메뉴 건너뛰기




Volumn 108, Issue 3, 2002, Pages 113-119

Cytogenetic and molecular genetic aspects of idiopathic myelofibrosis

Author keywords

13q; 20q; Cytogenetics; Idiopathic myelofibrosis; Prognosis; Trisomy 1q

Indexed keywords

ANDROGEN; CALMODULIN; FIBROBLAST GROWTH FACTOR; GROWTH FACTOR; PLATELET DERIVED GROWTH FACTOR; PROTEIN P53; RAS PROTEIN; STEM CELL FACTOR RECEPTOR; TRANSFORMING GROWTH FACTOR BETA; TUMOR PROTEIN; UNCLASSIFIED DRUG;

EID: 0036423705     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000064708     Document Type: Review
Times cited : (23)

References (89)
  • 2
    • 34447610836 scopus 로고
    • Zwei Fälle von leukämie mit eigentümlichem blut- resp. Knockenmarksbefund
    • Heuck G: Zwei Fälle von leukämie mit eigentümlichem blut- resp. Knockenmarksbefund. Virchows Archiv 1879;78:475-496.
    • (1879) Virchows Archiv , vol.78 , pp. 475-496
    • Heuck, G.1
  • 3
    • 0001639195 scopus 로고
    • Some speculations on the myeloproliferative syndromes
    • Dameshek W: Some speculations on the myeloproliferative syndromes. Blood 1951;6:372-375.
    • (1951) Blood , vol.6 , pp. 372-375
    • Dameshek, W.1
  • 4
    • 0035383813 scopus 로고    scopus 로고
    • Clinical correlates of splenic histopathology and splenic karyotype in myelofibrosis with myeloid metaplasia
    • Mesa RA, Li CY, Schroeder G, Tefferi A: Clinical correlates of splenic histopathology and splenic karyotype in myelofibrosis with myeloid metaplasia. Blood 2001;97:3665-3667.
    • (2001) Blood , vol.97 , pp. 3665-3667
    • Mesa, R.A.1    Li, C.Y.2    Schroeder, G.3    Tefferi, A.4
  • 5
    • 0035079648 scopus 로고    scopus 로고
    • Epidemiology of the myeloproliferative disorders: Essential thrombocythaemia, polycythaemia vera and idiopathic myelofibrosis
    • Kutti J, Ridell B: Epidemiology of the myeloproliferative disorders: Essential thrombocythaemia, polycythaemia vera and idiopathic myelofibrosis. Pathol Biol 2001;49:164-166.
    • (2001) Pathol Biol , vol.49 , pp. 164-166
    • Kutti, J.1    Ridell, B.2
  • 6
    • 0026649984 scopus 로고
    • High incidence of myeloproliferative disorders in Ashkenazi Jews in northern Israel
    • Chaiter Y, Brenner B, Aghai E, Tatarsky I: High incidence of myeloproliferative disorders in Ashkenazi Jews in northern Israel. Leuk Lymph 1992;7:251-255.
    • (1992) Leuk Lymph , vol.7 , pp. 251-255
    • Chaiter, Y.1    Brenner, B.2    Aghai, E.3    Tatarsky, I.4
  • 7
    • 0003088502 scopus 로고
    • Myelofibrosis with myeloid metaplasia in survivors of the atomic bomb in Hiroshima
    • Andersen RE, Hoshino T, Yamamoto T: Myelofibrosis with myeloid metaplasia in survivors of the atomic bomb in Hiroshima. Ann Intern Med 1964;60:1-18.
    • (1964) Ann Intern Med , vol.60 , pp. 1-18
    • Andersen, R.E.1    Hoshino, T.2    Yamamoto, T.3
  • 9
    • 0011319806 scopus 로고
    • Industrial solvents as possible etiologic agents in myeloid metaplasia
    • Rawson R, Parker F, Jackson H: Industrial solvents as possible etiologic agents in myeloid metaplasia. Science 1941;93:541-542.
    • (1941) Science , vol.93 , pp. 541-542
    • Rawson, R.1    Parker, F.2    Jackson, H.3
  • 10
    • 0023172009 scopus 로고
    • Benzene-associated myelofibrosis
    • Hu H: Benzene-associated myelofibrosis. Ann Intern Med 1987;106:171-173.
    • (1987) Ann Intern Med , vol.106 , pp. 171-173
    • Hu, H.1
  • 12
    • 0025820104 scopus 로고
    • Life expectancy of patients with chronic nonleukemic myeloproliferative disorders
    • Rozman C, Giralt M, Feliu E, Rubio D, Cortes MT: Life expectancy of patients with chronic nonleukemic myeloproliferative disorders. Cancer 1991;67:2658-2663.
