-
1
-
-
0021792205
-
The clinical significance of cytogenetic studies in 100 patients with multiple myeloma plasma cell leukemia, or amyloidosis
-
Dewald, G. W., Kyle, R. A., Hicks, G. A., and Greipp, P. R. The clinical significance of cytogenetic studies in 100 patients with multiple myeloma plasma cell leukemia, or amyloidosis. Blood, 66: 380-390, 1985.
-
(1985)
Blood
, vol.66
, pp. 380-390
-
-
Dewald, G.W.1
Kyle, R.A.2
Hicks, G.A.3
Greipp, P.R.4
-
2
-
-
0030211192
-
Multiple myeloma: Almost all patients are cytogenetically abnormal
-
Zandecki, M., Lai, J. L., and Facon, T. Multiple myeloma: almost all patients are cytogenetically abnormal. Br. J. Haematol., 94: 217-227, 1996.
-
(1996)
Br. J. Haematol.
, vol.94
, pp. 217-227
-
-
Zandecki, M.1
Lai, J.L.2
Facon, T.3
-
3
-
-
8944237001
-
Incidence of chromosome numerical changes in multiple myeloma: Fluorescence in situ hybridization analysis using 15 chromosome-specific probes
-
Tabernero, D., San Miguel, J. F., Garcia-Sanz, M., Najera, L., Garcia-Isidoro, M., Perez-Simon, J. A., Gonzalez, M., Wiegant, J., Raap, A. K., and Orfao, A. Incidence of chromosome numerical changes in multiple myeloma: fluorescence in situ hybridization analysis using 15 chromosome-specific probes. Am. J. Pathol., 149: 153-161, 1996.
-
(1996)
Am. J. Pathol.
, vol.149
, pp. 153-161
-
-
Tabernero, D.1
San Miguel, J.F.2
Garcia-Sanz, M.3
Najera, L.4
Garcia-Isidoro, M.5
Perez-Simon, J.A.6
Gonzalez, M.7
Wiegant, J.8
Raap, A.K.9
Orfao, A.10
-
4
-
-
0037085787
-
Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation
-
Avet-Loiseau, H., Facon, T., Grosbois, B., Magrangeas, F., Rapp, M. J., Harousseau, J. L., Minvielle, S., Bataille, R., and Intergroupe Francophone du Myelome. Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation. Blood, 99: 2185-2191, 2002.
-
(2002)
Blood
, vol.99
, pp. 2185-2191
-
-
Avet-Loiseau, H.1
Facon, T.2
Grosbois, B.3
Magrangeas, F.4
Rapp, M.J.5
Harousseau, J.L.6
Minvielle, S.7
Bataille, R.8
-
5
-
-
0029124130
-
Multiple myeloma: High incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization
-
Drach, J., Schuster, J., Nowotny, H., Angerler, J., Rosenthal, F., Fiegl, M., Rothermundt, C., Gsur, A., Jager, U., Heinz, R., Lechner, K., Ludwig, H., and Huber, H. Multiple myeloma: high incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization. Cancer Res., 55: 3854-3859, 1995.
-
(1995)
Cancer Res.
, vol.55
, pp. 3854-3859
-
-
Drach, J.1
Schuster, J.2
Nowotny, H.3
Angerler, J.4
Rosenthal, F.5
Fiegl, M.6
Rothermundt, C.7
Gsur, A.8
Jager, U.9
Heinz, R.10
Lechner, K.11
Ludwig, H.12
Huber, H.13
-
6
-
-
0013366763
-
Cytogenetic abnormalities in multiple myeloma and related plasma cell disorders; a comparison of conventional cytogenetic analysis to fluorescent in-situ hybridization with simultaneous cytoplasmic immunoglobulin staining
-
Fonseca, R., Ahmann, G. J., Juneau, A. L., Jalal, S. M., Dewald, G. W., Larson, D. M., Therneau, T. M., Gertz, M. A., and Greipp, P. R. Cytogenetic abnormalities in multiple myeloma and related plasma cell disorders; a comparison of conventional cytogenetic analysis to fluorescent in-situ hybridization with simultaneous cytoplasmic immunoglobulin staining (Meeting Abstract). Blood, 90: 349, 1997.
-
(1997)
Blood
, vol.90
, pp. 349
-
-
Fonseca, R.1
Ahmann, G.J.2
Juneau, A.L.3
Jalal, S.M.4
Dewald, G.W.5
Larson, D.M.6
Therneau, T.M.7
Gertz, M.A.8
Greipp, P.R.9
-
7
-
-
0037103287
-
Genomic abnormalities in monoclonal gammopathy of undetermined significance
-
Fonseca, R., Bailey, R. J., Ahmann, G. J., Rajkumar, S. V., Hoyer, J. D., Lust, J. A., Kyle, R. A., Gertz, M. A., Greipp, P. R., and Dewald, G. W. Genomic abnormalities in monoclonal gammopathy of undetermined significance. Blood, 100: 1417-1424, 2002.
-
(2002)
Blood
, vol.100
, pp. 1417-1424
-
-
Fonseca, R.1
Bailey, R.J.2
Ahmann, G.J.3
Rajkumar, S.V.4
Hoyer, J.D.5
Lust, J.A.6
Kyle, R.A.7
Gertz, M.A.8
Greipp, P.R.9
Dewald, G.W.10
-
8
-
-
0036512435
-
Multiple myeloma: Evolving genetic events and host interactions
-
Kuehl, W. M., and Bergsagel, P. L. Multiple myeloma: evolving genetic events and host interactions. Nat. Rev Cancer, 2: 175-187, 2002.
-
(2002)
Nat. Rev. Cancer
, vol.2
, pp. 175-187
-
-
Kuehl, W.M.1
Bergsagel, P.L.2
-
9
-
-
0035839841
-
Chromosome translocations in multiple myeloma
-
Bergsagel, P. L., and Kuehl, W. M. Chromosome translocations in multiple myeloma. Oncogene, 20: 5611-5622, 2001.
-
(2001)
Oncogene
, vol.20
, pp. 5611-5622
-
-
Bergsagel, P.L.1
Kuehl, W.M.2
-
10
-
-
0028880424
-
Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalities
-
Tricot, G., Barlogie, B., Jagannath, S., Bracy, D., Mattox, S., Vesole, D. H., Naucke, S., and Sawyer, J. R. Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalities. Blood, 86: 4250-4256, 1995.
-
(1995)
Blood
, vol.86
, pp. 4250-4256
-
-
Tricot, G.1
Barlogie, B.2
Jagannath, S.3
Bracy, D.4
Mattox, S.5
Vesole, D.H.6
Naucke, S.7
Sawyer, J.R.8
-
11
-
-
0035496928
-
Hypodiploidy is a major prognostic factor in multiple myeloma
-
Smadja, N. V., Bastard, C., Brigaudeau, C., Leroux, D., and Fruchart, C. Hypodiploidy is a major prognostic factor in multiple myeloma. Blood, 98: 2229-2238, 2001.
-
(2001)
Blood
, vol.98
, pp. 2229-2238
-
-
Smadja, N.V.1
Bastard, C.2
Brigaudeau, C.3
Leroux, D.4
Fruchart, C.5
-
12
-
-
0031861960
-
Chromosomal analysis in multiple myeloma: Cytogenetic evidence of two different diseases
-
Smadja, N. V., Fruchart, C., Isnard, F., Louvet, C., Dutel, J. L., Cheron, N., Grange, M. J., Monconduit, M., and Bastard, C. Chromosomal analysis in multiple myeloma: cytogenetic evidence of two different diseases. Leukemia (Baltimore), 12: 960-969, 1998.
-
(1998)
Leukemia (Baltimore)
, vol.12
, pp. 960-969
-
-
Smadja, N.V.1
Fruchart, C.2
Isnard, F.3
Louvet, C.4
Dutel, J.L.5
Cheron, N.6
Grange, M.J.7
Monconduit, M.8
Bastard, C.9
-
13
-
-
7144255524
-
Prognostic value of cytogenetics in multiple myeloma
-
Seong, C., Delasalle, K., Hayes, K., Weber, D., Dimopoulos, M., Swantkowski, J., Huh, Y., Glassman, A., Champlin, R., and Alexanian, R. Prognostic value of cytogenetics in multiple myeloma. Br. J. Haematol., 101: 189-194, 1998.
-
(1998)
Br. J. Haematol.
, vol.101
, pp. 189-194
-
-
Seong, C.1
Delasalle, K.2
Hayes, K.3
Weber, D.4
Dimopoulos, M.5
Swantkowski, J.6
Huh, Y.7
Glassman, A.8
Champlin, R.9
Alexanian, R.10
-
14
-
-
0037148921
-
A long-term study of prognosis in monoclonal gammopathy of undetermined significance
-
See comments
-
Kyle, R. A., Therneau, T. M., Rajkumar, S. V., Offord, J. R., Larson, D. R., Plevak, M. F., and Melton, L. J., III. A long-term study of prognosis in monoclonal gammopathy of undetermined significance. [See comments.]. N. Eng. J. Med., 346: 564-569, 2002.
-
(2002)
N. Eng. J. Med.
, vol.346
, pp. 564-569
-
-
Kyle, R.A.1
Therneau, T.M.2
Rajkumar, S.V.3
Offord, J.R.4
Larson, D.R.5
Plevak, M.F.6
Melton III, L.J.7
-
15
-
-
0038509089
-
Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: A report of the International Myeloma Working Group
-
International-Myeloma-Working-Group Criteria for the classification of monoclonal gammopathies, multiple myeloma and related disorders: a report of the International Myeloma Working Group. Br. J. Haematol., 121: 749-757, 2003.
-
(2003)
Br. J. Haematol.
, vol.121
, pp. 749-757
-
-
-
16
-
-
0032819014
-
Cytogenetic abnormalities correlate with the plasma cell labeling index and extent of bone marrow involvement in myeloma
-
Rajkumar, S. V., Fonseca, R., Dewald, G. W., Therneau, T. M., Lacy, M. Q., Kyle, R. A., Greipp, P. R., and Gertz, M. A. Cytogenetic abnormalities correlate with the plasma cell labeling index and extent of bone marrow involvement in myeloma. Cancer Genet Cytogenet., 113: 73-77, 1999.
-
(1999)
Cancer Genet. Cytogenet.
, vol.113
, pp. 73-77
-
-
Rajkumar, S.V.1
Fonseca, R.2
Dewald, G.W.3
Therneau, T.M.4
Lacy, M.Q.5
Kyle, R.A.6
Greipp, P.R.7
Gertz, M.A.8
-
17
-
-
0037087680
-
Prognostic factors for malignant transformation in monoclonal gammopathy of undetermined significance and smoldering multiple myeloma
-
Cesana, C., Klersy, C., Barbarano, L., Nosari, A. M., Crugnola, M., Pungolino, E., Gargantini, L., Granata, S., Valentini, M., and Morra, E. Prognostic factors for malignant transformation in monoclonal gammopathy of undetermined significance and smoldering multiple myeloma. J. Clin. Oncol., 20: 1625-1634, 2002.
-
(2002)
J. Clin. Oncol.
, vol.20
, pp. 1625-1634
-
-
Cesana, C.1
Klersy, C.2
Barbarano, L.3
Nosari, A.M.4
Crugnola, M.5
Pungolino, E.6
Gargantini, L.7
Granata, S.8
Valentini, M.9
Morra, E.10
-
18
-
-
0015830795
-
Immunoglobulin synthesis and tumor kinetics of multiple myeloma
-
Salmon, S. Immunoglobulin synthesis and tumor kinetics of multiple myeloma. Semin. Hematol., 10: 135-147, 1973.
-
(1973)
Semin. Hematol.
, vol.10
, pp. 135-147
-
-
Salmon, S.1
-
19
-
-
0029151758
-
The incidence and epidemiology of plasma cell neoplasms
-
Bergsagel, D. The incidence and epidemiology of plasma cell neoplasms. Stem Cells (Dayton), 13 (Suppl. 2): 1-9, 1995.
