-
1
-
-
58149095544
-
Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia
-
C.J. Harrison Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia Br J Haematol 144 2009 147 156
-
(2009)
Br J Haematol
, vol.144
, pp. 147-156
-
-
Harrison, C.J.1
-
2
-
-
34548027243
-
Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia
-
J.B. Nachman, N.A. Heerema, H. Sather Outcome of treatment in children with hypodiploid acute lymphoblastic leukemia Blood 110 2007 1112 1115
-
(2007)
Blood
, vol.110
, pp. 1112-1115
-
-
Nachman, J.B.1
Heerema, N.A.2
Sather, H.3
-
3
-
-
67650421868
-
High hyperdiploid childhood acute lymphoblastic leukemia
-
K. Paulsson, B. Johansson High hyperdiploid childhood acute lymphoblastic leukemia Genes Chromosomes Cancer 48 2009 637 660
-
(2009)
Genes Chromosomes Cancer
, vol.48
, pp. 637-660
-
-
Paulsson, K.1
Johansson, B.2
-
4
-
-
62849088473
-
Childhood acute lymphoblastic leukemia: Update on prognostic factors
-
L.M. Vrooman, L.B. Silverman Childhood acute lymphoblastic leukemia: update on prognostic factors Curr Opin Pediatr 21 2009 1 8
-
(2009)
Curr Opin Pediatr
, vol.21
, pp. 1-8
-
-
Vrooman, L.M.1
Silverman, L.B.2
-
5
-
-
0036344108
-
Cytogenetics and molecular genetics of acute lymphoblastic leukemia
-
C.J. Harrison, L. Foroni Cytogenetics and molecular genetics of acute lymphoblastic leukemia Rev Clin Exp Hematol 6 2002 91 113
-
(2002)
Rev Clin Exp Hematol
, vol.6
, pp. 91-113
-
-
Harrison, C.J.1
Foroni, L.2
-
6
-
-
0034981713
-
The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia
-
C.J. Harrison The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia Blood Rev 15 2001 49 59
-
(2001)
Blood Rev
, vol.15
, pp. 49-59
-
-
Harrison, C.J.1
-
7
-
-
27844581656
-
Molecular cytogenetics in haematological malignancy: Current technology and future prospects
-
L. Kearney, S.W. Horsley Molecular cytogenetics in haematological malignancy: current technology and future prospects Chromosoma 114 2005 286 294
-
(2005)
Chromosoma
, vol.114
, pp. 286-294
-
-
Kearney, L.1
Horsley, S.W.2
-
8
-
-
36549062445
-
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
-
K. Paulsson, A. Horvat, B. Strömbeck Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia Genes Chromosomes Cancer 47 2008 26 33
-
(2008)
Genes Chromosomes Cancer
, vol.47
, pp. 26-33
-
-
Paulsson, K.1
Horvat, A.2
Strömbeck, B.3
-
9
-
-
0031466118
-
Molecular cytogenetics of childhood hematological malignancies
-
J.A. Martinez-Climent Molecular cytogenetics of childhood hematological malignancies Leukemia 11 1997 1999 2021
-
(1997)
Leukemia
, vol.11
, pp. 1999-2021
-
-
Martinez-Climent, J.A.1
-
10
-
-
0342424184
-
Chromosomal rearrangements in childhood acute myeloid leukemia and myelodysplastic syndromes
-
J.A. Martinez-Climent, J. García-Conde Chromosomal rearrangements in childhood acute myeloid leukemia and myelodysplastic syndromes J Pediatr Hematol Oncol 21 1999 91 102
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, pp. 91-102
-
-
Martinez-Climent, J.A.1
García-Conde, J.2
-
11
-
-
0030795080
-
Molecular cytogenetics of childhood acute myelogenous leukaemias
-
T. Leblanc, R. Berger Molecular cytogenetics of childhood acute myelogenous leukaemias Eur J Haematol 59 1997 1 13
-
(1997)
Eur J Haematol
, vol.59
, pp. 1-13
-
-
Leblanc, T.1
Berger, R.2
-
12
-
-
0026748638
-
Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia
-