    • (1991) Cancer , vol.67 , pp. 2658-2663
    • Rozman, C.1    Giralt, M.2    Feliu, E.3    Rubio, D.4    Cortes, M.T.5
  • 13
    • 0017812507 scopus 로고
    • Agnogenic myeloid metaplasia: A clonal proliferation of hematopoietic stem cells with secondary myelofibrosis
    • Jacobson RJ, Salo A, Fialkow PJ: Agnogenic myeloid metaplasia: A clonal proliferation of hematopoietic stem cells with secondary myelofibrosis. Blood 1978;51:189-194.
    • (1978) Blood , vol.51 , pp. 189-194
    • Jacobson, R.J.1    Salo, A.2    Fialkow, P.J.3
  • 14
    • 0024445397 scopus 로고
    • The application of X chromosome gene probes to the diagnosis of myeloproliferative disease
    • Lucas GS, Padua RA, Masters GS, Oscier D, Jacobs A: The application of X chromosome gene probes to the diagnosis of myeloproliferative disease. Br J Haematol 1989;72:530-533.
    • (1989) Br J Haematol , vol.72 , pp. 530-533
    • Lucas, G.S.1    Padua, R.A.2    Masters, G.S.3    Oscier, D.4    Jacobs, A.5
  • 15
    • 0026091590 scopus 로고
    • Clonal granulocytes and marrow cells in the cellular phase of agnogenic myeloid metaplasia
    • Kreipe H, Jaquet K, Felgner J, Radzun H-J, Parwaresch MR: Clonal granulocytes and marrow cells in the cellular phase of agnogenic myeloid metaplasia. Blood 1991;78:1814-1817.
    • (1991) Blood , vol.78 , pp. 1814-1817
    • Kreipe, H.1    Jaquet, K.2    Felgner, J.3    Radzun, H.-J.4    Parwaresch, M.R.5
  • 18
    • 0028219438 scopus 로고
    • Tissue specificity of X-chromosome inactivation patterns
    • Gale RE, Wheadon H, Boulos P, Linch DC: Tissue specificity of X-chromosome inactivation patterns. Blood 1994;83:2899-2905.
    • (1994) Blood , vol.83 , pp. 2899-2905
    • Gale, R.E.1    Wheadon, H.2    Boulos, P.3    Linch, D.C.4
  • 19
    • 0028362575 scopus 로고
    • Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: Demonstration of heterogeneity in lineage involvement
    • Tsukamoto N, Morita K, Maehara T, Okamoto K, Sakai H, Karasawa M, Naruse T, Omine M: Clonality in chronic myeloproliferative disorders defined by X-chromosome linked probes: Demonstration of heterogeneity in lineage involvement. Br J Haematol 1994;86:253-258.
    • (1994) Br J Haematol , vol.86 , pp. 253-258
    • Tsukamoto, N.1    Morita, K.2    Maehara, T.3    Okamoto, K.4    Sakai, H.5    Karasawa, M.6    Naruse, T.7    Omine, M.8
  • 20
    • 0029842073 scopus 로고    scopus 로고
    • Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera
    • Asimakopoulos FA, Gilbert JG, Aldred MA, Pearson TC, Green AR: Interstitial deletion constitutes the major mechanism for loss of heterozygosity on chromosome 20q in polycythemia vera. Blood 1996;88:2690-2698.
    • (1996) Blood , vol.88 , pp. 2690-2698
    • Asimakopoulos, F.A.1    Gilbert, J.G.2    Aldred, M.A.3    Pearson, T.C.4    Green, A.R.5
  • 21
    • 0021266150 scopus 로고
    • Myeloid progenitor cells in the circulation of patients with myelofibrosis and other myeloproliferative disorders
    • Hibbin JA, Njoku OS, Matutes E, Lewis SM, Goldman JM: Myeloid progenitor cells in the circulation of patients with myelofibrosis and other myeloproliferative disorders. Br J Haematol 1984;57:495-503.
    • (1984) Br J Haematol , vol.57 , pp. 495-503
    • Hibbin, J.A.1    Njoku, O.S.2    Matutes, E.3    Lewis, S.M.4    Goldman, J.M.5
  • 23
    • 0023622360 scopus 로고
    • Effects of recombinant alpha and gamma interferons on the in vitro growth of circulating hematopoietic progenitor cells (CFU-GEMM, CFU-Mk, BFU-E and CFU-GM) from patients with myelofibrosis and myeloid metaplasia
    • Carlo-Stella C, Cazzola M, Gasner A, Barosi G, Dezza L, Meloni F, Pedrazzoli P, Hoelzer D, Ascari E: Effects of recombinant alpha and gamma interferons on the in vitro growth of circulating hematopoietic progenitor cells (CFU-GEMM, CFU-Mk, BFU-E and CFU-GM) from patients with myelofibrosis and myeloid metaplasia. Blood 1987;70:1014-1019.
