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Volumn 179, Issue 1, 2007, Pages 25-30

Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns

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EID: 35548989625     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2007.07.011     Document Type: Article
Times cited : (6)

References (32)
  • 1
    • 0024423029 scopus 로고
    • Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts
    • Dewald G.W., Brecher M., Travis L.B., and Stupca P.J. Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genet Cytogenet 42 (1989) 173-185
    • (1989) Cancer Genet Cytogenet , vol.42 , pp. 173-185
    • Dewald, G.W.1    Brecher, M.2    Travis, L.B.3    Stupca, P.J.4
  • 2
    • 0028846257 scopus 로고
    • Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature
    • Dierlamm J., Michaux L., Criel A., Wlodarska I., Zeller W., Louwagie A., Michaux J.L., Mecucci C., and Van den Berghe H. Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature. Br J Haematol 91 (1995) 885-891
    • (1995) Br J Haematol , vol.91 , pp. 885-891
    • Dierlamm, J.1    Michaux, L.2    Criel, A.3    Wlodarska, I.4    Zeller, W.5    Louwagie, A.6    Michaux, J.L.7    Mecucci, C.8    Van den Berghe, H.9
  • 3
    • 4344666221 scopus 로고
    • Isodicentric X chromosomes in human: origin, segregation behavior, and replication band patterns
    • Sandberg A.A. (Ed), Alan R. Liss, New York
    • Dewald G.W. Isodicentric X chromosomes in human: origin, segregation behavior, and replication band patterns. In: Sandberg A.A. (Ed). Cytogenetics of the mammalian X chromosome. Part A. Basic mechanisms of X chromosome behavior (1983), Alan R. Liss, New York 405-426
    • (1983) Cytogenetics of the mammalian X chromosome. Part A. Basic mechanisms of X chromosome behavior , pp. 405-426
    • Dewald, G.W.1
  • 4
    • 35548968543 scopus 로고    scopus 로고
    • Mitelman F, Johansson B, Mertens F, editors. Mitelman database of chromosome aberrations in cancer [Internet]. Updated Feb 2007. Accessed Feb. 16, 2007. Available at: http://www.cgap.nci.nih.gov/Chromosomes/Mitelman.
  • 6
    • 0019444548 scopus 로고
    • Cytogenetic follow-up of patients with nonlymphocytic leukemia. II. Acute nonlymphocytic leukemia
    • Hagemeijer A., Hahlen K., and Abels J. Cytogenetic follow-up of patients with nonlymphocytic leukemia. II. Acute nonlymphocytic leukemia. Cancer Genet Cytogenet 3 (1981) 109-124
    • (1981) Cancer Genet Cytogenet , vol.3 , pp. 109-124
    • Hagemeijer, A.1    Hahlen, K.2    Abels, J.3
  • 10
    • 0142217424 scopus 로고    scopus 로고
    • A case of Down syndrome with acute lymphoblastic leukemia and isochromosome Xp
    • Baker J.M., Coppes M.J., and Roland B. A case of Down syndrome with acute lymphoblastic leukemia and isochromosome Xp. Cancer Genet Cytogenet 147 (2003) 75-77
    • (2003) Cancer Genet Cytogenet , vol.147 , pp. 75-77
    • Baker, J.M.1    Coppes, M.J.2    Roland, B.3
  • 13
    • 0029031073 scopus 로고
    • Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes
    • Nacheva E., Holloway T., Carter N., Grace C., White N., and Green A.R. Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes. Cancer Genet Cytogenet 80 (1995) 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
  • 15
    • 0021180330 scopus 로고
    • Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromes
    • Knuutila S., Teerenhovi L., and Borgstrom G.H. Chromosome instability is associated with hypodiploid clones in myelodysplastic syndromes. Hereditas 101 (1984) 19-30
    • (1984) Hereditas , vol.101 , pp. 19-30
    • Knuutila, S.1    Teerenhovi, L.2    Borgstrom, G.H.3
  • 19
