-
1
-
-
33947709535
-
Characteristics of patients with TEL-AML1-positive acute lymphoblastic leukemia with single or multiple fusions
-
Al-Sweedan SA, Neglia JP, Steiner ME, Bostrom BC, Casey T, Hirsch BA. 2007. Characteristics of patients with TEL-AML1-positive acute lymphoblastic leukemia with single or multiple fusions. Pediatr Blood Cancer 48:510-514.
-
(2007)
Pediatr Blood Cancer
, vol.48
, pp. 510-514
-
-
Al-Sweedan, S.A.1
Neglia, J.P.2
Steiner, M.E.3
Bostrom, B.C.4
Casey, T.5
Hirsch, B.A.6
-
2
-
-
24644510719
-
Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia
-
Alvarez Y, Coll MD, Ortega JJ, Bastida P, Dastugue N, Robert A, Cervera J, Verdeguer A, Tasso M, Aventin A, Guitart M, Caballín MR. 2005. Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia. Cancer Genet Cytogenet 162:21-29.
-
(2005)
Cancer Genet Cytogenet
, vol.162
, pp. 21-29
-
-
Alvarez, Y.1
Coll, M.D.2
Ortega, J.J.3
Bastida, P.4
Dastugue, N.5
Robert, A.6
Cervera, J.7
Verdeguer, A.8
Tasso, M.9
Aventin, A.10
Guitart, M.11
Caballín, M.R.12
-
3
-
-
6344289461
-
Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: An interphase FISH analysis
-
Attarbaschi A, Mann G, Konig M, Dworzak MN, Trebo MM, Muhlegger N, Gadner H, Haas OA. 2004. Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: An interphase FISH analysis. Leukemia 18:1611-1616.
-
(2004)
Leukemia
, vol.18
, pp. 1611-1616
-
-
Attarbaschi, A.1
Mann, G.2
Konig, M.3
Dworzak, M.N.4
Trebo, M.M.5
Muhlegger, N.6
Gadner, H.7
Haas, O.A.8
-
4
-
-
33646589709
-
Near-tetraploidy in childhood B-cell precursor acute lymphoblastic leukemia is a highly specific feature of ETV6/RUNX1-positive leukemic cases
-
Attarbaschi A, Mann G, Konig M, Steiner M, Dworzak MN, Gadner H, Haas OA. 2006. Near-tetraploidy in childhood B-cell precursor acute lymphoblastic leukemia is a highly specific feature of ETV6/RUNX1-positive leukemic cases. Genes Chromosomes Cancer 45:608-611.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 608-611
-
-
Attarbaschi, A.1
Mann, G.2
Konig, M.3
Steiner, M.4
Dworzak, M.N.5
Gadner, H.6
Haas, O.A.7
-
5
-
-
33847204694
-
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, Konig M, Steiner M, Jeitler V, Lion T, Dworzak MN, Gadner H, Haas OA. 2007. Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia. Leukemia 21:584-586.
-
(2007)
Leukemia
, vol.21
, pp. 584-586
-
-
Attarbaschi, A.1
Mann, G.2
Strehl, S.3
Konig, M.4
Steiner, M.5
Jeitler, V.6
Lion, T.7
Dworzak, M.N.8
Gadner, H.9
Haas, O.A.10
-
6
-
-
33947430093
-
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
-
Forestier E, Andersen MK, Autio K, Blennow E, Borgstrom G, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kerndrup G, Nordgren A, Rosenquist R, Swolin B, Johansson B. 2007. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature. Genes Chromosomes Cancer 46:440-450.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 440-450
-
-
Forestier, E.1
Andersen, M.K.2
Autio, K.3
Blennow, E.4
Borgstrom, G.5
Golovleva, I.6
Heim, S.7
Heinonen, K.8
Hovland, R.9
Johannsson, J.H.10
Kerndrup, G.11
Nordgren, A.12
Rosenquist, R.13
Swolin, B.14
Johansson, B.15
-
7
-
-
0035003350
-
The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: A valuable resource for patient management
-
Harrison CJ, Martineau M, Secker-Walker LM. 2001. The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: A valuable resource for patient management. Br J Haematol 113:3-10.
