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Journal Abstract Search

290 related items for PubMed ID: 7553646

  • 1. Significance of chromosome 1p loss of heterozygosity in neuroblastoma.
    Maris JM, White PS, Beltinger CP, Sulman EP, Castleberry RP, Shuster JJ, Look AT, Brodeur GM.
    Cancer Res; 1995 Oct 15; 55(20):4664-9. PubMed ID: 7553646
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  • 2. 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
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  • 3. The 1p deletion is not a reliable marker for the prognosis of patients with neuroblastoma.
    Gehring M, Berthold F, Edler L, Schwab M, Amler LC.
    Cancer Res; 1995 Nov 15; 55(22):5366-9. PubMed ID: 7585602
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  • 4. 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
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  • 5. 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 15; 34(3):299-305. PubMed ID: 12007190
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  • 7. Distal chromosome 17 gains in neuroblastomas detected by comparative genomic hybridization (CGH) are associated with a poor clinical outcome.
    Brinkschmidt C, Christiansen H, Terpe HJ, Simon R, Lampert F, Boecker W, Dockhorn-Dworniczak B.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):11-3. PubMed ID: 11464859
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  • 9. Analysis of genomic imprinting at 1p35-36 in neuroblastoma.
    Hogarty MD, Maris JM, White PS, Guo C, Brodeur GM.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):52-5. PubMed ID: 11464906
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  • 11. Detection of MYCN gene amplification and deletions of chromosome 1p in neuroblastoma by in situ hybridization using routine histologic sections.
    Leong PK, Thorner P, Yeger H, Ng K, Zhang Z, Squire J.
    Lab Invest; 1993 Jul 15; 69(1):43-50. PubMed ID: 8331897
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  • 12. 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
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  • 13. 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 24; 36(1):32-6. PubMed ID: 11464900
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  • 14. Neuroblastoma: clinical significance of genetic abnormalities.
    Brodeur GM.
    Cancer Surv; 1990 Jan 24; 9(4):673-88. PubMed ID: 2101728
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  • 15. 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 24; 36(1):24-7. PubMed ID: 11464895
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  • 17. Genetic alterations involving chromosome 1p in children with neuroblastoma.
    Avigad S, Tamir Y, Yaniv I, Goshen J, Kaplinsky C, Cohen IJ, Zaizov R.
    Isr J Med Sci; 1994 Aug 24; 30(8):639-41. PubMed ID: 7913920
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  • 18. 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 24; 4(2):187-90. PubMed ID: 8102298
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