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Volumn 75, Issue 1, 2002, Pages 72-77

Establishment of a monosomy 7 leukemia cell line, MONO-7, with a ras gene mutation

Author keywords

Cell line; Leukemia; Monosomy 7; ras gene mutation

Indexed keywords

RECOMBINANT INTERLEUKIN 3; T LYMPHOCYTE RECEPTOR BETA CHAIN; DNA; GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; INTERLEUKIN 3; RECOMBINANT PROTEIN;

EID: 0036363474     PISSN: 09255710     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02981983     Document Type: Article
Times cited : (3)

References (27)
  • 1
    • 0028910402 scopus 로고
    • Childhood monosomy 7: Epidemiology, biology, and mechanistic implications
    • Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications. Blood. 1995; 85:1985-1999.
    • (1995) Blood , vol.85 , pp. 1985-1999
    • Luna-Fineman, S.1    Shannon, K.M.2    Lange, B.J.3
  • 2
    • 0026101050 scopus 로고
    • Mutations of the ras protooncogenes in childhood monosomy 7
    • Neubauer A, Shannon K, Liu E. Mutations of the ras protooncogenes in childhood monosomy 7. Blood. 1991;77:594-598.
    • (1991) Blood , vol.77 , pp. 594-598
    • Neubauer, A.1    Shannon, K.2    Liu, E.3
  • 4
    • 0023001165 scopus 로고
    • Simple monosomy 7 and myelodysplastic syndrome in thirteen patients without previous cytostatic treatment
    • Michiels JJ, Mallios-Zorbala H, Prins ME, Hahlen K, Hagemeijer A. Simple monosomy 7 and myelodysplastic syndrome in thirteen patients without previous cytostatic treatment. Br J Haematol. 1986;64:425-433.
    • (1986) Br J Haematol , vol.64 , pp. 425-433
    • Michiels, J.J.1    Mallios-Zorbala, H.2    Prins, M.E.3    Hahlen, K.4    Hagemeijer, A.5
  • 5
    • 0025355946 scopus 로고
    • Childhood myelodysplasia: Suggested classification as myelodysplastic syndromes based on laboratory and clinical findings
    • Brandwein JM, Horsman DE, Eaves AC, et al. Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings. Am J Pediatr Hematol Oncol. 1990;12:63-70.
    • (1990) Am J Pediatr Hematol Oncol , vol.12 , pp. 63-70
    • Brandwein, J.M.1    Horsman, D.E.2    Eaves, A.C.3
  • 6
    • 0027372507 scopus 로고
    • Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: A report on 408 cases
    • Morel P, Hebbar M, Lai JL, et al. Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: a report on 408 cases. Leukemia. 1993;7:1315-1323.
    • (1993) Leukemia , vol.7 , pp. 1315-1323
    • Morel, P.1    Hebbar, M.2    Lai, J.L.3
  • 7
    • 0019136268 scopus 로고
    • Clinical implications of monosomy 7 in acute nonlymphocytic leukemia
    • Borgstrom G, Teerenhovi L, Vuopio P, et al. Clinical implications of monosomy 7 in acute nonlymphocytic leukemia. Cancer Genet Cytogenet. 1980;2:115-126.
    • (1980) Cancer Genet Cytogenet , vol.2 , pp. 115-126
    • Borgstrom, G.1    Teerenhovi, L.2    Vuopio, P.3
  • 9
    • 0024501380 scopus 로고
    • Prognostic impact of cytogenetic abnormalities in patients with de novo acute nonlymphocytic leukemia
    • Schiffer CA, Lee EJ, Tomiyasu T, Wiernik PH, Testa JR. Prognostic impact of cytogenetic abnormalities in patients with de novo acute nonlymphocytic leukemia. Blood. 1989;73:263-270.
    • (1989) Blood , vol.73 , pp. 263-270
    • Schiffer, C.A.1    Lee, E.J.2    Tomiyasu, T.3    Wiernik, P.H.4    Testa, J.R.5
  • 10
    • 0023712566 scopus 로고
    • Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults
    • de Planque MM, Kluin-Nelemans HC, van Krieken HJ, et al. Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults. Br J Haematol. 1988;70:55-62.
    • (1988) Br J Haematol , vol.70 , pp. 55-62
    • De Planque, M.M.1    Kluin-Nelemans, H.C.2    Van Krieken, H.J.3
  • 11
    • 0028030712 scopus 로고
    • A review of 125 cases to determine the risk of myelodysplasia and leukemia in pediatric neutropenic patients after treatment with recombinant human granulocyte colony-stimulating factor
    • Imashuku S, Hibi S, Nakajima F, et al. A review of 125 cases to determine the risk of myelodysplasia and leukemia in pediatric neutropenic patients after treatment with recombinant human granulocyte colony-stimulating factor. Blood. 1994;84:2380-2381.
    • (1994) Blood , vol.84 , pp. 2380-2381
    • Imashuku, S.1    Hibi, S.2    Nakajima, F.3
  • 12
    • 0025818349 scopus 로고
    • Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL)
    • Johansson B, Mertens F, Heim S, Kristoffersson U, Mitelman F. Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL). Eur J Haematol. 1991;47:17-27.
    • (1991) Eur J Haematol , vol.47 , pp. 17-27
    • Johansson, B.1    Mertens, F.2    Heim, S.3    Kristoffersson, U.4    Mitelman, F.5
  • 13
    • 0022617302 scopus 로고
    • Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: Further evidence for characteristic abnormalities of chromosomes no. 5 and 7
