peroxisome

[pə'rɒksɪsəʊm]
  • peroxisome
  • n.

    过氧物酶体;

纠错 数据更新时间:2026-06-10 12:02:51
1、

The peroxisome proliferators-actived receptors ( PPAR) are a member of the nuclear receptors.

综述了过氧化物酶体增殖激活受体(PPAR)中α亚型的结构、功能和配体研究的最新进展。

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2、

Peroxisome proliferator-activated receptors increase human sebum production

过氧化物酶增殖活化受体增加皮脂分泌

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3、

Regulatory Effects of Tea Polyphenols on Peroxisome Proliferator-Activated Receptor α and Nuclear Factor-κ B in Alcoholic Liver Disease Models

茶多酚对酒精性肝病过氧化物酶体增殖物激活受体α及核因子-κB的调节作用

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4、

Peroxisome proliferator activated receptor γ ( PPAR γ) is a very important ligand activated nuclear transcription factor, belonging to nuclear hormone receptor superfamily.

过氧化物酶体增殖剂活化受体γ(PPARγ)是一个由配体激活的核转录因子,属于核激素受体(nuclear hormone receptor)超家族。

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5、

Background and Objective: Peroxisome proliferator-activated receptors ( PPARs) are a class of ligand-activated nuclear transcription factor belonging to the nuclear receptor superfamily.

研究背景和目的:过氧化物酶体增殖物激活受体(PPARs)是一类由配体激活的核转录因子,属于核内受体超家族成员。

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6、

Peroxisome proliferator activated receptor γ ( PPAR γ) is aberrantly expressed in pancreatic carcinoma

过氧化物酶体增殖因子活化受体γ在胰腺癌中的表达及其意义

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7、

PPAR ( Peroxisome proliferator-activated receptors), are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily that functions as critical regulators of lipid and energy homeostasis.

PPAR(peroxisome proliferator-activated receptor),即过氧化物酶体增殖剂激活受体,是一类由配体激活的核转录因子,为核受体家族的一员。PPAR在调节脂类代谢及机体能量代谢平衡方面有重要作用。

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8、

AIM: To investigate the effect of rosiglitazone on the binding activity of hepatic nuclear factor-kappa B ( NF-κ B) and the expression of peroxisome proliferator-activated receptor gamma ( PPAR γ) in mice with liver fibrosis caused by schistosoma japonicum infection.

目的:观察日本血吸虫病肝纤维化小鼠肝脏肝组织核因子-κB(NF-κB)的活性和过氧化物酶体增殖物激活受体γ(PPARγ)的表达,及PPARγ配体罗格列酮对其表达的影响。

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9、

Effects of peroxisome proliferators PFOA on immune system of mice

过氧化物酶体增殖剂PFOA对小鼠免疫系统的影响

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10、

Objective: To observe the expression of the peroxisome proliferators_ activated receptor γ( PPAR γ) in colonic mucosa of rat with ulcerative colitis ( UC).

目的:观察溃疡性结肠炎(Ulcerative colitis,UC)大鼠肠黏膜中过氧化物酶体增殖物激活受体γ(PPARγ)的表达。

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11、

Transcriptional Regulation of nephrin Gene by Peroxisome Proliferator-Activated Receptor γ Agonist in Nephridial Tissue in Nephropathy Rats

过氧化物酶体增殖物活化受体γ激动剂对肾病大鼠肾组织nephrin表达的调控

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12、

The results showed that the peroxisome mainly exists in the R-cell of hepatopancreas and the labyrinth epithelium of antennary gland.

过氧化物酶体主要存在于肝胰腺细胞和触角腺的迷路上皮细胞中。

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13、

Objective To study the regulatory ability of peroxisome proliferator-activated receptor γ( PPAR γ) ligands to the inflammatory response in human gallbladder epithelial cells.

目的初步探讨过氧化物酶体增殖体活化受体γ(PPARγ)之配体能否抑制人胆囊上皮细胞的炎症反应。

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14、

Objective: To observe effects of Huatan Huoxue Prescription on expressions of peroxisome proliferation substance activating receptor α ( PPAR α) and the target gene acetyl-CoA oxidase ( ACO) in the liver of the rat with hyperlipemia.

目的:观察化痰活血方对高脂血症大鼠肝脏过氧化物酶体增殖物激活受体α(PPARα)、乙酰辅酶A氧化酶(ACO)表达的影响。

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15、

Aims: To investigate the effect of peroxisome proliferator-activated receptor ( PPAR)-r li-gand rosiglitazone on dextran sulfate sodium ( DSS)-induced colitis of mice.

