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Other desmosomal proteins showed variable changes, but signal levels for the nondesmosomal adhesion molecule N-cadherin were normal in all subjects with ARVC.

其它的桥粒蛋白变化多样，但是在所有致心律失常右室心肌病患者的标本中，非桥粒连接分子的N-钙粘蛋白的信号水平都是正常的。

These structures are stable and the C〓 molecule does not desorb from the substrate even at 1000K.

这些吸附结构很稳定，即使温度升高到1000K也不脱附。

Results Bulbus alkaloids easily formed molecular ions(superscript + in MS and dimerized easily in alcohol solution, which did not dimerize in acidity solution. Collision induced dissociation made these alkaloids easily lose a molecule of H2O. The MS spectra of the extracts of five Bulbu Fritillartae species indicated that the major molecular ions were similar to each other, but different varieties showed very different relative abundances of these molecular ions.

结果 在正离子一级质谱中，贝母生物碱易形成带一个正电荷的准分子离子，并且在中性醇溶液中，贝母生物碱易形成二聚体，在酸性介质中则无此现象；二级碰撞诱导解离易使贝母生物碱脱去一分子水；5种贝母对照药材的总生物碱提取液的一级电喷雾质谱图显示，主要分子离子峰基本相同，但因品种不同相对丰度差异较大。

Some bifunctional agents can also cross-link each hemoglobin molecule internally to prevent its breakdown into dimers.

一些双功能试剂也能使每个血红蛋白分子内部交联，以防止分解成二聚体。

When infused into the body, a hemoglobin molecule breaks down into potentially toxic half molecules, or dimmers.

当被注射到体内以后，每个血红蛋白分子会分解成有潜在毒性的半分子，或二聚体。

We first identified new small-molecule enhancers and inhibitors of the cytostatic effects of rapamycin in Saccharomyces cerevisiae.

我们首次确认了rapamycin在酵母中引起细胞抑制效应的小分子增强因子和抑制剂。

We first identified new small-molecule enhancers and inhibitors of the cytostatic effects of rapamycin in Saccharomyces cerevisiae.

我们首先在酿酒酵母中识别雷帕霉素抑制细胞生长的作用的新的小分子增强剂和抑制剂。

The most stable geometry of C78O is the 73, 78-C78O molecule with an epoxide structure.

讨论了电子跃迁性质和73，78-C78O电子光谱的长波吸收峰与母体相比发生蓝移的原因。

Therefore,the researth of immunity molecule and genes correlated with the invision and metastasis of gastric cancer can provide assistants and evidents to early diagnosis and targeted therapy of the invision and metastasis of gastric cancer.

因此，对胃癌侵袭转移相关免疫分子和基因的研究，可以为胃癌侵袭转移的早期诊断和靶向治疗提供帮助和依据。

Highly active, small-molecule furin inhibitors are attractive drug candidates to fend off bacterial exotoxins and viral infection. Based on the 22-residue, active Lys fragment of the mung bean trypsin inhibitor, a series of furin inhibitors were designed and synthesized, and their inhibitory activity toward furin and kexin was evaluated using enzyme kinetic analysis. The most potent inhibitor, containing 16 amino acid residues with a Ki value of 2.45×10~(-9) M for furin and of 5.60×10~(-7) M for kexin, was designed by three incremental approaches.

本论文研究活性多肽类似物的设计、制备和功能，分为四个部分，采用多肽固相和液相合成的方法，分别合成了活性多肽绿豆胰蛋白酶抑制剂Lys片段长链16肽、天花粉胰蛋白酶抑制剂、癌胚抗原肽、甜味肽等一系列类似物，并测定了这些类似物的生物活性，有以下新的研究结果：1、furin酶抑制剂的设计、制备和功能；2、芳香氨基酸芳环之间的π-π共轭能部分补偿二硫键的作用；3、癌胚抗原肽Gly4被L-Pro替代可增加与HLA-A2分子的结合；4、肽键对甜味肽保持甜味是必须的。

You can do some assertiveness training.

你可以进行一些自信训练。

We were well on the path to making a rear-wheel-drive global platform," says Mays."

我们正致力于建立一个后轮驱动的平台，"Mays这样说道。"