    • Le Beau MM, Albain KS, Larson RA, et al. Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndromes and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7. J Clin Oncol. 1986;4:325-345.
    • (1986) J Clin Oncol , vol.4 , pp. 325-345
    • Le Beau, M.M.1    Albain, K.S.2    Larson, R.A.3
  • 14
    • 0023840866 scopus 로고
    • Cytogenetic studies in patients with secondary leukemia/dysmyelopoietic syndrome after different treatment modalities
    • Whang-Peng J, Young RC, Lee EC, Longo DL, Schlechter GP, DeVita VT Jr. Cytogenetic studies in patients with secondary leukemia/dysmyelopoietic syndrome after different treatment modalities. Blood. 1988;71:403-414.
    • (1988) Blood , vol.71 , pp. 403-414
    • Whang-Peng, J.1    Young, R.C.2    Lee, E.C.3    Longo, D.L.4    Schlechter, G.P.5    DeVita Jr., V.T.6
  • 15
    • 0026712424 scopus 로고
    • Morphologic, immunologic and cytogenetic studies in acute myeloid leukemia following occupational exposure to pesticides and organic solvents
    • Cuneo A, Fagioli F, Pazzi I, et al. Morphologic, immunologic and cytogenetic studies in acute myeloid leukemia following occupational exposure to pesticides and organic solvents. Leuk Res. 1992;16:789-796.
    • (1992) Leuk Res , vol.16 , pp. 789-796
    • Cuneo, A.1    Fagioli, F.2    Pazzi, I.3
  • 16
    • 0019943809 scopus 로고
    • Correlation of occupation and karyotype in adults with acute nonlymphocytic leukemia
    • Golomb HM, Alimena G, Rowley JD, Vardiman JW, Testa JR, Sovik C. Correlation of occupation and karyotype in adults with acute nonlymphocytic leukemia. Blood. 1982;60:404-411.
    • (1982) Blood , vol.60 , pp. 404-411
    • Golomb, H.M.1    Alimena, G.2    Rowley, J.D.3    Vardiman, J.W.4    Testa, J.R.5    Sovik, C.6
  • 18
    • 0026001690 scopus 로고
    • Monosomy 7 in multilineage and acute lymphoblastic leukaemia
    • Paietta E, Gucalp R, Wiernik PH. Monosomy 7 in multilineage and acute lymphoblastic leukaemia. Br J Haematol. 1991;79:152-155.
    • (1991) Br J Haematol , vol.79 , pp. 152-155
    • Paietta, E.1    Gucalp, R.2    Wiernik, P.H.3
  • 19
    • 0028358155 scopus 로고
    • Lymphoid blast crisis of B-lineage phenotype with monosomy 7 in a patient with juvenile chronic myelogenous leukemia (JCML)
    • Lau RC, Squire J, Brisson L, et al. Lymphoid blast crisis of B-lineage phenotype with monosomy 7 in a patient with juvenile chronic myelogenous leukemia (JCML). Leukemia. 1994;8:903-908.
    • (1994) Leukemia , vol.8 , pp. 903-908
    • Lau, R.C.1    Squire, J.2    Brisson, L.3
  • 20
    • 0023634906 scopus 로고
    • Juvenile monosomy 7 syndrome: Evidence that the disease originates in a pluripotent hemopoietic stem cell
    • Hogge DE, Shannon KM, Kalousek DK, et al. Juvenile monosomy 7 syndrome: evidence that the disease originates in a pluripotent hemopoietic stem cell. Leuk Res. 1987;11:705-709.
    • (1987) Leuk Res , vol.11 , pp. 705-709
    • Hogge, D.E.1    Shannon, K.M.2    Kalousek, D.K.3
  • 22
    • 0026525853 scopus 로고
    • Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders
    • Neuman WL, Rubin CM, Rios RB, et al. Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders. Blood. 1992;79:1501-1510.
    • (1992) Blood , vol.79 , pp. 1501-1510
    • Neuman, W.L.1    Rubin, C.M.2    Rios, R.B.3
  • 23
    • 0026708498 scopus 로고
    • Clonal analysis of myelodysplastic syndrome: Monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization
    • Gerritsen WR, Donohue J, Bauman J, et al. Clonal analysis of myelodysplastic syndrome: monosomy 7 is expressed in the myeloid lineage, but not in the lymphoid lineage as detected by fluorescent in situ hybridization. Blood. 1992;80:217-224.
    • (1992) Blood , vol.80 , pp. 217-224
    • Gerritsen, W.R.1    Donohue, J.2    Bauman, J.3
  • 25
    • 0022997075 scopus 로고
    • Monosomy 7 and acute mixed leukemia
    • Sanz GF, Gomis F, Sanz MA. Monosomy 7 and acute mixed leukemia. Br J Haematol. 1986;64:842-844.
    • (1986) Br J Haematol , vol.64 , pp. 842-844
    • Sanz, G.F.1    Gomis, F.2    Sanz, M.A.3
  • 26
    • 0032895213 scopus 로고    scopus 로고
    • Lineage switch in childhood leukemia with monosomy 7 and reverse of lineage switch in severe combined immunodeficient mice
    • Fujisaki H, Hara J, Takai K, et al. Lineage switch in childhood leukemia with monosomy 7 and reverse of lineage switch in severe combined immunodeficient mice. Exp Hematol. 1999;27: 826-833.
    • (1999) Exp Hematol , vol.27 , pp. 826-833
    • Fujisaki, H.1    Hara, J.2    Takai, K.3
  • 27
    • 0006166049 scopus 로고
    • ISCN 1985. Report of the Standing Committee on Human Cytogenetic Nomenclature
    • An International System for Human Cytogenetic Nomenclature (1985). ISCN 1985. Report of the Standing Committee on Human Cytogenetic Nomenclature. Birth Defects Orig Artic Ser. 1985;21:1-117.
    • (1985) Birth Defects Orig Artic Ser , vol.21 , pp. 1-117


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.