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391 related items for PubMed ID: 10490829

  • 1. Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas.
    Guo C, White PS, Weiss MJ, Hogarty MD, Thompson PM, Stram DO, Gerbing R, Matthay KK, Seeger RC, Brodeur GM, Maris JM.
    Oncogene; 1999 Sep 02; 18(35):4948-57. PubMed ID: 10490829
    [Abstract] [Full Text] [Related]

  • 2. Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma.
    Maris JM, Guo C, White PS, Hogarty MD, Thompson PM, Stram DO, Gerbing R, Matthay KK, Seeger RC, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 02; 36(1):24-7. PubMed ID: 11464895
    [Abstract] [Full Text] [Related]

  • 3. Loss of heterozygosity for chromosome 14q in neuroblastoma.
    Thompson PM, Seifried BA, Kyemba SK, Jensen SJ, Guo C, Maris JM, Brodeur GM, Stram DO, Seeger RC, Gerbing R, Matthay KK, Matise TC, White PS.
    Med Pediatr Oncol; 2001 Jan 02; 36(1):28-31. PubMed ID: 11464899
    [Abstract] [Full Text] [Related]

  • 4. Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas.
    Guo C, White PS, Hogarty MD, Brodeur GM, Gerbing R, Stram DO, Maris JM.
    Med Pediatr Oncol; 2000 Dec 02; 35(6):544-6. PubMed ID: 11107113
    [Abstract] [Full Text] [Related]

  • 5. Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms.
    Martinsson T, Sjöberg RM, Hedborg F, Kogner P.
    Cancer Res; 1995 Dec 01; 55(23):5681-6. PubMed ID: 7585654
    [Abstract] [Full Text] [Related]

  • 6. Analysis of genomic imprinting at 1p35-36 in neuroblastoma.
    Hogarty MD, Maris JM, White PS, Guo C, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):52-5. PubMed ID: 11464906
    [Abstract] [Full Text] [Related]

  • 7. Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas.
    Fong CT, White PS, Peterson K, Sapienza C, Cavenee WK, Kern SE, Vogelstein B, Cantor AB, Look AT, Brodeur GM.
    Cancer Res; 1992 Apr 01; 52(7):1780-5. PubMed ID: 1551108
    [Abstract] [Full Text] [Related]

  • 8. Sublocalization of putative tumor suppressor gene loci on chromosome arm 14q in neuroblastoma.
    Theobald M, Christiansen H, Schmidt A, Melekian B, Wolkewitz N, Christiansen NM, Brinkschmidt C, Berthold F, Lampert F.
    Genes Chromosomes Cancer; 1999 Sep 01; 26(1):40-6. PubMed ID: 10441004
    [Abstract] [Full Text] [Related]

  • 9. Comprehensive analysis of chromosome 1p deletions in neuroblastoma.
    Maris JM, Guo C, Blake D, White PS, Hogarty MD, Thompson PM, Rajalingam V, Gerbing R, Stram DO, Matthay KK, Seeger RC, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):32-6. PubMed ID: 11464900
    [Abstract] [Full Text] [Related]

  • 10. Biological characteristics of neuroblastoma with partial deletion in the short arm of chromosome 1.
    Hiyama E, Hiyama K, Ohtsu K, Yamaoka H, Fukuba I, Matsuura Y, Yokoyama T.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):67-74. PubMed ID: 11464909
    [Abstract] [Full Text] [Related]

  • 11. Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification.
    Caron H, van Sluis P, van Hoeve M, de Kraker J, Bras J, Slater R, Mannens M, Voûte PA, Westerveld A, Versteeg R.
    Nat Genet; 1993 Jun 01; 4(2):187-90. PubMed ID: 8102298
    [Abstract] [Full Text] [Related]

  • 12. Detailed deletion mapping of chromosome band 14q32 in human neuroblastoma defines a 1.1-Mb region of common allelic loss.
    Hoshi M, Otagiri N, Shiwaku HO, Asakawa S, Shimizu N, Kaneko Y, Ohi R, Hayashi Y, Horii A.
    Br J Cancer; 2000 Jun 01; 82(11):1801-7. PubMed ID: 10839294
    [Abstract] [Full Text] [Related]

  • 13. Deletions in chromosome arms 3p and 11q are new prognostic markers in localized and 4s neuroblastoma.
    Spitz R, Hero B, Ernestus K, Berthold F.
    Clin Cancer Res; 2003 Jan 01; 9(1):52-8. PubMed ID: 12538451
    [Abstract] [Full Text] [Related]

  • 14. Deletion map of chromosome 9 and p16 (CDKN2A) gene alterations in neuroblastoma.
    Takita J, Hayashi Y, Kohno T, Yamaguchi N, Hanada R, Yamamoto K, Yokota J.
    Cancer Res; 1997 Mar 01; 57(5):907-12. PubMed ID: 9041193
    [Abstract] [Full Text] [Related]

  • 15. Preoperative analysis of 11q loss using circulating tumor-released DNA in serum: a novel diagnostic tool for therapy stratification of neuroblastoma.
    Yagyu S, Iehara T, Gotoh T, Miyachi M, Katsumi Y, Kikuchi K, Tsuchiya K, Osone S, Kuroda H, Sugimoto T, Sawada T, Hosoi H.
    Cancer Lett; 2011 Oct 28; 309(2):185-9. PubMed ID: 21726937
    [Abstract] [Full Text] [Related]

  • 16. Expression of TSLC1, a candidate tumor suppressor gene mapped to chromosome 11q23, is downregulated in unfavorable neuroblastoma without promoter hypermethylation.
    Ando K, Ohira M, Ozaki T, Nakagawa A, Akazawa K, Suenaga Y, Nakamura Y, Koda T, Kamijo T, Murakami Y, Nakagawara A.
    Int J Cancer; 2008 Nov 01; 123(9):2087-94. PubMed ID: 18726896
    [Abstract] [Full Text] [Related]

  • 17. Detailed molecular analysis of 1p36 in neuroblastoma.
    White PS, Thompson PM, Seifried BA, Sulman EP, Jensen SJ, Guo C, Maris JM, Hogarty MD, Allen C, Biegel JA, Matise TC, Gregory SG, Reynolds CP, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):37-41. PubMed ID: 11464901
    [Abstract] [Full Text] [Related]

  • 18. Loss in chromosome 11q identifies tumors with increased risk for metastatic relapses in localized and 4S neuroblastoma.
    Spitz R, Hero B, Simon T, Berthold F.
    Clin Cancer Res; 2006 Jun 01; 12(11 Pt 1):3368-73. PubMed ID: 16740759
    [Abstract] [Full Text] [Related]

  • 19. An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis.
    Spieker N, Beitsma M, van Sluis P, Roobeek I, den Dunnen JT, Speleman F, Caron H, Versteeg R.
    Genes Chromosomes Cancer; 2000 Feb 01; 27(2):143-52. PubMed ID: 10612802
    [Abstract] [Full Text] [Related]

  • 20. Allelotype of neuroblastoma.
    Takita J, Hayashi Y, Kohno T, Shiseki M, Yamaguchi N, Hanada R, Yamamoto K, Yokota J.
    Oncogene; 1995 Nov 02; 11(9):1829-34. PubMed ID: 7478611
    [Abstract] [Full Text] [Related]

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