-
(2001)
Br J Haematol
, vol.113
, pp. 3-10
-
-
Harrison, C.J.1
Martineau, M.2
Secker-Walker, L.M.3
-
8
-
-
0003676646
-
-
ISCN, Schaffer LG, Slovak ML, Campbell LJ, editors. Basel: S. Karger
-
ISCN.2009. An International System for Human Cytogenetic Nomenclature. In: Schaffer LG, Slovak ML, Campbell LJ, editors. Basel: S. Karger, 2009.
-
(2009)
An International System for Human Cytogenetic Nomenclature
-
-
-
9
-
-
16844362747
-
Duplication or translocation? The origin of a second der(12)
-
Jalali GR, Barber KE, Broadfield ZJ, Cheung KL, Harris RL, Harrison CJ, Moorman AV, Robinson HM, Martineau M. 2003a. Duplication or translocation? The origin of a second der(12). Blood 102:867a.
-
(2003)
Blood
, vol.102
-
-
Jalali, G.R.1
Barber, K.E.2
Broadfield, Z.J.3
Cheung, K.L.4
Harris, R.L.5
Harrison, C.J.6
Moorman, A.V.7
Robinson, H.M.8
Martineau, M.9
-
10
-
-
0037851049
-
A unique variant of ETV6/AML1 fusion in a child with acute lymphoblastic leukemia
-
Jalali GR, Martineau M, Ford AM, Greaves M, Stevens RF, Harrison CJ. 2003b. A unique variant of ETV6/AML1 fusion in a child with acute lymphoblastic leukemia. Leukemia 17:993-995.
-
(2003)
Leukemia
, vol.17
, pp. 993-995
-
-
Jalali, G.R.1
Martineau, M.2
Ford, A.M.3
Greaves, M.4
Stevens, R.F.5
Harrison, C.J.6
-
11
-
-
38349056439
-
Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia
-
Jalali GR, An Q, Konn ZJ, Worley H, Wright SL, Harrison CJ, Strefford JC, Martineau M. 2008. Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia. Leukemia 22:114-123.
-
(2008)
Leukemia
, vol.22
, pp. 114-123
-
-
Jalali, G.R.1
An, Q.2
Konn, Z.J.3
Worley, H.4
Wright, S.L.5
Harrison, C.J.6
Strefford, J.C.7
Martineau, M.8
-
12
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N, Ogawa S, Zimmermann M, Kato M, Sanada M, Hemminki K, Yamatomo G, Nannya Y, Koehler R, Flohr T, Miller CW, Harbott J, Ludwig WD, Stanulla M, Schrappe M, Bartram CR, Koeffler HP. 2008. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood 111:776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
Kato, M.4
Sanada, M.5
Hemminki, K.6
Yamatomo, G.7
Nannya, Y.8
Koehler, R.9
Flohr, T.10
Miller, C.W.11
Harbott, J.12
Ludwig, W.D.13
Stanulla, M.14
Schrappe, M.15
Bartram, C.R.16
Koeffler, H.P.17
-
13
-
-
34548789577
-
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region
-
Lilljebjorn H, Heidenblad M, Nilsson B, Lassen C, Horvat A, Heldrup J, Behrendtz M, Johansson B, Andersson A, Fioretos T. 2007. Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq duplications and identify several putative target genes within the commonly gained region. Leukemia 21:2137-2144.