    • (1987) Blood , vol.70 , pp. 1014-1019
    • Carlo-Stella, C.1    Cazzola, M.2    Gasner, A.3    Barosi, G.4    Dezza, L.5    Meloni, F.6    Pedrazzoli, P.7    Hoelzer, D.8    Ascari, E.9
  • 24
    • 0033038171 scopus 로고    scopus 로고
    • Circulating haematopoietic progenitor cells in primary and secondary myelofibrosis: Relation to collagen and reticulin fibrosis
    • Colovic MD, Wiernik PH, Jankovic GM, Vidovic AD, Janosevic S, Basara NM: Circulating haematopoietic progenitor cells in primary and secondary myelofibrosis: Relation to collagen and reticulin fibrosis. Eur J Haematol 1999;62:155-159.
    • (1999) Eur J Haematol , vol.62 , pp. 155-159
    • Colovic, M.D.1    Wiernik, P.H.2    Jankovic, G.M.3    Vidovic, A.D.4    Janosevic, S.5    Basara, N.M.6
  • 25
    • 0035760303 scopus 로고    scopus 로고
    • Diagnostic and clinical relevance of the number of circulating CD34+ cells in myelofibrosis with myeloid metaplasia
    • Barosi G, Viarengo G, Pecci A, Rosti V, Piaggio G, Marchetti M, Frassoni F: Diagnostic and clinical relevance of the number of circulating CD34+ cells in myelofibrosis with myeloid metaplasia. Blood 2001;98:3249-3255
    • (2001) Blood , vol.98 , pp. 3249-3255
    • Barosi, G.1    Viarengo, G.2    Pecci, A.3    Rosti, V.4    Piaggio, G.5    Marchetti, M.6    Frassoni, F.7
  • 26
    • 0020085766 scopus 로고
    • Characteristics of bone marrow fibroblast colony forming cells and their progeny in patients with myeloproliferative disorders
    • Castro-Malaspina H, Gay RE, Thanwar SL: Characteristics of bone marrow fibroblast colony forming cells and their progeny in patients with myeloproliferative disorders. Blood 1982; 59:1046-1056.
    • (1982) Blood , vol.59 , pp. 1046-1056
    • Castro-Malaspina, H.1    Gay, R.E.2    Thanwar, S.L.3
  • 28
    • 0028041268 scopus 로고
    • Monocytic adhesion in patients with bone marrow fibrosis is required for the production of fibrogenic cytokines. Potential role for interleukin-1 and TGF-beta
    • Rameshwar P, Denny TN, Stein D, Gascon P: Monocytic adhesion in patients with bone marrow fibrosis is required for the production of fibrogenic cytokines. Potential role for interleukin-1 and TGF-beta. J Immunol 1994;15: 2819-2830.
    • (1994) J Immunol , vol.15 , pp. 2819-2830
    • Rameshwar, P.1    Denny, T.N.2    Stein, D.3    Gascon, P.4
  • 29
    • 0031454769 scopus 로고    scopus 로고
    • Idiopathic myelofibrosis: Pathogenesis, natural history and management
    • Reilly JT: Idiopathic myelofibrosis: Pathogenesis, natural history and management. Blood Rev 1997;11:233-242.
    • (1997) Blood Rev , vol.11 , pp. 233-242
    • Reilly, J.T.1
  • 30
    • 0026533908 scopus 로고
    • Cytogenetic studies of bone marrow fibroblasts cultured from patients with myelofibrosis and myeloid metaplasia
    • Wang JC, Lang HD, Lichter S, Weinstein M, Benn P: Cytogenetic studies of bone marrow fibroblasts cultured from patients with myelofibrosis and myeloid metaplasia. Br J Haematol 1992;80:184-188.
    • (1992) Br J Haematol , vol.80 , pp. 184-188
    • Wang, J.C.1    Lang, H.D.2    Lichter, S.3    Weinstein, M.4    Benn, P.5
  • 31
    • 0024353190 scopus 로고
    • The splenomegaly of myeloproliferative and lymphoproliferative disorders: Splenic cellularity and vascularity
    • Zhang B, Lewis SM: The splenomegaly of myeloproliferative and lymphoproliferative disorders: Splenic cellularity and vascularity. Eur J Haematol 1989;43:63-66.
