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遗传学

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Experiments of Genetics A is offered in combination with key experiments of Genetics A.

遗传学A实验》是配合《遗传学A》的实验课程。

This is the web page of the Atlas of Genetics and Cytogenetics in Oncology and Haematology.

这是《肿瘤学和血液学的遗传学与细胞遗传学图谱》的网页。

Topics of study include genetic factors in disease, immunogenetics, cytogenetics, and more.

课程包括疾病的遗传因素,免疫遗传学和细胞遗传学等。

On the basis of conventional cytogenetics analysis, FISH analysis technology can promote the positive rate andaccuracy in detecting.

在常规细胞遗传学分析的基础上,选用分子遗传学FISH技术可以明显提高染色体异常的检出率及准确率。

Florescence in situ hybridization, one of the most important molecular cytogenetic techniques, overcomes the main inconvenience in classical cytogenetic methods in solid tumors.

荧光原位杂交是当前分子细胞遗传学最重要的技术之一,克服了实体瘤经典细胞遗传学研究的主要障碍。

In 1937 he was made a member of the Supreme Soviet and head of the institute of Genetics of the Soviet Academy of Sciences.

在二十世纪的几十年的时间里,遗传学曾分为两派;西方遗传学和苏联遗传学

Department of Biological Sciences is primarily dedicated to teaching and research in biology including insect and vertebrate molecular ecology, historical biogeography and population genetics; conservation genetics, crustacean endocrinology, physiology and biochemistry of gametes, vertebrate physiology, systematics, ecology, and zoogeography of freshwater and marine fishes, molecular genetics, reproductive physiology, evolutionary genetics.

生物科学系主要致力于生物学的教学与研究,其研究领域包括昆虫和脊椎动物分子生态学,历史生物地理学和种群遗传学,保护遗传学,甲壳类内分泌学,配子生理生化,脊椎动物生理学,淡水和海洋鱼类系统学、生态学、动物地理学,分子遗传学,生殖生理学等。

To identify whether our previous founding were exist in the series of our newly established cell cultures with the same genetic background and different metastatic potentials, and to make clear what are congenerous and various traits in the chromosomal or DMA sequence levels between these cells, in this study, a combination of conventional G-banding, comparative genomic hybridization, multiplex fluorescence in situ hybridization and arm or locus-specific fluorescence in situ hybridization were used to comprehensively characterize molecular cytogenetics aberrations of the above cell cultures.

为查明我所新建立的这些具有同一遗传背景而又在肝癌的转移潜能上存在明显差异的细胞是否也具有8p的缺失,并弄清它们在其它染色体及其区段的DNA水平上有着怎样的相似和不同,这些相似与不同又有着怎样的意义,本课题联合应用G显带技术、比较基因组杂交技术、多重荧光原位杂交技术和位点或臂特异荧光原位杂交技术,对上述细胞进行细胞及分子遗传学研究,以期了解其分子细胞遗传学异常的特征、找出转移相关的遗传学标记,为探讨肝癌转移机制提供材料。

Methods Totally 173 patients diagnosed as MDS according to FAB or WHO criteria with complete clinical and cytogenetical data were included in this reseach.

方法应用骨髓细胞短期培养法和染色体G显带技术,部分病例联合应用荧光原位杂交技术,对42例细胞遗传学检查具有+8异常克隆,16例具有-7/7q-异常克隆,以及55例虽然经常规细胞遗传学检查未检出异常克隆,但是骨髓涂片原始细胞≥0.10,按照FAB或WHO标准既往诊断为MDS的病例进行了临床及血液形态学和细胞遗传学的系列研究。

Methods Totally 173 patients diagnosed as MDS according to FAB or WHO criteria with complete clinical and cytogenetical data were included in this reseach. Among them 42 had +8 chromosome aberration, 16 had -7/7q-, and 55 had normal karyotypes and more than 0.10 blast cells in the bone marrow. Short term culture and G-banding techniques and in some specimens fluorescence in situ hybridization method were used to do chromosome analysis.

方法应用骨髓细胞短期培养法和染色体G显带技术,部分病例联合应用荧光原位杂交技术,对42例细胞遗传学检查具有+8异常克隆,16例具有-7/7q-异常克隆,以及55例虽然经常规细胞遗传学检查未检出异常克隆,但是骨髓涂片原始细胞≥0.10,按照FAB或WHO标准既往诊断为MDS的病例进行了临床及血液形态学和细胞遗传学的系列研究。

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