논문KCI 등재
Pyrosequencing as a Fast and Reliable Method in Detecting the MYD88 p.L265P Mutation in Decalcified Formalin-Fixed and Paraffin-Embedded Tissues
대한진단검사의학회 (Korean Society For Laboratory Medicine)|2014.03|Annals of Laboratory Medicine|제34권 제2호|pp. 170-173
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주제분류병리학
초록
Dear Editor, MYD88 p.L265P has recently been identified as a considerably recurrent mutation in lymphoplasmacytic lymphomas with an IgM monoclonal protein (Waldenström’s macroglobulinemia [WM]). The mutation was also described as a common event in several other lymphoproliferative disorders, including diffuse large B-cell lymphoma and primary central nervous system (CNS) lymphoma [1].
Abstract
Dear Editor, MYD88 p.L265P has recently been identified as a considerably recurrent mutation in lymphoplasmacytic lymphomas with an IgM monoclonal protein (Waldenström’s macroglobulinemia [WM]). The mutation was also described as a common event in several other lymphoproliferative disorders, including diffuse large B-cell lymphoma and primary central nervous system (CNS) lymphoma [1].
참고문헌 (7)
- Ngo VN, "Oncogenically active MYD88 mutations in human lymphoma", Nature, 470, pp.115~119 (2011)
- Treon SP, "MYD88 L265P somatic mutation in Waldenstrom’s macroglobulinemia", N Engl J Med, 367, pp.826~833 (2012)
- Xu L, "MYD88 L265P in Waldenstrom macroglobulinemia, immunoglobulin M monoclonal gammopathy, and other B-cell lymphoproliferative disorders using conventional and quantitative allele-specific polymerase chain reaction", Blood, 121, pp.2051~2058 (2013)
- Poulain S, "MYD88 L265P mutation in Waldenstrom macroglobulinemia", Blood, 121, pp.4504~4511 (2013)
- Loiarro M, "Targeting the Toll-like receptor", interleukin 1 receptor pathway in human diseases: rational design of MYD88 inhibitors, 2013, pp.13, 222~226
- Wang CZ, "Development of high-resolution melting analysis for the detection of the MYD88 L265Pmutation", Clin Biochem, 46, pp.385~387 (2013)
- Bock O, "Aberrant collagenase expression in chronic idiopathic myelofibrosis is related to the stage of disease but not to the JAK2 mutation status", Am J Pathol, 169, pp.471~481 (2006)
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