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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

149 related items for PubMed ID: 9491318

  • 21. hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors.
    Rousseau-Merck MF, Versteege I, Legrand I, Couturier J, Mairal A, Delattre O, Aurias A.
    Cancer Res; 1999 Jul 01; 59(13):3152-6. PubMed ID: 10397258
    [Abstract] [Full Text] [Related]

  • 22. Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.
    Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N.
    Eur J Cancer; 1995 Jul 01; 31A(4):523-6. PubMed ID: 7576958
    [Abstract] [Full Text] [Related]

  • 23. Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.
    Srivatsan ES, Chakrabarti R, Zainabadi K, Pack SD, Benyamini P, Mendonca MS, Yang PK, Kang K, Motamedi D, Sawicki MP, Zhuang Z, Jesudasan RA, Bengtsson U, Sun C, Roe BA, Stanbridge EJ, Wilczynski SP, Redpath JL.
    Oncogene; 2002 Aug 15; 21(36):5631-42. PubMed ID: 12165862
    [Abstract] [Full Text] [Related]

  • 24. Chromosome translocations in breast cancer with breakpoints at 8p12.
    Courtay-Cahen C, Morris JS, Edwards PA.
    Genomics; 2000 May 15; 66(1):15-25. PubMed ID: 10843800
    [Abstract] [Full Text] [Related]

  • 25. Identification of candidate genes on chromosome band 20q12 by physical mapping of translocation breakpoints found in myeloid leukemia cell lines.
    MacGrogan D, Alvarez S, DeBlasio T, Jhanwar SC, Nimer SD.
    Oncogene; 2001 Jul 12; 20(31):4150-60. PubMed ID: 11464281
    [Abstract] [Full Text] [Related]

  • 26. Genomic deletions on other chromosomes involved in variant t(9;22) chronic myeloid leukemia cases.
    Albano F, Specchia G, Anelli L, Zagaria A, Storlazzi CT, Buquicchio C, Roberti MG, Liso V, Rocchi M.
    Genes Chromosomes Cancer; 2003 Apr 12; 36(4):353-60. PubMed ID: 12619159
    [Abstract] [Full Text] [Related]

  • 27. Identification and characterization of novel genes located at the t(1;15)(p36.2;q24) translocation breakpoint in the neuroblastoma cell line NGP.
    Amler LC, Bauer A, Corvi R, Dihlmann S, Praml C, Cavenee WK, Schwab M, Hampton GM.
    Genomics; 2000 Mar 01; 64(2):195-202. PubMed ID: 10729226
    [Abstract] [Full Text] [Related]

  • 28. Characterization of a recurrent t(1;2)(p36;p24) in human uterine leiomyoma.
    van Rijk A, Sweers M, Huys E, Kersten M, Merkx G, van Kessel AG, Debiec-Rychter M, Schoenmakers EF.
    Cancer Genet Cytogenet; 2009 Aug 01; 193(1):54-62. PubMed ID: 19602464
    [Abstract] [Full Text] [Related]

  • 29. Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
    Jin Y, Jin C, Wennerberg J, Mertens F, Höglund M.
    Cancer Res; 1998 Dec 15; 58(24):5859-65. PubMed ID: 9865746
    [Abstract] [Full Text] [Related]

  • 30. A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers.
    Filippova GN, Lindblom A, Meincke LJ, Klenova EM, Neiman PE, Collins SJ, Doggett NA, Lobanenkov VV.
    Genes Chromosomes Cancer; 1998 May 15; 22(1):26-36. PubMed ID: 9591631
    [Abstract] [Full Text] [Related]

  • 31. Analysis of chromosome 22q as an aid to the diagnosis of rhabdoid tumor: a case report.
    Simons J, Teshima I, Zielenska M, Edwards V, Taylor G, Squire J, Thorner P.
    Am J Surg Pathol; 1999 Aug 15; 23(8):982-8. PubMed ID: 10435570
    [Abstract] [Full Text] [Related]

  • 32. Complex chromosome rearrangements may locate the bcr/abl fusion gene sites other than 22q11.
    Sessarego M, Fugazza G, Bruzzone R, Ballestrero A, Miglino M, Bacigalupo A.
    Haematologica; 2000 Jan 15; 85(1):35-9. PubMed ID: 10629589
    [Abstract] [Full Text] [Related]

  • 33. Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.
    Popovici C, Basset C, Bertucci F, Orsetti B, Adélaide J, Mozziconacci MJ, Conte N, Murati A, Ginestier C, Charafe-Jauffret E, Ethier SP, Lafage-Pochitaloff M, Theillet C, Birnbaum D, Chaffanet M.
    Genes Chromosomes Cancer; 2002 Nov 15; 35(3):204-18. PubMed ID: 12353263
    [Abstract] [Full Text] [Related]

  • 34. Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.
    Loncarevic IF, Römer J, Starke H, Heller A, Bleck C, Ziegler M, Fiedler W, Liehr T, Clement JH, Claussen U.
    Genes Chromosomes Cancer; 2002 Jun 15; 34(2):193-200. PubMed ID: 11979553
    [Abstract] [Full Text] [Related]

  • 35. The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium.
    Lerman MI, Minna JD.
    Cancer Res; 2000 Nov 01; 60(21):6116-33. PubMed ID: 11085536
    [Abstract] [Full Text] [Related]

  • 36. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
    Berend SA, Spikes AS, Kashork CD, Wu JM, Daw SC, Scambler PJ, Shaffer LG.
    Am J Med Genet; 2000 Apr 10; 91(4):313-7. PubMed ID: 10766989
    [Abstract] [Full Text] [Related]

  • 37. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
    Van Roy N, Vandesompele J, Berx G, Staes K, Van Gele M, De Smet E, De Paepe A, Laureys G, van der Drift P, Versteeg R, Van Roy F, Speleman F.
    Genes Chromosomes Cancer; 2002 Oct 10; 35(2):113-20. PubMed ID: 12203774
    [Abstract] [Full Text] [Related]

  • 38. Deletion mapping of 6q21-26 and frequency of 1p36 deletion in childhood endodermal sinus tumors by microsatellite analysis.
    Hu J, Schuster AE, Fritsch MK, Schneider DT, Lauer S, Perlman EJ.
    Oncogene; 2001 Nov 29; 20(55):8042-4. PubMed ID: 11753688
    [Abstract] [Full Text] [Related]

  • 39. An 800-kb region of deletion at 13q14 in human prostate and other carcinomas.
    Chen C, Frierson HF, Haggerty PF, Theodorescu D, Gregory CW, Dong JT.
    Genomics; 2001 Oct 29; 77(3):135-44. PubMed ID: 11597138
    [Abstract] [Full Text] [Related]

  • 40. 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 29; 36(1):37-41. PubMed ID: 11464901
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 8.