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Journal Abstract Search

316 related items for PubMed ID: 12149226

  • 1. Genomic abnormalities in monoclonal gammopathy of undetermined significance.
    Fonseca R, Bailey RJ, Ahmann GJ, Rajkumar SV, Hoyer JD, Lust JA, Kyle RA, Gertz MA, Greipp PR, Dewald GW.
    Blood; 2002 Aug 15; 100(4):1417-24. PubMed ID: 12149226
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  • 5. Characterization of oncogene dysregulation in multiple myeloma by combined FISH and DNA microarray analyses.
    Fabris S, Agnelli L, Mattioli M, Baldini L, Ronchetti D, Morabito F, Verdelli D, Nobili L, Intini D, Callea V, Stelitano C, Lombardi L, Neri A.
    Genes Chromosomes Cancer; 2005 Feb 15; 42(2):117-27. PubMed ID: 15543617
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  • 7. The t(4;14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance.
    Fonseca R, Oken MM, Greipp PR, Eastern Cooperative Oncology Group Myeloma Group.
    Blood; 2001 Aug 15; 98(4):1271-2. PubMed ID: 11510469
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  • 9. Frequent occurrence of CCND1 deregulation in patients with early stages of plasma cell dyscrasia.
    Miura K, Iida S, Hanamura I, Kato M, Banno S, Ishida T, Kusumoto S, Takeuchi G, Miwa H, Nitta M, Inagaki H, Eimoto T, Nomura K, Taniwaki M, Ueda R.
    Cancer Sci; 2003 Apr 15; 94(4):350-4. PubMed ID: 12824903
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  • 10. Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia.
    Rasillo A, Tabernero MD, Sánchez ML, Pérez de Andrés M, Martín Ayuso M, Hernández J, Moro MJ, Fernández-Calvo J, Sayagués JM, Bortoluci A, San Miguel JF, Orfao A.
    Cancer; 2003 Feb 01; 97(3):601-9. PubMed ID: 12548602
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  • 12. Correlation between losses of IGH or its segments and deletions of 13q14 in t(11;14) (q13;q32) multiple myeloma.
    Trakhtenbrot L, Hardan I, Koren-Michowitz M, Oren S, Yshoev G, Rechavi G, Nagler A, Amariglio N.
    Genes Chromosomes Cancer; 2010 Jan 01; 49(1):17-27. PubMed ID: 19787791
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  • 16. Expression of fibroblast growth factor and FGF-receptor family genes in human myeloma cells, including lines possessing t(4;14)(q16.3;q32. 3) and FGFR3 translocation.
    Otsuki T, Yamada O, Yata K, Sakaguchi H, Kurebayashi J, Nakazawa N, Taniwaki M, Yawata Y, Ueki A.
    Int J Oncol; 1999 Dec 01; 15(6):1205-12. PubMed ID: 10568829
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  • 18. Cytogenetics of multiple myeloma: interpretation of fluorescence in situ hybridization results.
    Harrison CJ, Mazzullo H, Cheung KL, Gerrard G, Jalali GR, Mehta A, Osier DG, Orchard KH.
    Br J Haematol; 2003 Mar 01; 120(6):944-52. PubMed ID: 12648063
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  • 19. Detection of t(4;14)(p16.3;q32) chromosomal translocation in multiple myeloma by double-color fluorescent in situ hybridization.
    Finelli P, Fabris S, Zagano S, Baldini L, Intini D, Nobili L, Lombardi L, Maiolo AT, Neri A.
    Blood; 1999 Jul 15; 94(2):724-32. PubMed ID: 10397739
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  • 20. Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark.
    Christensen JH, Abildgaard N, Plesner T, Nibe A, Nielsen O, Sørensen AG, Kerndrup GB, Leukemia/Lymphoma Study Group, Region of Southern Denmark.
    Cancer Genet Cytogenet; 2007 Apr 15; 174(2):89-99. PubMed ID: 17452249
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