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Volumn 157, Issue 2, 2005, Pages 178-180

Cryptic 5′ MLL gene insertion in an X-chromosome in acute myeloblastic leukemia

Author keywords

[No Author keywords available]

Indexed keywords

MIXED LINEAGE LEUKEMIA PROTEIN; DNA BINDING PROTEIN; MLL PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

EID: 13844254011     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2004.08.015     Document Type: Article
Times cited : (8)

References (16)
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    • Y. Hayashi The molecular genetics of recurring chromosome abnormalities in acute myeloid leukemia Semin Hematol 37 2000 368 380
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    • Hayashi, Y.1
  • 5
    • 85044561752 scopus 로고    scopus 로고
    • An atlas on chromosomes in hematological malignancies. Example: 11q23 and MLL partners
    • J.L. Huret, P. Dessen, A. Bernheim, and the Groupe Francais de Cytogenetique Hematologique An atlas on chromosomes in hematological malignancies. Example: 11q23 and MLL partners Leukemia 15 2001 987 999
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  • 9
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    • Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe
    • M.J. Dyson, P.J. Talley, J.T. Reilly, D. Stevenson, E. Parsons, and J. Tighe Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe Cancer Genet Cytogenet 147 2003 81 83
    • (2003) Cancer Genet Cytogenet , vol.147 , pp. 81-83
    • Dyson, M.J.1    Talley, P.J.2    Reilly, J.T.3    Stevenson, D.4    Parsons, E.5    Tighe, J.6
  • 10
    • 0037532541 scopus 로고    scopus 로고
    • Insertion of MLL sequences into chromosome band 5q31 results in an MLL-AF5Q31 fusion and is a rare but recurrent abnormality associated with infant leukemia
    • R. Deveney, D.S. Chervinsky, S.N. Jani-Sait, M. Grossi, and P.D. Aplan Insertion of MLL sequences into chromosome band 5q31 results in an MLL-AF5Q31 fusion and is a rare but recurrent abnormality associated with infant leukemia Genes Chromosomes Cancer 37 2003 326 331
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    • Deveney, R.1    Chervinsky, D.S.2    Jani-Sait, S.N.3    Grossi, M.4    Aplan, P.D.5
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    • J. Bruch, M. Wilda, A. Teigler-Schlegel, J. Harbott, A. Borkhardt, and M. Metzler Occurrence of an MLL/LAF4 fusion gene caused by the insertion ins(11;2)(q23;q11.2q11.2) in an infant with acute lymphoblastic leukemia (ALL) Genes Chromosomes Cancer 37 2003 106 109
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    • Bruch, J.1    Wilda, M.2    Teigler-Schlegel, A.3    Harbott, J.4    Borkhardt, A.5    Metzler, M.6
  • 12
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    • MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site
    • D.J. Slater, E. Hilgenfeld, E.F. Rappaport, N. Shah, R.G. Meek, W.R. Williams, B.D. Lovett, N. Osheroff, R.S. Autar, T. Ried, and C.A. Felix MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site Oncogene 21 2002 4706 4714
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    • Slater, D.J.1    Hilgenfeld, E.2    Rappaport, E.F.3    Shah, N.4    Meek, R.G.5    Williams, W.R.6    Lovett, B.D.7    Osheroff, N.8    Autar, R.S.9    Ried, T.10    Felix, C.A.11
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    • SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24
    • R. Ono, T. Taki, T. Taketani, H. Kawaguchi, M. Taniwaki, T. Okamura, K. Kawa, R. Hanada, M. Kobayashi, and Y. Hayashi SEPTIN6, a human homologue to mouse Septin6, is fused to MLL in infant acute myeloid leukemia with complex chromosomal abnormalities involving 11q23 and Xq24 Cancer Res 62 2002 333 337
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    • Ono, R.1    Taki, T.2    Taketani, T.3    Kawaguchi, H.4    Taniwaki, M.5    Okamura, T.6    Kawa, K.7    Hanada, R.8    Kobayashi, M.9    Hayashi, Y.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.