    • (1989) Eur J Haematol , vol.43 , pp. 63-66
    • Zhang, B.1    Lewis, S.M.2
  • 32
    • 0035383813 scopus 로고    scopus 로고
    • Clinical correlates of splenic histopathology and splenic karyotype in myelofibrosis with myeloid metaplasia
    • Mesa RA, Li CY, Schroeder G, Tefferi A: Clinical correlates of splenic histopathology and splenic karyotype in myelofibrosis with myeloid metaplasia. Blood 2001;97:3665-3667.
    • (2001) Blood , vol.97 , pp. 3665-3667
    • Mesa, R.A.1    Li, C.Y.2    Schroeder, G.3    Tefferi, A.4
  • 33
  • 35
    • 0034988764 scopus 로고    scopus 로고
    • Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia
    • Tefferi A, Mesa RA, Schroeder G, Hanson CA, Li C-Y, Dewald GW: Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia. Br J Haematol 2001;113: 763-771.
    • (2001) Br J Haematol , vol.113 , pp. 763-771
    • Tefferi, A.1    Mesa, R.A.2    Schroeder, G.3    Hanson, C.A.4    Li, C.-Y.5    Dewald, G.W.6
  • 37
    • 0027970180 scopus 로고
    • Karyotypic and ras gene mutation analysis in idiopathic myelofibrosis
    • Reilly JT, Wilson J, Barnett D, Watmore A, Potter, A: Karyotypic and ras gene mutation analysis in idiopathic myelofibrosis. Br J Haematol 1994;88:575-581.
    • (1994) Br J Haematol , vol.88 , pp. 575-581
    • Reilly, J.T.1    Wilson, J.2    Barnett, D.3    Watmore, A.4    Potter, A.5
  • 38
    • 0029767865 scopus 로고    scopus 로고
    • Prognostic factors in agnogenic myeloid metaplasia: A report on 195 cases with a new scoring system
    • Dupriez B, Morel P, Demory J-L, Lai JL, Simon M, Plantier I, Bauters F: Prognostic factors in agnogenic myeloid metaplasia: A report on 195 cases with a new scoring system. Blood 1996;88:1013-1018.
    • (1996) Blood , vol.88 , pp. 1013-1018
    • Dupriez, B.1    Morel, P.2    Demory, J.-L.3    Lai, J.L.4    Simon, M.5    Plantier, I.6    Bauters, F.7
  • 40
    • 0025778675 scopus 로고
    • Trisomy 8 and an unbalanced t(5;17)(q11;p11) characterize two karyotypically independent clones in a case of idiopathic myelofibrosis evolving to acute nonlymphoid leukemia
    • Kerim S, Rege-Cambrin G, Scaravaglio P, Godio L, Saglio G, Aglietta M: Trisomy 8 and an unbalanced t(5;17)(q11;p11) characterize two karyotypically independent clones in a case of idiopathic myelofibrosis evolving to acute nonlymphoid leukemia. Cancer Genet Cytogenet 1991;52:63-69.
    • (1991) Cancer Genet Cytogenet , vol.52 , pp. 63-69
    • Kerim, S.1    Rege-Cambrin, G.2    Scaravaglio, P.3    Godio, L.4    Saglio, G.5    Aglietta, M.6
  • 42
    • 24244477715 scopus 로고
    • Impaired retinoblastoma suscepibility (Rb) gene expression in agnogenic myeloid metaplasia
    • Lebowitz P, Papac R, Ghosh PK: Impaired retinoblastoma suscepibility (Rb) gene expression in agnogenic myeloid metaplasia. Blood 1990;76(suppl 1): 236a.
    • (1990) Blood , vol.76 , Issue.SUPPL. 1
    • Lebowitz, P.1    Papac, R.2    Ghosh, P.K.3
  • 45
    • 0032820779 scopus 로고    scopus 로고
    • Frequent allelic loss of the RB, D13S319 and D13S25 locus in myeloid malignancies with deletion/translocation at 13q14 of chromosome 13, but not in lymphoid malignancies
    • Tanaka K, Arif M, Eguchi M, Guo SX, Hayashi Y, Asaoku H, Kyo T, Dohy H, Kamada N: Frequent allelic loss of the RB, D13S319 and D13S25 locus in myeloid malignancies with deletion/translocation at 13q14 of chromosome 13, but not in lymphoid malignancies. Leukemia 1999;13:1367-1373.
    • (1999) Leukemia , vol.13 , pp. 1367-1373
    • Tanaka, K.1    Arif, M.2    Eguchi, M.3    Guo, S.X.4    Hayashi, Y.5    Asaoku, H.6    Kyo, T.7    Dohy, H.8    Kamada, N.9
  • 46
    • 0035015773 scopus 로고    scopus 로고
    • Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: Monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14
    • Sinclair EJ, Forrest EC, Reilly JT, Watemore AE, Potter AM: Fluorescence in situ hybridization analysis of 25 cases of idiopathic myelofibrosis and two cases of secondary myelofibrosis: Monoallelic loss of RB1, D13S319 and D13S25 loci associated with cytogenetic deletion and translocation involving 13q14. Br J Haematology2001;113:365-368.