-
(1995)
Stem Cells (Dayton)
, vol.13
, Issue.SUPPL. 2
, pp. 1-9
-
-
Bergsagel, D.1
-
20
-
-
0033568514
-
14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma
-
Intergroupe Francophone du Myelome
-
Avet-Loiseau, H., Facon, T., Daviet, A., Godon, C., Rapp, M. J., Harousseau, J. L., Grosbois, B., and Bataille, R. 14q32 translocations and monosomy 13 observed in monoclonal gammopathy of undetermined significance delineate a multistep process for the oncogenesis of multiple myeloma. Intergroupe Francophone du Myelome. Cancer Res., 59: 4546-4550, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 4546-4550
-
-
Avet-Loiseau, H.1
Facon, T.2
Daviet, A.3
Godon, C.4
Rapp, M.J.5
Harousseau, J.L.6
Grosbois, B.7
Bataille, R.8
-
21
-
-
0028884252
-
Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance
-
Drach, J., Angerler, J., Schuster, J., Rothermundt, C., Thalhammer, R., Haas, O. A., Jager, U., Fiegl, M., Geissler, K., and Ludwig, H. Interphase fluorescence in situ hybridization identifies chromosomal abnormalities in plasma cells from patients with monoclonal gammopathy of undetermined significance. Blood, 86: 3915-3921, 1995.
-
(1995)
Blood
, vol.86
, pp. 3915-3921
-
-
Drach, J.1
Angerler, J.2
Schuster, J.3
Rothermundt, C.4
Thalhammer, R.5
Haas, O.A.6
Jager, U.7
Fiegl, M.8
Geissler, K.9
Ludwig, H.10
-
22
-
-
0029063966
-
Monoclonal gammopathy of undetermined significance: Chromosome changes are a common finding within bone marrow plasma cells
-
Zandecki, M., Obein, V., Bernardi, F., Soenen, V., Flactif, M., Lai, J. L., Francois, M., and Facon, T. Monoclonal gammopathy of undetermined significance: chromosome changes are a common finding within bone marrow plasma cells. Br. J. Haematol., 90: 693-696, 1995.
-
(1995)
Br. J. Haematol.
, vol.90
, pp. 693-696
-
-
Zandecki, M.1
Obein, V.2
Bernardi, F.3
Soenen, V.4
Flactif, M.5
Lai, J.L.6
Francois, M.7
Facon, T.8
-
23
-
-
0037302794
-
Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia
-
Rasillo, A., Tabernero, M. D., Sanchez, M. L., Perez de Andres, M., Martin Ayuso, M., Hernandez, J., Moro, M. J., Fernandez-Calvo, J., Sayagues, J. M., Bortoluci, A., San Miguel, J. F., and Orfao, A. Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia. Cancer (Phila.), 97: 601-609, 2003.
-
(2003)
Cancer (Phila.)
, vol.97
, pp. 601-609
-
-
Rasillo, A.1
Tabernero, M.D.2
Sanchez, M.L.3
Perez De Andres, M.4
Martin Ayuso, M.5
Hernandez, J.6
Moro, M.J.7
Fernandez-Calvo, J.8
Sayagues, J.M.9
Bortoluci, A.10
San Miguel, J.F.11
Orfao, A.12
-
24
-
-
0023240678
-
The spectrum of IgM monoclonal gammopathy in 430 cases
-
Kyle, R. A., and Garton, J. P. The spectrum of IgM monoclonal gammopathy in 430 cases. Mayo Clin. Proc., 62: 719-731, 1987.
-
(1987)
Mayo Clin. Proc.
, vol.62
, pp. 719-731
-
-
Kyle, R.A.1
Garton, J.P.2
-
25
-
-
0018848543
-
Smoldering multiple myeloma
-
Kyle, R. A., and Greipp, P. R. Smoldering multiple myeloma. N. Engl. J. Med., 302: 1347-1349, 1980.
-
(1980)
N. Engl. J. Med.
, vol.302
, pp. 1347-1349
-
-
Kyle, R.A.1
Greipp, P.R.2
-
26
-
-
0028235301
-
Detection of peripheral blood plasma cells as a predictor of disease course in patients with smouldering multiple myeloma
-
Witzig, T. E., Kyle, R. A., O'Fallon, W. M., and Greipp, P. R. Detection of peripheral blood plasma cells as a predictor of disease course in patients with smouldering multiple myeloma. Br. J. Haematol., 87: 266-272, 1994.
-
(1994)
Br. J. Haematol.
, vol.87
, pp. 266-272
-
-
Witzig, T.E.1
Kyle, R.A.2
O'Fallon, W.M.3
Greipp, P.R.4
-
27
-
-
0026720169
-
Malignant transformation and life expectancy in monoclonal gammopathy of undetermined significance
-
Blade, J., Lopez, G. A., Rozman, C., Cervantes, F., Salgado, C., Aguilar, J. L., Vives, C. J. L., and Montserrat, E. Malignant transformation and life expectancy in monoclonal gammopathy of undetermined significance. Br. J. Haematol., 81: 391-394, 1992.
-
(1992)
Br. J. Haematol.
, vol.81
, pp. 391-394
-
-
Blade, J.1
Lopez, G.A.2
Rozman, C.3
Cervantes, F.4
Salgado, C.5
Aguilar, J.L.6
Vives, C.J.L.7
Montserrat, E.8
-
29
-
-
0032857034
-
Monosomy 13 is associated with the transition of monoclonal gammopathy of undetermined significance to multiple myeloma
-
Intergroupe Francophone du Myelome
-
Avet-Loiseau, H., Li, J. Y., Morineau, N., Facon, T., Brigaudeau, C., Harousseau, J. L., Grosbois, B., and Bataille, R. Monosomy 13 is associated with the transition of monoclonal gammopathy of undetermined significance to multiple myeloma. Intergroupe Francophone du Myelome. Blood, 94: 2583-2589, 1999.
-
(1999)
Blood
, vol.94
, pp. 2583-2589
-
-
Avet-Loiseau, H.1
Li, J.Y.2
Morineau, N.3
Facon, T.4
Brigaudeau, C.5
Harousseau, J.L.6
Grosbois, B.7
Bataille, R.8
-
30
-
-
0032882448
-
Monoclonal gammopathy of undetermined significance (MGUS)-31 year follow up of a community study
-
Colls, B. M. Monoclonal gammopathy of undetermined significance (MGUS) -31 year follow up of a community study. Aust. N. Z. J. Med., 29: 500-504, 1999.
-
(1999)
Aust. N. Z. J. Med.
, vol.29
, pp. 500-504
-
-
Colls, B.M.1
-
31
-
-
0037307238
-
Gene expression profiling of human plasma cell differentiation and classification of multiple myeloma based on similarities to distinct stages of late-stage B-cell development
-
Zhan, F., Tian, E., Bumm, K., Smith, R., Barlogie, B., and Shaughnessy, J., Jr. Gene expression profiling of human plasma cell differentiation and classification of multiple myeloma based on similarities to distinct stages of late-stage B-cell development. Blood, 101: 1128-1140, 2003.
-
(2003)
Blood
, vol.101
, pp. 1128-1140
-
-
Zhan, F.1
Tian, E.2
Bumm, K.3
Smith, R.4
Barlogie, B.5
Shaughnessy Jr., J.6
-
32
-
-
0031929051
-
The myeloma cell antigen syndecan-1 is lost by apoptotic myeloma cells
-
Jourdan, M., Ferlin, M., Legouffe, E., Horvathova, M., Liautard, J., Rossi, J. F., Wijdenes, J., Brochier, J., and Klein, B. The myeloma cell antigen syndecan-1 is lost by apoptotic myeloma cells. Br. J. Haematol., 100: 637-646, 1998.
-
(1998)
Br. J. Haematol.
, vol.100
, pp. 637-646
-
-
Jourdan, M.1
Ferlin, M.2
Legouffe, E.3
Horvathova, M.4
Liautard, J.5
Rossi, J.F.6
Wijdenes, J.7
Brochier, J.8
Klein, B.9
-
33
-
-
0032005528
-
A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies
-
Ahmann, G. J., Jalal, S. M., Juneau, A. L., Christensen, E. R., Hanson, C. A., Dewald, G. W., and Greipp, P. R. A novel three-color, clone-specific fluorescence in situ hybridization procedure for monoclonal gammopathies. Cancer Genet Cytogenet., 101: 7-11, 1998.
-
(1998)
Cancer Genet Cytogenet.
, vol.101
, pp. 7-11
-
-
Ahmann, G.J.1
Jalal, S.M.2
Juneau, A.L.3
Christensen, E.R.4
Hanson, C.A.5
Dewald, G.W.6
Greipp, P.R.7
-
34
-
-
0028947460
-
Improved cytogenetics in multiple myeloma: A study of 151 patients including 117 patients at diagnosis
-
Review
-
Lai, J. L., Zandecki, M., Mary, J. Y., Bernardi, F., Izydorezyk, V., Flactif, M., Morel, P., Jouet, J. P., Bauters, F., and Facon, T. Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis. [Review]. Blood, 85: 2490-2497, 1995.
-
(1995)
Blood
, vol.85
, pp. 2490-2497
-
-
Lai, J.L.1
Zandecki, M.2
Mary, J.Y.3
Bernardi, F.4
Izydorezyk, V.5
Flactif, M.6
Morel, P.7
Jouet, J.P.8
Bauters, F.9
Facon, T.10
-
35
-
-
0023853845
-
Plasma cell karyotype in multiple myeloma
-
Gould, J., Alexanian, R., Goodacre, A., Pathak, S., Hecht, B., and Barlogie, B. Plasma cell karyotype in multiple myeloma. Blood, 71: 453-456, 1988.
-
(1988)
Blood
, vol.71
, pp. 453-456
-
-
Gould, J.1
Alexanian, R.2
Goodacre, A.3
Pathak, S.4
Hecht, B.5
Barlogie, B.6
-
36
-
-
0030211192
-
Multiple-myeloma-almost all patients are cytogenetically abnormal
-
Zandecki, M. Multiple-myeloma-almost all patients are cytogenetically abnormal. Br. J. Haematol., 94: 217-227, 1996.
-
(1996)
Br. J. Haematol.
, vol.94
, pp. 217-227
-
-
Zandecki, M.1
-
37
-
-
0029162938
-
Cytogenetic findings in 200 patients with multiple myeloma
-
Sawyer, J. R., Waldron, J. A., Jagannath, S., and Barlogie, B. Cytogenetic findings in 200 patients with multiple myeloma. Cancer Genet Cytogenet., 82: 41-49, 1995.
-
(1995)
Cancer Genet Cytogenet.
, vol.82
, pp. 41-49
-
-
Sawyer, J.R.1
Waldron, J.A.2
Jagannath, S.3
Barlogie, B.4
-
38
-
-
20244363331
-
Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma
-
Debes-Marun, C., Dewald, G., Bryant, S., Picken, E., Santana-Dá vila, S., González-Paz, N., Winkler, J. M., Kyle, R., Gertz, M., Witzig, T., Dispenzieri, A., Lacy, M., Rajkumar, S., Lust, J., Greipp, P., and Fonseca, R. Chromosome abnormalities clustering and its implications for pathogenesis and prognosis in myeloma. Leukemia (Baltimore), 17: 427-436, 2003.
-
(2003)
Leukemia (Baltimore)
, vol.17
, pp. 427-436
-
-
Debes-Marun, C.1
Dewald, G.2
Bryant, S.3
Picken, E.4
Santana-Dávila, S.5
González-Paz, N.6
Winkler, J.M.7
Kyle, R.8
Gertz, M.9
Witzig, T.10
Dispenzieri, A.11
Lacy, M.12
Rajkumar, S.13
Lust, J.14
Greipp, P.15
Fonseca, R.16
-
39
-
-
0030922231
-
Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3
-
Chesi, M., Nardini, E., Brents, L. A., Schrock, E., Ried, T., Kuehl, W. M., and Bergsagel, P. L. Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3. Nat. Genet., 16: 260-264, 1997.
-
(1997)
Nat. Genet.
, vol.16
, pp. 260-264
-
-
Chesi, M.1
Nardini, E.2
Brents, L.A.3
Schrock, E.4
Ried, T.5
Kuehl, W.M.6
Bergsagel, P.L.7
-
40
-
-
0031839633
-
Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma
-
Chesi, M., Bergsagel, P. L., Shonukan, O. O., Martelli, M. L., Brents, L. A., Chen, T., Schrock, E., Ried, T., and Kuehl, W. M. Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma. Blood, 91: 4457-4463, 1998.
