-
1
-
-
0027279295
-
Predictability of the t(1;19)(q23;p13) from surface antigen phenotype: Implications for screening cases of childhood acute lymphoblastic leukaemia for molecular analysis: A Pediatric Oncology Group study
-
Borowitz, M.J., Hunger, S.P., Carroll, A.J., Shuster, J.J., Pullen, D.J., Steuber, C.P. & Cleary, M.L. (1993) Predictability of the t(1;19)(q23;p13) from surface antigen phenotype: implications for screening cases of childhood acute lymphoblastic leukaemia for molecular analysis: a Pediatric Oncology Group study. Blood, 82, 1086-1091.
-
(1993)
Blood
, vol.82
, pp. 1086-1091
-
-
Borowitz, M.J.1
Hunger, S.P.2
Carroll, A.J.3
Shuster, J.J.4
Pullen, D.J.5
Steuber, C.P.6
Cleary, M.L.7
-
2
-
-
0042664120
-
New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia
-
Brockman, S.R., Paternoster, S.F., Ketterling, R.P. & Dewald, G.W. (2003) New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia. Cancer Genetics and Cytogenetics, 145, 144-151.
-
(2003)
Cancer Genetics and Cytogenetics
, vol.145
, pp. 144-151
-
-
Brockman, S.R.1
Paternoster, S.F.2
Ketterling, R.P.3
Dewald, G.W.4
-
3
-
-
0029035305
-
Expression of the E2A-PBX1 fusion transcripts in t(1;19)(q23;p13) and der(19)t(1;19) at diagnosis and in remission of acute lymphoblastic leukemia with different B lineage immunophenotypes
-
Devaraj, P.E., Foroni, L., Janossy, G., Hoffbrand, A.V. & Seeker-Walker, L.M. (1995) Expression of the E2A-PBX1 fusion transcripts in t(1;19)(q23;p13) and der(19)t(1;19) at diagnosis and in remission of acute lymphoblastic leukemia with different B lineage immunophenotypes. Leukemia, 9, 821-825.
-
(1995)
Leukemia
, vol.9
, pp. 821-825
-
-
Devaraj, P.E.1
Foroni, L.2
Janossy, G.3
Hoffbrand, A.V.4
Seeker-Walker, L.M.5
-
4
-
-
0036357502
-
Interphase FISH studies of chronic myeloid leukemia
-
(ed. by Y.-S. Fan). Humana Press Inc., Totowa, NJ
-
Dewald, G.W. (2002) Interphase FISH studies of chronic myeloid leukemia. In: Molecular Cytogenetics Protocols and Applications, Vol. 204 (ed. by Y.-S. Fan), pp. 311-342. Humana Press Inc., Totowa, NJ.
-
(2002)
Molecular Cytogenetics Protocols and Applications
, vol.204
, pp. 311-342
-
-
Dewald, G.W.1
-
5
-
-
0032079490
-
Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia
-
Dewald, G.W., Wyatt, W.A., Juneau, A.L., Carlson, R.O., Zinsmeister, A.R., Jalal, S.M., Spurbeck, J.L. & Silver, R.T. (1998) Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia. Blood, 91, 3357-3365.
-
(1998)
Blood
, vol.91
, pp. 3357-3365
-
-
Dewald, G.W.1
Wyatt, W.A.2
Juneau, A.L.3
Carlson, R.O.4
Zinsmeister, A.R.5
Jalal, S.M.6
Spurbeck, J.L.7
Silver, R.T.8
-
6
-
-
0036736503
-
Large deletions 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia
-
Godon, C., Proffitt, J., Dastugue, N., Lafage-Pochitaloff, M., Mozziconacci, M.J., Talmant, P., Hackbarth, M., Bataille, R. & Avet-Loiseau, H. (2002) Large deletions 5′ to the ETO breakpoint are recurrent events in patients with t(8;21) acute myeloid leukemia. Leukemia, 16, 1752-1754.