    • (2001) Br J Haematology , vol.113 , pp. 365-368
    • Sinclair, E.J.1    Forrest, E.C.2    Reilly, J.T.3    Watemore, A.E.4    Potter, A.M.5
  • 48
    • 0029154197 scopus 로고
    • Chromosome abnormalities in the myeloproliferative disorders
    • Dewald GW, Wright PI: Chromosome abnormalities in the myeloproliferative disorders. Semin Oncol 1995;22:341-354.
    • (1995) Semin Oncol , vol.22 , pp. 341-354
    • Dewald, G.W.1    Wright, P.I.2
  • 49
    • 0030930177 scopus 로고    scopus 로고
    • Cytogenetic, fluorescence in situ hybridisation and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphatic leukemia
    • Gardiner AC, Corcoran MM, Oscier DG: Cytogenetic, fluorescence in situ hybridisation and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphatic leukemia. Genes Chromosomes Cancer 1997;20:73-81.
    • (1997) Genes Chromosomes Cancer , vol.20 , pp. 73-81
    • Gardiner, A.C.1    Corcoran, M.M.2    Oscier, D.G.3
  • 50
    • 0027336301 scopus 로고
    • The consistent 13q14 translocation breakpoint in chronic B-cell leukemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene
    • Hawthorn LA, Chapman R, Oscier D, Cowell JK: The consistent 13q14 translocation breakpoint in chronic B-cell leukemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene. Oncogene 1993;8:1415-1419.
    • (1993) Oncogene , vol.8 , pp. 1415-1419
    • Hawthorn, L.A.1    Chapman, R.2    Oscier, D.3    Cowell, J.K.4
  • 51
    • 0033001469 scopus 로고    scopus 로고
    • A case of myelofibrosis with a t(4;13)(q25;q12): Evidence for involvement of a second 13q12 locus in chronic myeloproliferative disorders
    • Macdonald DHC, Lahiri D, Chase A, Sohal J, Goldman JM, Cross NCP: A case of myelofibrosis with a t(4;13)(q25;q12): Evidence for involvement of a second 13q12 locus in chronic myeloproliferative disorders. Br J Haematol 1999;105:771-774.
    • (1999) Br J Haematol , vol.105 , pp. 771-774
    • Macdonald, D.H.C.1    Lahiri, D.2    Chase, A.3    Sohal, J.4    Goldman, J.M.5    Cross, N.C.P.6
  • 52
    • 0025848934 scopus 로고
    • Karyotypic patterns in chronic myeloproliferative disorders: Report on 74 cases and review of the literature
    • Mertens F, Johansson B, Heim S, Kristoffersson U, Mitelman F: Karyotypic patterns in chronic myeloproliferative disorders: Report on 74 cases and review of the literature. Leukemia 1991;5:214-220.
    • (1991) Leukemia , vol.5 , pp. 214-220
    • Mertens, F.1    Johansson, B.2    Heim, S.3    Kristoffersson, U.4    Mitelman, F.5
  • 53
    • 0029031073 scopus 로고
    • Characterization of 20q deletions in patients with myeloproliferative disorders and myelodysplastic syndromes
    • Nacheva E, Holloway T, Carter N, Grace C, White N, Green AR: Characterization of 20q deletions in patients with myeloproliferative disorders and myelodysplastic syndromes. Cancer Genet Cytogenet 1995;80:87-94.
    • (1995) Cancer Genet Cytogenet , vol.80 , pp. 87-94
    • Nacheva, E.1    Holloway, T.2    Carter, N.3    Grace, C.4    White, N.5    Green, A.R.6
  • 54
    • 0027375437 scopus 로고
    • Molecular genetics of myeloid leukemia: Identification of the commonly deleted segment of chromosome 20
    • Roulston D, Espinosa R, Stoffel M, Bell GI, Le Beau MM: Molecular genetics of myeloid leukemia: Identification of the commonly deleted segment of chromosome 20. Blood 1993;82: 3424-3429.
    • (1993) Blood , vol.82 , pp. 3424-3429
    • Roulston, D.1    Espinosa, R.2    Stoffel, M.3    Bell, G.I.4    Le Beau, M.M.5
  • 55
    • 0034235673 scopus 로고    scopus 로고
    • Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map
    • Wang PW, Eisenbart JD, Espinosa R, Davis EM, Larson RA, Le Beau MM: Refinement of the smallest commonly deleted segment of chromosome 20 in malignant myeloid diseases and development of a PAC-based physical and transcription map. Genomics 2000;67:28-39.
