Detection of minimal residual cells carrying the t(14;18) by DNA sequence amplification.

Detection of minimal residual cells carrying the t(14;18) by DNA sequence amplification.
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通过 DNA 序列扩增检测携带 t(14;18) 的最小残留细胞。

DOI:
10.1126/science.3110950
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发表时间:
1987
期刊:
影响因子:
56.9
通讯作者:
S. Stass
S. Stass
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Ming;K. Chang;F. Cabanillas;E. Freireich;J. Trujillo;S. Stass

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通过聚合酶链反应(PCR)技术,扩增滤泡性淋巴瘤特征性染色体易位t(14;18)(q32;q21)交叉位点两侧的DNA序列。该技术允许检测以1:100,000稀释的携带t(14;18)杂合DNA序列的细胞。1例滤泡性淋巴瘤缓解期患者的骨髓和血液标本经形态学检查和常规Southern印迹分析均未发现t(14;18)异常。而PCR技术检测到t(14;18)杂合DNA序列。因此,该技术是检测携带t(14;18)的最小残留细胞的高度敏感的工具,并且具有鉴定具有亚临床疾病的患者亚群的潜力。
By means of the polymerase chain reaction (PCR) technique, DNA sequences were amplified that flank the crossover sites of a characteristic chromosomal translocation for follicular lymphomas, t(14;18)(q32;q21). This technique permitted the detection of cells carrying the t(14;18) hybrid DNA sequences at a dilution of 1:100,000. The remission marrow and blood samples of a patient with follicular lymphoma and the t(14;18) failed to show any abnormality by morphological examination and conventional Southern blot analysis. However, the t(14;18) hybrid DNA sequences were detected by the PCR technique. Thus, this technique is a highly sensitive tool to detect minimal residual cells carrying the t(14;18) and has the potential to identify a subpopulation of patients with subclinical disease.
DOI: 10.1126/science.6093263
发表时间: 1984-01-01
期刊: SCIENCE
影响因子: 56.9
作者:
TSUJIMOTO, Y;FINGER, LR;CROCE, CM
通讯作者: CROCE, CM
非霍奇金淋巴瘤中的循环单克隆 B 淋巴细胞。
DOI: 10.1056/nejm198412063112304
发表时间: 1984
期刊: The New England journal of medicine
影响因子: --
作者:
Smith,BR;Weinberg,DS;Robert,NJ;Towle,M;Luther,E;Pinkus,GS;Ault,KA
通讯作者: Ault,KA
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发表时间: 1986-07-01
影响因子: 11.1
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