分子性

Expression analyses identified increased expression of numerous TGF-beta-related genes that regulate cell proliferation and survival and plausibly contribute to myxomatous valve disease.

他们注意到，多数效应器分子的表达增加降低了TGF-β的信号作用，包括可诱导TGF-β的H3基因、内皮素-1、组织抑制因子金属蛋白酶1、致骨形态学发生的蛋白和&调节细胞增生和存活可能还有促进粘液瘤性疾病的基因&。

In D3 gene with 5 site mutations. There exists individual variation in the COII gene, but this variation is less than that among other members of Myzomyia Series such as An. aconitus, An. jeyporiensis, etc. In addition, one haplotype different from both An. minimus A and C was found in these 3 genes studied.②The genetic distance between An. minimus A and An. minimus C is less than that among other members of Myzomyia Series. Molecular trees based on different genes and different methods show that An.

种系发生研究表明，微小按蚊复合体亲缘种A、C间的遗传距离远小于与之近缘的同系其它成员间的距离。2个分子标记3种方法构建的基因树显示，微小按蚊A、C的种系地位非常固定，不同地域来源、不同变异类型的微小按蚊始终在同一分&枝&上，与迈蚊系其它成员相比，呈现其相对稳固的单源性。

Moutains of evidences from laboratary and clinical data show that gene abnormality is the major etiological factor of over 40% patients affected with epilepsy.There were also 6 epilepsy genes been cloned successfully, and mutations of over 1000 genes maybe related to epilepsy. These abnormal genes influence many aspects from molecular level to the neuronal plasticity, such as the development of brain,neuronic degeneration, remodeling of neural circuits, energy metabolism, ion channel and so on.These factors would at last affect the formation of epilepsy focus, propagations of epileptic potentials, vulnerability of epilepsy cells.

大量的实验和临床资料提示基因异常是40%以上癫痫患者的病因，有6种常见全身癫痫的基因已被成功克隆，1000种以上的基因突变可能与癫痫的发作有关，这些表达异常的基因分布在脑发育、神经元变性及神经环路重组、能量代谢、离子通道等多个环节，从分子、细胞、神经元可塑性等多个方面影响着癫痫灶的形成、痫性放电的扩布及癫痫细胞的损伤，构成了癫痫的基因机制。

It was confirmed that the mutation of nonconservative animo acids in DAF could improve the activities of DAF and the positive charges on the surface of DAF were necessary for its binding with

并证实了DAF分子的非保守性氨基酸突变可提高其活性。

Recombinatino polypeptide or chemically synthesized polypeptide antigen is used to immunize the mammal to obtain polyclonal antibody and the nonconservative amion acid sequence of the antiboby to N-terminal with recognition site qBrn-2 of development regulatory protein qBrn-2. The antibody does not recognize other POU structure domain protein, and recognizes specifically qunique protein in Western imprinting experiment. The qBrn-2 expression mode obtained immunohistochemistry process is identical with the resulted height of in-situ molecular hydridization.

以重组多肽或化学合成多肽为抗原免疫哺乳动物获得的多克隆抗体，这一抗体对发育调控蛋白qBrn－2的识别位点为qBrn－2的N－末端的非保守性的氨基酸序列，该抗体不识别其它POU结构域蛋白；在Western印记实验中，该抗体特异地识别单一的蛋白；利用免疫组织化学接示的qBrn－2表达模式与分子原位杂交的结果高度一致。

The lipid peroxidation of S. maxima cultured in the presence of 4 to 100mg Se/L analysed showed that the contents of free radicals by EPR and malondialdehyde increased, of which the latter was the products of lipid peroxidation. These resulted in the decrease of the contents of liposoluble matter and percentage of polyunsaturated fatty acids, and the increase of percentage of saturated fatty acids. Using dimethyl sulfoxide , which was oxidized by OH·to form the stable and nonradical compound, methane sulfinic acid , as a molecular probe, we found that the contents of MSA from S. maxima growing in the presence of selenium were higher than those without selenium added, i. e. selenium in vivo was able to scavenge OH. in this alga.

对4～100mg Se/L范围内培养的S.maxima进行脂质过氧化的分析结果表明，加硒条件下藻细胞EPR自由基的含量与脂质过氧化产物的含量增加，造成细胞脂溶性物质含量和不饱和脂肪酸百分含量下降，以及饱和脂肪酸的百分含量相对上升；使用DMSO作分子探针，用它与OH·的反应产物MSA来表示藻细胞OH·含量，发现加硒条件下藻细胞MSA含量低于未加硒的，即硒在藻细胞内具有清除OH·作用。

Under different initial total egg white lysozyme concentrations in urea solution, the refolding egg white lysozyme intermediates could be deduced to have a tendency to form a bimolecular intermediate aggregate, and this inference was further confirmed by their nonreducing SDS-PAGE and size exclusion chromatography.

当不同浓度蛋白溶菌酶在脲溶液中复性时，蛋白溶菌酶折叠中间体有形成二分子积聚体的趋势，这个推测得到了非还原电泳和体积排阻色谱结果的证实。

Rhinitis ; allergic ; nonseasonal ; Receptors ; neurokinin-1; Molecular biology ; Rat

鼻炎；变应性；常年性；受体；神经激肽1；分子生物学；大鼠

INTERPRETATION: Similar to molecular genetic studies, we showed evidence that schizophrenia and bipolar disorder partly share a common genetic cause. These results challenge the current nosological dichotomy between schizophrenia and bipolar disorder, and are consistent with a reappraisal of these disorders as distinct diagnostic entities.

解释：类似于分子遗传学的研究证实了精神分裂症和双相情感障碍具有部分共同的疾病基因，对当前疾病分类学上这两类疾病的独立分类提出了挑战，有必要对它们显著的和特征性的本质再次进行认识。

Scanning electron microscopy,transmission electron microscopy,circular dichroism and small-angle X-ray diffraction were used to analyze the aggregation mode of CSG in the organogel phase.A hierarchical self-assembly model was proposed to explain the transition from molecular to primary and secondary structure.It is shown from our results that CSG can aggregate into a micellar fibril nanostructure with high length-to-width ratio which is bundled and entangled to form a three-dimensional(3D) network that immobilize the fluid component probably by surface tension.Moreover,sol-gel polymerization of tetraethoxysilane was carried out using CSG in the gel phase.

通过扫描电镜(ScanningElectron Microscopy，SEM)、透射电镜(Transmission Electron Microscopy，TEM)、圆二色谱(Circular Dichroism，CD)和小角X—射线衍射仪(Small-angle X-rayDiffraction，SAXRD)考察CSG分子自组装行为结果表明，CSG形成的聚集体具有多级结构：首先CSG通过手性堆叠自组装形成直径在9—10nm的细纳米纤维，这些细的纳米纤维再以不规则的六方堆积的方式进行排列，构成直径在40—100nm的粗纳米纤维(即细纳米纤维的&捆束&)，最后粗纳米纤维互相粘连形成三维网络状结构，使有机溶剂&固定&，从而形成凝胶；以CSG有机凝胶为模板，四乙氧基硅烷为前体，通过溶胶—凝胶聚合的方法制备了直径大约为100nm的二氧化硅纳米管。3。

The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了，排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意，我建议我们在价格上大家各让一半。