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Chelerythrine (20 μM), a potent selective PKC inhibitor, also blocked the facilitation of NMDA/glycine-induce currents by sar-SP.

蛋白激酶广谱拮抗剂H-7(5 μM)有效地阻断sar-SP对NMDA/glycine诱发电流的加强作用;同样地,PKC选择性拮抗剂chelerythrine(50 μM)也完全阻断这一易化作用。

It helps in blocking the nervous impulse due to presence of cholinergic blocking .

它有助于在阻断神经冲动,由于在场的胆碱能阻断

Yesterday, in Qushan, a stricken area, Wen Jiabao told Hong Kong reporters,"It is possible to move a mountain, but not to shake the Chinese people's determination to carry out relief work. It is possible to stop a river, but not to repress the compatriotic love Hongkongers and mainlanders have for one another."

温家宝昨日在曲山镇赈灾现场接受香港记者访问时说:「山可以移动,但动摇不了广大人民抗震救灾的决心;水可以阻断,但阻断不了香港和内地的同胞之情。

Our results have shown that the analgesic effect of morphine administered to nucleus accumbens was blocked by intra-habenula injection of naloxone or ME antiserum, whereas the analgesic effect of morphine injected into habenula was attenuated by intra-PAG administration of naloxone or muscimol, and enhanced by bicuculline methochoride (BMC, an antagonist of GABA receptor).

本工作实验结果表明,在伏核内注射吗啡产生的镇痛作用可被缰核内注射NX或ME抗体所大部阻断,而缰核内注射吗啡产生的镇痛作用又可被PAG内注射NX或γ-氨基丁酸受体激动剂异鹅羔胺所削弱,被GABA受体阻断剂氯甲基荷包牡丹碱所增强。

Results are as followed:1 Exposure of HELF cells to BP caused c-Jun activation,and increased the activity of MAPK,PI-3K,p53 and cyclin D1 pathway.2 BP-induced c-Jun activation was inhibited by dominant negative mutants of extracellular signal-regulated protein kinase or c-Jun NH_2-terminal kinase,but not by p38,impling that JNK and ERK pathways medicate c-Jun activation induced by BP.3 Overexpression of dominant-negative mutants PI-3K and Akt potently blocked phosphorylations of c-Jun and ERK,but not JNK in response to BP,suggesting that PI-3K/Akt pathway positively regulates BP-induced c-Jun activation through ERK.4 Inhibition of p53 by its chemical or molecular inhibitor markedly increased the phosphorylation levels of c-Jun,Akt and ERK upon BP stimulation,indicating that p53 negatively medicates BP-induced c-Jun activation through PI-3K/Akt/ERK pathway.5 The cell lines expressed TAM67 exhibits no significant affecting normal cell growth properties.6 TAM67 was able to significantly block G_1-S transition and subsequent cell proliferation,suggesting that c-Jun is essential for cell cycle alternations elicited by BP.7 Overexpression of TAM67 impaired BP-induced cyclin D1 activation,decreasing expression of E2F1 and pRb,indicating that c-Jun participates in the modulation of BP-induced activation of cyclin D1/pRb/E2F1 pathway.8 Stably expression of TAM67 led to the increases in the expression levels of p53 and p21,elevating phosphorylation level of p53,clearly indicating that c-Jun regulates p53/p21 pathway activation induced by BRCollectively,PI3K/Akt/ERK pathway mediated BP-induced c-Jun activation through p53-dependent mechanism.

结果显示:1BP刺激细胞可促进c-Jun活化,并伴随着MAPK、PI-3K、p53和cyclinD1通路各组成成分的活性增强。2利用MAPK通路的显性失活突变体分别阻断细胞外信号调节激酶和c-Jun氨基末端激酶活性,均可明显抑制BP诱导的c-Jun活化,但阻断p38活性对BP引起的c-Jun活化无明显影响,提示JNK和ERK通路参与调控BP诱导的c-Jun活化。3过表达PI-3K和Akt的显性失活突变体也可显著抑制BP诱导的c-Jun活化,并降低磷酸化ERK的表达水平,但对磷酸化JNK的表达水平无明显影响,说明PI-3K/Akt通路通过ERK正性调控了BP诱导的c-Jun活化。4p53的化学/分子抑制剂能使BP作用的细胞内c-Jun活性明显增加,并同时诱导Akt和ERK的磷酸化水平的升高,表明p53可通过PI-3K/Akt/ERK通路对BP诱导的c-Jun活化进行负性调控。5随后观察转染细胞的生长情况,发现TAM67对细胞正常生长和形态无明显影响。6稳定表达TAM67可有效抑制BP诱导的S期细胞数的增加,提示c-Jun在BP致细胞周期改变的过程中发挥了重要作用。7TAM67过表达能够抑制BP诱导的cyclin D1活化,降低磷酸化Rb以及E2F1蛋白表达水平,表明c-Jun参与调控BP诱导的cyclin D1/Rb/E2F1通路的活化。8过表达TAM67可使BP刺激的细胞中p53、p21总蛋白以及p53磷酸化的表达水平明显升高,可见c-Jun也参与调控BP诱导的p53/p21通路活化。

Thus, a vanadate inhibitable event , presumably a phosphotyrosine dephosphorylation event, was required for the initiation of differentiation process.

在用DEX,M1X和insulin诱导3T3-L1前脂肪细胞分化过程中,酪氨酸磷酸酯酶专一性抑制剂Vanadate则能有效阻断细胞分化的进程,但这种阻断是有时间限制的。

Seauckthorn juice can be appropriate drinks afer the diluting, which could block the N-nitroso Synthesis and also can block N-dimethylnitrosaminewhich can lead to cancer.The flavone of Seabuckthorn contains coumarin, isocoumarin, furan coumarins, lignin, as well as bitter polyphenols, 5 - serotonin, which are benefited for anti-cancer.

沙棘汁经稀释成宜引用的浓度后,能阻断N-亚硝酸的合成,另外沙棘汁对致癌物N二甲基亚硝胺也有阻断与防护的作用;沙棘黄酮中含有香豆素,异香豆素,呋喃香豆素,苦木素以及多酚类,5-色胺等具有综合抗癌作用的成分。

Robertson and his colleagues discovered that isothiocyanates may block the activity of Akt3 protein, which is overactive in approximately 70% of melanoma tumors and thought to promote tumor growth by preventing cell death.

Robertson和他的同事发现了异硫氰酸盐类可能阻断Akt3蛋白的激活,Akt3蛋白可以激活接近70%的黑色素瘤而且通过阻断细胞死亡来促进肿瘤的生长。

The inhibitory effect of GABA could be blocked by GABAAreceptor antagonist bicuculline bicuculline methiodide and Cl- channel blocker picrotokin.

GABA的抑制效应大部分可被GABAA受体选择性拮抗剂荷苞牡丹碱甲基碘化物和Cl-通道阻断剂印防己毒素所阻断,而单独灌流BMI和PTX对RVLM神经元主要起兴奋作用。

WT5"HZResults [WT5"BZ]Peilan increased the resting tension of longitudinal and cicular muscule of fundus and longitudinal of bodys.atropine and hexamethonium inhibited the effect of peilan Partially.

结果 佩兰增高胃底纵、环行肌条和胃体纵行肌条的张力。阿托品和六烃季胺分别阻断佩兰增高胃底纵、环行肌张力的作用;佩兰增高胃体纵行肌张力的作用可被六烃季胺阻断

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