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Volumn 27, Issue 2, 2005, Pages 355-359

Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia

Author keywords

Acute myeloid leukemia; Comparative genomic hybridization

Indexed keywords

ACUTE DISEASE; ADOLESCENT; ADULT; AGED; ARTICLE; BLOOD; BONE MARROW; CELL PROLIFERATION; CHROMOSOME ABERRATION; CHROMOSOME BANDING PATTERN; COMPARATIVE STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; GENOME; HUMAN; KARYOTYPING; MALE; METABOLISM; METHODOLOGY; MYELOID LEUKEMIA; NUCLEIC ACID HYBRIDIZATION; PATHOLOGY; PILOT STUDY;

EID: 29244483599     PISSN: 10196439     EISSN: 17912423     Source Type: Journal    
DOI: 10.3892/ijo.27.2.355     Document Type: Article
Times cited : (5)

References (25)
  • 4
    • 0029912473 scopus 로고    scopus 로고
    • Karyotyping human chromosomes by combinatorial multi-fluor FISH
    • Speicher MR. Gwyn Ballard S and Ward DC: Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12: 368-375. 1996.
    • (1996) Nat Genet , vol.12 , pp. 368-375
    • Speicher, M.R.1    Gwyn Ballard, S.2    Ward, D.C.3
  • 6
    • 0036080006 scopus 로고    scopus 로고
    • FISH banding methods: Applications in research and diagnostics
    • Liehr T. Heller A. Starke H and Claussen U: FISH banding methods: applications in research and diagnostics. Expert Rev Mol Diagn 2:217-225.2002.
    • (2002) Expert Rev Mol Diagn , vol.2 , pp. 217-225
    • Liehr, T.1    Heller, A.2    Starke, H.3    Claussen, U.4
  • 7
    • 0027164414 scopus 로고
    • Use of fluorescence in situ hybridization (FISH) for the estimation of the aberrant cell clone in leukaemias with trisomy 8 or monosomy 7 detected by karyotyping
    • Gcbhart E. Trautmann U, Reichardt S and Liehr T: Use of fluorescence in situ hybridization (FISH) for the estimation of the aberrant cell clone in leukaemias with trisomy 8 or monosomy 7 detected by karyotyping. Int J Oncol 3: 191-195. 1993.
    • (1993) Int J Oncol , vol.3 , pp. 191-195
    • Gcbhart, E.1    Trautmann, U.2    Reichardt, S.3    Liehr, T.4
  • 8
    • 0027755235 scopus 로고
    • Chromosomal heterogenety of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH)
    • Gcbhart E. Trautmann U. Reichardt S and Liehr T: Chromosomal heterogenety of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH). Anticancer Res 13: 1857-1862. 1993.
    • (1993) Anticancer Res , vol.13 , pp. 1857-1862
    • Gcbhart, E.1    Trautmann, U.2    Reichardt, S.3    Liehr, T.4
  • 10
    • 0034146264 scopus 로고    scopus 로고
    • Microdissection based comparative genomic hybridization (micro-CGH) analysis of secondary acute myelogenous leukemias
    • Heller A. Chudoba I. Bleek C. Senger G. Claussen U and LichrT: Microdissection based comparative genomic hybridization (micro-CGH) analysis of secondary acute myelogenous leukemias. Int J Oncol 16: 461-468. 2000.
    • (2000) Int J Oncol , vol.16 , pp. 461-468
    • Heller, A.1    Chudoba, I.2    Bleek, C.3    Senger, G.4    Claussen, U.5    Lichr, T.6
  • 16
    • 0034133818 scopus 로고    scopus 로고
    • Patterns of genomic imbalances in human solid tumors (Review)
    • Gebhart E and Liehr T: Patterns of genomic imbalances in human solid tumors (Review). Int J Oncol 16: 383-399. 2000.
    • (2000) Int J Oncol , vol.16 , pp. 383-399
    • Gebhart, E.1    Liehr, T.2
  • 17