目的:观察过氧化物酶体增生物激活受体(PPAR)-r配体罗格列酮治疗葡聚糖硫酸钠(DSS)诱导小鼠结肠炎的疗效。

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16、

Peroxisome proliferator-activated receptors ( PPAR ) are a family of at least 3 nuclear receptors ( a, 8 , andy ) .

其中PPARγ在心脏中表达丰富,胰岛素增敏剂噻唑烷二酮类药物是 PPAR γ的合成配体.

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17、

Computational Analyses of MicroRNA Involved in Peroxisome Biogenesis and Proliferation

调控过氧化物酶体生物合成和增殖的microRNA的计算机分析

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18、

Effect of rosiglitazone on the activity of hepatic nuclear factor-kappa B and expression of peroxisome proliferator-activated receptor-γ in mice with liver fibrosis due to schistosoma japonicum infection

罗格列酮对日本血吸虫病肝纤维化小鼠肝组织核因子-κB和过氧化物酶体增殖物激活受体γ表达的影响

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19、

The Mechanism of Reactive Oxygen Species Forming and Clearance in Peroxisome

过氧化物酶体中活性氧的生成与清除机理

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20、

Chemotherapy given in combination with ligands for the peroxisome proliferator-activated receptor-( PPAR) synergistically inhibits the growth of lung and ovarian cancer cell lines.

化疗药物联合过氧化物酶体增殖物激活受体(PPAR)的配体能够协同抑制肺细胞癌及卵巢癌细胞。

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21、

Hormones and nutritional factor can regulate peroxisome proliferation response.

持续的过氧化物酶体增殖可导致肝癌.

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22、

Objective To express the fusion protein of glutathione S-transferase ( GST) and peroxisome proliferator-activated receptor-gamma coactivator-1 ( PPAR γ C1) in E.

目的在大肠杆菌中表达过氧化物酶体增殖物激活受体γ共激活因子-1(PPARγC1)与谷胱甘肽-S转移酶(GST)的融合蛋白,并制备抗PPARγC1的多克隆抗体。

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23、

Aim: To study the expressions of scavenger receptor class B type I ( SR-BI) and peroxisome proliferator-activated receptor γ( PPAR γ) in atherosclerotic mini swine and provide a new mechanism for investigating the pathogenesis of atherosclerosis.

目的:用贵州小香猪建立动脉粥样硬化(As)动物模型,探讨该模型中B类I型清道夫受体(SR-BI)和过氧化物酶体增殖物激活受体γ(PPARγ)表达的变化。

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24、

Objective To construct the target siRNA vector to peroxisome proliferator-activated receptor-γ( PPAR-γ).

目的构建靶向过氧化物酶体增殖活化受体-γ(PPAR-γ)基因的siRNA载体。

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25、

The distribution probability of RS was respectively 88%, 36%, 31.3%, 28% in nucleus, mitochondrial matrix space, microbody ( peroxisome), chloroplast thylakoid membrane.

RS在植物细胞中的细胞核、线粒体基质空间、微体(过氧化物酶体)、叶绿体类囊体膜中的分布概率分别为:88%、36%、31.3%、28%。

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26、

Objective To investigate the expression of peroxisome proliferator activated receptor γ ( PPAR γ) in atherosclerosis.

目的:探讨动脉粥样硬化病变组织中过氧化物酶体增殖激活受体γ(PPARγ)的表达。

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27、

AIM To study the expression peroxisome proliferator activated receptor γ( PPAR γ) in lung cancer cell and the mechnism of PPAR γ activated by ligands inhibiting human lung cancer cell growth.

目的研究肺癌细胞上过氧化物酶体增生物激活受体γ(PPARγ)的表达及其经配体(激动剂)活化后抑制肺癌细胞生长的机制。

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28、

The AD 7 C-NTP protein was predicted to have 3 potential transmembrane domains and locate on peroxisome's membrane.

AD7CNTP基因编码产物具有3个跨膜区,可能定位于过氧化物酶体.

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29、

Rosiglitazone is a peroxisome proliferator-activated receptor γ( PPAR γ) agonists, which can induce apoptosis in non-small cell lung cancer and inhibit non-small cell lung cancer cell invasion and metastasis.

罗格列酮是过氧化物酶体增殖激活受体γ(PPARγ)激动剂,它能够诱导非小细胞肺癌凋亡并抑制非小细胞肺癌细胞侵袭及转移。

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30、

Rosiglitazone belongs to a class of drugs known as peroxisome proliferator-actiated receptor ( PPAR ) agonists.

罗格列酮属于称为过氧化物酶体活化受体 ( PPAR )促效剂一类药物.

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