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Items: 1 to 20 of 101

1.

Long-term follow-up of ETV6-RUNX1 ALL reveals that NCI risk, rather than secondary genetic abnormalities, is the key risk factor.

Enshaei A, Schwab CJ, Konn ZJ, Mitchell CD, Kinsey SE, Wade R, Vora A, Harrison CJ, Moorman AV.

Leukemia. 2013 Nov;27(11):2256-9. doi: 10.1038/leu.2013.136. Epub 2013 May 2. No abstract available.

PMID:
23636228
2.

Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia.

Al-Shehhi H, Konn ZJ, Schwab CJ, Erhorn A, Barber KE, Wright SL, Gabriel AS, Harrison CJ, Moorman AV.

Genes Chromosomes Cancer. 2013 Feb;52(2):202-13. doi: 10.1002/gcc.22021. Epub 2012 Oct 18.

PMID:
23077088
3.

Excellent prognosis of late relapses of ETV6/RUNX1-positive childhood acute lymphoblastic leukemia: lessons from the FRALLE 93 protocol.

Gandemer V, Chevret S, Petit A, Vermylen C, Leblanc T, Michel G, Schmitt C, Lejars O, Schneider P, Demeocq F, Bader-Meunier B, Bernaudin F, Perel Y, Auclerc MF, Cayuela JM, Leverger G, Baruchel A; FRALLE Group.

Haematologica. 2012 Nov;97(11):1743-50. doi: 10.3324/haematol.2011.059584. Epub 2012 May 11.

4.

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. doi: 10.1080/08880010802237450.

PMID:
18728978
5.

Presenting features of 201 children with acute lymphoblastic leukemia: comparison according to presence or absence of ETV6/RUNX1 rearrangement.

Alvarez Y, Caballín MR, Gaitán S, Pérez A, Bastida P, Ortega JJ, Cervera J, Verdeguer A, Tasso M, Aventín A, Badell I, Guitart M, Melo M, Granada I, Javier G, Dastugue N, Robert A, Coll MD.

Cancer Genet Cytogenet. 2007 Sep;177(2):161-3. No abstract available.

PMID:
17854676
6.

Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia.

Bokemeyer A, Eckert C, Meyr F, Koerner G, von Stackelberg A, Ullmann R, Türkmen S, Henze G, Seeger K.

Haematologica. 2014 Apr;99(4):706-14. doi: 10.3324/haematol.2012.072470. Epub 2013 Nov 15.

7.

False positivity of ETV6/RUNX1 detected by FISH in healthy newborns and adults.

Kusk MS, Lausten-Thomsen U, Andersen MK, Olsen M, Hjalgrim H, Schmiegelow K.

Pediatr Blood Cancer. 2014 Sep;61(9):1704-6. doi: 10.1002/pbc.25050. Epub 2014 Apr 17.

PMID:
24740533
8.

Determination of ETV6-RUNX1 genomic breakpoint by next-generation sequencing.

Jin Y, Wang X, Hu S, Tang J, Li B, Chai Y.

Cancer Med. 2016 Feb;5(2):337-51. doi: 10.1002/cam4.579. Epub 2015 Dec 29.

9.

Coexistence of ETV6/RUNX1 and MLL aberrations in B-cell precursor acute lymphoblastic leukemia discloses a small subclass of BCP-ALL.

Amare Kadam PS, Raje GC, Pais AP, Banavali S.

Cancer Genet Cytogenet. 2008 Apr 1;182(1):27-32. doi: 10.1016/j.cancergencyto.2007.12.012.

PMID:
18328947
10.

Six cases of rare gene amplifications and multiple copy of fusion gene in childhood acute lymphoblastic leukemia.

Haltrich I, Csóka M, Kovács G, Török D, Alpár D, Ottoffy G, Fekete G.

Pathol Oncol Res. 2013 Jan;19(1):123-8. doi: 10.1007/s12253-012-9533-9. Epub 2012 Apr 24.