-
(2002)
Leukemia
, vol.16
, pp. 1752-1754
-
-
Godon, C.1
Proffitt, J.2
Dastugue, N.3
Lafage-Pochitaloff, M.4
Mozziconacci, M.J.5
Talmant, P.6
Hackbarth, M.7
Bataille, R.8
Avet-Loiseau, H.9
-
7
-
-
0030056354
-
Chromosomal translocations involving the E2A gene in acute lymphoblastic leukemia: Clinical features and molecular pathogenesis
-
Hunger, S.P. (1996) Chromosomal translocations involving the E2A gene in acute lymphoblastic leukemia: clinical features and molecular pathogenesis. Blood, 87, 1211-1224.
-
(1996)
Blood
, vol.87
, pp. 1211-1224
-
-
Hunger, S.P.1
-
8
-
-
0026069091
-
The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias
-
Hunger, S.P., Galili, N., Carroll, A.J., Crist, W.M., Link, M.P. & Cleary, M.L. (1991) The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias. Blood, 77, 687-693.
-
(1991)
Blood
, vol.77
, pp. 687-693
-
-
Hunger, S.P.1
Galili, N.2
Carroll, A.J.3
Crist, W.M.4
Link, M.P.5
Cleary, M.L.6
-
9
-
-
0027309284
-
Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: A comparison between cytogenetic and polymerase chain reaction analyses
-
Izraeli, S., Janssen, J.W., Haas, O.A., Harbott, J., Brok-Simoni, F., Walther, J.U., Kovar, H., Henn, T., Ludwig, W.D., Reiter, A., Rechavi, G., Bartram, C.R., Gadner, H. & Lion, T. (1993) Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses. Leukemia, 7, 671-678.
-
(1993)
Leukemia
, vol.7
, pp. 671-678
-
-
Izraeli, S.1
Janssen, J.W.2
Haas, O.A.3
Harbott, J.4
Brok-Simoni, F.5
Walther, J.U.6
Kovar, H.7
Henn, T.8
Ludwig, W.D.9
Reiter, A.10
Rechavi, G.11
Bartram, C.R.12
Gadner, H.13
Lion, T.14
-
10
-
-
0003477486
-
-
World Health Organization Classification of Tumours. IARC Press, Lyon
-
Jaffe, E.S., Stein, H.N. & Vardiman, J.W. (eds) (2001). World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. World Health Organization Classification of Tumours. IARC Press, Lyon, 111-114.
-
(2001)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues
, pp. 111-114
-
-
Jaffe, E.S.1
Stein, H.N.2
Vardiman, J.W.3
-
11
-
-
11844252527
-
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia
-
Kajsa Paulsson, A.H., Fioretos, T., Mitelman, F. & Johansson, B. (2005) Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia. Genes, Chromosomes and Cancer, 42, 144-148.
-
(2005)
Genes, Chromosomes and Cancer
, vol.42
, pp. 144-148
-
-
Kajsa Paulsson, A.H.1
Fioretos, T.2
Mitelman, F.3
Johansson, B.4
-
12
-
-
0025137176
-
A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL
-
Kamps, M.P., Murre, C., Sun, X.H. & Baltimore, D. (1990) A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL. Cell, 60, 547-555.
-
(1990)
Cell
, vol.60
, pp. 547-555
-
-
Kamps, M.P.1
Murre, C.2
Sun, X.H.3
Baltimore, D.4
-
13
-
-
0035383839
-
Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
-
Kolomietz, E., Al-Maghrabi, J., Brennan, S., Karaskova, J., Minkin, S., Lipton, J. & Squire, J.A. (2001) Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood, 97, 3581-3588.
-
(2001)
Blood
, vol.97
, pp. 3581-3588
-
-
Kolomietz, E.1
Al-Maghrabi, J.2
Brennan, S.3
Karaskova, J.4
Minkin, S.5
Lipton, J.6
Squire, J.A.7
-
14
-
-
0036121966
-
A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t(4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias
-
Konig, M., Reichel, M., Marschalek, R., Haas, O.A. & Strehl, S. (2002) A highly specific and sensitive fluorescence in situ hybridization assay for the detection of t(4;11)(q21;q23) and concurrent submicroscopic deletions in acute leukaemias. British Journal of Haematology, 116, 758-764.
