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324 related items for PubMed ID: 8102298

  • 1. 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; 4(2):187-90. PubMed ID: 8102298
    [Abstract] [Full Text] [Related]

  • 2. Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas.
    Cheng JM, Hiemstra JL, Schneider SS, Naumova A, Cheung NK, Cohn SL, Diller L, Sapienza C, Brodeur GM.
    Nat Genet; 1993 Jun; 4(2):191-4. PubMed ID: 8102299
    [Abstract] [Full Text] [Related]

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

  • 4. 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]

  • 5. Preferential amplification of the paternal allele in neuroblastomas with N-myc amplification.
    Cheng JM, Hiemstra JL, Schneider SS, Kaufman BA, Naumova A, Cheung NK, Cohn SL, Diller L, Sapienza C, Brodeur GM.
    Prog Clin Biol Res; 1994 Dec 01; 385():43-9. PubMed ID: 7972236
    [Abstract] [Full Text] [Related]

  • 6. Loss of the putative tumor suppressor-gene locus 1p36 as investigated by a PCR-assay and N-myc amplification in 48 neuroblastomas: results of the German Neuroblastoma Study Group.
    Christiansen H, Delattre O, Fuchs S, Theobald M, Christiansen NM, Berthold F, Lampert F.
    Prog Clin Biol Res; 1994 Dec 01; 385():19-25. PubMed ID: 7972212
    [Abstract] [Full Text] [Related]

  • 7. Deletion mapping in neuroblastoma cell lines suggests two distinct tumor suppressor genes in the 1p35-36 region, only one of which is associated with N-myc amplification.
    Cheng NC, Van Roy N, Chan A, Beitsma M, Westerveld A, Speleman F, Versteeg R.
    Oncogene; 1995 Jan 19; 10(2):291-7. PubMed ID: 7838528
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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]

  • 10. 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]

  • 11. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene.
    Barbashina V, Salazar P, Holland EC, Rosenblum MK, Ladanyi M.
    Clin Cancer Res; 2005 Feb 01; 11(3):1119-28. PubMed ID: 15709179
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification.
    Caron H, Peter M, van Sluis P, Speleman F, de Kraker J, Laureys G, Michon J, Brugières L, Voûte PA, Westerveld A.
    Hum Mol Genet; 1995 Apr 01; 4(4):535-9. PubMed ID: 7633401
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Fluorescence in situ hybridization analyses of chromosome band 1p36 in neuroblastoma detect two classes of alterations.
    Spitz R, Hero B, Westermann F, Ernestus K, Schwab M, Berthold F.
    Genes Chromosomes Cancer; 2002 Jul 01; 34(3):299-305. PubMed ID: 12007190
    [Abstract] [Full Text] [Related]

  • 16. Deletion mapping of chromosomes 14q and 1p in human neuroblastoma.
    Takayama H, Suzuki T, Mugishima H, Fujisawa T, Ookuni M, Schwab M, Gehring M, Nakamura Y, Sugimura T, Terada M.
    Oncogene; 1992 Jun 01; 7(6):1185-9. PubMed ID: 1594247
    [Abstract] [Full Text] [Related]

  • 17. No evidence for the presence of an imprinted neuroblastoma suppressor gene within chromosome sub-band 1p36.3.
    Hogarty MD, Winter CL, Liu X, Guo C, White PS, Look AT, Brodeur GM, Maris JM.
    Cancer Res; 2002 Nov 15; 62(22):6481-4. PubMed ID: 12438240
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 36(1):37-41. PubMed ID: 11464901
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 36(1):24-7. PubMed ID: 11464895
    [Abstract] [Full Text] [Related]

  • 20. Clinical investigation of neuroblastoma with partial deletion in the short arm of chromosome 1.
    Ohtsu K, Hiyama E, Ichikawa T, Matsuura Y, Yokoyama T.
    Clin Cancer Res; 1997 Jul 15; 3(7):1221-8. PubMed ID: 9815803
    [Abstract] [Full Text] [Related]


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