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Journal Abstract Search

417 related items for PubMed ID: 19602464

  • 1.
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  • 2. Identification of CUX1 as the recurrent chromosomal band 7q22 target gene in human uterine leiomyoma.
    Schoenmakers EF, Bunt J, Hermers L, Schepens M, Merkx G, Janssen B, Kersten M, Huys E, Pauwels P, Debiec-Rychter M, van Kessel AG.
    Genes Chromosomes Cancer; 2013 Jan; 52(1):11-23. PubMed ID: 22965931
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  • 3.
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  • 4. Uterine leiomyomata with t(10;17) disrupt the histone acetyltransferase MORF.
    Moore SD, Herrick SR, Ince TA, Kleinman MS, Dal Cin P, Morton CC, Quade BJ.
    Cancer Res; 2004 Aug 15; 64(16):5570-7. PubMed ID: 15313893
    [Abstract] [Full Text] [Related]

  • 5. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
    Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N.
    Oncogene; 1995 Mar 16; 10(6):1087-93. PubMed ID: 7700633
    [Abstract] [Full Text] [Related]

  • 6. [A preliminary cytogenetic study of uterine leiomyoma].
    Xiu ZF.
    Zhonghua Fu Chan Ke Za Zhi; 1993 Feb 16; 28(2):91-3, 123. PubMed ID: 8344090
    [Abstract] [Full Text] [Related]

  • 7. Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
    Schoenmakers EF, Kools PF, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong PJ, Van den Berghe H, Van de Ven WJ.
    Genomics; 1994 Mar 15; 20(2):210-22. PubMed ID: 8020967
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  • 8. Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP.
    Amler LC, Bauer A, Corvi R, Dihlmann S, Praml C, Cavenee WK, Schwab M, Hampton GM.
    Genomics; 2000 Mar 01; 64(2):195-202. PubMed ID: 10729226
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  • 9.
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  • 10. Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15.
    Quade BJ, Weremowicz S, Neskey DM, Vanni R, Ladd C, Dal Cin P, Morton CC.
    Cancer Res; 2003 Mar 15; 63(6):1351-8. PubMed ID: 12649198
    [Abstract] [Full Text] [Related]

  • 11. Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.
    Schoenmakers EF, Mols R, Wanschura S, Kools PF, Geurts JM, Bartnitzke S, Bullerdiek J, van den Berghe H, Van de Ven WJ.
    Genes Chromosomes Cancer; 1994 Oct 15; 11(2):106-18. PubMed ID: 7529547
    [Abstract] [Full Text] [Related]

  • 12. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS, Ludkovski O, Connors JM, Gascoyne RD, Lam WL, Horsman DE.
    Genes Chromosomes Cancer; 2003 Apr 15; 36(4):375-81. PubMed ID: 12619161
    [Abstract] [Full Text] [Related]

  • 13. Physical mapping of the uterine leiomyoma t(12;14)(q13-15;q24.1) breakpoint on chromosome 14 between SPTB and D14S77.
    Hug K, Doney MK, Tyler MJ, Grundy DA, Soukup S, Houseal TW, Menon AG.
    Genes Chromosomes Cancer; 1994 Dec 15; 11(4):263-6. PubMed ID: 7533530
    [Abstract] [Full Text] [Related]

  • 14. Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma.
    Bhugra B, Smolarek TA, Lynch RA, Meloni AM, Sandberg AA, Deaven L, Menon AG.
    Cancer Lett; 1998 Apr 24; 126(2):119-26. PubMed ID: 9585056
    [Abstract] [Full Text] [Related]

  • 15. Identification of the breakpoints at 1p36.2 and 3p21.3 in an AML(M3) patient who had t(1;3)(p36.2;p21.3) at the third relapse.
    Tri NK, Xinh PT, Nagao H, Izumi T, Ozawa K, Toyoda A, Hattori M, Sakaki Y, Tokunaga K, Sato Y.
    Genes Chromosomes Cancer; 2002 Dec 24; 35(4):365-7. PubMed ID: 12378531
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetics of parametrial leiomyoma.
    Dahlenfors R, Havel G, Wedell B, Mark J.
    Anticancer Res; 1997 Dec 24; 17(3C):2121-2. PubMed ID: 9216674
    [Abstract] [Full Text] [Related]

  • 17. Frequency and characterization of HMGA2 and HMGA1 rearrangements in mesenchymal tumors of the lower genital tract.
    Medeiros F, Erickson-Johnson MR, Keeney GL, Clayton AC, Nascimento AG, Wang X, Oliveira AM.
    Genes Chromosomes Cancer; 2007 Nov 24; 46(11):981-90. PubMed ID: 17654722
    [Abstract] [Full Text] [Related]

  • 18. Paratesticular leiomyoma with a der(14)t(12;14)(q15;q24).
    Gorunova L, Bjerkehagen B, Heim S.
    Cancer Genet; 2011 Aug 24; 204(8):465-8. PubMed ID: 21962898
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  • 19.
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  • 20. Gene fusion involving HMGIC is a frequent aberration in uterine leiomyomas.
    Mine N, Kurose K, Nagai H, Doi D, Ota Y, Yoneyama K, Konishi H, Araki T, Emi M.
    J Hum Genet; 2001 Aug 24; 46(7):408-12. PubMed ID: 11450849
    [Abstract] [Full Text] [Related]

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