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t(7;12)(q36;p13), a new recurrent translocation involving ETV6 in infant leukemia.
Tosi S, Harbott J, Teigler-Schlegel A, Haas OA, Pirc-Danoewinata H, Harrison CJ, Biondi A, Cazzaniga G, Kempski H, Scherer SW, Kearney L. Tosi S, et al. Among authors: kempski h. Genes Chromosomes Cancer. 2000 Dec;29(4):325-32. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1039>3.0.co;2-9. Genes Chromosomes Cancer. 2000. PMID: 11066076 Review.
Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia.
Kearney L, Gonzalez De Castro D, Yeung J, Procter J, Horsley SW, Eguchi-Ishimae M, Bateman CM, Anderson K, Chaplin T, Young BD, Harrison CJ, Kempski H, So CW, Ford AM, Greaves M. Kearney L, et al. Among authors: kempski h. Blood. 2009 Jan 15;113(3):646-8. doi: 10.1182/blood-2008-08-170928. Epub 2008 Oct 16. Blood. 2009. PMID: 18927438 Free article.
Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia.
van Delft FW, Horsley S, Colman S, Anderson K, Bateman C, Kempski H, Zuna J, Eckert C, Saha V, Kearney L, Ford A, Greaves M. van Delft FW, et al. Among authors: kempski h. Blood. 2011 Jun 9;117(23):6247-54. doi: 10.1182/blood-2010-10-314674. Epub 2011 Apr 11. Blood. 2011. PMID: 21482711 Free article.
Molecular cytogenetics in childhood leukemia.
Harrison CJ, Kempski H, Hammond DW, Kearney L. Harrison CJ, et al. Among authors: kempski h. Methods Mol Med. 2004;91:123-37. doi: 10.1385/1-59259-433-6:123. Methods Mol Med. 2004. PMID: 14573934 No abstract available.
Prospective gene expression analysis accurately subtypes acute leukaemia in children and establishes a commonality between hyperdiploidy and t(12;21) in acute lymphoblastic leukaemia.
van Delft FW, Bellotti T, Luo Z, Jones LK, Patel N, Yiannikouris O, Hill AS, Hubank M, Kempski H, Fletcher D, Chaplin T, Foot N, Young BD, Hann IM, Gammerman A, Saha V. van Delft FW, et al. Among authors: kempski h. Br J Haematol. 2005 Jul;130(1):26-35. doi: 10.1111/j.1365-2141.2005.05545.x. Br J Haematol. 2005. PMID: 15982341 Free article.
NOTCH1 mutation can be an early, prenatal genetic event in T-ALL.
Eguchi-Ishimae M, Eguchi M, Kempski H, Greaves M. Eguchi-Ishimae M, et al. Among authors: kempski h. Blood. 2008 Jan 1;111(1):376-8. doi: 10.1182/blood-2007-02-074690. Epub 2007 Sep 27. Blood. 2008. PMID: 17901244 Free article.
69 results