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Volumn 167, Issue 5, 2014, Pages 710-714

Quantification of rare NPM1 mutation subtypes by digital PCR

Author keywords

Digital PCR; Minimal residual disease (MRD); Rare NPM1 mutation subtypes; Real time PCR

Indexed keywords

COMPLEMENTARY DNA; MESSENGER RNA; NUCLEOPHOSMIN; NUCLEAR PROTEIN; TUMOR PROTEIN;

EID: 84925226324     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/bjh.13038     Document Type: Letter
Times cited : (39)

References (10)
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    • Evaluation of different NPM1 mutations in AML patients according to clinical, cytogenetic and molecular features and impact on outcome
    • Alpermann, T., Haferlach, C., Dicker, F., Eder, C., Kohlmann, A., Kern, W., Haferlach, T. & Schnittger, S. (2013) Evaluation of different NPM1 mutations in AML patients according to clinical, cytogenetic and molecular features and impact on outcome. Blood, 122, 51a.
    • (2013) Blood , vol.122 , pp. 51a
    • Alpermann, T.1    Haferlach, C.2    Dicker, F.3    Eder, C.4    Kohlmann, A.5    Kern, W.6    Haferlach, T.7    Schnittger, S.8
  • 6
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    • Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease
    • Schnittger, S., Schoch, C., Dugas, M., Kern, W., Staib, P., Wuchter, C., Loffler, H., Sauerland, C.M., Serve, H., Buchner, T., Haferlach, T. & Hiddemann, W. (2002) Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia: correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood, 100, 59-66.
    • (2002) Blood , vol.100 , pp. 59-66
    • Schnittger, S.1    Schoch, C.2    Dugas, M.3    Kern, W.4    Staib, P.5    Wuchter, C.6    Loffler, H.7    Sauerland, C.M.8    Serve, H.9    Buchner, T.10    Haferlach, T.11    Hiddemann, W.12
  • 7
    • 28444449081 scopus 로고    scopus 로고
    • Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype
    • Schnittger, S., Schoch, C., Kern, W., Mecucci, C., Tschulik, C., Martelli, M.F., Haferlach, T., Hiddemann, W. & Falini, B. (2005) Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. Blood, 106, 3733-3739.
    • (2005) Blood , vol.106 , pp. 3733-3739
    • Schnittger, S.1    Schoch, C.2    Kern, W.3    Mecucci, C.4    Tschulik, C.5    Martelli, M.F.6    Haferlach, T.7    Hiddemann, W.8    Falini, B.9
  • 8
    • 70349579540 scopus 로고    scopus 로고
    • Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML
    • Schnittger, S., Kern, W., Tschulik, C., Weiss, T., Dicker, F., Falini, B., Haferlach, C. & Haferlach, T. (2009) Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. Blood, 114, 2220-2231.
    • (2009) Blood , vol.114 , pp. 2220-2231
    • Schnittger, S.1    Kern, W.2    Tschulik, C.3    Weiss, T.4    Dicker, F.5    Falini, B.6    Haferlach, C.7    Haferlach, T.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.