17号染色体,chromosome 17英语短句,例句大全

17号染色体,chromosome 17
1)chromosome 1717号染色体
1.The purpose of this study is to investigate the status of p16 gene deletion and chromosome 17 aneuploidy change in EGIST and the relationship with p16 and p53 protein expression, and to analyse the correlation between the three types of multi-drug resistance gene product(P-gp,GST-πand TopoⅡ),to provide valuable reference information for related drug treatment of EGIST after operation.本研究旨在探讨p16基因缺失及17号染色体的非整倍性改变在EGIST中的发生情况,并进一步研究二者的改变与p16、p53蛋白表达之间的关系以及与三种多药耐药基因产物(P-gp、GST-π和TopoⅡ)的相关性分析,为EGIST预后及术后应用相关药物治疗提供有价值的参考信息。
2.Chromosome 17 polysomy was correlated to HER2 protein expression(P<0.目的:比较免疫组织化学法(IHC)、荧光原位杂交法(FISH)与显色原位杂交法(CISH)检测乳腺癌HER2基因状态的一致性,探讨FISH法与CISH法检测乳腺癌HER2基因状态的临床意义、FISH法检测17号染色体多体的发生情况及其意义。

英文短句/例句

1.Study on the Relationship between Microsatellite Abnormity at Chromosome 17 and Lung Cncer17号染色体微卫星异常与肺癌相关性的研究
2.Advance of Studies on Loss of Heterozygosity of 17p and Tumor;第17号染色体短臂杂合性缺失与肿瘤的研究进展
3.Study on the Loss of Heterozygosity on Chromosome 3,7,8,9,17 in Clear Cell Renal Carcinoma肾透明细胞癌3、7、8、9、17号染色体的杂合性缺失研究
4.The Research on the Application of Fluorescence in Situ Hybridization in Chromosome 9 and 17 in Diagnosis of Urinary Bladder Cancer荧光原位杂交在9、17号染色体诊断膀胱癌中的应用研究
5.Transitional cell carcinoma of urinary bladder related loss of heterozygosity of microsatellite loci on chromosomes 9 and 17 in Chinese国人9号和17号染色体膀胱移行细胞癌相关微卫星位点的杂合性丢失
6.Detection and Clinical Implication of Aneuploid of Chromosomes 8,17 and Overexpression of TP53, TOP2A in Gastric Adenocarcinoma;胃癌8、17号染色体异倍体及TP53、TOP2A蛋白过表达与临床病理相关性研究
7.The transgenes were localized on chromosome 8, 1, 17 and 2. The results indicated that transgene APP_SWE were integrated stably into the chromosomes of transgenic mice and could be transmitted to offsprings through germ cells.转基因分别整合在 8号、1号、17号和2号染色体上。
8.The analyisis of genetic effects for pericentric inversions of chromosome 9 in 17 case of children.9号染色体臂间倒位17例患儿的遗传效应分析
9.To Identify the Deletion of Chromosome 13 in 17 Patients with Multiple Myeloma17例多发性骨髓瘤患者13号染色体缺失的检测
10.304 Examples of Chromosome Abnormal and 17 Examples of Chromosome Abnormal Nuclear Type of the First Report in the World;304例染色体异常与17例世界首报染色体异常核型
11.Studies on the Inheritance Law of 13/17 Robertsonian Translocation Chromosomes in the Domestic Pig家猪13/17罗伯逊易位染色体遗传规律的研究
12.The Polymorphisms were diseovered in 13th,14th, 15th, 17th and 18th pairs of chromsomes in Duroc;其中杜洛克猪的第13、14、15、17和18对染色体;
13.Detection of 13/17 Robertsonian Translocation Chromosome Centromeric DNA by FISH in the Domestic Pig家猪13/17罗伯逊易位染色体着丝粒DNA的FISH检测
14.Significance of Monosome 7 or Deletion of the Long Arm of Chromosome 7单体7或7号染色体长臂缺失的意义
15.The chromosome evolution of wild pig and the domestic pig and the applications of 13/17 Robertsonian translocation chromosomes were discussed.本文还讨论了家猪和野猪的染色体进化，13／17 罗伯逊易位染色体的应用。
16.Fingerprinting Analysis on the Homozygous 13/17 Robertsonian Translocation Pig Population by RAPD;13/17染色体易位纯合子猪群随机扩增多态性DNA指纹分析
17.Microdissection and Microcloning of Swine 13/17 Robertsonian Translocation Chromosome;猪13/17罗伯逊易位染色体的显微分离与微克隆研究
18.Polymorphism of 17 Y-chromosomal Short Tandem Repeats Loci in 10 Minority Populations in Guangxi of China广西10个少数民族Y染色体17个STR基因座的遗传多态性

相关短句/例句

chromosome 8,9,178、9、17号染色体
3)chromosome 1818号染色体
4)Chromosome 11号染色体
1.Transcriptional Analysis of Chromosome 1 in Diffuse Large B-Cell Lymphoma;弥漫大B细胞淋巴瘤1号染色体的基因表达分析
2.Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population;中国人群中家族性精神分裂症与1号染色体的连锁分析
3.Objective To explore the molecular genetic relationship between chromosome 1 and quantitative trait loci for familial schizophrenia.目的　探讨家族性精神分裂症的定量性状位点与 1号染色体的分子遗传学关系。
5)Chromosome 99号染色体
1.Genetic Effect of Pericentric Inversion of Chromosome 9;9号染色体臂间倒位的遗传效应研究
2.Genetic polymorphism of 10 STR loci on chromosome 9 and its forensic application in Chinese population;中国人群9号染色体10个STR基因座的遗传多态性及其在法医学中的应用
3.To understand the genetic polymorphism of 10 STR loci on chromosome 9 and reveal the difference on the linkage maps of different populations, the author used a set of nine tetranucleotide ?and one tritranucleotide repeat STR markers on chromosome 9 chosen from Genome Data Bank.18个无关汉族 3代家系共 131份血样采自甘肃省白银地区 ,常规PCR扩增 9号染色体的 10个STR基因座 ,采用非变性聚丙烯酰胺凝胶电泳分析。
6)Chromosome 77号染色体
1.Analysis of Pericentric Inversion of Chromosome 7 Associated with Turner Syndrome in Family;7号染色体臂间倒位伴Turner综合征家系分析(英文)