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Journal Abstract Search

319 related items for PubMed ID: 11417483

  • 1. Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia.
    Lezon-Geyda K, Najfeld V, Johnson EM.
    Leukemia; 2001 Jun; 15(6):954-62. PubMed ID: 11417483
    [Abstract] [Full Text] [Related]

  • 2. PURA, the gene encoding Pur-alpha, member of an ancient nucleic acid-binding protein family with mammalian neurological functions.
    Daniel DC, Johnson EM.
    Gene; 2018 Feb 15; 643():133-143. PubMed ID: 29221753
    [Abstract] [Full Text] [Related]

  • 3. Polymerase chain reaction-based diagnosis of del (5q) in acute myeloid leukemia and myelodysplastic syndrome identifies a minimal deletion interval.
    Horrigan SK, Westbrook CA, Kim AH, Banerjee M, Stock W, Larson RA.
    Blood; 1996 Oct 01; 88(7):2665-70. PubMed ID: 8839861
    [Abstract] [Full Text] [Related]

  • 4. Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.
    Puda A, Milosevic JD, Berg T, Klampfl T, Harutyunyan AS, Gisslinger B, Rumi E, Pietra D, Malcovati L, Elena C, Doubek M, Steurer M, Tosic N, Pavlovic S, Guglielmelli P, Pieri L, Vannucchi AM, Gisslinger H, Cazzola M, Kralovics R.
    Am J Hematol; 2012 Mar 01; 87(3):245-50. PubMed ID: 22190018
    [Abstract] [Full Text] [Related]

  • 5. dic(5;17): a recurring abnormality in malignant myeloid disorders associated with mutations of TP53.
    Wang P, Spielberger RT, Thangavelu M, Zhao N, Davis EM, Iannantuoni K, Larson RA, Le Beau MM.
    Genes Chromosomes Cancer; 1997 Nov 01; 20(3):282-91. PubMed ID: 9365836
    [Abstract] [Full Text] [Related]

  • 6. Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.
    Gao Q, Horwitz M, Roulston D, Hagos F, Zhao N, Freireich EJ, Golomb HM, Olopade OI.
    Genes Chromosomes Cancer; 2000 Jun 01; 28(2):164-72. PubMed ID: 10825001
    [Abstract] [Full Text] [Related]

  • 7. Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype.
    Cuneo A, Bigoni R, Cavazzini F, Bardi A, Roberti MG, Agostini P, Tammiso E, Ciccone N, Mancini M, Nanni M, De Cuia R, Divona M, La Starza R, Crescenzi B, Testoni N, Rege Cambrin G, Mecucci C, Lo Coco F, Saglio G, Castoldi G.
    Leukemia; 2002 Sep 01; 16(9):1745-51. PubMed ID: 12200689
    [Abstract] [Full Text] [Related]

  • 8. Hidden chromosomal aberrations are rare in primary myelodysplastic syndromes with evolution to acute myeloid leukaemia and normal cytogenetics.
    Trost D, Hildebrandt B, Müller N, Germing U, Royer-Pokora B.
    Leuk Res; 2004 Feb 01; 28(2):171-7. PubMed ID: 14654082
    [Abstract] [Full Text] [Related]

  • 9. Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation.
    Liu TX, Becker MW, Jelinek J, Wu WS, Deng M, Mikhalkevich N, Hsu K, Bloomfield CD, Stone RM, DeAngelo DJ, Galinsky IA, Issa JP, Clarke MF, Look AT.
    Nat Med; 2007 Jan 01; 13(1):78-83. PubMed ID: 17159988
    [Abstract] [Full Text] [Related]

  • 10. Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.
    Fischer K, Fröhling S, Scherer SW, McAllister Brown J, Scholl C, Stilgenbauer S, Tsui LC, Lichter P, Döhner H.
    Blood; 1997 Mar 15; 89(6):2036-41. PubMed ID: 9058725
    [Abstract] [Full Text] [Related]

  • 11. Localization of PURA, the gene encoding the sequence-specific single-stranded-DNA-binding protein Pur alpha, to chromosome band 5q31.
    Ma ZW, Pejovic T, Najfeld V, Ward DC, Johnson EM.
    Cytogenet Cell Genet; 1995 Mar 15; 71(1):64-7. PubMed ID: 7606931
    [Abstract] [Full Text] [Related]

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  • 13. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21.
    Preudhomme C, Warot-Loze D, Roumier C, Grardel-Duflos N, Garand R, Lai JL, Dastugue N, Macintyre E, Denis C, Bauters F, Kerckaert JP, Cosson A, Fenaux P.
    Blood; 2000 Oct 15; 96(8):2862-9. PubMed ID: 11023523
    [Abstract] [Full Text] [Related]

  • 14. C/EBP-epsilon: chromosomal mapping and mutational analysis of the gene in leukemia and preleukemia.
    Koike M, Chumakov AM, Takeuchi S, Tasaka T, Yang R, Nakamaki T, Tsuruoka N, Koeffler HP.
    Leuk Res; 1997 Sep 15; 21(9):833-9. PubMed ID: 9393598
    [Abstract] [Full Text] [Related]

  • 15. FISH investigation of 5q and 7q deletions in MDS/AML reveals hidden translocations, insertions and fragmentations of the same chromosomes.
    Lessard M, Herry A, Berthou C, Léglise MC, Abgrall JF, Morice P, Flandrin G.
    Leuk Res; 1998 Apr 15; 22(4):303-12. PubMed ID: 9669835
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetic analysis of de novo acute myeloid leukemia with trilineage myelodysplasia in comparison with myelodysplastic syndrome evolving to acute myeloid leukemia.
    Tamura S, Takemoto Y, Hashimoto-Tamaoki T, Mimura K, Sugahara Y, Senoh J, Furuyama JI, Kakishita E.
    Int J Oncol; 1998 Jun 15; 12(6):1259-62. PubMed ID: 9592183
    [Abstract] [Full Text] [Related]

  • 17. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.
    Cancer Genet Cytogenet; 2007 Jun 15; 175(2):125-31. PubMed ID: 17556068
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