N. Onodera, N.R. McCabe, C.M. Rubin Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia Blood 80 1992 203 208
-
(1992)
Blood
, vol.80
, pp. 203-208
-
-
Onodera, N.1
McCabe, N.R.2
Rubin, C.M.3
-
13
-
-
0032928401
-
Fish analysis at diagnosis in acute lymphoblastic leukemia
-
H. Avet-Loiseau Fish analysis at diagnosis in acute lymphoblastic leukemia Leuk Lymphoma 33 1999 441 449
-
(1999)
Leuk Lymphoma
, vol.33
, pp. 441-449
-
-
Avet-Loiseau, H.1
-
15
-
-
0242719886
-
Hidden aberrations diagnosed by interphase fluorescence in situ hybridisation and spectral karyotyping in childhood acute lymphoblastic leukaemia
-
A. Nordgren Hidden aberrations diagnosed by interphase fluorescence in situ hybridisation and spectral karyotyping in childhood acute lymphoblastic leukaemia Leuk Lymphoma 44 2003 2039 2053
-
(2003)
Leuk Lymphoma
, vol.44
, pp. 2039-2053
-
-
Nordgren, A.1
-
17
-
-
0031729221
-
Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line: A DNA ploidy and fluorescence in-situ hybridization study
-
S.K. Ma, G.C. Chan, T.S. Wan Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line: a DNA ploidy and fluorescence in-situ hybridization study Br J Haematol 103 1998 750 755
-
(1998)
Br J Haematol
, vol.103
, pp. 750-755
-
-
Ma, S.K.1
Chan, G.C.2
Wan, T.S.3
-
18
-
-
11844252527
-
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia
-
K. Paulsson, A. Horvat, T. Fioretos Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia Genes Chromosomes Cancer 42 2005 144 148
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 144-148
-
-
Paulsson, K.1
Horvat, A.2
Fioretos, T.3
-
19
-
-
0026094623
-
Near haploid acute lymphoblastic leukemia: Seven new cases and a review of the literature
-
B. Gibbons, P. MacCallum, E. Watts Near haploid acute lymphoblastic leukemia: seven new cases and a review of the literature Leukemia 5 1991 738 743
-
(1991)
Leukemia
, vol.5
, pp. 738-743
-
-
Gibbons, B.1
MacCallum, P.2
Watts, E.3
-
20
-
-
0035878530
-
Near haploid childhood acute lymphoblastic leukemia masked by hyperdiploid line: Detection by fluorescence in situ hybridization
-
B. Stark, M. Jeison, R. Gobuzov Near haploid childhood acute lymphoblastic leukemia masked by hyperdiploid line: detection by fluorescence in situ hybridization Cancer Genet Cytogenet 128 2001 108 113
-
(2001)
Cancer Genet Cytogenet
, vol.128
, pp. 108-113
-
-
Stark, B.1
Jeison, M.2
Gobuzov, R.3
-
21
-
-
0028910402
-
Childhood monosomy 7: Epidemiology, biology, and mechanistic implications
-
S. Luna-Fineman, K.M. Shannon, B.J. Lange Childhood monosomy 7: epidemiology, biology, and mechanistic implications Blood 85 1995 1985 1999
-
(1995)
Blood
, vol.85
, pp. 1985-1999
-
-
Luna-Fineman, S.1
Shannon, K.M.2
Lange, B.J.3
-
22
-
-
1842295700
-
Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias
-
K. Fischer, S. Fröhling, S.W. Scherer Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias Blood 89 1997 2036 2041
-
(1997)
Blood
, vol.89
, pp. 2036-2041
-
-
Fischer, K.1
Fröhling, S.2
Scherer, S.W.3
-
23
-
-
0032915689
-
Allelotyping of acute myelogenous leukemia: Loss of heterozygosity at 7q31.1 (D7S486) and q33-34 (D7S498, D7S505)
-
M. Koike, T. Tasaka, S. Spira Allelotyping of acute myelogenous leukemia: loss of heterozygosity at 7q31.1 (D7S486) and q33-34 (D7S498, D7S505) Leuk Res 23 1999 307 310
-
(1999)
Leuk Res
, vol.23
, pp. 307-310
-
-
Koike, M.1
Tasaka, T.2
Spira, S.3
-
24
-
-
0029821113
-
Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases
-
M.M. Le Beau, R. Espinosa 3rd, E.M. Davis Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases Blood 88 1996 1930 1935
-
(1996)
Blood
, vol.88
, pp. 1930-1935
-
-
Le Beau, M.M.1
Espinosa III, R.2
Davis, E.M.3
-
25
-
-
0032188805
-
The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1,612 patients entered into the MRC AML 10 trial the Medical Research Council Adult and Children's Leukaemia Working Parties
-
D. Grimwade, H. Walker, F. Oliver The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial The Medical Research Council Adult And Children's Leukaemia Working Parties Blood 92 1998 2322 2333
-
(1998)
Blood
, vol.92
, pp. 2322-2333
-
-
Grimwade, D.1
Walker, H.2
Oliver, F.3
-
26
-
-
70349939681
-
Cytogenetics of pediatric acute myeloid leukemia
-
K.N. Manola Cytogenetics of pediatric acute myeloid leukemia Eur J Haematol 83 2009 391 405
-
(2009)
Eur J Haematol
, vol.83
, pp. 391-405
-
-
Manola, K.N.1
-
28
-
-
38949098169
-
Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: An iBFM-SG study
-
E. Forestier, S. Izraeli, B. Beverloo Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study Blood 11 2008 1575 1583
-
(2008)
Blood
, vol.11
, pp. 1575-1583
-
-
Forestier, E.1
Izraeli, S.2
Beverloo, B.3
-
30
-
-
0031438731
-
The AML1 gene: A transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias
-
F. Lo Coco, S. Pisegna, D. Diverio The AML1 gene: a transcription factor involved in the pathogenesis of myeloid and lymphoid leukemias Haematologica 82 1997 364 370
-
(1997)
Haematologica
, vol.82
, pp. 364-370
-
-
Lo Coco, F.1
Pisegna, S.2
Diverio, D.3
-
31
-
-
0037358377
-
Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions
-
U. Gamerdinger, A. Teigler-Schlegel, S. Pils Cryptic chromosomal aberrations leading to an AML1/ETO rearrangement are frequently caused by small insertions Genes Chromosomes Cancer 36 2003 261 272
-
(2003)
Genes Chromosomes Cancer
, vol.36
, pp. 261-272
-
-
Gamerdinger, U.1
Teigler-Schlegel, A.2
Pils, S.3
-
32
-
-
0027933398
-
The AML1 and ETO genes in acute myeloid leukemia with a t(8;21)
-
G. Nucifora, J.D. Rowley The AML1 and ETO genes in acute myeloid leukemia with a t(8;21) Leuk Lymphoma 14 1994 353 362
-
(1994)
Leuk Lymphoma
, vol.14
, pp. 353-362
-
-
Nucifora, G.1
Rowley, J.D.2
-
33
-
-
33646703059
-
Prenatal origin of childhood AML occurs less frequently than in childhood ALL
-
T. Burjanivova, J. Madzo, K. Muzikova Prenatal origin of childhood AML occurs less frequently than in childhood ALL BMC Cancer 6 2006 100 107
-
(2006)
BMC Cancer
, vol.6
, pp. 100-107
-
-
Burjanivova, T.1
Madzo, J.2
Muzikova, K.3
-
35
-
-
80052493235
-
Importance of c-kit mutation detection method sensitivity in prognostic analyses of t(8;21)(q22;q22) acute myeloid leukemia
-
S. Wakita, H. Yamaguchi, K. Miyake Importance of c-kit mutation detection method sensitivity in prognostic analyses of t(8;21)(q22;q22) acute myeloid leukemia Leukemia 25 2011 1423 1432
-
(2011)
Leukemia
, vol.25
, pp. 1423-1432
-
-
Wakita, S.1
Yamaguchi, H.2
Miyake, K.3
-
36
-
-
54049106547
-
Transcriptional repression of the RUNX3/AML2 gene by the t(8;21) and inv(16) fusion proteins in acute myeloid leukemia
-
C.K. Cheng, L. Li, S.H. Cheng Transcriptional repression of the RUNX3/AML2 gene by the t(8;21) and inv(16) fusion proteins in acute myeloid leukemia Blood 112 2008 3391 3402
-
(2008)
Blood
, vol.112
, pp. 3391-3402
-
-
Cheng, C.K.1