-
(2002)
British Journal of Haematology
, vol.116
, pp. 758-764
-
-
Konig, M.1
Reichel, M.2
Marschalek, R.3
Haas, O.A.4
Strehl, S.5
-
15
-
-
0024465836
-
The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias
-
Mellentin, J.D., Murre, C., Donion, T.A., McCaw, P.S., Smith, S.D., Carroll, A.J., McDonald, M.E., Baltimore, D. & Cleary, M.L. (1989) The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias. Science, 246, 379-382.
-
(1989)
Science
, vol.246
, pp. 379-382
-
-
Mellentin, J.D.1
Murre, C.2
Donion, T.A.3
McCaw, P.S.4
Smith, S.D.5
Carroll, A.J.6
McDonald, M.E.7
Baltimore, D.8
Cleary, M.L.9
-
16
-
-
0025185904
-
Molecular analysis of the t(1;19) breakpoint cluster region in pre-B cell acute lymphoblastic leukemias
-
Mellentin, J.D., Nourse, J., Hunger, S.P., Smith, S.D. & Cleary, M.L. (1990) Molecular analysis of the t(1;19) breakpoint cluster region in pre-B cell acute lymphoblastic leukemias. Genes, Chromosomes and Cancer, 2, 239-247.
-
(1990)
Genes, Chromosomes and Cancer
, vol.2
, pp. 239-247
-
-
Mellentin, J.D.1
Nourse, J.2
Hunger, S.P.3
Smith, S.D.4
Cleary, M.L.5
-
17
-
-
0025064238
-
Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor
-
Nourse, J., Mellentin, J.D., Galili, N., Wilkinson, J., Stanbridge, E., Smith, S.D. & Cleary, M.L. (1990) Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor. Cell, 60, 535-545.
-
(1990)
Cell
, vol.60
, pp. 535-545
-
-
Nourse, J.1
Mellentin, J.D.2
Galili, N.3
Wilkinson, J.4
Stanbridge, E.5
Smith, S.D.6
Cleary, M.L.7
-
18
-
-
10744228486
-
CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy
-
Pardanani, A., Ketterling, R.P., Brockman, S.R., Flynn, H.C., Paternoster, S.F., Shearer, B.M., Reeder, T.L., Li, C.Y., Cross, N.C., Cools, J., Gilliland, D.G., Dewald, G.W. & Tefferi, A. (2003) CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy. Blood, 102, 3093-3096.
-
(2003)
Blood
, vol.102
, pp. 3093-3096
-
-
Pardanani, A.1
Ketterling, R.P.2
Brockman, S.R.3
Flynn, H.C.4
Paternoster, S.F.5
Shearer, B.M.6
Reeder, T.L.7
Li, C.Y.8
Cross, N.C.9
Cools, J.10
Gilliland, D.G.11
Dewald, G.W.12
Tefferi, A.13
-
19
-
-
0027961005
-
Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t(1;19) (q23;p13) or its derivative
-
Pui, C.H., Raimondi, S.C., Hancock, M.L., Rivera, G.K., Ribeiro, R.C., Mahmoud, H.H., Sandlund, J.T., Crist, W.M. & Behm, F.G. (1994) Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t(1;19) (q23;p13) or its derivative. Journal of Clinical Oncology, 12, 2601-2606.
-
(1994)
Journal of Clinical Oncology
, vol.12
, pp. 2601-2606
-
-
Pui, C.H.1
Raimondi, S.C.2
Hancock, M.L.3
Rivera, G.K.4
Ribeiro, R.C.5
Mahmoud, H.H.6
Sandlund, J.T.7
Crist, W.M.8
Behm, F.G.9
-
20
-
-
2142819411
-
Acute lymphoblastic leukaemia
-
Pui, C.H., Relling, M.V. & Downing, J.R. (2004) Acute lymphoblastic leukaemia [see comment]. New England Journal of Medicine, 350, 1535-1548.
-
(2004)
New England Journal of Medicine
, vol.350
, pp. 1535-1548
-
-
Pui, C.H.1
Relling, M.V.2
Downing, J.R.3
-
21
-
-
0025914808
-
New recurring chromosomal translocations in childhood acute lymphoblastic leukemia
-
Raimondi, S.C., Privitera, E., Williams, D.L., Look, A.T., Behm, F., Rivera, G.K., Crist, W.M. & Pui, C.H. (1991) New recurring chromosomal translocations in childhood acute lymphoblastic leukemia. Blood, 77, 2016-2022.
