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Volumn 37, Issue 2, 2007, Pages 153-154

FIP1L1/PDGFRA is a molecular marker of chronic eosinophilic leukaemia but not for systemic mastocytosis [1]

Author keywords

[No Author keywords available]

Indexed keywords

FIP1L1 PLATELET DERIVED GROWTH FACTOR ALPHA RECEPTOR FUSION PROTEIN; HYBRID PROTEIN; IMATINIB; STEM CELL FACTOR; UNCLASSIFIED DRUG;

EID: 33846099538     PISSN: 00142972     EISSN: 13652362     Source Type: Journal    
DOI: 10.1111/j.1365-2362.2007.01757.x     Document Type: Letter
Times cited : (14)

References (11)
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    • The FIP1L1-PDGFRalpha fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: Implications for diagnosis, classification, and management
    • Gotlib J, Cools J, Malone JM, Schrier SL, Gilliland DG, Coutre SE. The FIP1L1-PDGFRalpha fusion tyrosine kinase in hypereosinophilic syndrome and chronic eosinophilic leukemia: implications for diagnosis, classification, and management. Blood 2004;103:2879-91.
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  • 3
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    • CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy
    • Pardanani A, Ketterling RP, Brockman SR, Flynn HC, Paternoster SF, Shearer BM et al. CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy. Blood 2003;102:3093-6.
    • (2003) Blood , vol.102 , pp. 3093-3096
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  • 4
    • 0023695019 scopus 로고
    • Significance of systemic mast cell disease with associated hematologic disorders
    • Travis WD, Li CY, Yam LT, Bergstralh EJ, Swee RG. Significance of systemic mast cell disease with associated hematologic disorders. Cancer 1988;62:965-72.
    • (1988) Cancer , vol.62 , pp. 965-972
    • Travis, W.D.1    Li, C.Y.2    Yam, L.T.3    Bergstralh, E.J.4    Swee, R.G.5
  • 5
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    • (1990) Br J Haematol , vol.76 , pp. 186-193
    • Horny, H.-P.1    Ruck, M.2    Wehrmann, M.3    Kaiserling, E.4
  • 6
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    • Classification and diagnosis of mastocytosis: Current status
    • Metcalfe DD. Classification and diagnosis of mastocytosis: current status. J Invest Dermatol 1991;96:2S-4S.
    • (1991) J Invest Dermatol , vol.96
    • Metcalfe, D.D.1
  • 7
    • 0028856070 scopus 로고
    • Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder
    • Nagata H, Worobec AS, Oh CK, Chowdhury BA, Tannenbaum S, Suzuki Y et al. Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder. Proc Natl Acad Sci USA 1995;92:10560-4.
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    • Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia
    • Sotlar K, Marafioti T, Griesser H, Theil J, Aepinus C, Jaussi R et al. Detection of c-kit mutation Asp 816 to Val in microdissected bone marrow infiltrates in a case of systemic mastocytosis associated with chronic myelomonocytic leukaemia. Mol Pathol 2000;53:188-93.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.