Li, L.2
Cheng, S.H.3
-
37
-
-
20244389694
-
Favorable impact of the t(9;11) in childhood acute myeloid leukemia
-
J.E. Rubnitz, S.C. Raimondi, X. Tong Favorable impact of the t(9;11) in childhood acute myeloid leukemia J Clin Oncol 20 2002 2302 2309
-
(2002)
J Clin Oncol
, vol.20
, pp. 2302-2309
-
-
Rubnitz, J.E.1
Raimondi, S.C.2
Tong, X.3
-
38
-
-
0041400392
-
-
inv16(p13q22);t(16;16)(p13;q22);del(16)(q22) Accessed: May 1, 2012
-
J.L. Huret inv16(p13q22);t(16;16)(p13;q22);del(16)(q22) Atlas Genet Cytogenet Oncol Haematol June 1999 http://AtlasGeneticsOncology.org/Anomalies/ inv16.html Accessed: May 1, 2012
-
(1999)
Atlas Genet Cytogenet Oncol Haematol
-
-
Huret, J.L.1
-
39
-
-
70349754444
-
Philadelphia chromosome-positive acute lymphoblastic leukemia
-
F. Ravandi, P. Kebriaei Philadelphia chromosome-positive acute lymphoblastic leukemia Hematol Oncol Clin North Am 23 2009 1043 1063
-
(2009)
Hematol Oncol Clin North Am
, vol.23
, pp. 1043-1063
-
-
Ravandi, F.1
Kebriaei, P.2
-
40
-
-
77956902000
-
Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia
-
J. Lazic, N. Tosic, L. Dokmanovic Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia Med Oncol 27 2010 449 453
-
(2010)
Med Oncol
, vol.27
, pp. 449-453
-
-
Lazic, J.1
Tosic, N.2
Dokmanovic, L.3
-
41
-
-
41849145759
-
Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia
-
N. Shah, M.T. Leaker, I. Teshima Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia Pediatr Blood Cancer 50 2008 1052 1053
-
(2008)
Pediatr Blood Cancer
, vol.50
, pp. 1052-1053
-
-
Shah, N.1
Leaker, M.T.2
Teshima, I.3
-
43
-
-
84655170213
-
Duplication of Philadelphia chromosome and trisomy of chromosome 21 in a pediatric patient with acute lymphoblastic leukemia
-
K. Katsibardi, M. Braoudaki, S.I. Papadhimitriou Duplication of Philadelphia chromosome and trisomy of chromosome 21 in a pediatric patient with acute lymphoblastic leukemia Med Oncol 28 Suppl 1 2011 S501 S504
-
(2011)
Med Oncol
, vol.28
, Issue.SUPPL. 1
-
-
Katsibardi, K.1
Braoudaki, M.2
Papadhimitriou, S.I.3
-
44
-
-
73949159219
-
Karyotyping, FISH, and PCR in acute lymphoblastic leukemia: Competing or complementary diagnostics?
-
L. Olde Nordkamp, C. Mellink, E. van der Schoot Karyotyping, FISH, and PCR in acute lymphoblastic leukemia: competing or complementary diagnostics? J Pediatr Hematol Oncol 31 2009 930 935
-
(2009)
J Pediatr Hematol Oncol
, vol.31
, pp. 930-935
-
-
Olde Nordkamp, L.1
Mellink, C.2
Van Der Schoot, E.3
-
45
-
-
73849107115
-
Treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia
-
J.H. Milone, A. Enrico Treatment of Philadelphia chromosome-positive acute lymphoblastic leukemia Leuk Lymphoma 50 Suppl 2 2009 9 15
-
(2009)
Leuk Lymphoma
, vol.50
, Issue.SUPPL. 2
, pp. 9-15
-
-
Milone, J.H.1
Enrico, A.2
-
46
-
-
0025043959
-
The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor alpha gene to a novel transcribed locus
-
H. de Thé, C. Chomienne, M. Lanotte The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor alpha gene to a novel transcribed locus Nature 347 1990 558 561
-
(1990)
Nature
, vol.347
, pp. 558-561
-
-
De Thé, H.1
Chomienne, C.2
Lanotte, M.3
-
47
-
-
0025981102
-
Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus
-
1977-781
-
M. Alcalay, D. Zangrilli, P.P. Pandolfi Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus Proc Natl Acad Sci U S A 88 1991 1977-781
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