    • (2000) Genomics , vol.67 , pp. 28-39
    • Wang, P.W.1    Eisenbart, J.D.2    Espinosa, R.3    Davis, E.M.4    Larson, R.A.5    Le Beau, M.M.6
  • 56
    • 0035849797 scopus 로고    scopus 로고
    • Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines
    • MacGrogan D, Alvarez S, DeBlasio T, Jhanwar SC, Nimer SD: Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines. Oncogene 2001; 20:4150-4160.
    • (2001) Oncogene , vol.20 , pp. 4150-4160
    • MacGrogan, D.1    Alvarez, S.2    DeBlasio, T.3    Jhanwar, S.C.4    Nimer, S.D.5
  • 57
    • 84920215150 scopus 로고
    • Abnormalities of chromosome no 1 in haematological malignancies
    • Rowley JD: Abnormalities of chromosome no 1 in haematological malignancies. Lancet 1978;i:554-555.
    • (1978) Lancet
    • Rowley, J.D.1
  • 58
    • 0017876801 scopus 로고
    • Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblastic leukemia
    • Gahrton G, Friburg K, Lindsten J, Zech L: Duplication of part of the long arm of chromosome 1 in myelofibrosis terminating in acute myeloblastic leukemia. Hereditas 1978;88:1-5.
    • (1978) Hereditas , vol.88 , pp. 1-5
    • Gahrton, G.1    Friburg, K.2    Lindsten, J.3    Zech, L.4
  • 60
    • 0027957970 scopus 로고
    • A hematopoietic protein tyrosine phosphatase (hePTP) gene that is amplified and overexpressed in myeloid malignancies maps to chromosome 1q32.1
    • Zanke B, Squire J, Griesser H, Henry M, Suzuki H, Patterson B, Minden M, Mak TW: A hematopoietic protein tyrosine phosphatase (hePTP) gene that is amplified and overexpressed in myeloid malignancies maps to chromosome 1q32.1. Leukemia 1994;8:236-244.
    • (1994) Leukemia , vol.8 , pp. 236-244
    • Zanke, B.1    Squire, J.2    Griesser, H.3    Henry, M.4    Suzuki, H.5    Patterson, B.6    Minden, M.7    Mak, T.W.8
  • 61
    • 0018908108 scopus 로고
    • An identical translocation between chromosome 1 and 7 in three patients with myelofibrosis and myeloid metaplasia
    • Geraedts JPM, den Ottolander GJ, Ploem JE, Muntinghe OG: An identical translocation between chromosome 1 and 7 in three patients with myelofibrosis and myeloid metaplasia. Br J Haematol 1980;44:569-575.
    • (1980) Br J Haematol , vol.44 , pp. 569-575
    • Geraedts, J.P.M.1    Den Ottolander, G.J.2    Ploem, J.E.3    Muntinghe, O.G.4
  • 63
    • 0018083019 scopus 로고
    • Cytogenetic studies in patients with myelofibrosis and myeloid metaplasia
    • Whang-Peng J, Lee E, Knutsen T, et al: Cytogenetic studies in patients with myelofibrosis and myeloid metaplasia. Leuk Res 1978;2:41-56.
    • (1978) Leuk Res , vol.2 , pp. 41-56
    • Whang-Peng, J.1    Lee, E.2    Knutsen, T.3
  • 64
    • 0021925745 scopus 로고
    • The pattern and clinical significance of karyotypic abnormalities in patients with idiopathic and postpolycythemic myelofibrosis
    • Miller JB, Testa JR, Lindgren V, Rowley JD: The pattern and clinical significance of karyotypic abnormalities in patients with idiopathic and postpolycythemic myelofibrosis. Cancer 1985;55:582-591.
    • (1985) Cancer , vol.55 , pp. 582-591
    • Miller, J.B.1    Testa, J.R.2    Lindgren, V.3    Rowley, J.D.4
  • 65
    • 0021047288 scopus 로고
    • The syndrome of idiopathic myelofibrosis: A clinicopathologic review with emphasis on the prognostic variables predicting survival
    • Varki A, Lottenberg R, Griffith R, Reinhard E: The syndrome of idiopathic myelofibrosis: A clinicopathologic review with emphasis on the prognostic variables predicting survival. Medicine 1983;62:353-371.
    • (1983) Medicine , vol.62 , pp. 353-371
    • Varki, A.1    Lottenberg, R.2    Griffith, R.3    Reinhard, E.4
  • 69
    • 0020041538 scopus 로고
    • Analysis of the androgen response of 23 patients with agnogenic myeloid metaplasia: The value of chromosomal studies predicting response and survival
    • Besa EC, Nowell PC, Geller NL, Gardner FH: Analysis of the androgen response of 23 patients with agnogenic myeloid metaplasia: The value of chromosomal studies predicting response and survival. Cancer 1982;49:308-313.
