非霍奇金淋巴瘤遗传标记的分子分析

Lynette M. Sholl, Janina Longtine, Frank C. Kuo
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引用次数: 3

摘要

分子分析补充临床和组织病理学工具用于诊断和细分血液恶性肿瘤。克隆抗原受体基因重排的存在有助于确认B细胞或T细胞淋巴瘤的诊断,并可作为该肿瘤的指纹,用于识别不同部位的并发疾病或未来时间点的复发。某些淋巴细胞恶性肿瘤具有特征性的染色体易位,这一发现可能对个体的预后或治疗反应具有重要意义。聚合酶链反应(PCR)通常用于检测抗原-受体基因重排以及可通过荧光原位杂交(FISH)和核型分析补充的特定易位。©2017 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Analysis of Genetic Markers for Non-Hodgkin Lymphomas

Molecular analysis complements the clinical and histopathologic tools used to diagnose and subclassify hematologic malignancies. The presence of clonal antigen-receptor gene rearrangements can help to confirm the diagnosis of a B or T cell lymphoma and can serve as a fingerprint of that neoplasm to be used in identifying concurrent disease at disparate sites or recurrence at future time points. Certain lymphoid malignancies harbor a characteristic chromosomal translocation, a finding that may have significant implications for an individual's prognosis or response to therapy. The polymerase chain reaction (PCR) is typically used to detect antigen-receptor gene rearrangements as well as specific translocations that can be supplemented by fluorescence in situ hybridization (FISH) and karyotype analysis. © 2017 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Human Genetics
Current Protocols in Human Genetics Biochemistry, Genetics and Molecular Biology-Genetics
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期刊介绍: Current Protocols in Human Genetics is the resource for designing and running successful research projects in all branches of human genetics.
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