    • 0037238483 scopus 로고    scopus 로고
    • Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: A multicolor and locus-specific fluorescence in situ hybridization study
    • Paulsson K. Fioretos T. Strömbeek B. Mauritzson N. Tanke HJ and Johansson B: Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study. Cancer Genet Cytogenet 140: 66-69. 2003.
    • (2003) Cancer Genet Cytogenet , vol.140 , pp. 66-69
    • Paulsson, K.1    Fioretos, T.2    Strömbeek, B.3    Mauritzson, N.4    Tanke, H.J.5    Johansson, B.6
  • 18
    • 0141676607 scopus 로고    scopus 로고
    • Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: A comprehensive molecular cytogenetic analysis reveals no cryptic aberrations
    • Heller A. Brecevic L. Glaser M. Lonearevic I. Gebhart E. Claussen U and Liehr T: Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. Cancer Genet Cytogenet 146: 81-83. 2003.
    • (2003) Cancer Genet Cytogenet , vol.146 , pp. 81-83
    • Heller, A.1    Brecevic, L.2    Glaser, M.3    Lonearevic, I.4    Gebhart, E.5    Claussen, U.6    Liehr, T.7
  • 19
    • 0030200537 scopus 로고    scopus 로고
    • Trisomy 15 in hematological malignancies: Six cases and review of the literature
    • Smith SR and Rowe D: Trisomy 15 in hematological malignancies: six cases and review of the literature. Cancer Genet Cytogenet 89: 27-30. 1996.
    • (1996) Cancer Genet Cytogenet , vol.89 , pp. 27-30
    • Smith, S.R.1    Rowe, D.2
  • 22
    • 84887117495 scopus 로고    scopus 로고
    • M7 acute non lymphocytic leukemia (M7-ANLL). Atlas Genet Cytogenet Oncol Haematol. November
    • Cunco A. Cavazzini F and Castoldi G: Acute megakaryoblaslic leukemia (AMegL). M7 acute non lymphocytic leukemia (M7-ANLL). Atlas Genet Cytogenet Oncol Haematol. November 2003. URL: http://www.infobiogen.fr/services/ chromcancer/ Anomalies/M7ANLLID1100.html
    • (2003) Acute Megakaryoblaslic Leukemia (AMegL)
    • Cunco, A.1    Cavazzini, F.2    Castoldi, G.3
  • 23
    • 84887117931 scopus 로고    scopus 로고
    • Van Dyke DL: +18 or trisomy 18 in lymphoproliferative disorders. September
    • Van Dyke DL: +18 or trisomy 18 in lymphoproliferative disorders. Allas Genet Cytogenet Oncol Haematol. September 2003 URL: http://www.infobiogen.fr/ services/chromcancer/ Anomalies/Tri 18ID2030.hlml
    • (2003) Allas Genet Cytogenet Oncol Haematol
  • 24
    • 0030800135 scopus 로고    scopus 로고
    • Frequent gains and losses of specific chromosome segments in human ovarian carcinomas shown by comparative genomic hybridization
    • Wolff E. Liehr T. Vordcrwülbecke U. Tulusan AH. Husslein EM and Gebhart E: Frequent gains and losses of specific chromosome segments in human ovarian carcinomas shown by comparative genomic hybridization. Int J Oncol 11: 19-23. 1997.
    • (1997) Int J Oncol , vol.11 , pp. 19-23
    • Wolff, E.1    Liehr, T.2    Vorderwülbecke, U.3    Tulusan, A.H.4    Husslein, E.M.5    Gebhart, E.6
  • 25
    • 0033672795 scopus 로고    scopus 로고
    • Comparative genomic hybridization study of de novo myeloid neoplasia
    • Castuma MV. Rao PH. Acevedo SH and Larripa IB: Comparative genomic hybridization study of de novo myeloid neoplasia. Acta Haematol 104: 25-30. 2000.
    • (2000) Acta Haematol , vol.104 , pp. 25-30
    • Castuma, M.V.1    Rao, P.H.2    Acevedo, S.H.3    Larripa, I.B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.