-
(2007)
Leukemia
, vol.21
, pp. 2137-2144
-
-
Lilljebjorn, H.1
Heidenblad, M.2
Nilsson, B.3
Lassen, C.4
Horvat, A.5
Heldrup, J.6
Behrendtz, M.7
Johansson, B.8
Andersson, A.9
Fioretos, T.10
-
14
-
-
0032907413
-
Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion
-
Loncarevic IF, Roitzheim B, Ritterbach J, Viehmann S, Borkhardt A, Lampert F, Harbott J. 1999. Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion. Genes Chromosomes Cancer 24:272-277.
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 272-277
-
-
Loncarevic, I.F.1
Roitzheim, B.2
Ritterbach, J.3
Viehmann, S.4
Borkhardt, A.5
Lampert, F.6
Harbott, J.7
-
15
-
-
20144387358
-
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. 2005. ETV6/RUNX1 fusion at diagnosis and relapse: Some prognostic indications. Genes Chromosomes Cancer 43:54-71.
-
(2005)
Genes Chromosomes Cancer
, vol.43
, pp. 54-71
-
-
Martineau, M.1
Jalali, G.R.2
Barber, K.E.3
Broadfield, Z.J.4
Cheung, K.L.5
Lilleyman, J.6
Moorman, A.V.7
Richards, S.8
Robinson, H.M.9
Ross, F.10
Harrison, C.J.11
-
16
-
-
33746237628
-
Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: Association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable outcome
-
Raimondi SC, Zhou Y, Shurtleff SA, Rubnitz JE, Pui CH, Behm FG. 2006. Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: Association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable outcome. Cancer Genet Cytogenet 169:50-57.
-
(2006)
Cancer Genet Cytogenet
, vol.169
, pp. 50-57
-
-
Raimondi, S.C.1
Zhou, Y.2
Shurtleff, S.A.3
Rubnitz, J.E.4
Pui, C.H.5
Behm, F.G.6
-
17
-
-
33644554828
-
Incidence of additional genetic changes in the TEL and AML1 genes in DCOG and COALL-treated t(12;21)-positive pediatric ALL, and their relation with drug sensitivity and clinical outcome
-
Stams WA, Beverloo HB, den Boer ML, de Menezes RX, Stigter RL, van Drunen E, Ramakers-van-Woerden NL, Loonen AH, van Wering ER, Janka-Schaub GE, Pieters R. 2006. Incidence of additional genetic changes in the TEL and AML1 genes in DCOG and COALL-treated t(12;21)-positive pediatric ALL, and their relation with drug sensitivity and clinical outcome. Leukemia 20:410-416.
-
(2006)
Leukemia
, vol.20
, pp. 410-416
-
-
Stams, W.A.1
Beverloo, H.B.2
den Boer, M.L.3
de Menezes, R.X.4
Stigter, R.L.5
van Drunen, E.6
Ramakers-van-Woerden, N.L.7
Loonen, A.H.8
van Wering, E.R.9
Janka-Schaub, G.E.10
Pieters, R.11
-
18
-
-
76649121278
-
Clinical relevance of complex chromosomal aberrations in bone marrow Cells of 107 children with ETV6/RUNX1 positive acute lymphoblastic leukemia (ALL)
-
Zemanova Z, Michalova K, Babicka L, Pavlistova L, Jarosova M, Holzerova M, Oltova A, Hruba M, Muzikova K, Zuna J, Trka J, Mihal V, Sterba J, Formankova R, Sedlacek P, Vrzalova A, Stary J. 2006. Clinical relevance of complex chromosomal aberrations in bone marrow Cells of 107 children with ETV6/RUNX1 positive acute lymphoblastic leukemia (ALL). Blood 108:2278a.
-
(2006)
Blood
, vol.108
-
-
Zemanova, Z.1
Michalova, K.2
Babicka, L.3
Pavlistova, L.4
Jarosova, M.5
Holzerova, M.6
Oltova, A.7
Hruba, M.8
Muzikova, K.9
Zuna, J.10
Trka, J.11
Mihal, V.12
Sterba, J.13
Formankova, R.14
Sedlacek, P.15
Vrzalova, A.16
Stary, J.17
|