-
(1998)
Blood
, vol.91
, pp. 4457-4463
-
-
Chesi, M.1
Bergsagel, P.L.2
Shonukan, O.O.3
Martelli, M.L.4
Brents, L.A.5
Chen, T.6
Schrock, E.7
Ried, T.8
Kuehl, W.M.9
-
41
-
-
0032402134
-
Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping
-
Sawyer, J. R., Lukacs, J. L., Munshi, N., Desikan, K. R., Singhal, S., Mehta, J., Siegel, D., Shaughnessy, J., and Barlogie, B. Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping. Blood, 92: 4269-4278, 1998.
-
(1998)
Blood
, vol.92
, pp. 4269-4278
-
-
Sawyer, J.R.1
Lukacs, J.L.2
Munshi, N.3
Desikan, K.R.4
Singhal, S.5
Mehta, J.6
Siegel, D.7
Shaughnessy, J.8
Barlogie, B.9
-
42
-
-
0035133202
-
Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma
-
Sawyer, J. R., Lukacs, J. L., Thomas, E. L., Swanson, C. M., Goosen, L. S., Sammartino, G., Gilliland, J. C., Munshi, N. C., Tricot, G., Shaughnessy, J. D., Jr., and Barlogie, B. Multicolour spectral karyotyping identifies new translocations and a recurring pathway for chromosome loss in multiple myeloma. Br. J. Haematol. 112: 167-174, 2001.
-
(2001)
Br. J. Haematol.
, vol.112
, pp. 167-174
-
-
Sawyer, J.R.1
Lukacs, J.L.2
Thomas, E.L.3
Swanson, C.M.4
Goosen, L.S.5
Sammartino, G.6
Gilliland, J.C.7
Munshi, N.C.8
Tricot, G.9
Shaughnessy Jr., J.D.10
Barlogie, B.11
-
43
-
-
0032170964
-
Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma
-
Rao, P. H., Cigudosa, J. C., Ning, Y., Calasanz, M. J., Iida, S., Tagawa, S., Michaeli, J., Klein, B., Dalla-Favera, R., Jhanwar, S. C., Ried, T., and Chaganti, R. S. Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma. Blood, 92: 1743-1748, 1998.
-
(1998)
Blood
, vol.92
, pp. 1743-1748
-
-
Rao, P.H.1
Cigudosa, J.C.2
Ning, Y.3
Calasanz, M.J.4
Iida, S.5
Tagawa, S.6
Michaeli, J.7
Klein, B.8
Dalla-Favera, R.9
Jhanwar, S.C.10
Ried, T.11
Chaganti, R.S.12
-
44
-
-
0032532610
-
Detection of nonrandom chromosomal changes in multiple myeloma by comparative genomic hybridization
-
Avet-Loiseau, H., and Bataille, R. Detection of nonrandom chromosomal changes in multiple myeloma by comparative genomic hybridization. Blood, 92: 2997-2998, 1998.
-
(1998)
Blood
, vol.92
, pp. 2997-2998
-
-
Avet-Loiseau, H.1
Bataille, R.2
-
45
-
-
0032522947
-
Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization
-
Cigudosa, J. C., Rao, P. H., Calasanz, M. J., Odero, M. D., Michaeli, J., Jhanwar, S. C., and Chaganti, R. S. Characterization of nonrandom chromosomal gains and losses in multiple myeloma by comparative genomic hybridization. Blood, 91: 3007-3010, 1998.
-
(1998)
Blood
, vol.91
, pp. 3007-3010
-
-
Cigudosa, J.C.1
Rao, P.H.2
Calasanz, M.J.3
Odero, M.D.4
Michaeli, J.5
Jhanwar, S.C.6
Chaganti, R.S.7
-
46
-
-
0034997505
-
Differences in genetic changes between multiple myeloma and plasma cell leukemia demonstrated by comparative genomic hybridization
-
Gutierrez, N. C., Hernandez, J. M., Garcia, J. L., Canizo, M. C., Gonzalez, M., Hernandez, J., Gonzalez, M. B., Garcia-Marcos, M. A., and San Miguel, J. F. Differences in genetic changes between multiple myeloma and plasma cell leukemia demonstrated by comparative genomic hybridization. Leukemia (Baltimore), 15: 840-845, 2001.
-
(2001)
Leukemia (Baltimore)
, vol.15
, pp. 840-845
-
-
Gutierrez, N.C.1
Hernandez, J.M.2
Garcia, J.L.3
Canizo, M.C.4
Gonzalez, M.5
Hernandez, J.6
Gonzalez, M.B.7
Garcia-Marcos, M.A.8
San Miguel, J.F.9
-
47
-
-
0030957791
-
Molecular cytogenetic abnormalities in multiple myeloma and plasma cell leukemia measured using comparative genomic hybridization
-
Avet-Loiseau, H., Andree-Ashley, L. E., Moore, D., II, Mellerin, M. P., Feusner, J., Bataille, R., and Pallavicini, M. G. Molecular cytogenetic abnormalities in multiple myeloma and plasma cell leukemia measured using comparative genomic hybridization. Genes Chromosomes Cancer, 19: 124-133, 1997.
-
(1997)
Genes Chromosomes Cancer
, vol.19
, pp. 124-133
-
-
Avet-Loiseau, H.1
Andree-Ashley, L.E.2
Moore II, D.3
Mellerin, M.P.4
Feusner, J.5
Bataille, R.6
Pallavicini, M.G.7
-
48
-
-
0035496937
-
Translocations involving heavy-chain locus are possible early genetic events in patients with primary systemic amyloidosis
-
Hayman, S. R., Bailey, R. J., Jalal, S. M., Ahmann, G. J., Dispenzieri, A., Gertz, M. A., Greipp, P. R., Kyle, R. A., Lacy, M. Q., Rajkumar, V., Witzig, T. E., Lust, J. A., and Fonseca, R. Translocations involving heavy-chain locus are possible early genetic events in patients with primary systemic amyloidosis. Blood, 98: 2266-2268, 2001.
-
(2001)
Blood
, vol.98
, pp. 2266-2268
-
-
Hayman, S.R.1
Bailey, R.J.2
Jalal, S.M.3
Ahmann, G.J.4
Dispenzieri, A.5
Gertz, M.A.6
Greipp, P.R.7
Kyle, R.A.8
Lacy, M.Q.9
Rajkumar, V.10
Witzig, T.E.11
Lust, J.A.12
Fonseca, R.13
-
49
-
-
0037092981
-
Myeloma and the t(11;14)(q13;q32) represents a uniquely defined biological subset of patients
-
Fonseca, R., Harrington, D., Oken, M., Kyle, R., Dewald, G., Bailey, R., Van Wier, S., Henderson, K., Hoyer, J., Blood, E., Kay, N., Van Ness, B., and Greipp, P. Myeloma and the t(11;14)(q13;q32) represents a uniquely defined biological subset of patients. Blood, 99: 3735-3741, 2002.
-
(2002)
Blood
, vol.99
, pp. 3735-3741
-
-
Fonseca, R.1
Harrington, D.2
Oken, M.3
Kyle, R.4
Dewald, G.5
Bailey, R.6
Van Wier, S.7
Henderson, K.8
Hoyer, J.9
Blood, E.10
Kay, N.11
Van Ness, B.12
Greipp, P.13
-
50
-
-
0036468246
-
Biologic and prognostic significance of interphase FISH detection of chromosome 13 abnormalities (Δ13) in multiple myeloma: An Eastern Cooperative Oncology Group (ECOG) Study
-
Fonseca, R., Harrington, D., Oken, M., Dewald, G., Bailey, R., Van Wier, S., Henderson, K., Blood, E., Rajkumar, S., Kay, N., Van Ness, B., and Greipp, P. Biologic and prognostic significance of interphase FISH detection of chromosome 13 abnormalities (Δ13) in multiple myeloma: an Eastern Cooperative Oncology Group (ECOG) Study. Cancer Res., 62: 715-720, 2002.
-
(2002)
Cancer Res.
, vol.62
, pp. 715-720
-
-
Fonseca, R.1
Harrington, D.2
Oken, M.3
Dewald, G.4
Bailey, R.5
Van Wier, S.6
Henderson, K.7
Blood, E.8
Rajkumar, S.9
Kay, N.10
Van Ness, B.11
Greipp, P.12
-
51
-
-
0035883062
-
The t(4;14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathies of undetermined significance
-
Fonseca, R., Oken, M., and Greipp, P. The t(4;14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathies of undetermined significance. Blood, 98: 1271-1272, 2001.
-
(2001)
Blood
, vol.98
, pp. 1271-1272
-
-
Fonseca, R.1
Oken, M.2
Greipp, P.3
-
52
-
-
0034988904
-
Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q-arm or monosomy
-
Fonseca, R., Oken, M., Harrington, D., Bailey, R., Van Wier, S., Henderson, K., Kay, N., Van Ness, B., Greipp, P., and Dewald, G. Deletions of chromosome 13 in multiple myeloma identified by interphase FISH usually denote large deletions of the q-arm or monosomy. Leukemia (Baltimore), 15: 981-986, 2001.
-
(2001)
Leukemia (Baltimore)
, vol.15
, pp. 981-986
-
-
Fonseca, R.1
Oken, M.2
Harrington, D.3
Bailey, R.4
Van Wier, S.5
Henderson, K.6
Kay, N.7
Van Ness, B.8
Greipp, P.9
Dewald, G.10
-
53
-
-
0038142356
-
Clinical and biologic implications of recurrent genomic aberrations in myeloma
-
Fonseca, R., Blood, E., Rue, M., Harrington, D., Oken, M. M., Kyle, R. A., Dewald, G. W., Van Ness, B., Van Wier, S. A., Henderson, K. J., Bailey, R. J., and Greipp, P. R. Clinical and biologic implications of recurrent genomic aberrations in myeloma. Blood, 101: 4569-4575, 2003.
-
(2003)
Blood
, vol.101
, pp. 4569-4575
-
-
Fonseca, R.1
Blood, E.2
Rue, M.3
Harrington, D.4
Oken, M.M.5
Kyle, R.A.6
Dewald, G.W.7
Van Ness, B.8
Van Wier, S.A.9
Henderson, K.J.10
Bailey, R.J.11
Greipp, P.R.12
-
54
-
-
0032889633
-
High incidence of cryptic translocations involving the Ig heavy chain gene in multiple myeloma, as shown by fluorescence in situ hybridization
-
Avet-Loiseau, H., Brigaudeau, C., Morineau, N., Talmant, P., Lai, J. L., Daviet, A., Li, J. Y., Praloran, V., Rapp, M. J., Harousseau, J. L., Facon, T., and Bataille, R. High incidence of cryptic translocations involving the Ig heavy chain gene in multiple myeloma, as shown by fluorescence in situ hybridization. Genes Chromosomes Cancer, 24: 9-15, 1999.
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 9-15
-
-
Avet-Loiseau, H.1
Brigaudeau, C.2
Morineau, N.3
Talmant, P.4
Lai, J.L.5
Daviet, A.6
Li, J.Y.7
Praloran, V.8
Rapp, M.J.9
Harousseau, J.L.10
Facon, T.11
Bataille, R.12
-
55
-
-
0034490134
-
Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13
-
Avet-Loiseau, H., Daviet, A., Saunier, S., and Bataille, R. Chromosome 13 abnormalities in multiple myeloma are mostly monosomy 13. Br. J. Haematol., 111: 1116-1117, 2000.
-
(2000)
Br. J. Haematol.
, vol.111
, pp. 1116-1117
-
-
Avet-Loiseau, H.1
Daviet, A.2
Saunier, S.3
Bataille, R.4
-
56
-
-
0343355828
-
High incidence of translocations t(11;14)(q13;q32) and t(4;14)(p16;q32)
-
Avet-Loiseau, H., Li, J. Y., Facon, T., Brigaudeau, C., Morineau, N., Maloisel, F., Rapp, M. J., Talmant, P., Trimoreau, F., Jaccard, A., Harousseau, J. L., and Bataille, R. High incidence of translocations t(11;14)(q13;q32) and t(4;14)(p16;q32). Cancer Res., 58: 5640-5645, 1998.
-
(1998)
Cancer Res.
