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Journal Abstract Search

151 related items for PubMed ID: 8037210

  • 21. 17q gain in neuroblastoma predicts adverse clinical outcome. U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group.
    Bown N, Lastowska M, Cotterill S, O'Neill S, Ellershaw C, Roberts P, Lewis I, Pearson AD, U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group.
    Med Pediatr Oncol; 2001 Jan; 36(1):14-9. PubMed ID: 11464868
    [Abstract] [Full Text] [Related]

  • 22. Balanced translocation in a neuroblastoma patient disrupts a cluster of small nuclear RNA U1 and tRNA genes in chromosomal band 1p36.
    van der Drift P, Chan A, Laureys G, van Roy N, Sickmann G, den Dunnen J, Westerveld A, Speleman F, Versteeg R.
    Genes Chromosomes Cancer; 1995 Sep; 14(1):35-42. PubMed ID: 8527382
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  • 23. Comparative genomic hybridization analysis of human neuroblastomas: detection of distal 1p deletions and further molecular genetic characterization of neuroblastoma cell lines.
    Van Roy N, Jauch A, Van Gele M, Laureys G, Versteeg R, De Paepe A, Cremer T, Speleman F.
    Cancer Genet Cytogenet; 1997 Sep; 97(2):135-42. PubMed ID: 9283597
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  • 25. Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation.
    Panarello C, Morerio C, Russo I, Pasquali F, Rapella A, Corrias MV, Morando A, Rosanda C.
    Cancer Genet Cytogenet; 2000 Jan 15; 116(2):124-32. PubMed ID: 10640144
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  • 27. Allelic loss of chromosome 1 and additional chromosome 17 material are both unfavourable prognostic markers in neuroblastoma.
    Caron H.
    Med Pediatr Oncol; 1995 Apr 15; 24(4):215-21. PubMed ID: 7700165
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  • 28. Reciprocal translocation at 1p36.2/D1S160 in a neuroblastoma cell line: isolation of a YAC clone at the break.
    Amler LC, Corvi R, Praml C, Savelyeva L, Le Paslier D, Schwab M.
    Eur J Cancer; 1995 Apr 15; 31A(4):527-30. PubMed ID: 7576959
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  • 29. 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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  • 31. Cytogenetic and molecular studies on the neuroblastoma cell line NGP: identification of a reciprocal t(1;15) involving the "consensus region" 1p36.1.
    Muresu R, Casciano I, Volpi EV, Siniscalco M, Romani M.
    Genes Chromosomes Cancer; 1995 May 01; 13(1):66-71. PubMed ID: 7541646
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  • 32. Molecular and genetic studies on the region of translocation and duplication in the neuroblastoma cell line NGP at the 1p36.13-p36.32 chromosomal site.
    Casciano I, Marchi JV, Muresu R, Volpi EV, Rozzo C, Opdenakker G, Romani M.
    Oncogene; 1996 May 16; 12(10):2101-8. PubMed ID: 8668335
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  • 33. Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma?
    Stallings RL, Howard J, Dunlop A, Mullarkey M, McDermott M, Breatnach F, O'Meara A.
    Cancer Genet Cytogenet; 2003 Jan 15; 140(2):133-7. PubMed ID: 12645651
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  • 34. Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.
    Abel F, Ejeskär K, Kogner P, Martinsson T.
    Br J Cancer; 1999 Dec 15; 81(8):1402-9. PubMed ID: 10604740
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  • 35. Molecular analysis of the region of distal 1p commonly deleted in neuroblastoma.
    White PS, Maris JM, Sulman EP, Jensen SJ, Kyemba SM, Beltinger CP, Allen C, Kramer DL, Biegel JA, Brodeur GM.
    Eur J Cancer; 1997 Oct 15; 33(12):1957-61. PubMed ID: 9516832
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  • 36. Monosomy 1p36.31-33-->pter due to a paternal reciprocal translocation: prognostic significance of FISH analysis.
    Blennow E, Bui TH, Wallin A, Kogner P.
    Am J Med Genet; 1996 Oct 02; 65(1):60-7. PubMed ID: 8914743
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  • 37. Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
    Van Gele M, Van Roy N, Ronan SG, Messiaen L, Vandesompele J, Geerts ML, Naeyaert JM, Blennow E, Bar-Am I, Das Gupta TK, van der Drift P, Versteeg R, Leonard JH, Speleman F.
    Genes Chromosomes Cancer; 1998 Sep 02; 23(1):67-71. PubMed ID: 9713999
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  • 38. Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma.
    Laureys G, Speleman F, Opdenakker G, Benoit Y, Leroy J.
    Genes Chromosomes Cancer; 1990 Sep 02; 2(3):252-4. PubMed ID: 2078517
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  • 39. Loss of heterozygosity for chromosome 1p in familial neuroblastoma.
    Tonini GP, Lo Cunsolo C, Cusano R, Iolascon A, Dagnino M, Conte M, Milanaccio C, De Bernardi B, Mazzocco K, Scaruffi P.
    Eur J Cancer; 1997 Oct 02; 33(12):1953-6. PubMed ID: 9516831
    [Abstract] [Full Text] [Related]

  • 40. Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization.
    Anamthawat-Jónsson K, Eyfjörd JE, Ogmundsdóttir HM, Pétursdóttir I, Steinarsdóttir M.
    Cancer Genet Cytogenet; 1996 May 02; 88(1):1-7. PubMed ID: 8630972
    [Abstract] [Full Text] [Related]

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