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358 related items for PubMed ID: 9218994

  • 1. Promiscuous translocations of chromosome arm 17q in human neuroblastomas.
    Lastowska M, Roberts P, Pearson AD, Lewis I, Wolstenholme J, Bown N.
    Genes Chromosomes Cancer; 1997 Jul; 19(3):143-9. PubMed ID: 9218994
    [Abstract] [Full Text] [Related]

  • 2. Distinct cytogenetic pathways of advanced-stage neuroblastoma tumors, detected by spectral karyotyping.
    Stark B, Jeison M, Bar-Am I, Glaser-Gabay L, Mardoukh J, Luria D, Feinmesser M, Goshen Y, Stein J, Abramov A, Zaizov R, Yaniv I.
    Genes Chromosomes Cancer; 2002 Jul; 34(3):313-24. PubMed ID: 12007192
    [Abstract] [Full Text] [Related]

  • 3. Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.
    Schleiermacher G, Bourdeaut F, Combaret V, Picrron G, Raynal V, Aurias A, Ribeiro A, Janoueix-Lerosey I, Delattre O.
    Oncogene; 2005 May 05; 24(20):3377-84. PubMed ID: 15735707
    [Abstract] [Full Text] [Related]

  • 4. MYCN amplification and 17q in neuroblastoma: evidence for structural association.
    O'Neill S, Ekstrom L, Lastowska M, Roberts P, Brodeur GM, Kees UR, Schwab M, Bown N.
    Genes Chromosomes Cancer; 2001 Jan 05; 30(1):87-90. PubMed ID: 11107180
    [Abstract] [Full Text] [Related]

  • 5. Molecular cytogenetic analysis of recurrent unbalanced t(11;17) in neuroblastoma.
    Stallings RL, Carty P, McArdle L, Mullarkey M, McDermott M, Breatnach F, O'Meara A.
    Cancer Genet Cytogenet; 2004 Oct 01; 154(1):44-51. PubMed ID: 15381371
    [Abstract] [Full Text] [Related]

  • 6. Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.
    Lastowska M, Van Roy N, Bown N, Speleman F, Roberts P, Lunec J, Strachan T, Pearson AD, Jackson MS.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):20-3. PubMed ID: 11464884
    [Abstract] [Full Text] [Related]

  • 7. Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore.
    Yong MH, Hwang WS, Knight LA, Fung W, Chan MY, Seow WT, Chui CH.
    Singapore Med J; 2009 Nov 01; 50(11):1090-4. PubMed ID: 19960166
    [Abstract] [Full Text] [Related]

  • 8. Gain of distal chromosome arm 17q is not associated with poor prognosis in neuroblastoma.
    Spitz R, Hero B, Ernestus K, Berthold F.
    Clin Cancer Res; 2003 Oct 15; 9(13):4835-40. PubMed ID: 14581355
    [Abstract] [Full Text] [Related]

  • 9. Variety and complexity of chromosome 17 translocations in neuroblastoma.
    Schleiermacher G, Raynal V, Janoueix-Lerosey I, Combaret V, Aurias A, Delattre O.
    Genes Chromosomes Cancer; 2004 Feb 15; 39(2):143-50. PubMed ID: 14695994
    [Abstract] [Full Text] [Related]

  • 10. der(11)t(11;17): a distinct cytogenetic pathway of advanced stage neuroblastoma (NBL) - detected by spectral karyotyping (SKY).
    Stark B, Jeison M, Glaser-Gabay L, Bar-Am I, Mardoukh J, Ash S, Atias D, Stein J, Zaizov R, Yaniv I.
    Cancer Lett; 2003 Jul 18; 197(1-2):75-9. PubMed ID: 12880963
    [Abstract] [Full Text] [Related]

  • 11. Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma.
    Bown N, Cotterill S, Lastowska M, O'Neill S, Pearson AD, Plantaz D, Meddeb M, Danglot G, Brinkschmidt C, Christiansen H, Laureys G, Speleman F, Nicholson J, Bernheim A, Betts DR, Vandesompele J, Van Roy N.
    N Engl J Med; 1999 Jun 24; 340(25):1954-61. PubMed ID: 10379019
    [Abstract] [Full Text] [Related]

  • 12. Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.
    Van Roy N, Cheng NC, Laureys G, Opdenakker G, Versteeg R, Speleman F.
    Eur J Cancer; 1995 Jun 24; 31A(4):530-5. PubMed ID: 7576960
    [Abstract] [Full Text] [Related]

  • 13. Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.
    Van Roy N, Laureys G, Van Gele M, Opdenakker G, Miura R, van der Drift P, Chan A, Versteeg R, Speleman F.
    Eur J Cancer; 1997 Oct 24; 33(12):1974-8. PubMed ID: 9516836
    [Abstract] [Full Text] [Related]

  • 14. [The neuroblastoma, "enfant terrible" among pediatric tumors].
    Laureys G.
    Verh K Acad Geneeskd Belg; 2003 Oct 24; 65(1):5-23; discussion 23-8. PubMed ID: 12802894
    [Abstract] [Full Text] [Related]

  • 15. Human neuroblastomas and abnormalities of chromosomes 1 and 17.
    Gilbert F, Feder M, Balaban G, Brangman D, Lurie DK, Podolsky R, Rinaldt V, Vinikoor N, Weisband J.
    Cancer Res; 1984 Nov 24; 44(11):5444-9. PubMed ID: 6488196
    [Abstract] [Full Text] [Related]

  • 16. Numerical and structural aberrations in advanced neuroblastoma tumours by CGH analysis; survival correlates with chromosome 17 status.
    Cunsolo CL, Bicocchi MP, Petti AR, Tonini GP.
    Br J Cancer; 2000 Nov 24; 83(10):1295-300. PubMed ID: 11044353
    [Abstract] [Full Text] [Related]

  • 17. Regions syntenic to human 17q are gained in mouse and rat neuroblastoma.
    Łastowska M, Chung YJ, Cheng Ching N, Haber M, Norris MD, Kees UR, Pearson AD, Jackson MS.
    Genes Chromosomes Cancer; 2004 Jun 24; 40(2):158-63. PubMed ID: 15101050
    [Abstract] [Full Text] [Related]

  • 18. Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas.
    Meddeb M, Danglot G, Chudoba I, Vénuat AM, Bénard J, Avet-Loiseau H, Vasseur B, Le Paslier D, Terrier-Lacombe MJ, Hartmann O, Bernheim A.
    Genes Chromosomes Cancer; 1996 Nov 24; 17(3):156-65. PubMed ID: 8946194
    [Abstract] [Full Text] [Related]

  • 19. Detection of single-copy chromosome 17q gain in human neuroblastomas using real-time quantitative polymerase chain reaction.
    Morowitz M, Shusterman S, Mosse Y, Hii G, Winter CL, Khazi D, Wang Q, King R, Maris JM.
    Mod Pathol; 2003 Dec 24; 16(12):1248-56. PubMed ID: 14681326
    [Abstract] [Full Text] [Related]

  • 20. 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]

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