, vol.58
, pp. 5640-5645
-
-
Avet-Loiseau, H.1
Li, J.Y.2
Facon, T.3
Brigaudeau, C.4
Morineau, N.5
Maloisel, F.6
Rapp, M.J.7
Talmant, P.8
Trimoreau, F.9
Jaccard, A.10
Harousseau, J.L.11
Bataille, R.12
-
57
-
-
0033763998
-
Deletions of chromosome 13q in monoclonal gammopathy of undetermined significance
-
Konigsberg, R., Ackermann, J., Kaufmann, H., Zojer, N., Urbauer, E., Kromer, E., Jager, U., Gisslinger, H., Schreiber, S., Heinz, R., Ludwig, H., Huber, H., and Drach, J. Deletions of chromosome 13q in monoclonal gammopathy of undetermined significance. Leukemia (Baltimore), 14: 1975-1979, 2000.
-
(2000)
Leukemia (Baltimore)
, vol.14
, pp. 1975-1979
-
-
Konigsberg, R.1
Ackermann, J.2
Kaufmann, H.3
Zojer, N.4
Urbauer, E.5
Kromer, E.6
Jager, U.7
Gisslinger, H.8
Schreiber, S.9
Heinz, R.10
Ludwig, H.11
Huber, H.12
Drach, J.13
-
58
-
-
0031760617
-
Chromosomal abnormalities in systemic amyloidosis
-
Fonseca, R., Ahmann, G. J., Jalal, S. M., Dewald, G. W., Larson, D. R., Therneau, T. M., Gertz, M. A., Kyle, R. A., and Goipp, P. R. Chromosomal abnormalities in systemic amyloidosis. Br. J. Haematol., 103: 704-710, 1998.
-
(1998)
Br. J. Haematol.
, vol.103
, pp. 704-710
-
-
Fonseca, R.1
Ahmann, G.J.2
Jalal, S.M.3
Dewald, G.W.4
Larson, D.R.5
Therneau, T.M.6
Gertz, M.A.7
Kyle, R.A.8
Goipp, P.R.9
-
59
-
-
0032971585
-
Insertion of excised IgH switch sequences causes overexpression of cyclin D1 in a myeloma tumor cell
-
Gabrea, A., Bergsagel, P. L., Chesi, M., Shou, Y., and Kuehl, W. M. Insertion of excised IgH switch sequences causes overexpression of cyclin D1 in a myeloma tumor cell. Mol. Cell, 3: 119-123, 1999.
-
(1999)
Mol. Cell
, vol.3
, pp. 119-123
-
-
Gabrea, A.1
Bergsagel, P.L.2
Chesi, M.3
Shou, Y.4
Kuehl, W.M.5
-
60
-
-
0037441747
-
In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expression
-
Keats, J. J., Reiman, T., Maxwell, C. A., Taylor, B. J., Larratt, L. M., Mant, M. J., Belch, A. R., and Pilarski, L. M. In multiple myeloma, t(4;14)(p16;q32) is an adverse prognostic factor irrespective of FGFR3 expression. Blood, 101: 1520-1529, 2003.
-
(2003)
Blood
, vol.101
, pp. 1520-1529
-
-
Keats, J.J.1
Reiman, T.2
Maxwell, C.A.3
Taylor, B.J.4
Larratt, L.M.5
Mant, M.J.6
Belch, A.R.7
Pilarski, L.M.8
-
61
-
-
0037443417
-
A subset of multiple myeloma harboring the t(4;14)(p16;q32) translocation lacks FGFR3 expression but maintains an IGH/MMSET fusion transcript
-
Santra, M., Zhan, F., Tian, E., Barlogie, B., and Shaughnessy, J., Jr. A subset of multiple myeloma harboring the t(4;14)(p16;q32) translocation lacks FGFR3 expression but maintains an IGH/MMSET fusion transcript. Blood, 101: 2374-2376, 2003.
-
(2003)
Blood
, vol.101
, pp. 2374-2376
-
-
Santra, M.1
Zhan, F.2
Tian, E.3
Barlogie, B.4
Shaughnessy Jr., J.5
-
62
-
-
0036493522
-
Global gene expression profiling of multiple myeloma, monoclonal gammopathy of undetermined significance, and normal bone marrow plasma cells
-
Zhan, F., Hardin, J., Kordsmeier, B., Bumm, K., Zheng, M., Tian, E., Sanderson, R., Yang, Y., Wilson, C., Zangari, M., Anaissie, E., Morris, C., Muwalla, F., van Rhee, F., Fassas, A., Crowley, J., Tricot, G., Barlogie, B., and Shaughnessy, J., Jr. Global gene expression profiling of multiple myeloma, monoclonal gammopathy of undetermined significance, and normal bone marrow plasma cells. Blood, 99: 1745-1757, 2002.
-
(2002)
Blood
, vol.99
, pp. 1745-1757
-
-
Zhan, F.1
Hardin, J.2
Kordsmeier, B.3
Bumm, K.4
Zheng, M.5
Tian, E.6
Sanderson, R.7
Yang, Y.8
Wilson, C.9
Zangari, M.10
Anaissie, E.11
Morris, C.12
Muwalla, F.13
Van Rhee, F.14
Fassas, A.15
Crowley, J.16
Tricot, G.17
Barlogie, B.18
Shaughnessy Jr., J.19
-
63
-
-
0035437195
-
Identifying intercellular signaling genes expressed in malignant plasma cells by using complementary DNA arrays
-
De Vos, J., Couderc, G., Tarte, K., Jourdan, M., Requirand, G., Delteil, M-C., Rossi, J-F., Mechti, N., and Klein, B. Identifying intercellular signaling genes expressed in malignant plasma cells by using complementary DNA arrays. Blood, 98: 771-780, 2001.
-
(2001)
Blood
, vol.98
, pp. 771-780
-
-
De Vos, J.1
Couderc, G.2
Tarte, K.3
Jourdan, M.4
Requirand, G.5
Delteil, M.-C.6
Rossi, J.-F.7
Mechti, N.8
Klein, B.9
-
64
-
-
0037103205
-
Generation of polyclonal plasmablasts from peripheral blood B cells: A normal counterpart of malignant plasmablasts
-
See comments
-
Tarte, K., De Vos, J., Thykjaer, T., Zhan, F., Fiol, G., Costes, V., Reme, T., Legouffe, E., Rossi, J. F., Shaughnessy, J., Jr., Orntoft, T. F., and Klein, B. Generation of polyclonal plasmablasts from peripheral blood B cells: a normal counterpart of malignant plasmablasts. [See comments.]. Blood, 100: 1113-1122, 2002.
-
(2002)
Blood
, vol.100
, pp. 1113-1122
-
-
Tarte, K.1
De Vos, J.2
Thykjaer, T.3
Zhan, F.4
Fiol, G.5
Costes, V.6
Reme, T.7
Legouffe, E.8
Rossi, J.F.9
Shaughnessy Jr., J.10
Orntoft, T.F.11
Klein, B.12
-
65
-
-
0037105582
-
A molecular compendium of genes expressed in multiple myeloma
-
Claudio, J. O., Masih-Khan, E., Tang, H., Goncalves, J., Voralia, M., Li, Z. H., Nadeem, V., Cukerman, E., Francisco-Pabalan, O., Liew, C. C., Woodgett, J. R., and Stewart, A. K. A molecular compendium of genes expressed in multiple myeloma. Blood, 100: 2175-2186, 2002.
-
(2002)
Blood
, vol.100
, pp. 2175-2186
-
-
Claudio, J.O.1
Masih-Khan, E.2
Tang, H.3
Goncalves, J.4
Voralia, M.5
Li, Z.H.6
Nadeem, V.7
Cukerman, E.8
Francisco-Pabalan, O.9
Liew, C.C.10
Woodgett, J.R.11
Stewart, A.K.12
-
66
-
-
10744221725
-
Gene expression profiling of multiple myeloma reveals molecular portraits in relation to the pathogenesis of the disease
-
Magrangeas, F., Nasser. V., Avet-Loiseau, H., Loriod, B., Decaux, O., Granjeaud, S., Bertucci, F., Birnbaum, D., Nguyen, C., Harousseau, J-L., Bataille, R., Houlgatte, R., and Minvielle, S. Gene expression profiling of multiple myeloma reveals molecular portraits in relation to the pathogenesis of the disease. Blood, 101: 4998-5006, 2003.
-
(2003)
Blood
, vol.101
, pp. 4998-5006
-
-
Magrangeas, F.1
Nasser, V.2
Avet-Loiseau, H.3
Loriod, B.4
Decaux, O.5
Granjeaud, S.6
Bertucci, F.7
Birnbaum, D.8
Nguyen, C.9
Harousseau, J.-L.10
Bataille, R.11
Houlgatte, R.12
Minvielle, S.13
-
67
-
-
0020036477
-
Ploidy and proliferative characteristics in monoclonal gammopathies
-
Latreille, J., Barlogie, B., Johnston, D., Drewinko, B., and Alexanian, R. Ploidy and proliferative characteristics in monoclonal gammopathies. Blood, 59: 43-51, 1982.
-
(1982)
Blood
, vol.59
, pp. 43-51
-
-
Latreille, J.1
Barlogie, B.2
Johnston, D.3
Drewinko, B.4
Alexanian, R.5
-
68
-
-
0028289637
-
Image analysis in multiple myeloma at diagnosis. Correlation with cytogenetic study
-
Zandecki, M., Bernardi, F., Lai, J., Facon, T., Izydorczyk, V., Bauters, F., and Cosson, A. Image analysis in multiple myeloma at diagnosis. Correlation with cytogenetic study. Cancer Genet. Cytogenet., 74: 115-119, 1994.
-
(1994)
Cancer Genet. Cytogenet.
, vol.74
, pp. 115-119
-
-
Zandecki, M.1
Bernardi, F.2
Lai, J.3
Facon, T.4
Izydorczyk, V.5
Bauters, F.6
Cosson, A.7
-
69
-
-
0030834970
-
Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this condition
-
Zandecki, M., Lai, J. L., Genevieve, F., Bernardi, F., Volle-Remy, H., Blanchet, O., Francois, M., Cosson, A., Bauters, F., and Facon, T. Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this condition. Blood, 90: 3682-3690, 1997.
-
(1997)
Blood
, vol.90
, pp. 3682-3690
-
-
Zandecki, M.1
Lai, J.L.2
Genevieve, F.3
Bernardi, F.4
Volle-Remy, H.5
Blanchet, O.6
Francois, M.7
Cosson, A.8
Bauters, F.9
Facon, T.10
-
70
-
-
0003071187
-
Clonal chromosomal aberrations in plasma cells from patients with monoclonal gammopathy of undetermined significance (MGUS)
-
Drach, J., Angerler, J., Schuster, J., Thalhammer, R., Jager, U., Geissler, K., Lechner K., Ludwig, H., and Huber, H. Clonal chromosomal aberrations in plasma cells from patients with monoclonal gammopathy of undetermined significance (MGUS). Proc Am. Assoc. Cancer Res., 36: 144, 1995.
-
(1995)
Proc Am. Assoc. Cancer Res.
, vol.36
, pp. 144
-
-
Drach, J.1
Angerler, J.2
Schuster, J.3
Thalhammer, R.4
Jager, U.5
Geissler, K.6
Lechner, K.7
Ludwig, H.8
Huber, H.9
-
71
-
-
0033571630
-
Primary plasma cell leukemia and multiple myeloma: One or two diseases according to the methodology
-
Smadja, N. V., Bastard, C., and Brgaudeau, C. Primary plasma cell leukemia and multiple myeloma: one or two diseases according to the methodology [Letter; comment]. Blood, 94: 3607-3609, 1999.
-
(1999)
Blood
, vol.94
, pp. 3607-3609
-
-
Smadja, N.V.1
Bastard, C.2
Brgaudeau, C.3
-
72
-
-
0032866976
-
Is flow cytometric DNA content hypodiploidy prognostic in multiple myeloma?
-
Greipp, P. R., Trendle, M. C., Leong, T., Oken, M. M., Kay, N. E., Van Ness, B., and Kyle, R. A. Is flow cytometric DNA content hypodiploidy prognostic in multiple myeloma? Leuk. Lymphoma., 35: 83-89, 1999.