    • (1982) Cancer , vol.49 , pp. 308-313
    • Besa, E.C.1    Nowell, P.C.2    Geller, N.L.3    Gardner, F.H.4
  • 70
    • 0018358319 scopus 로고
    • Trisomy 13 in bone marrow cells in acute myelocytic leukemia and myelofibrosis
    • Hsu LY, Greenberg ML, Kohan S, Wittman R: Trisomy 13 in bone marrow cells in acute myelocytic leukemia and myelofibrosis. Clin Genet 1979;15:327-331.
    • (1979) Clin Genet , vol.15 , pp. 327-331
    • Hsu, L.Y.1    Greenberg, M.L.2    Kohan, S.3    Wittman, R.4
  • 72
    • 0028825769 scopus 로고
    • Trisomy 13 in a case of myelofibrosis with myeloid metaplasia with early blastic transformation
    • Ferrara F, Vicari L, Festa B, Di Noto R, Pane F, Sebastio L, Cimino R: Trisomy 13 in a case of myelofibrosis with myeloid metaplasia with early blastic transformation. Haematologica 1995;80:434-436.
    • (1995) Haematologica , vol.80 , pp. 434-436
    • Ferrara, F.1    Vicari, L.2    Festa, B.3    Di Noto, R.4    Pane, F.5    Sebastio, L.6    Cimino, R.7
  • 74
    • 84966178234 scopus 로고
    • Defective erythropoiesis in primary myelofibrosis associated with a chromosome 11 abnormality
    • Patton WN, Bunce CM, Larkins S, Brown G: Defective erythropoiesis in primary myelofibrosis associated with a chromosome 11 abnormality. Br J Cancer 1991;64:128-131.
    • (1991) Br J Cancer , vol.64 , pp. 128-131
    • Patton, W.N.1    Bunce, C.M.2    Larkins, S.3    Brown, G.4
  • 75
    • 0031841069 scopus 로고    scopus 로고
    • Myelofibrosis with myeloid metaplasia in young individuals: Disease characteristics, prognostic factors and identification of risk groups
    • Cervantes F, Barosi G, Demory J-L, Reilly J, Guarnone R, Dupriez B, Pereira A, Montserrat E: Myelofibrosis with myeloid metaplasia in young individuals: Disease characteristics, prognostic factors and identification of risk groups. Br J Haematol 1998;102:684-690.
    • (1998) Br J Haematol , vol.102 , pp. 684-690
    • Cervantes, F.1    Barosi, G.2    Demory, J.-L.3    Reilly, J.4    Guarnone, R.5    Dupriez, B.6    Pereira, A.7    Montserrat, E.8
  • 76
    • 0034971782 scopus 로고    scopus 로고
    • Myelofibrosis with myeloid metaplasia in adult individuals 30 years old or younger: Presenting features, evolution and survival
    • Cervantes F, Barosi G, Hernández-Boluda J-C, Marchetti M, Montserrat E: Myelofibrosis with myeloid metaplasia in adult individuals 30 years old or younger: Presenting features, evolution and survival. Eur J Haematol 2001;66: 324-327.
    • (2001) Eur J Haematol , vol.66 , pp. 324-327
    • Cervantes, F.1    Barosi, G.2    Hernández-Boluda, J.-C.3    Marchetti, M.4    Montserrat, E.5
  • 77
    • 0034042464 scopus 로고    scopus 로고
    • Long-term survival of infants with idiopathic myelofibrosis
    • Altura RA, Head DR, Wang WC: Long-term survival of infants with idiopathic myelofibrosis. Br J Haematol 2000;109:459-462.
    • (2000) Br J Haematol , vol.109 , pp. 459-462
    • Altura, R.A.1    Head, D.R.2    Wang, W.C.3
  • 78
    • 0035723703 scopus 로고    scopus 로고
    • Comparison of peripheral blood interphase cytogenetics with bone marrow karyotype analysis in myelofibrosis with myeloid metaplasia
    • Tefferi A, Meyer RG, Wyatt WA, Dewald GW: Comparison of peripheral blood interphase cytogenetics with bone marrow karyotype analysis in myelofibrosis with myeloid metaplasia. Br J Haematol 2001;115:316-319.