-
-
Alcalay, M.1
Zangrilli, D.2
Pandolfi, P.P.3
-
49
-
-
23044479837
-
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner
-
S. Hayette, P. Cornillet-Lefebvre, I. Tigaud AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner Cancer Res 65 2005 6521 6525
-
(2005)
Cancer Res
, vol.65
, pp. 6521-6525
-
-
Hayette, S.1
Cornillet-Lefebvre, P.2
Tigaud, I.3
-
50
-
-
35648954058
-
Acute lymphoblastic leukemia in infancy
-
L.B. Silverman Acute lymphoblastic leukemia in infancy Pediatr Blood Cancer 49 2007 1070 1073
-
(2007)
Pediatr Blood Cancer
, vol.49
, pp. 1070-1073
-
-
Silverman, L.B.1
-
51
-
-
85014198406
-
Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia
-
H. Van Limbergen, B. Poppe, A. Janssens Molecular cytogenetic analysis of 10;11 rearrangements in acute myeloid leukemia Leukemia 16 2002 344 351
-
(2002)
Leukemia
, vol.16
, pp. 344-351
-
-
Van Limbergen, H.1
Poppe, B.2
Janssens, A.3
-
52
-
-
0041568468
-
Children's cancer group prognostic implications of t(10;11) translocations in childhood acute myelogenous leukemia: A report from the Children's Cancer Group
-
J.N. Casillas, W.G. Woods, S.P. Hunger Children's cancer group prognostic implications of t(10;11) translocations in childhood acute myelogenous leukemia: a report from the Children's Cancer Group J Pediatr Hematol Oncol 25 2003 594 600
-
(2003)
J Pediatr Hematol Oncol
, vol.25
, pp. 594-600
-
-
Casillas, J.N.1
Woods, W.G.2
Hunger, S.P.3
-
53
-
-
0345701514
-
Prognostic impact of t(9;11) in childhood acute myeloid leukemia (AML)
-
L. Lo Nigro, D. Bottino, C. Panarello Prognostic impact of t(9;11) in childhood acute myeloid leukemia (AML) Leukemia 17 2003 636
-
(2003)
Leukemia
, vol.17
, pp. 636
-
-
Lo Nigro, L.1
Bottino, D.2
Panarello, C.3
-
54
-
-
0032697175
-
Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities
-
S. Mathew, F. Behm, J. Dalton Comparison of cytogenetics, Southern blotting, and fluorescence in situ hybridization as methods for detecting MLL gene rearrangements in children with acute leukemia and with 11q23 abnormalities Leukemia 13 1999 1713 1720
-
(1999)
Leukemia
, vol.13
, pp. 1713-1720
-
-
Mathew, S.1
Behm, F.2
Dalton, J.3
-
55
-
-
2942616592
-
ETV6/RUNX1 rearrangement in childhood B-precursor acute lymphoblastic leukemia with normal karyotypes or without cytogenetic results
-
Y. Alvarez, S. Gaitán, A. Perez ETV6/RUNX1 rearrangement in childhood B-precursor acute lymphoblastic leukemia with normal karyotypes or without cytogenetic results Cancer Genet Cytogenet 52 2004 77 80
-
(2004)
Cancer Genet Cytogenet
, vol.52
, pp. 77-80
-
-
Alvarez, Y.1
Gaitán, S.2
Perez, A.3
-
56
-
-
9244221153
-
The 12;21 translocation involving TEL and deletion of the other TEL allele: Two frequently associated alterations found in childhood acute lymphoblastic leukemia
-
S. Raynaud, H. Cave, M. Baens The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia Blood 87 1996 2891 2899
-
(1996)
Blood
, vol.87
, pp. 2891-2899
-
-
Raynaud, S.1
Cave, H.2
Baens, M.3
-
57
-
-
17544401894
-
The role of TEL and AML1 genes in the pathogenesis of hematologic malignancies
-
J. Zuna The role of TEL and AML1 genes in the pathogenesis of hematologic malignancies Cas Lek Cesk 140 2001 131 137
-
(2001)
Cas Lek Cesk
, vol.140
, pp. 131-137
-
-
Zuna, J.1
-
58
-
-
58749097408
-
A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: A genome-wide classification study
-
