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Journal Abstract Search

219 related items for PubMed ID: 31399558

  • 1. An acquired high-risk chromosome instability phenotype in multiple myeloma: Jumping 1q Syndrome.
    Sawyer JR, Tian E, Walker BA, Wardell C, Lukacs JL, Sammartino G, Bailey C, Schinke CD, Thanendrarajan S, Davies FE, Morgan GJ, Barlogie B, Zangari M, van Rhee F.
    Blood Cancer J; 2019 Aug 09; 9(8):62. PubMed ID: 31399558
    [Abstract] [Full Text] [Related]

  • 2. Evidence of an epigenetic origin for high-risk 1q21 copy number aberrations in multiple myeloma.
    Sawyer JR, Tian E, Heuck CJ, Johann DJ, Epstein J, Swanson CM, Lukacs JL, Binz RL, Johnson M, Sammartino G, Zangari M, Davies FE, van Rhee F, Morgan GJ, Barlogie B.
    Blood; 2015 Jun 11; 125(24):3756-9. PubMed ID: 25943786
    [Abstract] [Full Text] [Related]

  • 3. Jumping translocations of 1q12 in multiple myeloma: a novel mechanism for deletion of 17p in cytogenetically defined high-risk disease.
    Sawyer JR, Tian E, Heuck CJ, Epstein J, Johann DJ, Swanson CM, Lukacs JL, Johnson M, Binz R, Boast A, Sammartino G, Usmani S, Zangari M, Waheed S, van Rhee F, Barlogie B.
    Blood; 2014 Apr 17; 123(16):2504-12. PubMed ID: 24497533
    [Abstract] [Full Text] [Related]

  • 4. Genomic instability in multiple myeloma: evidence for jumping segmental duplications of chromosome arm 1q.
    Sawyer JR, Tricot G, Lukacs JL, Binz RL, Tian E, Barlogie B, Shaughnessy J.
    Genes Chromosomes Cancer; 2005 Jan 17; 42(1):95-106. PubMed ID: 15472896
    [Abstract] [Full Text] [Related]

  • 5. Centromeric instability of chromosome 1 resulting in multibranched chromosomes, telomeric fusions, and "jumping translocations" of 1q in a human immunodeficiency virus-related non-Hodgkin's lymphoma.
    Sawyer JR, Swanson CM, Koller MA, North PE, Ross SW.
    Cancer; 1995 Oct 01; 76(7):1238-44. PubMed ID: 8630904
    [Abstract] [Full Text] [Related]

  • 6. Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage-fusion-bridge cycles of a 1q12 approximately 23 amplicon.
    Sawyer JR, Tian E, Thomas E, Koller M, Stangeby C, Sammartino G, Goosen L, Swanson C, Binz RL, Barlogie B, Shaughnessy J.
    Br J Haematol; 2009 Nov 01; 147(4):484-94. PubMed ID: 19744130
    [Abstract] [Full Text] [Related]

  • 7. Jumping translocations of chromosome 1q in multiple myeloma: evidence for a mechanism involving decondensation of pericentromeric heterochromatin.
    Sawyer JR, Tricot G, Mattox S, Jagannath S, Barlogie B.
    Blood; 1998 Mar 01; 91(5):1732-41. PubMed ID: 9473240
    [Abstract] [Full Text] [Related]

  • 8. Novel evidence of a role for chromosome 1 pericentric heterochromatin in the pathogenesis of B-cell lymphoma and multiple myeloma.
    Le Baccon P, Leroux D, Dascalescu C, Duley S, Marais D, Esmenjaud E, Sotto JJ, Callanan M.
    Genes Chromosomes Cancer; 2001 Nov 01; 32(3):250-64. PubMed ID: 11579465
    [Abstract] [Full Text] [Related]

