1)Chromosome 88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。
英文短句/例句
1.The Study of Microsatellite Alterations on Chromsome 8 in Colorectal Cancer;结直肠癌患者8号染色体微卫星改变的研究
2.Functional Localization of Metastasis Suppressor Gene for Liver Cancer on Human Chromosome 8 and Relation Studies;8号染色体上肝癌转移抑制基因的功能性定位及相关研究
3.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
4.Fluorescence In Situ Hybridization on Bone Marrow Smear in the Detection of Cytogenetic Aberrations of Multiple Myeloma骨髓涂片荧光原位杂交法在检测多发性骨髓瘤细胞8号染色体遗传学异常的应用
5.Evolution of the Isochore Structure on Human Chromosome 18;人类18号染色体同质段的进化研究
6.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。
7.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
8.Detection of Hyperdiploid Malignant Cells in Breas Cancer with a-satellite DNA Probe of Chromosome 8 and Fluorescence in Situ Hybridization;应用8号人染色体α-卫星探针和FISH技术检测乳腺肿瘤中的超二倍体细胞
9.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
10.Aneuploid analysis of chromosomes 3, 8, 10, 20 and Y in esophageal squamous cell carcinoma食管鳞癌3、8、10、20和Y染色体的非整倍性分析
11.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
12.Microdissection and Microcloning of Swine Chromosome 12;猪12号染色体显微切割与微克隆研究
13.Chromosome 1q amplification and multiple myeloma1号染色体长臂扩增与多发性骨髓瘤
14.Analysis on karyotype of Galega orientalis cv. Xinyin No.1新引1号东方山羊豆染色体核型分析
15.Prenatal Diagnosis of Ring Chromosome 15.15号环状染色体综合征的产前诊断
16.simultaneous del(13q) and 14q32 rearrangement in 26.1%.13号和14号染色体异常同时存在的检出率为26.1%;
17.Obtaining and Identification of Chinese Cabbage Alien Addition Lines with Chromosome 3, 6 and 9 of Cabbage;附加甘蓝3号、6号、9号染色体的大白菜异附加系获得与鉴定
18.Study on Chromosome Preparation of Single Blastomere from Mouse 4、8-Cell Stage Embryos;小鼠4、8-细胞期胚胎单卵裂球染色体标本制备的研究
相关短句/例句
trisomy 88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。
3)chromosomes 8p8号染色体短臂
4)chromosome 8 aberration8号染色体异常
5)chromosome 8,9,178、9、17号染色体
6)8 chromosome.8染色体
延伸阅读
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。