M.L. Den Boer, M. van Slegtenhorst, R.X. De Menezes A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study Lancet Oncol 10 2009 125 134
-
(2009)
Lancet Oncol
, vol.10
, pp. 125-134
-
-
Den Boer, M.L.1
Van Slegtenhorst, M.2
De Menezes, R.X.3
-
59
-
-
79955716719
-
MicroRNA characterize genetic diversity and drug resistance in pediatric acute lymphoblastic leukemia
-
D. Schotte, R.X. De Menezes, F.A. Moqadam MicroRNA characterize genetic diversity and drug resistance in pediatric acute lymphoblastic leukemia Haematologica 96 2011 703 711
-
(2011)
Haematologica
, vol.96
, pp. 703-711
-
-
Schotte, D.1
De Menezes, R.X.2
Moqadam, F.A.3
-
60
-
-
0031440492
-
Incidence of TEL/AML1 fusion gene analyzed consecutively in children with acute lymphoblastic leukemia in relapse
-
J. Harbott, S. Viehmann, A. Borkhardt Incidence of TEL/AML1 fusion gene analyzed consecutively in children with acute lymphoblastic leukemia in relapse Blood 90 1997 4933 4937
-
(1997)
Blood
, vol.90
, pp. 4933-4937
-
-
Harbott, J.1
Viehmann, S.2
Borkhardt, A.3
-
61
-
-
14844334150
-
Molecular cytogenetic analysis of gene rearrangements in childhood acute lymphoblastic leukemia
-
H.Y. Woo, D.W. Kim, H. Park Molecular cytogenetic analysis of gene rearrangements in childhood acute lymphoblastic leukemia J Korean Med Sci 20 2005 36 41
-
(2005)
J Korean Med Sci
, vol.20
, pp. 36-41
-
-
Woo, H.Y.1
Kim, D.W.2
Park, H.3
-
62
-
-
33744465219
-
Prospective analysis of TEL/AML1-positive patients treated on Dana-Farber Cancer Institute consortium protocol 95-01
-
M.L. Loh, M.A. Goldwasser, L.B. Silverman Prospective analysis of TEL/AML1-positive patients treated on Dana-Farber Cancer Institute consortium protocol 95-01 Blood 107 2006 4508 4513
-
(2006)
Blood
, vol.107
, pp. 4508-4513
-
-
Loh, M.L.1
Goldwasser, M.A.2
Silverman, L.B.3
-
63
-
-
0037246483
-
Recent advances in pediatric acute lymphoblastic and myeloid leukemia
-
Y. Ravindranath Recent advances in pediatric acute lymphoblastic and myeloid leukemia Curr Opin Oncol 15 2003 23 35
-
(2003)
Curr Opin Oncol
, vol.15
, pp. 23-35
-
-
Ravindranath, Y.1
-
64
-
-
0030056354
-
Chromosomal translocations involving the E2A gene in acute lymphoblastic leukemia: Clinical features and molecular pathogenesis
-
S.P. Hunger Chromosomal translocations involving the E2A gene in acute lymphoblastic leukemia: clinical features and molecular pathogenesis Blood 87 1996 1211 1224
-
(1996)
Blood
, vol.87
, pp. 1211-1224
-
-
Hunger, S.P.1
-
65
-
-
76549104445
-
Clinical features and prognostic implications of TCF3-PBX1 and ETV6-RUNX1 in adult acute lymphoblastic leukemia
-
T. Burmeister, N. Gökbuget, S. Schwartz Clinical features and prognostic implications of TCF3-PBX1 and ETV6-RUNX1 in adult acute lymphoblastic leukemia Haematologica 95 2010 241 246
-
(2010)
Haematologica
, vol.95
, pp. 241-246
-
-
Burmeister, T.1
Gökbuget, N.2
Schwartz, S.3
-
66
-
-
33845508795
-
HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32)
-
X.Y. Su, V. Della-Valle, I. Andre-Schmutz HOX11L2/TLX3 is transcriptionally activated through T-cell regulatory elements downstream of BCL11B as a result of the t(5;14)(q35;q32) Blood 108 2006 4198 4201
-
(2006)
Blood
, vol.108
, pp. 4198-4201
-
-
Su, X.Y.1
Della-Valle, V.2
Andre-Schmutz, I.3
-
67
-
-
9144253121
-
Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: Results of EORTC studies 58881 and 58951
-