  • 9. Molecular cytogenetic analysis of genomic instability at the 1q12-22 chromosomal site in B-cell non-Hodgkin lymphoma.
    Itoyama T, Nanjungud G, Chen W, Dyomin VG, Teruya-Feldstein J, Jhanwar SC, Zelenetz AD, Chaganti RS.
    Genes Chromosomes Cancer; 2002 Dec 01; 35(4):318-28. PubMed ID: 12378526
    [Abstract] [Full Text] [Related]

  • 10. Progression in smoldering myeloma is independently determined by the chromosomal abnormalities del(17p), t(4;14), gain 1q, hyperdiploidy, and tumor load.
    Neben K, Jauch A, Hielscher T, Hillengass J, Lehners N, Seckinger A, Granzow M, Raab MS, Ho AD, Goldschmidt H, Hose D.
    J Clin Oncol; 2013 Dec 01; 31(34):4325-32. PubMed ID: 24145347
    [Abstract] [Full Text] [Related]

  • 11. Trisomy 1q generating translocations in Wilms tumor.
    Betts DR, Ilg EC, Oezahin H, von der Weid N, Niggli FK.
    Cancer Genet Cytogenet; 1999 Jul 15; 112(2):138-43. PubMed ID: 10686941
    [Abstract] [Full Text] [Related]

  • 12. Chromosome 1 abnormalities in multiple myeloma.
    Marzin Y, Jamet D, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, Berthou C, De Braekeleer M.
    Anticancer Res; 2006 Jul 15; 26(2A):953-9. PubMed ID: 16619492
    [Abstract] [Full Text] [Related]

  • 13. [Comparative study of genetic aberrations in human multiple myeloma cell lines and newly diagnosed MM by fluorescence in situ hybridization].
    An G, Xie ZQ, Li CH, Li Q, Yi SH, Qiu LG.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Dec 15; 18(6):1505-10. PubMed ID: 21176360
    [Abstract] [Full Text] [Related]

  • 14. Hypomethylation of chromosome 1 heterochromatin DNA correlates with q-arm copy gain in human hepatocellular carcinoma.
    Wong N, Lam WC, Lai PB, Pang E, Lau WY, Johnson PJ.
    Am J Pathol; 2001 Aug 15; 159(2):465-71. PubMed ID: 11485905
    [Abstract] [Full Text] [Related]

  • 15. Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms.
    Rudolph C, Liehr T, Steinemann D, Emura M, Daibata M, Matsuo Y, Emi N, Abe M, Lai R, Mrasek K, Claussen U, Schlegelberger B.
    Cytogenet Genome Res; 2006 Aug 15; 112(3-4):213-21. PubMed ID: 16484775
    [Abstract] [Full Text] [Related]

  • 16. Chromosome instability in ICF syndrome: formation of micronuclei from multibranched chromosomes 1 demonstrated by fluorescence in situ hybridization.
    Sawyer JR, Swanson CM, Wheeler G, Cunniff C.
    Am J Med Genet; 1995 Mar 27; 56(2):203-9. PubMed ID: 7625446
    [Abstract] [Full Text] [Related]

  • 17. Gain of chromosome arm 1q in patients in relapse and progression of multiple myeloma.
    Balcárková J, Urbánková H, Scudla V, Holzerová M, Bacovský J, Indrák K, Jarosová M.
    Cancer Genet Cytogenet; 2009 Jul 15; 192(2):68-72. PubMed ID: 19596256
    [Abstract] [Full Text] [Related]

  • 18. Recurrent involvement of heterochromatic regions in multiple myeloma-a multicolor FISH study.
    Lange K, Gadzicki D, Schlegelberger B, Göhring G.
    Leuk Res; 2010 Aug 15; 34(8):1002-6. PubMed ID: 20022374
    [Abstract] [Full Text] [Related]

  • 19. Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
    Parada LA, Limon J, Iliszko M, Czauderna P, Gisselsson D, Höglund M, Kullendorff CM, Wiebe T, Mertens F, Johansson B.
    Med Pediatr Oncol; 2000 Mar 15; 34(3):165-70. PubMed ID: 10696121
    [Abstract] [Full Text] [Related]

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