Introducetion: in human cytogenetics, the advent of fluorescence molecular techniques has brought forth new procedures for chromosome investigation and diagnosis.
前言：在人类细胞遗传学中，荧光分子技术的出现带来了一些染色体研究和诊断的新方法。
Objective To provide a useful tool based on molecular level for clinical diagnosis and classification by detecting gene products encoded by disease genes of muscular dystrophy.
目的对导致肌营养不良症的基因编码产物进行检测，从分子水平为临床诊断和分型提供依据。
The VHL gene may be useful as a marker gene for the diagnosis of RCC and as a target gene for molecular therapy.
VHL基因可作为临床诊断指标，并可望成为肾透明细胞癌基因治疗的重要目的基因。
Such use of non-invasive imaging to determine unique molecular characteristics of disease could lead to more individualized diagnosis and treatment of patients, according to the researchers.
按照研究人员所说，运用无创成像以确定疾病的分子特征能够导致更多的个体化诊断和治疗。
To investigate the molecular mechanism of th may reveal the pathogenic mechanism of mitochondrial diseases and provide the molecular basis for diagnosis and gene therapy.
TH分子机制的研究将有助于揭示这些线粒体疾病的致病机理以及为其诊断和基因治疗提供分子依据。
These promising diagnostic and prognostic molecular biomarkers as well as therapeutic targets may bring new energy for the diagnosis and management of HCC.
这些有潜在价值的用于HCC诊断和预后的分子标记物和治疗的药物靶点，能够给HCC的诊断和治疗带来新的动力。
Objective To discuss the diagnosis, treatments and the mechanism of the molecular biology for multiple renal cell carcinoma (RCC).
目的探讨多发性肾细胞癌发生的分子生物学机制以及多发性肾细胞癌的诊断与治疗情况。
This assay provided basis for the establishment of rapid and available goat and sheep pox diagnosis methods and for the study of CPV molecular properties.
本试验为羊痘病快速有效诊断方法的建立和CPV的分子生物学特性的研究奠定了基础。
AIM: To investigate the hypermethylation of the BLU and ARF promoter in nasal NK/T cell lymphoma from nasopharyngeal mucosa and its roles in tumor genesis and molecular pathological diagnosis.
目的：检测BLU与ARF基因启动子在鼻NK/T细胞淋巴瘤中的甲基化状态，探讨其在肿瘤发生中的作用与分子病理诊断中的应用价值。
Conclusion the determination of molecular markers of PTS has important value for the diagnosis and treatment of high coagulation state in CHD patients, especially in those with T2DM.
结论PTS分子标志物的检测对冠心病尤其是合并T2DM患者高凝状态的诊断和治疗具有指导意义。
The molecular genetic research on OSA can assist us in understanding the pathogenesis of OSA and promote genetic diagnosis and prevention of OSA.
对OSA的分子遗传学研究可帮助理解OSA的病因和发病机理，并能促进对OSA的基因诊断和预防。
Extracellular RNA is a group of RNA that is bound or free, which can not only play an important role in life, but also be the useful molecular markers for disease diagnosis.
细胞外RNA是存在于细胞外以结合或游离形式存在的一类RNA分子，它不仅在生命过程中起着非常重要的作用，而且可以作为疾病诊断有力的分子标志。
Detection of the low molecular weight RNA associated with the tobacco bushy top disease is the main method of the disease diagnosis.
与病害特异的小分子rna的检测是烟草丛顶病的主要诊断方法。
It is a new way for the study of multidrug resistance of leukemia. RNAi may be a new research tool of molecular diagnosis and molecular therapy on leukemia in the future.
该技术为白血病多药耐药的基础和临床研究开辟了新思路，也为新的分子诊断和分子治疗提供可能。
Recent findings regarding the roles of immunohistochemistry and molecular testing in the diagnosis, prognosis, and personalized treatment of gastric cancer are also reviewed.
免疫组织化学和分子检测在胃癌诊断、预后判断及个体化治疗中作用的最新进展也有所讨论。
With clinical trials and the development of cardiovascular progress in the study of molecular biology, hypotension pathogenesis, diagnosis and treatment of in-depth studies are continuously.
随着临床实验的开展和心血管分子生物学研究的进展，对低血压发病机制、临床诊断及治疗的研究正在不断地深入。
Although clinical management has not received major attention recently, laboratory technology has improved in areas of molecular diagnosis and epidemiology.
虽然近来该病的治疗方面未引起重视，但在分子诊断和流行病学研究方面的实验技术提高了。
Microscopic examination of tumor specimens cannot always predict a cancer's aggressiveness, leading to increased interest in molecular approaches to diagnosis.
肿瘤样本的镜检结果不是总能预测肿瘤的侵蚀性，使用有针对性的分子手段可以增加诊断的正确性。
This is a review of recent research progress in molecular biology of antigens for immunization and diagnosis of cysticercosis.
该文就近年来猪囊尾蚴病免疫和诊断抗原的分子生物学研究进展进行了综述。
The high molecular protein which plays an important role in the cardiovascular disease has an significance to the happen of sudden cardiac death, and even to its diagnosis.
在心血管疾病发病机制中起重要作用的蛋白质大分子，对于心脏性猝死的发生及确诊具有十分重要的意义。
Molecular diagnosis has important significance for development of tumor pathology from morphological to molecular level as it is the main contents and methods of molecular pathology.
分子诊断是分子病理研究的最主要内容和手段，对肿瘤病理学研究由形态学深入到分子水平具有十分重要的意义。
In this review we described the molecular structure, epidemiology, pathogenesis, clinical manifestations, diagnosis, treatment and prevention of parvovirus B19 associated non immune fetal hydrops.
本文就细小病毒B19的生物学特性和感染特征，引起非免疫性胎儿水肿的流行病学，发病机制与临床表现，诊断治疗及预防作一综述。
A small amount of the remaining material is washed and sent for molecular diagnosis; the rest of the sample is saved.
一小部分剩余的标本冲洗下来可用来行分子学检查，保存剩余的标本。
Understand specific molecular mechanisms of this pathway in the process of tumor help provide the basis for clinical diagnosis and the methods for early intervention.
了解这条通路在肿瘤发生过程中具体的分子机制有助于为临床诊断提供依据，为早期干预治疗提供方法。
Conclusion: The alteration of thrombus molecular markers would reveal a higher sensitivity for diagnosis of high coagulation state in DM patients.
结论：血栓分子标志物的检测对DM病人高凝状态的诊断具有很高的临床指导意义。
Conclusions SYT-SSX is a reliable index for the molecular pathological diagnosis of synovial sarcoma.
结论SYT SSX融合基因表达可作为诊断滑膜肉瘤新的分子诊断指标。
TB achieve rapid and early diagnosis of the technical bottlenecks are too little known molecular identity.
实现结核病快速、早期诊断的技术瓶颈问题是已知的分子标识太少。
Methods: Using methods of field epidemiological investigation as well as serological, immunological and molecular-biological diagnosis to determine this outbreak.
方法采用现场流行病学调查的方法并依据血清学、免疫学以及分子生物学实验结果确认。
Therefore, it is of great significance to elucidate molecular mechanisms of CRC metastasis for its diagnosis and treatment.
因此，积极开展结直肠癌转移机制的研究对于结直肠癌的诊治具有十分重要的现实意义。
Therefore, it is of great significance to elucidate molecular mechanisms of CRC metastasis for its diagnosis and treatment.
因此，积极开展结直肠癌转移机制的研究对于结直肠癌的诊治具有十分重要的现实意义。
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