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Volumn 71, Issue 2, 2002, Pages 131-133

N-ras and p53 gene mutations in Japanese patients with myeloproliferative disorders

Author keywords

Essential thrombocythemia; Gene mutation; Myeloproliferative disorder; N ras; P53; Polycythemia vera

Indexed keywords

PROTEIN P53;

EID: 0036785106     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajh.10188     Document Type: Article
Times cited : (13)

References (13)
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  • 2
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    • Mutations in the P53 and RAS family genes are associated with tumor progression of BCR/ABL negative chronic myeloproliferative disorders
    • Gaidano G, Guerrasio A, Serra A, Carozzi F, Cambrin GR, Petroni D, Saglio G. Mutations in the P53 and RAS family genes are associated with tumor progression of BCR/ABL negative chronic myeloproliferative disorders. Leukemia 1993;7:946-953.
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    • Gaidano, G.1    Guerrasio, A.2    Serra, A.3    Carozzi, F.4    Cambrin, G.R.5    Petroni, D.6    Saglio, G.7
  • 4
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    • Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: High proportion of cases with 17p deletion
    • Sterkers Y, Preudhomme C, Lai J-L, Demory J-L, Caulier M-T, Wattel E, Bordessoule D, Bauters F, Fenaux P. Acute myeloid leukemia and myelodysplastic syndromes following essential thrombocythemia treated with hydroxyurea: high proportion of cases with 17p deletion. Blood 1998;91:616-622.
    • (1998) Blood , vol.91 , pp. 616-622
    • Sterkers, Y.1    Preudhomme, C.2    Lai, J.-L.3    Demory, J.-L.4    Caulier, M.-T.5    Wattel, E.6    Bordessoule, D.7    Bauters, F.8    Fenaux, P.9
  • 5
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    • Berlin, N.1
  • 6
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    • Essential thrombocythemia: An interim report from the Polycythemia Vera Study Group
    • Murphy S, Iland H, Rosenthal D, Laszlo J. Essential thrombocythemia: an interim report from the Polycythemia Vera Study Group. Semin Hematol 1986;23:117-182.
    • (1986) Semin Hematol , vol.23 , pp. 117-182
    • Murphy, S.1    Iland, H.2    Rosenthal, D.3    Laszlo, J.4
  • 7
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    • Primary chronic myelofibrosis: Clinical and prognostic evaluation in 336 Japanese patients
    • Okamura T, Kinukawa N, Niho Y, Mizoguchi H. Primary chronic myelofibrosis: clinical and prognostic evaluation in 336 Japanese patients. Int J Hematol 2001;73:194-198.
    • (2001) Int J Hematol , vol.73 , pp. 194-198
    • Okamura, T.1    Kinukawa, N.2    Niho, Y.3    Mizoguchi, H.4
  • 12
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    • Karyotypic and ras gene mutational analysis in idiopathic myelofibrosis
    • Reilly JT, Wilson G, Barnett D, Watmore A, Potter A. Karyotypic and ras gene mutational analysis in idiopathic myelofibrosis. Br J Haematol 1994;88:575-581.
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    • Reilly, J.T.1    Wilson, G.2    Barnett, D.3    Watmore, A.4    Potter, A.5
  • 13
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    • Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: Clonal analysis of a case characterized by a N-ras gene mutation
    • Buschle M, Janssen JW, Drexler H, Lyons J, Anger B, Bartram CR. Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: clonal analysis of a case characterized by a N-ras gene mutation. Leukemia 1988;2:658-660.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.