2) chromosome 17
17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。
3) Chromosome 9
9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。
4) Chromosome 8
8号染色体
1.
Study of Microsatellite Instability and Loss of Heterozygosity on Chromosome 8 in Leukemia;
白血病患者8号染色体微卫星不稳定性和杂合性缺失的研究
2.
Objective: To detect the status of loss of heterozygosity (LOH) on chromosome 8 in prostate carcinoma and high grade prostatic intraepithelial neoplasia (PIN).
目的 :分析原发性前列腺癌及高级别前列腺上皮内肿瘤 (PIN) 8号染色体等位基因杂合性缺失 (LOH)并探讨其意义。
3.
Methods Interphase FISH using Spectrum Red labeled chromosome 8 centromere specific probe was carried out to detect trisomy 8 in 59 cases of ALL and 8 normal controls.
方法 采用荧光素SpectrumRed直接标记 8号染色体着丝粒探针 ,检测了 5 9例ALL病例和 8例正常对照组骨髓细胞 ,并与细胞遗传学 (CG)结果相比较。
5) trisomy 8
8号染色体三体
1.
Clinical and experimental study of 38 cases with trisomy 8;
8号染色体三体38例临床及实验研究
2.
To evaluate the impact of trisomy 8 on cytobiological and clinical features of acute myelomonocytic and monocytic leukemia (M_4, M_5), a total of 56 cases of acute myelomonocytic and monocytic leukemia were investigated.
为了探讨8号染色体三体(8三体)对急性粒单、单核细胞白血病(M4、M5)细胞生物学及临床特征的影响,应用G显带或R显带技术及流式细胞仪对56例M4、M5患者进行核型及免疫表型检测,并对其临床特征进行回顾性分析。
3.
This study was purposed to characterize the first case of acute promyelocitic leukemia (AML-M_3a) with t(15;17) , trisomy 8 and tetrasomy 8,and explore its characteristics of morphology,cytogenetics,molecular biology,immunology and clinical features.
本研究报道首例伴有 8号染色体四体 (四体 8)、8号染色体三体 (三体 8)异常的t(15 ;17)急性早幼粒白血病 (AML M3 a) ,并探讨其形态学、细胞遗传学、分子生物学、免疫学及临床特点。
6) derivative chromosome 9
衍生9号染色体
1.
Application of dual-color fluorescence in situ hybridization to study on deletions of derivative chromosome 9 in chronic myelogenous leukemia.;
应用双色荧光原位杂交检测慢性粒细胞白血病衍生9号染色体缺失的研究
2.
To investigate the frequency of derivative chromosome 9 [der(9)] deletions in patients with chronic myelogenous leukemia(CML),karyotype analysis in 138 patients with CML was performed with R-banding technique,and dual fusion fluorescence in situ hybridization(FISH)was used to detect der(9)deletion.
为研究慢性髓系白血病(CML)患者衍生9号染色体[der(9)]部分序列缺失情况,对138例CML患者的骨髓应用R显带技术进行核型分析,并应用bcr-abl1双色双融合DNA探针荧光原位杂交(FISH)检测der(9)部分序列缺失。
补充资料：21号染色体部分缺失综合征
21号染色体部分缺失综合征
病名。即21q-综合征。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条