    • (2001) Br J Haematol , vol.115 , pp. 316-319
    • Tefferi, A.1    Meyer, R.G.2    Wyatt, W.A.3    Dewald, G.W.4
  • 80
    • 0023753816 scopus 로고
    • Evidence for pluripotent stem cell origin of idiopathic myelofibrosis: Clonal analysis of a case characterised 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 characterised by a N-ras gene mutation. Leukemia 1988;2:658-660.
    • (1988) Leukemia , vol.2 , pp. 658-660
    • Buschle, M.1    Janssen, J.W.2    Drexler, H.3    Lyons, J.4    Anger, B.5    Bartram, C.R.6
  • 81
    • 0027275593 scopus 로고
    • Mutations in the p53 and ras family genes are associated with tumour progression of bcr/abl negative chronic myeloproliferative disorders
    • Gaidano G, Guerrasio A, Serra A, Carozzi F, Cambrin GR, Petroni D: Mutations in the p53 and ras family genes are associated with tumour progression of bcr/abl negative chronic myeloproliferative disorders. Leukemia 1993; 7:946-953.
    • (1993) Leukemia , vol.7 , pp. 946-953
    • Gaidano, G.1    Guerrasio, A.2    Serra, A.3    Carozzi, F.4    Cambrin, G.R.5    Petroni, D.6
  • 82
    • 0028281042 scopus 로고
    • Expression of the c-kit proto-oncogene in myeloproliferative disorders and myelodysplastic syndromes
    • Siitonen T, Savolainen ER, Koistinen P: Expression of the c-kit proto-oncogene in myeloproliferative disorders and myelodysplastic syndromes. Leukemia 1994;8:631-637.
    • (1994) Leukemia , vol.8 , pp. 631-637
    • Siitonen, T.1    Savolainen, E.R.2    Koistinen, P.3
  • 83
    • 0029922912 scopus 로고    scopus 로고
    • Spontaneous granulocyte-macrophage colony growth by peripheral blood mononuclear cells in myeloproliferative disorders
    • Siitonen T, Zheng A, Savolainen E-R, Koistinen P: Spontaneous granulocyte-macrophage colony growth by peripheral blood mononuclear cells in myeloproliferative disorders. Leuk Res 1996;20:187-195.
    • (1996) Leuk Res , vol.20 , pp. 187-195
    • Siitonen, T.1    Zheng, A.2    Savolainen, E.-R.3    Koistinen, P.4
  • 85
    • 0030914402 scopus 로고    scopus 로고
    • c-kit mutations in patients with myeloproliferative disorders
    • Kimura A, Nakata Y, Katoh O, Hyodo H: c-kit mutations in patients with myeloproliferative disorders. Leuk Lymph 1997;25:281-287.
    • (1997) Leuk Lymph , vol.25 , pp. 281-287
    • Kimura, A.1    Nakata, Y.2    Katoh, O.3    Hyodo, H.4
  • 86
    • 0032227241 scopus 로고    scopus 로고
    • A novel thrombopoietin signaling defect in polycythemia vera platelets
    • Moliterno AR, Siebel KE, Sun AY, Hankins WD, Spivak JL: A novel thrombopoietin signaling defect in polycythemia vera platelets. Stem Cells 1998;16(suppl 2): 185-192.
    • (1998) Stem Cells , vol.16 , Issue.SUPPL. 2 , pp. 185-192
    • Moliterno, A.R.1    Siebel, K.E.2    Sun, A.Y.3    Hankins, W.D.4    Spivak, J.L.5
  • 88
    • 0036008494 scopus 로고    scopus 로고
    • Hypermethylation of the P15INK4b and P16INK4a in agnogenic myeloid metaplasia (AMM) and AMM in leukemic transformation
    • Wang JC, Chen W, Nallusamy S, Chen C, Nov-etsky AD: Hypermethylation of the P15INK4b and P16INK4a in agnogenic myeloid metaplasia (AMM) and AMM in leukemic transformation. Br J Haematol 2002;116:582-586.
    • (2002) Br J Haematol , vol.116 , pp. 582-586
    • Wang, J.C.1    Chen, W.2    Nallusamy, S.3    Chen, C.4    Novetsky, A.D.5
  • 89
    • 79960971619 scopus 로고    scopus 로고
    • Detection of aberrant signalling pathways in CD34+ cells from patients with myelofibrosis with myeloid metaplasia using oligonucleotide microarrays
    • Jones LC, Tefferi A, Wachsman W, Hofmann WK, Koeffler HP: Detection of aberrant signalling pathways in CD34+ cells from patients with myelofibrosis with myeloid metaplasia using oligonucleotide microarrays. Blood 2001; 98(suppl):626a.
    • (2001) Blood , vol.98 , Issue.SUPPL.
    • Jones, L.C.1    Tefferi, A.2    Wachsman, W.3    Hofmann, W.K.4    Koeffler, H.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.