    • 0023848323 scopus 로고
    • Immunological and molecular studies in a case of follicular lymphoma with an extra chromosome 12 and t(2;8) translocation
    • Donti E., Falini B., Giuseppe Pelicci P., Venti Donti G., Rosetti A., Martelli M., and Grignani F. Immunological and molecular studies in a case of follicular lymphoma with an extra chromosome 12 and t(2;8) translocation. Leukemia 2 (1988) 41-44
    • (1988) Leukemia , vol.2 , pp. 41-44
    • Donti, E.1    Falini, B.2    Giuseppe Pelicci, P.3    Venti Donti, G.4    Rosetti, A.5    Martelli, M.6    Grignani, F.7
  • 21
    • 0025160230 scopus 로고
    • Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity
    • Sharp C.B., Bedford H.M., and Willard H.F. Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity. Hum Genet 85 (1990) 330-336
    • (1990) Hum Genet , vol.85 , pp. 330-336
    • Sharp, C.B.1    Bedford, H.M.2    Willard, H.F.3
  • 22
    • 0026047793 scopus 로고
    • Detection and analysis of origin of i(12p), a diagnostic marker of human male germ cell tumors, by fluorescence in situ hybridization
    • Mukherjee A.B., Murty V.V., Rodriguez E., Reuter V.E., Bosl G.J., and Chaganti R.S. Detection and analysis of origin of i(12p), a diagnostic marker of human male germ cell tumors, by fluorescence in situ hybridization. Genes Chromosomes Cancer 3 (1991) 300-307
    • (1991) Genes Chromosomes Cancer , vol.3 , pp. 300-307
    • Mukherjee, A.B.1    Murty, V.V.2    Rodriguez, E.3    Reuter, V.E.4    Bosl, G.J.5    Chaganti, R.S.6
  • 23
    • 0029656085 scopus 로고    scopus 로고
    • Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation
    • Wolff D.J., Miller A.P., Van Dyke D.L., Schwartz S., and Willard H.F. Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation. Am J Hum Genet 58 (1996) 154-160
    • (1996) Am J Hum Genet , vol.58 , pp. 154-160
    • Wolff, D.J.1    Miller, A.P.2    Van Dyke, D.L.3    Schwartz, S.4    Willard, H.F.5
  • 25
    • 0033659742 scopus 로고    scopus 로고
    • Centromere cleavage is a mechanism underlying isochromosome formation in skin and head and neck carcinomas
    • Jin Y., Jin C., Salemark L., Martins C., Wennerberg J., and Mertens F. Centromere cleavage is a mechanism underlying isochromosome formation in skin and head and neck carcinomas. Chromosoma 109 (2000) 476-481
    • (2000) Chromosoma , vol.109 , pp. 476-481
    • Jin, Y.1    Jin, C.2    Salemark, L.3    Martins, C.4    Wennerberg, J.5    Mertens, F.6
  • 27
    • 0035869185 scopus 로고    scopus 로고
    • Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature
    • Uehara S., Hanew K., Harada N., Yamamori S., Nata M., Niikawa N., and Okamura K. Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature. Am J Med Genet 99 (2001) 196-199
    • (2001) Am J Med Genet , vol.99 , pp. 196-199
    • Uehara, S.1    Hanew, K.2    Harada, N.3    Yamamori, S.4    Nata, M.5    Niikawa, N.6    Okamura, K.7
  • 29
    • 0035858882 scopus 로고    scopus 로고
    • Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation
    • Csankovszki G., Nagy A., and Jaenisch R. Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation. J Cell Biol 153 (2001) 773-784
    • (2001) J Cell Biol , vol.153 , pp. 773-784
    • Csankovszki, G.1    Nagy, A.2    Jaenisch, R.3
  • 30
    • 0020053658 scopus 로고
    • Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia
    • Dewald G.W., Pierre R.V., and Phyliky R.L. Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia. Blood 59 (1982) 100-105
    • (1982) Blood , vol.59 , pp. 100-105
    • Dewald, G.W.1    Pierre, R.V.2    Phyliky, R.L.3
  • 31


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.