H. Cavé, S. Suciu, C. Preudhomme Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951 Blood 103 2004 442 450
-
(2004)
Blood
, vol.103
, pp. 442-450
-
-
Cavé, H.1
Suciu, S.2
Preudhomme, C.3
-
68
-
-
0032190079
-
NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia
-
S.Z. Raza-Egilmez, S.N. Jani-Sait, M. Grossi NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia Cancer Res 58 1998 4269 4273
-
(1998)
Cancer Res
, vol.58
, pp. 4269-4273
-
-
Raza-Egilmez, S.Z.1
Jani-Sait, S.N.2
Grossi, M.3
-
70
-
-
0035883090
-
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
-
R.J. Jaju, C. Fidler, O.A. Haas A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia Blood 98 2001 1264 1267
-
(2001)
Blood
, vol.98
, pp. 1264-1267
-
-
Jaju, R.J.1
Fidler, C.2
Haas, O.A.3
-
71
-
-
21244447565
-
Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization
-
K. Nebral, M. König, H.H. Schmidt Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization Haematologica 90 2005 746 752
-
(2005)
Haematologica
, vol.90
, pp. 746-752
-
-
Nebral, K.1
König, M.2
Schmidt, H.H.3
-
72
-
-
0033854646
-
T(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: Characterization of a new subset of T acute lymphoblastic leukaemia
-
C. Mecucci, R. La Starza, M. Negrini t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia Br J Haematol 109 2000 788 793
-
(2000)
Br J Haematol
, vol.109
, pp. 788-793
-
-
Mecucci, C.1
La Starza, R.2
Negrini, M.3
-
73
-
-
0033568581
-
The (4;11)(q21;p15) translocation fuses the NUP98 and RAP1GDS1 genes and is recurrent in T-cell acute lymphocytic leukemia
-
D.J. Hussey, M. Nicola, S. Moore The (4;11)(q21;p15) translocation fuses the NUP98 and RAP1GDS1 genes and is recurrent in T-cell acute lymphocytic leukemia Blood 94 1999 2072 2079
-
(1999)
Blood
, vol.94
, pp. 2072-2079
-
-
Hussey, D.J.1
Nicola, M.2
Moore, S.3
-
74
-
-
0032526056
-
Frequent loss of heterozygosity on the long arm of chromosome 6: Identification of two distinct regions of deletion in childhood acute lymphoblastic leukemia
-
S. Takeuchi, M. Koike, T. Seriu Frequent loss of heterozygosity on the long arm of chromosome 6: identification of two distinct regions of deletion in childhood acute lymphoblastic leukemia Cancer Res 58 1998 2618 2623
-
(1998)
Cancer Res
, vol.58
, pp. 2618-2623
-
-
Takeuchi, S.1
Koike, M.2
Seriu, T.3
-
76
-
-
0032079325
-
6q deletions in acute lymphoblastic leukemia and non-Hodgkin's lymphomas
-
M. Merup, T.C. Moreno, M. Heyman 6q deletions in acute lymphoblastic leukemia and non-Hodgkin's lymphomas Blood 91 1998 3397 3400
-
(1998)
Blood
, vol.91
, pp. 3397-3400
-
-
Merup, M.1
Moreno, T.C.2
Heyman, M.3
-
79
-
-
0025915835
-
The t(1;22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: A Pediatric Oncology Group study
-
A. Carroll, C. Civin, N. Schneider The t(1;22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group study Blood 78 1991 748 752
-
(1991)
Blood
, vol.78
, pp. 748-752
-
-
Carroll, A.1
Civin, C.2
Schneider, N.3
-
80
-
-
0027491334
-
Acute megakaryocytic leukemia with the t(1;22)(p13; Q13)
-
T. Lion, O.A. Haas Acute megakaryocytic leukemia with the t(1;22)(p13; q13) Leuk Lymphoma 11 1993 15 20
-
(1993)
Leuk Lymphoma
, vol.11
, pp. 15-20
-
-
Lion, T.1
Haas, O.A.2
-
81
-
-
36249010942
-
FISH panels for hematologic malignancies
-
C. Sreekantaiah FISH panels for hematologic malignancies Cytogenet Genome Res 118 2007 284 296
-
(2007)
Cytogenet Genome Res
, vol.118
, pp. 284-296
-
-
Sreekantaiah, C.1
|