本研究为分子诊断用于调控新型脱氨氮工艺提供了技术基础。
This study could supply basis for the process control of new ammonia removal technology by using molecular diagnosis.
在很多研究与分子诊断领域,PNA技术已成为一项基本研究工具。
The PNA technology is already used as an essential tool in a wide range of research and diagnostic molecular protocols.
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。
Conclusions SYT-SSX is a reliable index for the molecular pathological diagnosis of synovial sarcoma.
根据分子诊断结果优化了悬浮填料生物膜反应器的工艺参数,提高了脱氨氮效能。
According to the molecular diagnosis results, the operational parameters of the bioreactor were optimized and the ammonia removal efficiency was increased.
不过,带有分子诊断方法的来临,在食物传染疾病爆发里的病毒的角色正开始被理解。
However, with the advent of molecular diagnostic methods, the role of viruses in foodborne disease outbreaks is beginning to be understood.
研究结果在由美国癌症研究协会举办的第一届癌症治疗进展中的分子诊断大会上发表。
Results were presented at the first meeting on Molecular Diagnostics in Cancer Therapeutic Development, organized by the American Association for Cancer Research.
罗氏分子诊断中心的WalterKoch说到“从多个基因标记来诊断是未来的趋势。”
"Looking at multiple markers is the future of diagnostics," says Walter Koch of Roche Molecular diagnostics.
该公司的技术平台也将用于一种新的分子诊断产品的开发以及用于药物研发的药效诊断方面。
The Company's technology platform will also be used to develop a new family of molecular diagnostics products and has applications in pharmacodiagnostics of drug discovery and development.
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。
Although clinical management has not received major attention recently, laboratory technology has improved in areas of molecular diagnosis and epidemiology.
由于临床WES的分子诊断率约为30%,它是一种结束昂贵和耗时的诊断过程的有效方式。
With a molecular diagnosis rate of about 30%, clinical WES is an effective way of ending the expensive and time-consuming diagnostic Odyssey.
目的对3名来自不同家系的肾上腺脑白质营养不良(ALD)携带者所怀胎儿进行产前分子诊断。
Objective To carry out prenatal molecular diagnosis on 3 fetuses from different pedigrees with X-linked adrenoleukodystrophy (ALD).
在基因组DNA水平,应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。
The molecular diagnosis for X linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important.
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。
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.
“我认为所有的其他技术不能很容易地在我们这样一个实验室实施”约翰iafrate博士说,在医院的分子诊断董事。
"I think all the other technologies could not be easily implemented in a lab like ours," said Dr. John Iafrate, director of molecular diagnostics at the hospital.
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。
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.
许多村庄都没有清洁的饮水或基础卫生建设,要谈诊所和医生、现代科技的巫术、例如分子诊断和数位医疗纪录,还真是天方夜谭。
With many villages having no clean water or basic sanitation, let alone reliable access to clinics and doctors, modern wizardry like molecular diagnostics and digital medical records seem irrelevant.
结论对BRMS1基因的深入研究有助于进一步深化对乳腺癌转移的认识,为肿瘤转移的分子诊断和基因治疗提供新的思路。
Conclusion Further studies on BRMS1 may be helpful to understand the metastasis of breast cancer, which may provide a new way for the diagnosis and treatment of breast cancer.
方法:在这次调查中,我们阐述了可实现分子诊断工具的特点,并讨论了在基础设施条件较低的地点置备这些工具所带来的挑战。
Methods: in this review, we describe the characteristics of accessible molecular diagnostic tools and discuss the challenges associated with implementing such tools at low infrastructure sites.
雅培分子诊断事务部的负责人Staffordo'Kelly说,“与肿瘤免疫治疗研究领域中占领导地位的公司合作,这是一个令人兴奋的消息。”
"This is an exciting collaboration with a leading company in cancer immunotherapy research," said Stafford o 'kelly, head of Abbott's molecular diagnostics business.
我们探讨原位分子杂交法诊断尖锐湿疣的敏感性与特异性。
We explore the sensitivity and specificity of in situ hybridization in human papillomavirus in condyloma acuminata tissues.
“这些口袋结构可以被塑造成适合一定的细胞特征,”Shih说,“这样就可以用来设计针对单一类型细胞的药物传输或诊断分子。”
Those pockets could be molded to fit specific cellular features, said Shih, allowing for the design of drug-delivering or diagnostic molecules targeted at a single type of cell.
病人诊断为左下肢DVT,并使用低分子肝素(那曲肝素0·4mL,一日两次)持续治疗两周。
The patient was diagnosed with DVT of the left leg, and low-molecular-weight heparin (nadroparin 0·4 mL, two times per day) was started, lasting 2 weeks.
这些标本可以为与肺癌早期诊断有关的分子标记研究提供丰富的资料。Aberle说。
These specimens will provide a rich resource to validate molecular markers that may compliment imaging to detect early lung cancer, Aberle said.
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。
Introducetion: in human cytogenetics, the advent of fluorescence molecular techniques has brought forth new procedures for chromosome investigation and diagnosis.
这些发现之所以重要是因为它们揭示了精神分裂症的病因,并为临床诊断和治疗干预所需的分子测试提供了第一个要素。
These findings are important because they shed light on its causes and provide a first component to a molecular test to aid in clinical diagnosis and intervention.
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。
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.
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。
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。
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.
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