-
(1999)
Leuk. Lymphoma
, vol.35
, pp. 83-89
-
-
Greipp, P.R.1
Trendle, M.C.2
Leong, T.3
Oken, M.M.4
Kay, N.E.5
Van Ness, B.6
Kyle, R.A.7
-
73
-
-
0028033750
-
A new method for the analysis of plasma cell DNA content in multiple myeloma samples using a CD38/propidium iodide double staining technique
-
Orfao, A., Garcia-Sanz, R., Lopez-Berges, M. C., Belen Vidriales, M., Gonzalez, M., Caballero, M. D., and San Miguel, J. F. A new method for the analysis of plasma cell DNA content in multiple myeloma samples using a CD38/propidium iodide double staining technique. Cytometry, 17: 332-339, 1994.
-
(1994)
Cytometry
, vol.17
, pp. 332-339
-
-
Orfao, A.1
Garcia-Sanz, R.2
Lopez-Berges, M.C.3
Belen Vidriales, M.4
Gonzalez, M.5
Caballero, M.D.6
San Miguel, J.F.7
-
74
-
-
0018899398
-
Cellular DNA content as a marker of human multiple myeloma
-
Latreille, J., Barlogie, B., Dosik, G., Johnston, D. A., Drewinko, B., and Alexanian, R. Cellular DNA content as a marker of human multiple myeloma. Blood, 55: 403-408, 1980.
-
(1980)
Blood
, vol.55
, pp. 403-408
-
-
Latreille, J.1
Barlogie, B.2
Dosik, G.3
Johnston, D.A.4
Drewinko, B.5
Alexanian, R.6
-
75
-
-
0141481984
-
The recurrent IgH translocations are highly associated with nonhyperdiploid variant multiple myeloma
-
Fonseca, R., Debes-Marun, C., Picken, E., Dewald, G., Bryant, S., Winkler, J., Blood, E., Oken, M. M., Santana-Dávila, R., González-Paz, N., Kyle, R., Gertz, M., Dispenzieri, A., Lacy, M., and Greipp, P. The recurrent IgH translocations are highly associated with nonhyperdiploid variant multiple myeloma. Blood, 102: 2562-2567, 2003.
-
(2003)
Blood
, vol.102
, pp. 2562-2567
-
-
Fonseca, R.1
Debes-Marun, C.2
Picken, E.3
Dewald, G.4
Bryant, S.5
Winkler, J.6
Blood, E.7
Oken, M.M.8
Santana-Dávila, R.9
González-Paz, N.10
Kyle, R.11
Gertz, M.12
Dispenzieri, A.13
Lacy, M.14
Greipp, P.15
-
76
-
-
0141993685
-
Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid patients
-
Smadja, N. V., Leroux, D., Soulier, J., Dumont, S., Arnould, C., Taviaux, S., Taillemite, J. L., and Bastard, C. Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid patients. Genes Chromosomes Cancer, 38: 234-239, 2003.
-
(2003)
Genes Chromosomes Cancer
, vol.38
, pp. 234-239
-
-
Smadja, N.V.1
Leroux, D.2
Soulier, J.3
Dumont, S.4
Arnould, C.5
Taviaux, S.6
Taillemite, J.L.7
Bastard, C.8
-
77
-
-
2642617778
-
Prognostic value of numerical chromosome aberrations in multiple myeloma: A FISH analysis of 15 different chromosomes
-
Perez-Simon, J. A., Garcia-Sanz, R., Tabernero, M. D., Almeida, J., Gonzalez, M., Fernandez-Calvo, J., Moro, M. J., Hernandez, J. M., San Miguel, J. F., and Orfao, A. Prognostic value of numerical chromosome aberrations in multiple myeloma: A FISH analysis of 15 different chromosomes. Blood, 91: 3366-3371, 1998.
-
(1998)
Blood
, vol.91
, pp. 3366-3371
-
-
Perez-Simon, J.A.1
Garcia-Sanz, R.2
Tabernero, M.D.3
Almeida, J.4
Gonzalez, M.5
Fernandez-Calvo, J.6
Moro, M.J.7
Hernandez, J.M.8
San Miguel, J.F.9
Orfao, A.10
-
78
-
-
0022472775
-
Biclonal and hypodiploid multiple myeloma
-
Smith, L., Barlogie, B., and Alexanian, R. Biclonal and hypodiploid multiple myeloma. Am. J. Med., 80: 841-843, 1986.
-
(1986)
Am. J. Med.
, vol.80
, pp. 841-843
-
-
Smith, L.1
Barlogie, B.2
Alexanian, R.3
-
79
-
-
0030825598
-
Hypodiploidy and 22q11 rearrangements at diagnosis are associated with poor prognosis in patients with multiple myeloma
-
Calasanz, M. J., Cigudosa, J. C., Odero, M. D., Garcia-Foncillas, J., Marin, J., Ardanaz, M. T., Rocha, E., and Gullon, A. Hypodiploidy and 22q11 rearrangements at diagnosis are associated with poor prognosis in patients with multiple myeloma. Br. J. Haematol., 98: 418-425, 1997.
-
(1997)
Br. J. Haematol.
, vol.98
, pp. 418-425
-
-
Calasanz, M.J.1
Cigudosa, J.C.2
Odero, M.D.3
Garcia-Foncillas, J.4
Marin, J.5
Ardanaz, M.T.6
Rocha, E.7
Gullon, A.8
-
80
-
-
18544363372
-
Both hypodiploidy and deletion of chromosome 13 independently confer poor prognosis in multiple myeloma
-
Fassas, A. B., Spencer, T., Sawyer, J., Zangari, M., Lee, C. K., Anaissie, E., Muwalla, F., Morris, C., Barlogie, B., and Tricot, G. Both hypodiploidy and deletion of chromosome 13 independently confer poor prognosis in multiple myeloma. Br. J. Haematol., 118: 1041-1047, 2002.
-
(2002)
Br. J. Haematol.
, vol.118
, pp. 1041-1047
-
-
Fassas, A.B.1
Spencer, T.2
Sawyer, J.3
Zangari, M.4
Lee, C.K.5
Anaissie, E.6
Muwalla, F.7
Morris, C.8
Barlogie, B.9
Tricot, G.10
-
81
-
-
0033928972
-
The biology of multiple myeloma
-
Review
-
Drach, J., Kaufmann, H., Urbauer, E., Schreiber, S., Ackermann, J., and Huber, H. The biology of multiple myeloma. [Review]. J. Cancer Res. Clin. Oncol., 126: 441-447, 2000.
-
(2000)
J. Cancer Res. Clin. Oncol.
, vol.126
, pp. 441-447
-
-
Drach, J.1
Kaufmann, H.2
Urbauer, E.3
Schreiber, S.4
Ackermann, J.5
Huber, H.6
-
82
-
-
10744225707
-
Translocations involving 14q32 are common in patients with the monoclonal gammopathy of undetermined significance
-
in press
-
Fonseca, R., Bailey, R., Ahmann, G., Aguayo, P., Jalal, S., Rajkumar, S., Kyle, R., Gertz, M., Dispenzieri, A., Lust, J., Lacy, M., Witzig, T., Greipp, P., and Dewald, G. Translocations involving 14q32 are common in patients with the monoclonal gammopathy of undetermined significance. Blood, in press, 2003.
-
(2003)
Blood
-
-
Fonseca, R.1
Bailey, R.2
Ahmann, G.3
Aguayo, P.4
Jalal, S.5
Rajkumar, S.6
Kyle, R.7
Gertz, M.8
Dispenzieri, A.9
Lust, J.10
Lacy, M.11
Witzig, T.12
Greipp, P.13
Dewald, G.14
-
83
-
-
17344395438
-
Deletion of 13q14 remains an independent adverse prognostic variable in multiple myeloma despite its frequent detection by interphase fluorescence in situ hybridization
-
Zojer, N., Konigsberg, R., Ackermann, J., Fritz, E., Dallinger, S., Kromer, E., Kaufmann, H., Riedl, L., Gisslinger, H., Schreiber, S., Heinz, R., Ludwig, H., Huber, H., and Drach, J. Deletion of 13q14 remains an independent adverse prognostic variable in multiple myeloma despite its frequent detection by interphase fluorescence in situ hybridization. Blood, 95: 1925-1930, 2000.
-
(2000)
Blood
, vol.95
, pp. 1925-1930
-
-
Zojer, N.1
Konigsberg, R.2
Ackermann, J.3
Fritz, E.4
Dallinger, S.5
Kromer, E.6
Kaufmann, H.7
Riedl, L.8
Gisslinger, H.9
Schreiber, S.10
Heinz, R.11
Ludwig, H.12
Huber, H.13
Drach, J.14
-
84
-
-
0035869257
-
Chromosome 13 abnormalities identified by FISH analysis and serum β-2-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy
-
Facon, T., Avet-Loiseau, H., Guillerm, G., Moreau, P., Geneviève, F., Zandecki, M., Laï, J., Leleu, X., Jouet, J., Bauters, F., Harousseau, J., Bataille, R., Mary, J. Y., and Intergroupe Francophone du Myelome. Chromosome 13 abnormalities identified by FISH analysis and serum β-2-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy. Blood, 97: 1566-1571, 2001.
-
(2001)
Blood
, vol.97
, pp. 1566-1571
-
-
Facon, T.1
Avet-Loiseau, H.2
Guillerm, G.3
Moreau, P.4
Geneviève, F.5
Zandecki, M.6
Laï, J.7
Leleu, X.8
Jouet, J.9
Bauters, F.10
Harousseau, J.11
Bataille, R.12
Mary, J.Y.13
-
85
-
-
0033977476
-
Multiple myeloma: Monoallelic deletions of the tumor suppressor genes TP53 and RB1 in long-term follow-up
-
Carlebach, M., Amiel, A., Gaber, E., Radnay, J., Manor, Y., Fejgin, M., and Lishner, M. Multiple myeloma: monoallelic deletions of the tumor suppressor genes TP53 and RB1 in long-term follow-up. Cancer Genet. Cytogenet., 117: 57-60, 2000.
-
(2000)
Cancer Genet. Cytogenet.
, vol.117
, pp. 57-60
-
-
Carlebach, M.1
Amiel, A.2
Gaber, E.3
Radnay, J.4
Manor, Y.5
Fejgin, M.6
Lishner, M.7
-
86
-
-
0034663292
-
High incidence of chromosome 13 deletion in multiple myeloma detected by multiprobe interphase FISH
-
Shaughnessy, J., Tian, E., Sawyer, J., Bumm, K., Landes, R., Badros, A., Morris, C., Tricot, G., Epstein, J., and Barlogie, B. High incidence of chromosome 13 deletion in multiple myeloma detected by multiprobe interphase FISH. Blood, 96: 1505-1511, 2000.
-
(2000)
Blood
, vol.96
, pp. 1505-1511
-
-
Shaughnessy, J.1
Tian, E.2
Sawyer, J.3
Bumm, K.4
Landes, R.5
Badros, A.6
Morris, C.7
Tricot, G.8
Epstein, J.9
Barlogie, B.10
-
87
-
-
18544409610
-
Results of high-dose therapy for 1000 patients with multiple myeloma: Durable complete remissions and superior survival in the absence of chromosome 13 abnormalities
-
Desikan, R., Barlogie, B., Sawyer, J., Ayers, D., Tricot, G., Badros, A., Zangari, M., Munshi, N. C., Anaissie, E., Spoon, D., Siegel, D., Jagannath, S., Vesole, D., Epstein, J., Shaughnessy, J., Fassas, A., Lim, S., Roberson, P., and Crowley, J. Results of high-dose therapy for 1000 patients with multiple myeloma: durable complete remissions and superior survival in the absence of chromosome 13 abnormalities. Blood, 95: 4008-4010, 2000.
