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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2018.1
- 수록면
- 147 - 154 (8page)
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Background: JAK2 V617F is the most common mutation in myeloproliferative neoplasms (MPNs) and is a major diagnostic criterion. Mutation quantification is useful for classifying patients with MPN into subgroups and for prognostic prediction. Droplet digital PCR (ddPCR) can provide accurate and reproducible quantitative analysis of DNA. This study was designed to verify the correlation of ddPCR with pyrosequencing results in the diagnosis of MPN and to investigate clinical implications of the mutational burden.
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참고문헌 (31)
참고문헌 신청
Swerdlow S / 2008 / WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues / IARC
Cankovic M / 2009 / Clinical performance of JAK2 V617F mutation detection assays in a molecular diagnostics laboratory: evaluation of screening and quantitation methods / Am J Clin Pathol 132:713~721
Kralovics R / 2005 / A gain-of-function mutation of JAK2 in myeloproliferative disorders / N Engl J Med 352:1779~1790
Steensma DP / 2005 / The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both atypical myeloproliferative disorders and myelodysplastic syndromes / Blood 106:1207~1209
Busque L / 2016 / Laboratory investigation of myeloproliferative neoplasms (MPNs): recommendations of the Canadian Mpn Group / Am J Clin Pathol 146:408~422
Cankovic M / 2009 / Clinical performance of JAK2 V617F mutation detection assays in a molecular diagnostics laboratory: evaluation of screening and quantitation methods / Am J Clin Pathol 132:713~721
Kralovics R / 2005 / A gain-of-function mutation of JAK2 in myeloproliferative disorders / N Engl J Med 352:1779~1790
Steensma DP / 2005 / The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both atypical myeloproliferative disorders and myelodysplastic syndromes / Blood 106:1207~1209
Busque L / 2016 / Laboratory investigation of myeloproliferative neoplasms (MPNs): recommendations of the Canadian Mpn Group / Am J Clin Pathol 146:408~422
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