These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 12800152)

  • 1. Prenatal chromosomal diversification of leukemia in monozygotic twins.
    Kempski H; Mensa-Bonsu KA; Kearney L; Jalali GR; Hann I; Khurshid M; Greaves M
    Genes Chromosomes Cancer; 2003 Aug; 37(4):406-11. PubMed ID: 12800152
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complex chromosomal abnormalities in utero, 5 years before leukaemia.
    Broadfield ZJ; Hain RD; Harrison CJ; Reza Jalali G; McKinley M; Michalová K; Robinson HM; Zemanová Z; Martineau M
    Br J Haematol; 2004 Aug; 126(3):307-12. PubMed ID: 15257702
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pre-natal, clonal origin of t(1;11)(p32;q23) acute lymphoblastic leukemia in monozygotic twins.
    Kotecha RS; Murch A; Kees U; Cole CH
    Leuk Res; 2012 Jan; 36(1):46-50. PubMed ID: 21474181
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Protracted postnatal natural histories in childhood leukemia.
    Maia AT; Koechling J; Corbett R; Metzler M; Wiemels JL; Greaves M
    Genes Chromosomes Cancer; 2004 Apr; 39(4):335-40. PubMed ID: 14978794
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chromosome changes associated with childhood leukaemia occur prenatally].
    Olsen M; Hjalgrim LL; Madsen HO; Hjalgrim H; Schmiegelow K
    Ugeskr Laeger; 2006 May; 168(22):2152-7. PubMed ID: 16768953
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clonal origins of ETV6-RUNX1⁺ acute lymphoblastic leukemia: studies in monozygotic twins.
    Alpar D; Wren D; Ermini L; Mansur MB; van Delft FW; Bateman CM; Titley I; Kearney L; Szczepanski T; Gonzalez D; Ford AM; Potter NE; Greaves M
    Leukemia; 2015 Apr; 29(4):839-46. PubMed ID: 25388957
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ETV6/RUNX1 fusion at diagnosis and relapse: some prognostic indications.
    Martineau M; Jalali GR; Barber KE; Broadfield ZJ; Cheung KL; Lilleyman J; Moorman AV; Richards S; Robinson HM; Ross F; Harrison CJ
    Genes Chromosomes Cancer; 2005 May; 43(1):54-71. PubMed ID: 15704129
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins.
    Bang B; Eisfeldt J; Barbany G; Harila-Saari A; Heyman M; Zachariadis V; Taylan F; Nordgren A
    Blood Adv; 2022 Apr; 6(7):2275-2289. PubMed ID: 34982829
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cytogenetic characterization of rearrangements involving 12p in leukemia.
    Vieira L; Marques B; Cavaleiro C; Ambrósio AP; Jorge M; Neto A; Costa JM; Júnior EC; Boavida MG
    Cancer Genet Cytogenet; 2005 Mar; 157(2):134-9. PubMed ID: 15721634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Two pairs of monozygotic twins with concordant acute lymphoblastic leukemia (ALL): case report.
    Li X; Sun N; Huang X; Ju X
    J Pediatr Hematol Oncol; 2014 Jul; 36(5):e299-303. PubMed ID: 24807006
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins.
    Maia AT; van der Velden VH; Harrison CJ; Szczepanski T; Williams MD; Griffiths MJ; van Dongen JJ; Greaves MF
    Leukemia; 2003 Nov; 17(11):2202-6. PubMed ID: 12931229
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TEL deletion analysis supports a novel view of relapse in childhood acute lymphoblastic leukemia.
    Zuna J; Ford AM; Peham M; Patel N; Saha V; Eckert C; Köchling J; Panzer-Grümayer R; Trka J; Greaves M
    Clin Cancer Res; 2004 Aug; 10(16):5355-60. PubMed ID: 15328172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
    Tosi S; Hughes J; Scherer SW; Nakabayashi K; Harbott J; Haas OA; Cazzaniga G; Biondi A; Kempski H; Kearney L
    Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ETV6-RUNX1
    Ford AM; Greaves M
    Adv Exp Med Biol; 2017; 962():217-228. PubMed ID: 28299660
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institution.
    Pérez-Vera P; Montero-Ruiz O; Frías S; Ulloa-Avilés V; Cárdenas-Cardós R; Paredes-Aguilera R; Rivera-Luna R; Carnevale A
    Cancer Genet Cytogenet; 2005 Oct; 162(2):140-5. PubMed ID: 16213362
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new complex rearrangement involving the ETV6, LOC115548, and MN1 genes in a case of acute myeloid leukemia.
    Belloni E; Trubia M; Mancini M; Derme V; Nanni M; Lahortiga I; Riccioni R; Confalonieri S; Lo-Coco F; Di Fiore PP; Pelicci PG
    Genes Chromosomes Cancer; 2004 Nov; 41(3):272-7. PubMed ID: 15334551
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Concordant childhood acute lymphoblastic leukemia in monozygotic twins.
    Chin YM; Wan Ariffin A; Lin HP; Chan YS
    Med J Malaysia; 1996 Mar; 51(1):145-8. PubMed ID: 10967997
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RUNX1 aberrations in ETV6/RUNX1-positive and ETV6/RUNX1-negative patients: its hemato-pathological and prognostic significance in a large cohort (619 cases) of ALL.
    Pais AP; Amare Kadam PS; Raje GC; Banavali S; Parikh P; Kurkure P; Arora B; Gujral S; Kumar SA; Badrinath Y
    Pediatr Hematol Oncol; 2008 Sep; 25(6):582-97. PubMed ID: 18728978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
    Strehl S; Nebral K; König M; Harbott J; Strobl H; Ratei R; Struski S; Bielorai B; Lessard M; Zimmermann M; Haas OA; Izraeli S
    Clin Cancer Res; 2008 Feb; 14(4):977-83. PubMed ID: 18281529
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.