-
(2000)
Blood
, vol.95
, pp. 4008-4010
-
-
Desikan, R.1
Barlogie, B.2
Sawyer, J.3
Ayers, D.4
Tricot, G.5
Badros, A.6
Zangari, M.7
Munshi, N.C.8
Anaissie, E.9
Spoon, D.10
Siegel, D.11
Jagannath, S.12
Vesole, D.13
Epstein, J.14
Shaughnessy, J.15
Fassas, A.16
Lim, S.17
Roberson, P.18
Crowley, J.19
-
88
-
-
0037217603
-
Prognostic impact of cytogenetic and interphase fluorescence in situ hybridization-defined chromosome 13 deletion in multiple myeloma: Early results of total therapy II
-
Shaughnessy, J., Jr., Tian, E., Sawyer, J., McCoy, J., Tricot, G., Jacobson, J., Anaissie, E., Zangari, M., Fassas, A., Muwalla, F., Morris, C., and Barlogie, B. Prognostic impact of cytogenetic and interphase fluorescence in situ hybridization-defined chromosome 13 deletion in multiple myeloma: early results of total therapy II. Br. J. Haematol., 120: 44-52, 2003.
-
(2003)
Br. J. Haematol.
, vol.120
, pp. 44-52
-
-
Shaughnessy Jr., J.1
Tian, E.2
Sawyer, J.3
McCoy, J.4
Tricot, G.5
Jacobson, J.6
Anaissie, E.7
Zangari, M.8
Fassas, A.9
Muwalla, F.10
Morris, C.11
Barlogie, B.12
-
89
-
-
0038495926
-
Continuous absence of metaphase-defined cytogenetic abnormalities, especially of chromosome 13 and hypodiploidy, ensures long-term survival in multiple myeloma treated with Total Therapy 1: Interpretation in the context of global gene expression
-
Shaughnessy, J., Jacobson, J., Sawyer, J., McCoy, J., Fassas, A., Zhan, F., Bumm, K., Epstein, J., Anaissie, E., Jagannath, S., Vesole, D., Siegel, D., Desikan, R., Munshi, N., Badros, A., Tian, E., Zangari, M., Tricot, G., Crowley, J., and Barlogie, B. Continuous absence of metaphase-defined cytogenetic abnormalities, especially of chromosome 13 and hypodiploidy, ensures long-term survival in multiple myeloma treated with Total Therapy 1: interpretation in the context of global gene expression. Blood, 101: 3849-3856, 2003.
-
(2003)
Blood
, vol.101
, pp. 3849-3856
-
-
Shaughnessy, J.1
Jacobson, J.2
Sawyer, J.3
McCoy, J.4
Fassas, A.5
Zhan, F.6
Bumm, K.7
Epstein, J.8
Anaissie, E.9
Jagannath, S.10
Vesole, D.11
Siegel, D.12
Desikan, R.13
Munshi, N.14
Badros, A.15
Tian, E.16
Zangari, M.17
Tricot, G.18
Crowley, J.19
Barlogie, B.20
more..
-
90
-
-
17144433568
-
Unique role of cytogenetics in the prognosis of patients with myeloma receiving high-dose therapy and autotransplants
-
Tricot, G., Sawyer, J. R., Jagannath, S., Desikan, K. R., Siegel, D., Naucke, S., Mattox, S., Bracy, D., Munshi, N., and Barlogie, B. Unique role of cytogenetics in the prognosis of patients with myeloma receiving high-dose therapy and autotransplants. J. Clin. Oncol., 15: 2659-2666, 1997.
-
(1997)
J. Clin. Oncol.
, vol.15
, pp. 2659-2666
-
-
Tricot, G.1
Sawyer, J.R.2
Jagannath, S.3
Desikan, K.R.4
Siegel, D.5
Naucke, S.6
Mattox, S.7
Bracy, D.8
Munshi, N.9
Barlogie, B.10
-
91
-
-
0036721371
-
Recurrent 14q32 translocations determine the prognosis of multiple myeloma, especially in patients receiving intensive chemotherapy
-
Moreau, P., Facon, T., Leleu, X., Morineau, N., Huyghe, P., Harousseau, J. L., Bataille, R., and Avet-Loiseau, H. Recurrent 14q32 translocations determine the prognosis of multiple myeloma, especially in patients receiving intensive chemotherapy. Blood, 100: 1579-1583, 2002.
-
(2002)
Blood
, vol.100
, pp. 1579-1583
-
-
Moreau, P.1
Facon, T.2
Leleu, X.3
Morineau, N.4
Huyghe, P.5
Harousseau, J.L.6
Bataille, R.7
Avet-Loiseau, H.8
-
92
-
-
0033776742
-
Multiple myeloma with deletion of chromosome 13q is characterized by increased bone marrow neovascularization
-
Schreiber, S., Ackermann, J., Obermair, A., Kaufmann, H., Urbauer, E., Aletaha, K., Gisslinger, H., Chott, a., Huber, H., and Drach, J. Multiple myeloma with deletion of chromosome 13q is characterized by increased bone marrow neovascularization. Br. J. Haematol., 110: 605-609, 2000.
-
(2000)
Br. J. Haematol.
, vol.110
, pp. 605-609
-
-
Schreiber, S.1
Ackermann, J.2
Obermair, A.3
Kaufmann, H.4
Urbauer, E.5
Aletaha, K.6
Gisslinger, H.7
Chott, A.8
Huber, H.9
Drach, J.10
-
93
-
-
0006125491
-
Translocations into IgH switch regions - The genetic hallmark of multiple myeloma
-
Bergsagel, P. L., Chesi, M., Brents, L. A., and Kuehl, W. M. Translocations into IgH switch regions - the genetic hallmark of multiple myeloma. Blood, 86: 223-223, 1995.
-
(1995)
Blood
, vol.86
, pp. 223-223
-
-
Bergsagel, P.L.1
Chesi, M.2
Brents, L.A.3
Kuehl, W.M.4
-
94
-
-
0030464093
-
Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma
-
Bergsagel, P. L., Chesi, M., Nardini, E., Brents, L. A., Kirby, S. L., and Kuehl, W. M. Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma. Proc. Natl. Acad. Sci. USA, 93: 13931-13936, 1996.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 13931-13936
-
-
Bergsagel, P.L.1
Chesi, M.2
Nardini, E.3
Brents, L.A.4
Kirby, S.L.5
Kuehl, W.M.6
-
95
-
-
0030792866
-
The Ig heavy chain gene is frequently involved in chromosomal translocations in multiple myeloma and plasma cell leukemia as detected by in situ hybridization
-
Nishida, K., Tamura, A., Nakazawa, N., Ueda, Y., Abe, T., Matsuda, F., Kashima, K., and Taniwaki, M. The Ig heavy chain gene is frequently involved in chromosomal translocations in multiple myeloma and plasma cell leukemia as detected by in situ hybridization. Blood, 90: 526-534, 1997.
-
(1997)
Blood
, vol.90
, pp. 526-534
-
-
Nishida, K.1
Tamura, A.2
Nakazawa, N.3
Ueda, Y.4
Abe, T.5
Matsuda, F.6
Kashima, K.7
Taniwaki, M.8
-
96
-
-
0034602691
-
Diverse karyotypic abnormalities of the c-myc locus associated with c-myc dysregulation and tumor progression in multiple myeloma
-
Shou, Y., Martelli, M. L., Gabrea, A., Qi, Y., Brents, L. A., Roschke, A., Dewald, G., Kirsch, I. R., Bergsagel, P. L., and Kuehl, W. M. Diverse karyotypic abnormalities of the c-myc locus associated with c-myc dysregulation and tumor progression in multiple myeloma. Proc. Natl. Acad. Sci. USA, 97: 228-233, 2000.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 228-233
-
-
Shou, Y.1
Martelli, M.L.2
Gabrea, A.3
Qi, Y.4
Brents, L.A.5
Roschke, A.6
Dewald, G.7
Kirsch, I.R.8
Bergsagel, P.L.9
Kuehl, W.M.10
-
97
-
-
0035892119
-
Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors
-
Avet-Loiseau, H., Gerson, F., Magrangeas, F., Minvielle, S., Harousseau, J. L., and Bataille, R. Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors. Blood, 98: 3082-3086, 2001.
-
(2001)
Blood
, vol.98
, pp. 3082-3086
-
-
Avet-Loiseau, H.1
Gerson, F.2
Magrangeas, F.3
Minvielle, S.4
Harousseau, J.L.5
Bataille, R.6
-
98
-
-
17444440946
-
Common chromosomal fragile site FRA16D sequence: Identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
-
Ried, K., Finnis, M., Hobson, L., Mangelsdorf, M., Dayan, S., Nancarrow, J. K., Woollatt, E., Kremmidiotis, G., Gardner, A., Venter, D., Baker, E., and Richards, R. I. Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells. Hum. Mol. Genet., 9: 1651-1663, 2000.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1651-1663
-
-
Ried, K.1
Finnis, M.2
Hobson, L.3
Mangelsdorf, M.4
Dayan, S.5
Nancarrow, J.K.6
Woollatt, E.7
Kremmidiotis, G.8
Gardner, A.9
Venter, D.10
Baker, E.11
Richards, R.I.12
-
99
-
-
0034306548
-
The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations
-
Krummel, K. A., Roberts, L. R., Kawakami, M., Glover, T. W., and Smith, D. I. The characterization of the common fragile site FRA16D and its involvement in multiple myeloma translocations. Genomics, 69: 37-46, 2000.
-
(2000)
Genomics
, vol.69
, pp. 37-46
-
-
Krummel, K.A.1
Roberts, L.R.2
Kawakami, M.3
Glover, T.W.4
Smith, D.I.5
-
100
-
-
0031985198
-
Multiple myeloma: Increasing evidence for a multistep transformation process
-
Hallek, M., Leif Bergsagel, P., and Anderson, K. C. Multiple myeloma: increasing evidence for a multistep transformation process. Blood, 91: 3-21, 1998.
-
(1998)
Blood
, vol.91
, pp. 3-21
-
-
Hallek, M.1
Leif Bergsagel, P.2
Anderson, K.C.3
-
101
-
-
0034254687
-
The role of immunoglobulin translocations in the pathogenesis of B-cell malignancies
-
Willis, T. G., and Dyer, M. J. The role of immunoglobulin translocations in the pathogenesis of B-cell malignancies. Blood, 96: 808-822, 2000.
-
(2000)
Blood
, vol.96
, pp. 808-822
-
-
Willis, T.G.1
Dyer, M.J.2
-
102
-
-
0035253869
-
Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia: A study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique
-
Avet-Loiseau, H., Daviet, A., Brigaudeau, C., Callet-Bauchu, E., Terre, C., Lafage-Pochitaloff, M., Desangles, F., Ramond, S., Talmant, P., and Bataille, R. Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myelome and the Groupe Francais de Cytogenetique Hematologique. Blood, 97: 822-825, 2001.
-
(2001)
Blood
, vol.97
, pp. 822-825
-
-
Avet-Loiseau, H.1
Daviet, A.2
Brigaudeau, C.3
Callet-Bauchu, E.4
Terre, C.5
Lafage-Pochitaloff, M.6
Desangles, F.7
Ramond, S.8
Talmant, P.9
Bataille, R.10
-
103
-
-
0038675193
-
Critical roles for immunoglobulin translocations and cyclin D dysregulation in multiple myeloma
-
Bergsagel, P., and Kuehl, W. Critical roles for immunoglobulin translocations and cyclin D dysregulation in multiple myeloma. Immunol Rev., 194: 96-104, 2003.
-
(2003)
Immunol Rev.
, vol.194
, pp. 96-104
-
-
Bergsagel, P.1
Kuehl, W.2
-
104
-
-
0035412392
-
Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma
-
Shaughnessy, J., Jr., Gabrea, A., Qi, Y., Brents, L., Zhan, F., Tian, E., Sawyer, J., Barlogie, B., Bergsagel, P. L., and Kuehl, M. Cyclin D3 at 6p21 is dysregulated by recurrent chromosomal translocations to immunoglobulin loci in multiple myeloma. Blood, 98: 217-223, 2001.
-
(2001)
Blood
, vol.98
, pp. 217-223
-
-
Shaughnessy Jr., J.1
Gabrea, A.2
Qi, Y.3
Brents, L.4
Zhan, F.5
Tian, E.6
Sawyer, J.7
Barlogie, B.8
Bergsagel, P.L.9
Kuehl, M.10
-
105
-
-
0033887241
-
Detection of t(4;14)(p16.3;q32) chromosomal translocation in multiple myeloma by reverse transcription-polymerase chain reaction analysis of IGH-MMSET fusion transcripts
-
Malgeri, U., Baldini, L., Perfetti, V., Fabris, S., Vignarelli, M. C., Colombo, G., Lotti, V., Compasso, S., Bogni, S., Lombardi, L., Maiolo, A. T., and Neri, A. Detection of t(4;14)(p16.3;q32) chromosomal translocation in multiple myeloma by reverse transcription-polymerase chain reaction analysis of IGH-MMSET fusion transcripts. Cancer Res., 60: 4058-4061, 2000.