-
(1991)
Blood
, vol.77
, pp. 2016-2022
-
-
Raimondi, S.C.1
Privitera, E.2
Williams, D.L.3
Look, A.T.4
Behm, F.5
Rivera, G.K.6
Crist, W.M.7
Pui, C.H.8
-
22
-
-
0026716252
-
Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia
-
Seeker-Walker, L.M., Berger, R., Fenaux, P., Lai, J.L., Nelken, B., Garson, M., Michael, P.M., Hagemeijer, A., Harrison, C.J., Kaneko, Y. & Rubin, C.M. (1992) Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia. Leukemia, 6, 363-369.
-
(1992)
Leukemia
, vol.6
, pp. 363-369
-
-
Seeker-Walker, L.M.1
Berger, R.2
Fenaux, P.3
Lai, J.L.4
Nelken, B.5
Garson, M.6
Michael, P.M.7
Hagemeijer, A.8
Harrison, C.J.9
Kaneko, Y.10
Rubin, C.M.11
-
23
-
-
0023029814
-
Balanced and unbalanced 1;19 translocation-associated acute lymphoblastic leukemias
-
Shikano, T., Kaneko, Y., Takazawa, M., Ueno, N., Ohkawa, M. & Fujimoto, T. (1986) Balanced and unbalanced 1;19 translocation-associated acute lymphoblastic leukemias. Cancer, 58, 2239-2243.
-
(1986)
Cancer
, vol.58
, pp. 2239-2243
-
-
Shikano, T.1
Kaneko, Y.2
Takazawa, M.3
Ueno, N.4
Ohkawa, M.5
Fujimoto, T.6
-
24
-
-
12944295358
-
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
-
Sinclair, P.B., Nacheva, E.P., Leversha, M., Telford, N., Chang, J., Reid, A., Bench, A., Champion, K., Huntly, B. & Green, A.R. (2000) Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia [see comment]. Blood, 95, 738-743.
-
(2000)
Blood
, vol.95
, pp. 738-743
-
-
Sinclair, P.B.1
Nacheva, E.P.2
Leversha, M.3
Telford, N.4
Chang, J.5
Reid, A.6
Bench, A.7
Champion, K.8
Huntly, B.9
Green, A.R.10
-
25
-
-
0346250817
-
A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t(9;22)(q34;q11.2) associated with deletion of DNA on the derivative chromosome 9 in chronic myelocytic leukemia
-
Smoley, S.A., Brockman, S.R., Paternoster, S.F., Meyer, R.G. & Dewald, G.W. (2004) A novel tricolor, dual-fusion fluorescence in situ hybridization method to detect BCR/ABL fusion in cells with t(9;22)(q34;q11.2) associated with deletion of DNA on the derivative chromosome 9 in chronic myelocytic leukemia. Cancer Genetics and Cytogenetics, 148, 1-6.
-
(2004)
Cancer Genetics and Cytogenetics
, vol.148
, pp. 1-6
-
-
Smoley, S.A.1
Brockman, S.R.2
Paternoster, S.F.3
Meyer, R.G.4
Dewald, G.W.5
-
26
-
-
0023881064
-
Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques
-
Spurbeck, J.L., Carlson, R.O., Allen, J.E. & Dewald, G.W. (1988) Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques. Cancer Genetics and Cytogenetics, 32, 59-66.
-
(1988)
Cancer Genetics and Cytogenetics
, vol.32
, pp. 59-66
-
-
Spurbeck, J.L.1
Carlson, R.O.2
Allen, J.E.3
Dewald, G.W.4
-
27
-
-
0028905495
-
Heterogeneity of t(1;19)(q23;p13) acute leukaemias
-
French Haematological Cytology Group
-
Troussard, X., Rimokh, R., Valensi, F., Leboeuf, D., Fenneteau, O., Guitard, A.M., Manel, A.M., Schillinger, F., Leglise, C., Brizard, A., Gardais, J., Lessard, M., Flandrin, G. & Macintyre, E. (1995) Heterogeneity of t(1;19)(q23;p13) acute leukaemias. French Haematological Cytology Group. British Journal of Haematology, 89, 516-526.
