These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
455 related articles for article (PubMed ID: 11464909)
21. Homozygous deletion of CDKN2A (p16INK4a/p14ARF) but not within 1p36 or at other tumor suppressor loci in neuroblastoma. Thompson PM; Maris JM; Hogarty MD; Seeger RC; Reynolds CP; Brodeur GM; White PS Cancer Res; 2001 Jan; 61(2):679-86. PubMed ID: 11212268 [TBL] [Abstract][Full Text] [Related]
22. 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; 36(1):28-31. PubMed ID: 11464899 [TBL] [Abstract][Full Text] [Related]
23. 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; 55(20):4664-9. PubMed ID: 7553646 [TBL] [Abstract][Full Text] [Related]
24. 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; 18(35):4948-57. PubMed ID: 10490829 [TBL] [Abstract][Full Text] [Related]
25. 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; 26(1):40-6. PubMed ID: 10441004 [TBL] [Abstract][Full Text] [Related]
26. 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; 83(10):1295-300. PubMed ID: 11044353 [TBL] [Abstract][Full Text] [Related]
27. 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; 385():19-25. PubMed ID: 7972212 [TBL] [Abstract][Full Text] [Related]
28. 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; 36(1):24-7. PubMed ID: 11464895 [TBL] [Abstract][Full Text] [Related]
30. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. Caron H; van Sluis P; de Kraker J; Bökkerink J; Egeler M; Laureys G; Slater R; Westerveld A; Voûte PA; Versteeg R N Engl J Med; 1996 Jan; 334(4):225-30. PubMed ID: 8531999 [TBL] [Abstract][Full Text] [Related]
31. Survival analysis of clinical, pathologic, and genetic features in neuroblastoma presenting as locoregional disease. Mora J; Cheung NK; Chen L; Qin J; Gerald W Cancer; 2001 Jan; 91(2):435-42. PubMed ID: 11180092 [TBL] [Abstract][Full Text] [Related]
32. 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; 57(5):907-12. PubMed ID: 9041193 [TBL] [Abstract][Full Text] [Related]
33. 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; 50(11):1090-4. PubMed ID: 19960166 [TBL] [Abstract][Full Text] [Related]
34. 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; 69(1):43-50. PubMed ID: 8331897 [TBL] [Abstract][Full Text] [Related]
36. 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 [TBL] [Abstract][Full Text] [Related]
37. Imbalances of chromosome arm 1p in pediatric and adult germ cell tumors are caused by true allelic loss: a combined comparative genomic hybridization and microsatellite analysis. Zahn S; Sievers S; Alemazkour K; Orb S; Harms D; Schulz WA; Calaminus G; Göbel U; Schneider DT Genes Chromosomes Cancer; 2006 Nov; 45(11):995-1006. PubMed ID: 16897744 [TBL] [Abstract][Full Text] [Related]
38. Molecular analysis of the putative tumour-suppressor gene EXTL1 in neuroblastoma patients and cell lines. Mathysen D; Van Roy N; Van Hul W; Laureys G; Ambros P; Speleman F; Wuyts W Eur J Cancer; 2004 May; 40(8):1255-61. PubMed ID: 15110891 [TBL] [Abstract][Full Text] [Related]