤组织标本中提取RNA进行逆转录PCR的研究
2.
Characterization of thermomechanical behavior of skin tissue:Ⅱ.Viscoelastic behavior;
皮肤组织的热力学行为表征:Ⅱ.黏弹性行为
3.
Characterization of thermomechanical behavior of skin tissue:Ⅰ.Tensile and compressive behavior;
皮肤组织的热力学行为表征:Ⅰ.拉压行为
5) skin
[英][skɪn] [美][skɪn]
皮肤组织
1.
To obtain the mathematical description and the properties of biology skin tissue conduction under various heat condition,a single-layer model and a multi-layer model of skin conduction are established respectively in one-dimensional Cartesian and cylindrical coordinates.
为了获得生物皮肤组织在不同条件下传热特性的数学模型及其传热规律,分别在一维直角坐标系和一维圆柱坐标系下,建立了稳态条件下基于皮肤组织单层结构和多层结构的传热数学模型。
2.
The experiment was aimed to study the correlation of skin deiodinase and cashmere growth and guard hair under natural condition in cashmere goats.
因此,皮肤组织中MD活性与绒山羊绒毛生长的生理过程具有相关关系。
6) tissue engineering artificial skin
组织工程化人工皮肤
1.
Objective To analysis the dynamic change of synthesis and content of collagen which is an extra cellular matrix of tissue engineering artificial skin.
目的检测组织工程化人工皮肤的细胞外基质成分——胶原蛋白的合成和含量的动态变化,为组织工程化人工皮肤的研究提供生物化学依据。
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