BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

466 related articles for article (PubMed ID: 8630904)

  • 1. 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; 76(7):1238-44. PubMed ID: 8630904
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 56(2):203-9. PubMed ID: 7625446
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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.
    Polito P; Canzonieri V; Cilia AM; Gloghini A; Carbone A; Gaidano G
    Cancer; 1996 Sep; 78(5):1142-4. PubMed ID: 8780557
    [No Abstract]   [Full Text] [Related]  

  • 4. 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; 91(5):1732-41. PubMed ID: 9473240
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Jumping translocations of 11q in acute myeloid leukemia and 1q in follicular lymphoma.
    Fan YS; Rizkalla K; William BF; Engel CJ
    Cancer Genet Cytogenet; 2000 Apr; 118(1):35-41. PubMed ID: 10731588
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
    Tuck-Muller CM; Narayan A; Tsien F; Smeets DF; Sawyer J; Fiala ES; Sohn OS; Ehrlich M
    Cytogenet Cell Genet; 2000; 89(1-2):121-8. PubMed ID: 10894953
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorescence in situ hybridization assessment of the telomeric regions of jumping translocations in a case of aggressive B-cell non-Hodgkin lymphoma.
    Gray BA; Bent-Williams A; Wadsworth J; Maiese RL; Bhatia A; Zori RT
    Cancer Genet Cytogenet; 1997 Oct; 98(1):20-7. PubMed ID: 9309114
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A role for telomeric and centromeric instability in the progression of chromosome aberrations in meningioma patients.
    Sawyer JR; Husain M; Pravdenkova S; Krisht A; Al-Mefty O
    Cancer; 2000 Jan; 88(2):440-53. PubMed ID: 10640979
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 9(8):62. PubMed ID: 31399558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 32(3):250-64. PubMed ID: 11579465
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
    Turleau C; Cabanis MO; Girault D; Ledeist F; Mettey R; Puissant H; Prieur M; de Grouchy J
    Am J Med Genet; 1989 Mar; 32(3):420-4. PubMed ID: 2729362
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Spectral karyotyping identifies new rearrangements, translocations, and clinical associations in diffuse large B-cell lymphoma.
    Nanjangud G; Rao PH; Hegde A; Teruya-Feldstein J; Donnelly G; Qin J; Jhanwar SC; Zelenetz AD; Chaganti RS
    Blood; 2002 Apr; 99(7):2554-61. PubMed ID: 11895793
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Pathogenesis of jumping translocations: a molecular cytogenetics study.
    Wan TS; Ma SK; Chow EY; Li YH; Lin SY; Chan LC
    Leuk Res; 2004 Oct; 28(10):1075-9. PubMed ID: 15289020
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A; Viaggi S; Ottaggio L; Fronza G; Schenone A; Roncella S; Abbondandolo A
    Haematologica; 2000 Mar; 85(3):250-5. PubMed ID: 10702812
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
    Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
    Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome.
    Maraschio P; Zuffardi O; Dalla Fior T; Tiepolo L
    J Med Genet; 1988 Mar; 25(3):173-80. PubMed ID: 3351904
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Jumping translocation of chromosome 1q associated with good clinical outcome in a case of Burkitt leukemia.
    Bessenyei B; Ujfalusi A; Balogh E; Olah E; Szegedi I; Kiss C
    Cancer Genet; 2011 Apr; 204(4):207-10. PubMed ID: 21536239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unbalanced 1q whole-arm translocation resulting in der(14)t(1;14)(q11-12;p11) in myelodysplastic syndrome.
    Fogu G; Campus PM; Cambosu F; Moro MA; Sanna R; Fozza C; Nieddu RM; Longinotti M; Montella A
    Cytogenet Genome Res; 2012; 136(4):256-63. PubMed ID: 22571950
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of complex chromosomal abnormalities in B-cell lymphoma by a combined spectral karyotyping (SKY) analysis and fluorescence in situ hybridization (FISH) using a 14q telomere probe.
    Kakazu N; Kito K; Hitomi T; Oita J; Nishida K; Masuda K; Miki T; Abe T
    Am J Hematol; 2000 Dec; 65(4):291-7. PubMed ID: 11074557
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.