-
(1995)
British Journal of Haematology
, vol.89
, pp. 516-526
-
-
Troussard, X.1
Rimokh, R.2
Valensi, F.3
Leboeuf, D.4
Fenneteau, O.5
Guitard, A.M.6
Manel, A.M.7
Schillinger, F.8
Leglise, C.9
Brizard, A.10
Gardais, J.11
Lessard, M.12
Flandrin, G.13
Macintyre, E.14
-
28
-
-
0031918423
-
Clinical significance of translocation t(1;19) in childhood acute lymphoblastic leukemia in the context of contemporary therapies: A report from the Children's Cancer Group
-
Uckun, P.M., Sensel, M.G., Sather, H.N., Gaynon, P.S., Arthur, D.C., Lange, B.J., Steinherz, P.G., Kraft, P., Hutchinson, R., Nachman, J.B., Reaman, G.H. & Heerema, N.A. (1998) Clinical significance of translocation t(1;19) in childhood acute lymphoblastic leukemia in the context of contemporary therapies: a report from the Children's Cancer Group. Journal of Clinical Oncology, 16, 527-535.
-
(1998)
Journal of Clinical Oncology
, vol.16
, pp. 527-535
-
-
Uckun, P.M.1
Sensel, M.G.2
Sather, H.N.3
Gaynon, P.S.4
Arthur, D.C.5
Lange, B.J.6
Steinherz, P.G.7
Kraft, P.8
Hutchinson, R.9
Nachman, J.B.10
Reaman, G.H.11
Heerema, N.A.12
-
29
-
-
0027176915
-
Pbx1 is converted into a transcriptional activator upon acquiring the N-terminal region of E2A in pre-B-cell acute lymphoblastoid leukemia
-
Van Dijk, M.A., Voorhoeve, P.M. & Murre, C. (1993) Pbx1 is converted into a transcriptional activator upon acquiring the N-terminal region of E2A in pre-B-cell acute lymphoblastoid leukemia. Proceedings of the National Academy of Sciences of the United States of America, 90, 6061-6065.
-
(1993)
Proceedings of the National Academy of Sciences of the United States of America
, vol.90
, pp. 6061-6065
-
-
Van Dijk, M.A.1
Voorhoeve, P.M.2
Murre, C.3
-
30
-
-
0033619452
-
Prenatal origin of acute lymphoblastic leukaemia in children
-
Wiemels, J.L., Cazzaniga, G., Daniotti, M., Eden, O.B., Addison, G.M., Masera, G., Saha, V., Biondi, A. & Greaves, M.F. (1999) Prenatal origin of acute lymphoblastic leukaemia in children [see comment]. Lancet, 354, 1499-1503.
-
(1999)
Lancet
, vol.354
, pp. 1499-1503
-
-
Wiemels, J.L.1
Cazzaniga, G.2
Daniotti, M.3
Eden, O.B.4
Addison, G.M.5
Masera, G.6
Saha, V.7
Biondi, A.8
Greaves, M.F.9
-
31
-
-
18744372705
-
Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia
-
Wiemels, J.L., Leonard, B.C., Wang, Y., Segal, M.R., Hunger, S.P., Smith, M.T., Grouse, V., Ma, X., Buffler, P.A. & Pine, S.R. (2002) Site-specific translocation and evidence of postnatal origin of the t(1;19) E2A-PBX1 fusion in childhood acute lymphoblastic leukemia. Proceedings of the National Academy of Sciences of the United States of America, 99, 15101-15106.
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, pp. 15101-15106
-
-
Wiemels, J.L.1
Leonard, B.C.2
Wang, Y.3
Segal, M.R.4
Hunger, S.P.5
Smith, M.T.6
Grouse, V.7
Ma, X.8
Buffler, P.A.9
Pine, S.R.10
-
32
-
-
3042642320
-
Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1;19)(q23;p13)
-
Yuki, Y., Imoto, I., Imaizumi, M., Hibi, S., Kaneko, Y., Amagasa, T. & Inazawa, J. (2004) Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1;19)(q23;p13). Cancer Science, 95, 503-507.
-
(2004)
Cancer Science
, vol.95
, pp. 503-507
-
-
Yuki, Y.1
Imoto, I.2
Imaizumi, M.3
Hibi, S.4
Kaneko, Y.5
Amagasa, T.6
Inazawa, J.7
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