• 自然界中有一类名为转录因子蛋白调节(升高或者降低)基因活性技术正是基于该机理。

    The technique relies on a natural process by which the activity of genes is raised or lowered by proteins called transcription factors.

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  • 作为活性关键决定因子,端粒酶逆转录酶的调控研究取得了重大进展具体机制清楚

    As a critical factor of telomerase activity, much progression has been achieved in the study of regulation of human telomerase reverse transcriptase, but the detail mechanism is still not clear.

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  • 具体地,本发明显E2-EPF5活性抑制降低VEGF以及其他低氧应答转录因子HIF-1调节蛋白质的产生。

    In particular, inhibition of E2-EPF5 activity is shown to reduce the production VEGF, as well as other proteins regulated the transcription factor HIF-1, in response to hypoxia.

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  • 雌激素反应元件荧光素酶(ERE -LUC)为报告基因通过检测荧光素酶活性来确定MDM2是否ER转录调节因子作用

    The effect of MDM2 on the transcriptional activity of er was detected by the reporter gene containing estrogen responsive elements luciferase (ERE-LUC).

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  • 紫外辐射后第315位丝氨酸发生磷酸化观察到,而且Ser315Ala突变p53能够减少作为转录因子活性17)。

    In vivo phosphorylation at Ser315 has been observed following UV-irradiation, and a Ser315Ala mutant p53 has reduced activity as a transcription factor (17).

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  • 目的探讨表面活性蛋白BSP-B甲状腺转录因子TTF-1新生儿肺透明病中的表达及其意义。

    Objectives To study the expression of surfactant protein B(SP-B)and thyroid transcription factor 1(TTF-1)and evaluate the role in neonatal hyaline membrane disease(NHMD).

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  • 目的探讨甲状腺转录因子1 (TTF 1)表面活性蛋白a、B (SP A,SP B)硬化性血管瘤(PSH)中表达生物学意义

    Objective to investigate the biologic significance of thyroid transcription factor-1 (TTF-1) and surfactant protein a (SP-A) and SP-B expression in pulmonary sclerosing hemangioma (PSH).

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  • 目的探讨内毒素(LPS)诱导急性损伤(ALI大鼠组织甲状腺转录因子-1(TTF-1)、肺表面活性物质相关蛋白-A(SP-A)表达变化

    Objective To investigate the change of the expression of TTF-1 and SP-A in lung tissue of ALI rats induced by LPS.

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  • 前言: 近年来,一些不依赖于转录因子活性新型杂交系统相继建立,分离的泛素系统、 蛋白质片段互补分析阻遏重构分析SOS恢复系统等。

    Some new type of two-hybrid systems, such as split-ubiquitin system, protein-fragment complementation assay, repressor reconstitution assay and SOS recruitment system, have been developed recently.

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  • 1985年Aaron先生发现了一类具有转录因子类似功能新的蛋白;蛋白能够识别特定DNA区域并且结合上去,从而导致基因活性上升或者下降

    In 1985 Sir Aaron discovered a new class of proteins that mimic this function and can recognise specific stretches of DNA and bind to them, boosting the activity of genes or damping them down.

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  • 此外活性增强转录因子- kB被逆转

    Additionally, increased activity of nuclear factor-kB was not reversed.

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  • 此外活性增强转录因子- kB被逆转

    Additionally, increased activity of nuclear factor-kB was not reversed.

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