1) loss of heterozygosity
杂合性缺失
1.
Identification of some macrosatillite sites of chromosome 19 in primary gastric carcinoma with loss of heterozygosity;
19号染色体微卫星杂合性缺失与原发性胃癌的临床关系
2.
Analysis of loss of heterozygosity in tk gene of L5178Y mouse lymphoma cells induced by colchicine and vincristine;
秋水仙碱和长春新碱诱导L5178Y小鼠淋巴瘤细胞tk基因杂合性缺失分析
3.
Study of loss of heterozygosity and microsatellite instabilities of fragile histidine triad gene in gastric carcinoma;
胃癌FHIT基因杂合性缺失及微卫星不稳定性的研究
2) LOH
杂合性缺失
1.
Study on 10q23 LOH and Both Mutation and Expression of PTEN Gene of the Oesophageal Squamous Cell Carcinomas in Chinese Population;
中国人食管癌10q23杂合性缺失和PTEN基因突变及表达研究
2.
Methods PCR-denaturing polyacrylamide gel electrophoresis-silver staining method was used to detect LOH of three mic- rusatellite locus located in the WWOX gene site of 31 breast cancer tissues.
目的检测乳腺癌组织中WWOX基因的杂合性缺失(LOH)状况及WWOX蛋白的表达状况,并探讨其与乳腺癌临床病理参数之间的关系。
3.
Objective:To detect the loss of heterozygosity(LOH) of ING1 gene microsatellite and the expression of p33ING1b protein in lung carcinoma and to investigate their association with the carcinogenesis of lung cancer.
目的:检测肺癌中抑癌基因ING1微卫星杂合性缺失(LOH)及其主要蛋白产物p33ING1b的表达情况,以探讨ING1基因改变与肺癌发生发展的关系。
3) LOH
杂合性缺失(LOH)
1.
Studies show that loss of heterozygosity (LOH) on multiple genetic LOH in clear cell renal carcinoma in 10 genetic locus and to find clues for tumor suppressor genes associated with cc-RCC.
本研究检测肾透明细胞癌等位基因杂合性缺失(LOH)情况,为寻找与肾透明细胞癌相关的抑癌基因提供线索。
2.
Objective:To compare the LOH rate of allelomorphic gene on chromosome 9 at the identical district and site between esophageal squamous carcinoma and cervical squamous carcinoma to explore the related anti-oncogene in common.
目的:比较食管和宫颈鳞状细胞癌组织中9号染色体相同区域七个微卫星位点的等位基因杂合性缺失(LOH)率,探寻与两种鳞癌发生、发展共同相关的抑癌基因。
5) 1p loss of heterozygosity
1p杂合性缺失
1.
Objective To set up the clinical examination method for 1p loss of heterozygosity(LOH).
目的建立临床检测少突胶质细胞瘤1p杂合性缺失的手段。
6) loss of heterozygosity
杂合缺失
1.
Loss of heterozygosity of chromosome 22 in sporadic colorectal carcinoma;
散发性结直肠癌22号染色体等位基因杂合缺失
2.
Methods: Mutation in exon 3 of β-catenin gene and mutation cluster region of APC gene, loss of heterozygosity and methylation status of promoter 1A of APC gene in breast cancer and normal tissue around tumor were detected by polymerase chain reaction-single strand conformation polymorphism, microsatellite analysis and methylation specific PCR.
方法:应用PCR-SSCP、微卫星标记、甲基化特异性PCR方法检测乳腺癌和癌旁正常乳腺组织中β-catenin基因外显子3和APC基因突变密集区突变、APC基因杂合缺失(LOH)和启动子1A区甲基化状态,用RT-PCR检测APC基因mRNA表达;并用免疫组织化学法检测APC和β-catenin蛋白表达。
3.
Objective Loss of heterozygosity (LOH) of tumor suppressor gene(TSG) is believed to play a key role in carcinogenesis of colorectal cancer (CRC).
目的抑癌基因的杂合缺失(LOH)被认为是结直肠癌形成的通路之一,本实验拟通过对染色体10q23～24区的LOH分析,发现高频杂合缺失区域并筛查与结直肠癌相关的抑癌基因。
补充资料：中枢性感觉缺失
中枢性感觉缺失
central anesthesia
脊髓或脑病变引起的感觉障碍。可分为传导束型(脊髓脑干损伤伤及感觉传导束）、丘脑型(丘脑痛）、内囊型(三偏症）和皮质型(单肢麻木）等不同类型。
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