PMID:
22528566
11.
12.

Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia.

Attarbaschi A, Mann G, Strehl S, König M, Steiner M, Jeitler V, Lion T, Dworzak MN, Gadner H, Haas OA.

Leukemia. 2007 Mar;21(3):584-6. Epub 2007 Jan 11. No abstract available. Erratum in: Leukemia. 2007 May;21(5):1135.

PMID:
17215856
13.

ETV6/RUNX1 fusion lacking prognostic effect in pediatric patients with acute lymphoblastic leukemia.

Zen PR, Capra ME, Silla LM, Loss JF, Fernandes MS, Jacques SM, Paskulin GA.

Cancer Genet Cytogenet. 2009 Jan 15;188(2):112-7. doi: 10.1016/j.cancergencyto.2008.09.005.

PMID:
19100516
14.

ETV6-RUNX1 fusion gene and additional genetic changes in infant leukemia: a genome-wide analysis.

Emerenciano M, Bungaro S, Cazzaniga G, Dorea MD, Coser VM, Magalhães IQ, Biondi A, Pombo-de-Oliveira MS.

Cancer Genet Cytogenet. 2009 Sep;193(2):86-92. doi: 10.1016/j.cancergencyto.2009.04.021.

PMID:
19665068
15.

ETV6/RUNX1 rearrangement in childhood B-precursor acute lymphoblastic leukemia with normal karyotypes or without cytogenetic results.

Alvarez Y, Gaitán S, Perez A, Bastida P, Ortega JJ, Dastugue N, Robert A, Aventín A, Badell I, Guitart M, Melo M, Caballín MR, Coll MD.

Cancer Genet Cytogenet. 2004 Jul 1;152(1):77-80.

PMID:
15193447
16.

Analysis of gene rearrangements using a fluorescence in situ hybridization method in Mexican patients with acute lymphoblastic leukemia: experience at a single institution.

Pérez-Vera P, Salas C, Montero-Ruiz O, Frías S, Dehesa G, Jarquín B, Rivera-Luna R.

Cancer Genet Cytogenet. 2008 Jul 15;184(2):94-8. doi: 10.1016/j.cancergencyto.2008.04.003.

PMID:
18617057
17.

Prevalence of ETV6-RUNX1 fusion gene in children with acute lymphoblastic leukemia in China.

Gao YJ, Zhu XH, Yang Y, Wu Y, Lu FJ, Zhai XW, Wang HS.

Cancer Genet Cytogenet. 2007 Oct 1;178(1):57-60.

PMID:
17889709
18.

Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival.

Forestier E, Heyman M, Andersen MK, Autio K, Blennow E, Borgström G, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kerndrup G, Nordgren A, Rosenquist R, Swolin B, Johansson B; Nordic Society of Paediatric Haematology, Oncology (NOPHO); Swedish Cytogenetic Leukaemia Study Group (SCLSG); NOPHO Leukaemia Cytogenetic Study Group (NLCSG).

Br J Haematol. 2008 Mar;140(6):665-72. doi: 10.1111/j.1365-2141.2008.06980.x. Epub 2008 Feb 1.

PMID:
18241254
19.

Clonotypic analysis of acute lymphoblastic leukemia with a double TEL-AML1 fusion at onset and relapse.

Inukai T, Yokota S, Okamoto T, Nemoto A, Akahane K, Takahashi K, Sato H, Goi K, Nakazawa S, Sugita K.

Leukemia. 2006 Feb;20(2):363-5. No abstract available.

PMID:
16357830
20.

Febrile infections in young children do not frequently induce translocation ETV6-RUNX1.

Olsen M, Nielsen NK, Birkballe S, Hjalgrim H, Madsen HO, Schmiegelow K.

Blood Cells Mol Dis. 2011 Feb 15;46(2):175-6. doi: 10.1016/j.bcmd.2010.11.003. Epub 2010 Dec 8. No abstract available.

PMID:
21145270

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