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162 related items for PubMed ID: 9119409

  • 1. ECK, a human EPH-related gene, maps to 1p36.1, a common region of alteration in human cancers.
    Sulman EP, Tang XX, Allen C, Biegel JA, Pleasure DE, Brodeur GM, Ikegaki N.
    Genomics; 1997 Mar 01; 40(2):371-4. PubMed ID: 9119409
    [Abstract] [Full Text] [Related]

  • 2. The gene encoding LERK-7 (EPLG7, Epl7), a ligand for the Eph-related receptor tyrosine kinases, maps to human chromosome 5 at band q21 and to mouse chromosome 17.
    Cerretti DP, Copeland NG, Gilbert DJ, Jenkins NA, Kuefer MU, Valentine V, Shapiro DN, Cui X, Morris SW.
    Genomics; 1996 Jul 15; 35(2):376-9. PubMed ID: 8661153
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36.
    Shapiro DN, Sublett JE, Li B, Valentine MB, Morris SW, Noll M.
    Genomics; 1993 Sep 01; 17(3):767-9. PubMed ID: 7902328
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Reassignment of the human ARH9 RAS-related gene to chromosome 1p13-p21.
    Morris SW, Valentine MB, Kirstein MN, Huebner K.
    Genomics; 1993 Mar 01; 15(3):677-9. PubMed ID: 8468062
    [Abstract] [Full Text] [Related]

  • 8. Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1.
    Spieker N, Beitsma M, Van Sluis P, Chan A, Caron H, Versteeg R.
    Genes Chromosomes Cancer; 2001 Jun 01; 31(2):172-81. PubMed ID: 11319804
    [Abstract] [Full Text] [Related]

  • 9. The Eck receptor tyrosine kinase is implicated in pattern formation during gastrulation, hindbrain segmentation and limb development.
    Ganju P, Shigemoto K, Brennan J, Entwistle A, Reith AD.
    Oncogene; 1994 Jun 01; 9(6):1613-24. PubMed ID: 8183555
    [Abstract] [Full Text] [Related]

  • 10. Translocation junctions cluster at the distal short arm of chromosome 1 (1p36.1-2) in human neuroblastoma cells.
    Barker PE, Savelyeva L, Schwab M.
    Oncogene; 1993 Dec 01; 8(12):3353-8. PubMed ID: 8247537
    [Abstract] [Full Text] [Related]

  • 11. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
    van Gils W, Kilic E, Brüggenwirth HT, Vaarwater J, Verbiest MM, Beverloo B, van Til-Berg ME, Paridaens D, Luyten GP, de Klein A.
    Melanoma Res; 2008 Feb 01; 18(1):10-5. PubMed ID: 18227702
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours.
    Ejeskär K, Sjöberg RM, Abel F, Kogner P, Ambros PF, Martinsson T.
    Med Pediatr Oncol; 2001 Jan 01; 36(1):61-6. PubMed ID: 11464908
    [Abstract] [Full Text] [Related]

  • 14. Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis.
    Reddy UR, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA.
    Genomics; 1997 Apr 15; 41(2):283-5. PubMed ID: 9143508
    [Abstract] [Full Text] [Related]

  • 15. An integrated transcript map of human chromosome 1p35-p36.
    Jensen SJ, Sulman EP, Maris JM, Matise TC, Vojta PJ, Barrett JC, Brodeur GM, White PS.
    Genomics; 1997 May 15; 42(1):126-36. PubMed ID: 9177782
    [Abstract] [Full Text] [Related]

  • 16. Evolutionary breakpoints on human chromosome 21.
    Davisson MT, Bechtel LJ, Akeson EC, Fortna A, Slavov D, Gardiner K.
    Genomics; 2001 Nov 15; 78(1-2):99-106. PubMed ID: 11707078
    [Abstract] [Full Text] [Related]

  • 17. The genes encoding the eph-related receptor tyrosine kinase ligands LERK-1 (EPLG1, Epl1), LERK-3 (EPLG3, Epl3), and LERK-4 (EPLG4, Epl4) are clustered on human chromosome 1 and mouse chromosome 3.
    Cerretti DP, Lyman SD, Kozlosky CJ, Copeland NG, Gilbert DJ, Jenkins NA, Valentine V, Kirstein MN, Shapiro DN, Morris SW.
    Genomics; 1996 Apr 15; 33(2):277-82. PubMed ID: 8660976
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. The human PECAM1 gene maps to 17q23.
    Gumina RJ, Kirschbaum NE, Rao PN, vanTuinen P, Newman PJ.
    Genomics; 1996 Jun 01; 34(2):229-32. PubMed ID: 8661055
    [Abstract] [Full Text] [Related]


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