说明:双击或选中下面任意单词,将显示该词的音标、读音、翻译等;选中中文或多个词,将显示翻译。
您的位置:首页 -> 词典 -> 孕烷受体
1)  Pregnane X receptor
孕烷受体
1.
SD (sprague-dawley) rat(Rattus norvegicus) hepatocytes were treated with clofibrate and the express levels of its PXR (pregnane X receptor) and CYP3A1 (cytochrome P450 3A1) were determined by Western blot and RT-PCR.
安妥明处理SD(sprague-dawley)大鼠(Rattus norvegicus)的原代肝细胞,Western blot和RT-PCR检测孕烷受体(PXR)和细胞色素酶P4503A1(CYP3A1)的表达情况。
2)  pregnane X receptor
孕烷X受体
1.
Genetic variants of pregnane X receptor in Chinese healthy Han;
中国健康汉族人孕烷X受体的基因多态性
2.
Recently identified nuclear receptors,such as the pregnane X receptor,the constitutive androstane receptor,and the vitamin D-binding receptor,play an important role in the induction of metabolizing enzymes an.
近年来一些研究表明,孕烷X受体(pregnane X receptor,PXR)、组成型雄烷受体(constitutive andro-stane receptor,CAR)、维生素D结合受体(vitamin D-binding receptor,VDR)在代谢酶和药物转运蛋白的诱导中扮演着重要角色。
3.
The pregnane X receptor(PXR;NR1I2) is an important component of the body′s adaptive defense against xenobiotics including drugs.
孕烷X受体(pregnane X recep-tor,PXR)是新发现的孤儿核受体(系统名:NR1 I2)。
3)  hPXR
人孕烷X受体
1.
Method: Transient cotransfection reporter gene assays were performed with pCI-hPXR-neo,pGL3-CYP3A4-Luc and β-galactosidase expression plasmid in HepG2 cells.
目的:从中药中筛选通过激活人孕烷X受体(PXR)诱导细胞色素P450 3A4(CYP3A4)转录表达的中药;研究其诱导能力与药物浓度和作用时间之间的关系。
4)  Progesterone receptor
孕酮受体
1.
Effects of Jingqianping granule on expression levels of estradiol receptor alpha and progesterone receptor in hypothalamus of premenstrual syndrome model rats with liver-qi invasion;
经前平颗粒对经前期综合征肝气逆证模型大鼠下丘脑雌二醇α和孕酮受体表达的影响
2.
Research of 5-Aza-2′-deoxycytidine inducing progesterone receptor demethylation;
5-Aza Dc诱导孕酮受体基因启动子脱甲基化可能与DNMT_1表达下调有关
3.
Demethylation of progesterone receptor in leukemia cell line induced by DNMT1 antisense oligonucleotide wrapped in liposome;
脂质体包裹DNMT1反义寡核苷酸诱导白血病细胞株孕酮受体去甲基化的实验研究
5)  PR [英][,pi: 'ɑ:(r)]  [美]['pi 'ɑr]
孕酮受体
1.
Methods The expression of P33ING1b,P53,oestrogen receptor(ER),and progesterone receptor(PR) of 86 primary invasive breast cancers and 19 juxtacancerous tissue were detected with immunohistochemical methods.
方法运用免疫组化方法检测86例乳腺癌标本(乳腺癌组)及19例癌旁正常组织(对照组)中P33ING1b、P53、雌二醇受体(ER)、孕酮受体(PR)的表达情况。
2.
OBJECTIVE:To discuss the effects of Rujieping capsule on estrogen receptor(ER) and progesteron receptor(PR) of pathological tissues in rats with hyperplasia of mammary glands.
目的:探讨乳结平胶囊对乳腺增生大鼠病理组织雌激素受体(ER)和孕酮受体(PR)表达的影响。
6)  progesterone receptor
孕激素受体
1.
Expression of matrix metalloproteinase-2 and progesterone receptor in endometrial carcinoma;
基质金属蛋白酶-2及孕激素受体在子宫内膜癌组织中的表达及其意义
2.
Estrogen and progesterone receptor expressions in 122 cases of paraffin-embeded gastric adenocarcinoma;
胃腺癌雌、孕激素受体检测研究
3.
Effects of progesterone on progesterone receptor c-fos and c-jun expression in MG-63 cells;
孕激素对MG-63细胞株孕激素受体和c-fos、c-jun的影响
补充资料:米那索龙 , 胺乙氧孕烷酮 ,明醇酮,羟胺孕烷
药物名称:明醇酮

英文名:Minaxolone

别名:米那索龙 , 胺乙氧孕烷酮 ,明醇酮,羟胺孕烷
药理作用: 本品麻醉效能强,无镇痛作用。其麻醉发生迅速,用药后10~15秒钟神志消失。作用持续6~84分钟。它对呼吸、循环系统影响很小。
适应症: 可用于全身麻醉诱导或小手术。
用法用量:诱导麻醉时静注一般剂量为0.5mg/kg;最大剂量为1mg/kg。
不良反应: 麻醉过程中可出现兴奋现象。可能发生过敏反应。
规格:注射液,每支5mg(1ml)。


类别:全身麻醉药\静脉麻醉药
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