-
(2000)
Cancer Res.
, vol.60
, pp. 4058-4061
-
-
Malgeri, U.1
Baldini, L.2
Perfetti, V.3
Fabris, S.4
Vignarelli, M.C.5
Colombo, G.6
Lotti, V.7
Compasso, S.8
Bogni, S.9
Lombardi, L.10
Maiolo, A.T.11
Neri, A.12
-
106
-
-
0029978550
-
Dysregulation of cyclin D1 by translocation into an IgH γ switch region in two multiple myeloma cell lines
-
Chesi, M., Bergsagel, P. L., Brents, L. A., Smith, C. M., Gerhard, D. S., and Kuehl, W. M. Dysregulation of cyclin D1 by translocation into an IgH γ switch region in two multiple myeloma cell lines. Blood, 88: 674-681, 1996.
-
(1996)
Blood
, vol.88
, pp. 674-681
-
-
Chesi, M.1
Bergsagel, P.L.2
Brents, L.A.3
Smith, C.M.4
Gerhard, D.S.5
Kuehl, W.M.6
-
107
-
-
0031838436
-
Multiple myeloma and the translocation t(11;14)(q13;q32) - A report on 13 cases
-
Fonseca, R., Witzig, T. E., Gertz, M. A., Kyle, R. A., Hoyer, J. D., Jalal, S. M., and Greipp, P. R. Multiple myeloma and the translocation t(11;14)(q13;q32) - a report on 13 cases. Br. J. Haematol., 101: 296-301, 1998.
-
(1998)
Br. J. Haematol.
, vol.101
, pp. 296-301
-
-
Fonseca, R.1
Witzig, T.E.2
Gertz, M.A.3
Kyle, R.A.4
Hoyer, J.D.5
Jalal, S.M.6
Greipp, P.R.7
-
108
-
-
0009931298
-
Chromosomal abnormalities in systemic amyloidosis
-
Banff, Alberta, Canada
-
Harrison, C., Mazullo, H., Cheung, K., Mehta, A., Lachmann, H., Hawkins, P., and Orchard, K. Chromosomal abnormalities in systemic amyloidosis. In: Proceedings of the VIII International Myeloma Workshop, Banff, Alberta, Canada, 2001, p. P18.
-
(2001)
Proceedings of the VIII International Myeloma Workshop
, pp. 18
-
-
Harrison, C.1
Mazullo, H.2
Cheung, K.3
Mehta, A.4
Lachmann, H.5
Hawkins, P.6
Orchard, K.7
-
109
-
-
0034656068
-
Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32)
-
Janssen, J. W., Vaandrager, J. W., Heuser, T., Jauch, A., Kluin, P. M., Geelen, E., Bergsagel, P. L., Kuehl, W. M., Drexler, H. G., Otsuki, T., Bartram, C. R., and Schuuring, E. Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32). Blood, 95: 2691-2698, 2000.
-
(2000)
Blood
, vol.95
, pp. 2691-2698
-
-
Janssen, J.W.1
Vaandrager, J.W.2
Heuser, T.3
Jauch, A.4
Kluin, P.M.5
Geelen, E.6
Bergsagel, P.L.7
Kuehl, W.M.8
Drexler, H.G.9
Otsuki, T.10
Bartram, C.R.11
Schuuring, E.12
-
110
-
-
0031033513
-
The t(11;14) (q13;q32) in multiple myeloma cell line KMS12 has its 11q13 breakpoint 330 kb centromeric from the cyclin D1 gene
-
Vaandrager, J. W., Kluin, P., and Schuuring, E. The t(11;14) (q13;q32) in multiple myeloma cell line KMS12 has its 11q13 breakpoint 330 kb centromeric from the cyclin D1 gene [Letter]. Blood, 89: 349-350, 1997.
-
(1997)
Blood
, vol.89
, pp. 349-350
-
-
Vaandrager, J.W.1
Kluin, P.2
Schuuring, E.3
-
111
-
-
0029099733
-
Molecular breakpoints of t(11;14)(q13;q32) in multiple myeloma
-
Meeus, P., Stul, M. S., Mecucci, C., Cassiman, J. J., and Van den Berghe, H. Molecular breakpoints of t(11;14)(q13;q32) in multiple myeloma. Cancer Genet Cytogenet., 83: 25-27, 1995.
-
(1995)
Cancer Genet. Cytogenet.
, vol.83
, pp. 25-27
-
-
Meeus, P.1
Stul, M.S.2
Mecucci, C.3
Cassiman, J.J.4
Van Den Berghe, H.5
-
112
-
-
0033557950
-
Molecular analysis of 11q13 breakpoints in multiple myeloma
-
Ronchetti, D., Finelli, P., Richelda, R., Baldini, L., Rocchi, M., Viggiano, L., Cuneo, A., Bogni, S., Fabris, S., Lombardi, L., Maiolo, A., and Neri, A. Molecular analysis of 11q13 breakpoints in multiple myeloma. Blood, 93: 1330-1337, 1999.
-
(1999)
Blood
, vol.93
, pp. 1330-1337
-
-
Ronchetti, D.1
Finelli, P.2
Richelda, R.3
Baldini, L.4
Rocchi, M.5
Viggiano, L.6
Cuneo, A.7
Bogni, S.8
Fabris, S.9
Lombardi, L.10
Maiolo, A.11
Neri, A.12
-
113
-
-
0027434804
-
Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B-cell malignancies
-
Raynaud, S. D., Bekri, S., Leroux, D., Grosgeorge, J., Klein, B., Bastard, C., Gaudray, P., and Simon, M. P. Expanded range of 11q13 breakpoints with differing patterns of cyclin D1 expression in B-cell malignancies. Genes Chromosomes Cancer, 8: 80-87, 1993.
-
(1993)
Genes Chromosomes Cancer
, vol.8
, pp. 80-87
-
-
Raynaud, S.D.1
Bekri, S.2
Leroux, D.3
Grosgeorge, J.4
Klein, B.5
Bastard, C.6
Gaudray, P.7
Simon, M.P.8
-
114
-
-
0034502263
-
The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study
-
Hoyer, J. D., Hanson, C. A., Fonseca, R., Greipp, P. R., Dewald, G. W., and Kurtin, P. J. The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical study. Am. J. Clin. Pathol., 113: 831-837, 2000.
-
(2000)
Am. J. Clin. Pathol.
, vol.113
, pp. 831-837
-
-
Hoyer, J.D.1
Hanson, C.A.2
Fonseca, R.3
Greipp, P.R.4
Dewald, G.W.5
Kurtin, P.J.6
-
115
-
-
0030810392
-
Cyclin D1 protein in multiple myeloma and plasmacytoma: An immunohistochemical study using fixed, paraffin-embedded tissue sections
-
Vasef, M. A., Medeiros, L. J., Yospur, L. S., Sun, N. C., McCourty, A., and Brynes, R. K. Cyclin D1 protein in multiple myeloma and plasmacytoma: an immunohistochemical study using fixed, paraffin-embedded tissue sections. Mod. Pathol., 10: 927-932, 1997.
-
(1997)
Mod. Pathol.
, vol.10
, pp. 927-932
-
-
Vasef, M.A.1
Medeiros, L.J.2
Yospur, L.S.3
Sun, N.C.4
McCourty, A.5
Brynes, R.K.6
-
116
-
-
0013224058
-
The proliferation gene expression signature is a quantitative integrator of oncogenic events that predicts survival in mantle cell lymphoma
-
Rosenwald, A., Wright, G., Wiestner, A., Chan, W. C., Connors, J. M., Campo, E., Gascoyne, R. D., Grogan, T. M., Muller-Hermelink, H. K., Smeland, E. B., Chiorazzi, M., Giltnane, J. M., Hurt, E. M., Zhao, H., Averett, L., Henrickson, S., Yang, L., Powell, J., Wilson, W. H., Jaffe, E. S., Simon, R., Klausner, R. D., Montserrat, E., Bosch, F., Greiner, T. C., Weisenburger, D. D., Sanger, W. G., Dave, B. J., Lynch, J. C., Vose, J., Armitage, J. O., Fisher, R. I., Miller, T. P., LeBlanc, M., Ott, G., Kvaloy, S., Holte, H., Delabie, J., and Staudt, L. M. The proliferation gene expression signature is a quantitative integrator of oncogenic events that predicts survival in mantle cell lymphoma. Cancer Cell., 3: 185-197, 2003.
-
(2003)
Cancer Cell.
, vol.3
, pp. 185-197
-
-
Rosenwald, A.1
Wright, G.2
Wiestner, A.3
Chan, W.C.4
Connors, J.M.5
Campo, E.6
Gascoyne, R.D.7
Grogan, T.M.8
Muller-Hermelink, H.K.9
Smeland, E.B.10
Chiorazzi, M.11
Giltnane, J.M.12
Hurt, E.M.13
Zhao, H.14
Averett, L.15
Henrickson, S.16
Yang, L.17
Powell, J.18
Wilson, W.H.19
Jaffe, E.S.20
Simon, R.21
Klausner, R.D.22
Montserrat, E.23
Bosch, F.24
Greiner, T.C.25
Weisenburger, D.D.26
Sanger, W.G.27
Dave, B.J.28
Lynch, J.C.29
Vose, J.30
Armitage, J.O.31
Fisher, R.I.32
Miller, T.P.33
LeBlanc, M.34
Ott, G.35
Kvaloy, S.36
Holte, H.37
Delabie, J.38
Staudt, L.M.39
more..
-
117
-
-
0343049149
-
Predictive role of interphase cytogenetics for survival of patients with multiple myeloma
-
Konigsberg, R., Zojer, N., Ackermann, J., Kromer, E., Kittler, H., Fritz, E., Kaufmann, H., Nosslinger, T., Riedl, L., Gisslinger, H., Jager, U., Simonitsch, I., Heinz, R., Ludwig, H., Huber, H., and Drach, J. Predictive role of interphase cytogenetics for survival of patients with multiple myeloma. J. Clin. Oncol., 18: 804-812, 2000.
-
(2000)
J. Clin. Oncol.
, vol.18
, pp. 804-812
-
-
Konigsberg, R.1
Zojer, N.2
Ackermann, J.3
Kromer, E.4
Kittler, H.5
Fritz, E.6
Kaufmann, H.7
Nosslinger, T.8
Riedl, L.9
Gisslinger, H.10
Jager, U.11
Simonitsch, I.12
Heinz, R.13
Ludwig, H.14
Huber, H.15
Drach, J.16
-
118
-
-
0042744766
-
CD20 is associated with a small mature plasma cell morphology and t(11;14) in multiple myeloma
-
Robillard, N., Avet-Loiseau, H., Garand, R., Moreau, P., Pineau, D., Rapp, M-J., Harousseau, J-L., and Bataille, R. CD20 is associated with a small mature plasma cell morphology and t(11;14) in multiple myeloma. Blood, 102: 1070-1071, 2003.
-
(2003)
Blood
, vol.102
, pp. 1070-1071
-
-
Robillard, N.1
Avet-Loiseau, H.2
Garand, R.3
Moreau, P.4
Pineau, D.5
Rapp, M.-J.6
Harousseau, J.-L.7
Bataille, R.8
-
119
-
-
0037441892
-
Translocation t(11;14)(q13;q32) is the hallmark of IgM, IgE, and nonsecretory multiple myeloma variants
-
Avet-Loiseau, H., Garand, R., Lode, L., Harousseau, J-L., and Bataille, R. Translocation t(11;14)(q13;q32) is the hallmark of IgM, IgE, and nonsecretory multiple myeloma variants. Blood, 101: 1570-1571, 2003.
-
(2003)
Blood
, vol.101
, pp. 1570-1571
-
-
Avet-Loiseau, H.1
Garand, R.2
Lode, L.3
Harousseau, J.-L.4
Bataille, R.5
-
120
-
-
0032212243
-
The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts
-
Chesi, M., Nardini, E., Lim, R., Smith, K., Kuehl, W., and Bergsagel, P. The t(4;14) translocation in myeloma dysregulates both FGFR3 and a novel gene, MMSET, resulting in IgH/MMSET hybrid transcripts. Blood, 92: 3025-3034, 1998.
