BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 12070048)

  • 21. Differences in immunoglobulin heavy chain gene rearrangmeent patterns between bone marrow and blood samples in childhood precursor B-acute lymphoblastic leaukemia at diagnosis.
    Beishuizen A; Verhoeven MA; Hählen K; van Wering ER; van Dongen JJ
    Leukemia; 1993 Jun; 7(6):60-3. PubMed ID: 8315958
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Lymphocytic progenitor cell origin and clonal evolution of human B-lineage acute lymphoblastic leukemia.
    Davi F; Gocke C; Smith S; Sklar J
    Blood; 1996 Jul; 88(2):609-21. PubMed ID: 8695809
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Submicroscopic deletions of immunoglobulin heavy chain gene (IGH) in precursor B lymphoblastic leukemia with IGH rearrangements.
    Huh J; Mun YC; Yoo ES; Seong CM; Chung WS
    Ann Lab Med; 2015 Jan; 35(1):128-31. PubMed ID: 25553293
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Simultaneous immunoglobulin/T-cell receptor gene rearrangements and multiclonality in childhood acute lymphoblastic leukemia.
    Forestier E; Nordenson I; Lindström A; Roos G; Lindh J
    Acta Paediatr; 1994 Mar; 83(3):319-26. PubMed ID: 8038538
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Characteristics of immunoglobulin heavy chain variable region genes in childhood B-cell acute lymphoblastic leukemia].
    Liu Y; Zhu P; Hu YM
    Zhonghua Xue Ye Xue Za Zhi; 2004 Jan; 25(1):8-12. PubMed ID: 14990068
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An investigation of the t(12;21) rearrangement in children with B-precursor acute lymphoblastic leukaemia using cytogenetic and molecular methods.
    Kempski H; Chalker J; Chessells J; Sturt N; Brickell P; Webb J; Clink JM; Reeves B
    Br J Haematol; 1999 Jun; 105(3):684-9. PubMed ID: 10354132
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Detailed clonality analysis of relapsing precursor B acute lymphoblastic leukemia: implications for minimal residual disease detection.
    Li AH; Rosenquist R; Forestier E; Lindh J; Roos G
    Leuk Res; 2001 Dec; 25(12):1033-45. PubMed ID: 11684274
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical relevance of T-cell receptor delta gene rearrangements in childhood B-precursor cell acute lymphoblastic leukaemia.
    Díaz MA; Garcia-Sanchez F; Vicario JL; Ramirez M; Balas A; Madero L
    Br J Haematol; 1997 Nov; 99(2):308-13. PubMed ID: 9375746
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Oligoclonal immunoglobulin heavy-chain and T-cell receptor delta rearrangements persist in a recurrent acute lymphoblastic leukemia with one immunoglobulin kappa rearrangement as a clonal marker.
    Stolz F; Panzer S; Fischer S; Panzer-Grümayer ER
    Mod Pathol; 1999 Aug; 12(8):819-26. PubMed ID: 10463485
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatal origin of childhood acute lymphoblastic leukemia, association with birth weight and hyperdiploidy.
    Gruhn B; Taub JW; Ge Y; Beck JF; Zell R; Häfer R; Hermann FH; Debatin KM; Steinbach D
    Leukemia; 2008 Sep; 22(9):1692-7. PubMed ID: 18548099
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia.
    Onodera N; McCabe NR; Nachman JB; Johnson FL; Le Beau MM; Rowley JD; Rubin CM
    Genes Chromosomes Cancer; 1992 Jun; 4(4):331-6. PubMed ID: 1377941
    [TBL] [Abstract][Full Text] [Related]  

  • 32. In multiple myeloma, circulating hyperdiploid B cells have clonotypic immunoglobulin heavy chain rearrangements and may mediate spread of disease.
    Pilarski LM; Giannakopoulos NV; Szczepek AJ; Masellis AM; Mant MJ; Belch AR
    Clin Cancer Res; 2000 Feb; 6(2):585-96. PubMed ID: 10690543
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Detection of hyperdiploid karyotypes (>50 chromosomes) in childhood acute lymphoblastic leukemia (ALL) using fluorescence in situ hybridization (FISH).
    Ritterbach J; Hiddemann W; Beck JD; Schrappe M; Janka-Schaub G; Ludwig WD; Harbott J; Lampert F
    Leukemia; 1998 Mar; 12(3):427-33. PubMed ID: 9529139
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia.
    Onodera N; McCabe NR; Rubin CM
    Blood; 1992 Jul; 80(1):203-8. PubMed ID: 1351763
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia.
    Mkrtchyan H; Garcia Ney DR; de Ventura ES; Liehr T; Felix GR; Marques-Salles Tde J; Abdelhay E; Macedo Silva ML
    Cancer Genet Cytogenet; 2010 Feb; 197(1):71-4. PubMed ID: 20113840
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Double CEBPE-IGH rearrangement due to chromosome duplication and cryptic insertion in an adult with B-cell acute lymphoblastic leukemia.
    Pierini V; Nofrini V; La Starza R; Barba G; Vitale A; Di Raimondo F; Matteucci C; Crescenzi B; Elia L; Gorello P; Storlazzi CT; Mecucci C
    Cancer Genet; 2011 Oct; 204(10):563-8. PubMed ID: 22137487
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Analysis of clonality with immunoglobulin heavy chain gene rearrangement fingerprinting map in childhood acute lymphoblastic leukemia].
    Liu J; Lu S; Zhu P; Xue H
    Zhonghua Xue Ye Xue Za Zhi; 1997 Jan; 18(1):21-4. PubMed ID: 15622745
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Multiple rearranged immunoglobulin genes in childhood acute lymphoblastic leukemia of precursor B-cell origin.
    Beishuizen A; Hählen K; Hagemeijer A; Verhoeven MA; Hooijkaas H; Adriaansen HJ; Wolvers-Tettero IL; van Wering ER; van Dongen JJ
    Leukemia; 1991 Aug; 5(8):657-67. PubMed ID: 1909409
    [TBL] [Abstract][Full Text] [Related]  

  • 39. IGH@ translocations co-exist with other primary rearrangements in B-cell precursor acute lymphoblastic leukemia.
    Jeffries SJ; Jones L; Harrison CJ; Russell LJ
    Haematologica; 2014 Aug; 99(8):1334-42. PubMed ID: 24816234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes.
    Spinella JF; Healy J; Saillour V; Richer C; Cassart P; Ouimet M; Sinnett D
    BMC Cancer; 2015 Jul; 15():539. PubMed ID: 26201965
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.