-
(1998)
Blood
, vol.92
, pp. 3025-3034
-
-
Chesi, M.1
Nardini, E.2
Lim, R.3
Smith, K.4
Kuehl, W.5
Bergsagel, P.6
-
121
-
-
0030842266
-
A novel chromosomal translocation t(4;14)(p16.3;q32) in multiple myeloma involves the fibroblast growth-factor receptor 3 gene
-
Richelda, R., Ronchetti, D., Baldini, L., Cro, L., Viggiano, L., Marzella, R., Rocchi, M., Otsuki, T., Lombardi, L., Maiolo, A. T., and Neri, A. A novel chromosomal translocation t(4;14)(p16.3;q32) in multiple myeloma involves the fibroblast growth-factor receptor 3 gene. Blood, 90: 4062-4070, 1997.
-
(1997)
Blood
, vol.90
, pp. 4062-4070
-
-
Richelda, R.1
Ronchetti, D.2
Baldini, L.3
Cro, L.4
Viggiano, L.5
Marzella, R.6
Rocchi, M.7
Otsuki, T.8
Lombardi, L.9
Maiolo, A.T.10
Neri, A.11
-
122
-
-
0034888840
-
Analysis of FGFR3 gene mutations in multiple myeloma patients with t(4;14)
-
Intini, D., Baldini, L., Fabris, S., Lombardi, L., Ciceri, G., Maiolo, A. T., and Neri, A. Analysis of FGFR3 gene mutations in multiple myeloma patients with t(4;14). Br. J. Haematol., 114: 362-364, 2001.
-
(2001)
Br. J. Haematol.
, vol.114
, pp. 362-364
-
-
Intini, D.1
Baldini, L.2
Fabris, S.3
Lombardi, L.4
Ciceri, G.5
Maiolo, A.T.6
Neri, A.7
-
123
-
-
0035254612
-
Activated fibroblast growth factor receptor 3 is an oncogene that contributes to tumor progression in multiple myeloma
-
Chesi, M., Brents, L. A., Ely, S. A., Bais, C., Robbiani, D. F., Mesri, E. A., Kuehl, W. M., and Bergsagel, P. L. Activated fibroblast growth factor receptor 3 is an oncogene that contributes to tumor progression in multiple myeloma. Blood, 97: 729-736, 2001.
-
(2001)
Blood
, vol.97
, pp. 729-736
-
-
Chesi, M.1
Brents, L.A.2
Ely, S.A.3
Bais, C.4
Robbiani, D.F.5
Mesri, E.A.6
Kuehl, W.M.7
Bergsagel, P.L.8
-
124
-
-
0035858985
-
Deregulated FGFR3 mutants in multiple myeloma cell lines with t(4;14):
-
Ronchetti, D., Greco, A., Compasso, S., Colombo, G., Dell'Era, P., Otsuki, T., Lombardi, L., and Neri, A. Deregulated FGFR3 mutants in multiple myeloma cell lines with t(4;14): comparative analysis of Y373C, K650E and the novel G384D mutations. Oncogene, 20: 3553-3562, 2001.
-
(2001)
Oncogene
, vol.20
, pp. 3553-3562
-
-
Ronchetti, D.1
Greco, A.2
Compasso, S.3
Colombo, G.4
Dell'Era, P.5
Otsuki, T.6
Lombardi, L.7
Neri, A.8
-
125
-
-
0035024746
-
Translocation t(4;14)(p16.3;q32) is a recurrent genetic lesion in primary amyloidosis
-
Perfetti, V., Coluccia, A., Intini, D., Malgeri, U., Colli Vignarelli, M., Casarini, S., Merlini, G., and Neri, A. Translocation t(4;14)(p16.3;q32) is a recurrent genetic lesion in primary amyloidosis. Leukemia (Baltimore), 158: 1599-1603, 2001.
-
(2001)
Leukemia (Baltimore)
, vol.158
, pp. 1599-1603
-
-
Perfetti, V.1
Coluccia, A.2
Intini, D.3
Malgeri, U.4
Colli Vignarelli, M.5
Casarini, S.6
Merlini, G.7
Neri, A.8
-
126
-
-
0034935624
-
Ectopic expression of MAFB gene in human myeloma cells carrying (14;20)(q32;q11) chromosomal translocations
-
Hanamura, I., Iida, S., Akano, Y., Hayami, Y., Kato, M., Miura, K., Harada, S., Banno, S., Wakita, A., Kiyoi, H., Naoe, T., Shimizu, S., Sonta, S. I., Nitta, M., Taniwaki, M., and Ueda, R. Ectopic expression of MAFB gene in human myeloma cells carrying (14;20)(q32;q11) chromosomal translocations. Jpn J Cancer Res., 92: 638-644, 2001.
-
(2001)
Jpn J. Cancer Res.
, vol.92
, pp. 638-644
-
-
Hanamura, I.1
Iida, S.2
Akano, Y.3
Hayami, Y.4
Kato, M.5
Miura, K.6
Harada, S.7
Banno, S.8
Wakita, A.9
Kiyoi, H.10
Naoe, T.11
Shimizu, S.12
Sonta, S.I.13
Nitta, M.14
Taniwaki, M.15
Ueda, R.16
-
127
-
-
84984756503
-
Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma
-
Iida, S., Rao, P. H., Butler, M., Corradini, P., Boccadoro, M., Klein, B., Chaganti, R. S., and Dalla-Favera, R. Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma. Nat. Genet., 17: 226-230, 1997.
-
(1997)
Nat. Genet.
, vol.17
, pp. 226-230
-
-
Iida, S.1
Rao, P.H.2
Butler, M.3
Corradini, P.4
Boccadoro, M.5
Klein, B.6
Chaganti, R.S.7
Dalla-Favera, R.8
-
128
-
-
0032697261
-
Detection of MUM1/IRF4-IgH fusion in multiple myeloma
-
Yoshida, S., Nakazawa, N., Iida, S., Hayami, Y., Sato, S., Wakita, A., Shimizu, S., Taniwaki, M., and Ueda, R. Detection of MUM1/IRF4-IgH fusion in multiple myeloma. Leukemia (Baltimore), 13: 1812-1816, 1999.
-
(1999)
Leukemia (Baltimore)
, vol.13
, pp. 1812-1816
-
-
Yoshida, S.1
Nakazawa, N.2
Iida, S.3
Hayami, Y.4
Sato, S.5
Wakita, A.6
Shimizu, S.7
Taniwaki, M.8
Ueda, R.9
-
129
-
-
0029819604
-
Activating mutations of N- and K-ras in multiple myeloma show different clinical associations: Analysis of the Eastern Cooperative Oncology Group Phase III Trial
-
Liu, P., Leong, T., Quam, L., Billadeau, D., Kay, N. E., Greipp, P., Kyle, R. A., Oken, M. M., and Van Ness, B. Activating mutations of N- and K-ras in multiple myeloma show different clinical associations: analysis of the Eastern Cooperative Oncology Group Phase III Trial. Blood, 88: 2699-2706, 1996.
-
(1996)
Blood
, vol.88
, pp. 2699-2706
-
-
Liu, P.1
Leong, T.2
Quam, L.3
Billadeau, D.4
Kay, N.E.5
Greipp, P.6
Kyle, R.A.7
Oken, M.M.8
Van Ness, B.9
-
130
-
-
0034876702
-
High incidence of N- and K-Ras activating mutations in multiple myeloma and primary plasma cell leukemia at diagnosis
-
Bezieau, S., Devilder, M. C., Avet-Loiseau, H., Mellerin, M. P., Puthier, D., Pennarun, E., Rapp, M. J., Harousseau, J. L., Moisan, J. P., and Bataille, R. High incidence of N- and K-Ras activating mutations in multiple myeloma and primary plasma cell leukemia at diagnosis. Hum. Mutat., 18: 212-224, 2001.
-
(2001)
Hum. Mutat.
, vol.18
, pp. 212-224
-
-
Bezieau, S.1
Devilder, M.C.2
Avet-Loiseau, H.3
Mellerin, M.P.4
Puthier, D.5
Pennarun, E.6
Rapp, M.J.7
Harousseau, J.L.8
Moisan, J.P.9
Bataille, R.10
-
131
-
-
85117739053
-
Activating Ras mutations in patients with plasma-cell disorders: A reappraisal
-
Bezieau, S., Avet-Loiseau, H., Moisan, J. P., and Bataille, R. Activating Ras mutations in patients with plasma-cell disorders: a reappraisal. Blood, 100: 1101-1102, 2003.
-
(2003)
Blood
, vol.100
, pp. 1101-1102
-
-
Bezieau, S.1
Avet-Loiseau, H.2
Moisan, J.P.3
Bataille, R.4
-
132
-
-
0027212420
-
Mutational activation of N- and K-ras oncogenes in plasma cell dyscrasias
-
Corradini, P., Ladetto, M., Voena, C., Palumbo, A., Inghirami, G., Knowles, D. M., Boccadoro, M., and Pileri, A. Mutational activation of N- and K-ras oncogenes in plasma cell dyscrasias. Blood, 81: 2708-2713, 1993.
-
(1993)
Blood
, vol.81
, pp. 2708-2713
-
-
Corradini, P.1
Ladetto, M.2
Voena, C.3
Palumbo, A.4
Inghirami, G.5
Knowles, D.M.6
Boccadoro, M.7
Pileri, A.8
-
133
-
-
0024811225
-
Ras oncogene mutation in multiple myeloma
-
Neri, A., Murphy, J. P., Cro, L., Ferrero, D., Tarella, C., Baldini, L., and Dalla-Favera, R. Ras oncogene mutation in multiple myeloma. J. Exp. Med., 170: 1715-1725, 1989.
-
(1989)
J. Exp. Med.
, vol.170
, pp. 1715-1725
-
-
Neri, A.1
Murphy, J.P.2
Cro, L.3
Ferrero, D.4
Tarella, C.5
Baldini, L.6
Dalla-Favera, R.7
-
134
-
-
0026110957
-
RAS gene mutations in multiple myeloma and related monoclonal gammopathies
-
Matozaki, S., Nakagawa, T., Nakao, Y., and Fujita, T. RAS gene mutations in multiple myeloma and related monoclonal gammopathies. Kobe J. Med. Sci., 37: 35-45, 1991.
-
(1991)
Kobe J. Med. Sci.
, vol.37
, pp. 35-45
-
-
Matozaki, S.1
Nakagawa, T.2
Nakao, Y.3
Fujita, T.4
-
135
-
-
0037421964
-
An unusual H-Ras mutant isolated from a human multiple myeloma line leads to transformation and factor-independent cell growth
-
Crowder, C., Kopantzev, E., Williams, K., Lengel, C., Miki, T., and Rudikoff, S. An unusual H-Ras mutant isolated from a human multiple myeloma line leads to transformation and factor-independent cell growth. Oncogene, 22: 649-659, 2003.
-
(2003)
Oncogene
, vol.22
, pp. 649-659
-
-
Crowder, C.1
Kopantzev, E.2
Williams, K.3
Lengel, C.4
Miki, T.5
Rudikoff, S.6
-
136
-
-
0032147210
-
Presence of a p53 gene deletion in patients with multiple myeloma predicts for short survival after conventional-dose chemotherapy
-
Drach, J., Ackermann, J., Fritz, E., Kromer, E., Schuster, R., Gisslinger, H., DeSantis, M., Zojer, N., Fiegl, M., Roka, S., Schuster, J., Heinz, R., Ludwig, H., and Huber, H. Presence of a p53 gene deletion in patients with multiple myeloma predicts for short survival after conventional-dose chemotherapy. Blood, 92: 802-809, 1998.
-
(1998)
Blood
, vol.92
, pp. 802-809
-
-
Drach, J.1
Ackermann, J.2
Fritz, E.3
Kromer, E.4
Schuster, R.5
Gisslinger, H.6
DeSantis, M.7
Zojer, N.8
Fiegl, M.9
Roka, S.10
Schuster, J.11
Heinz, R.12
Ludwig, H.13
Huber, H.14
-
137
-
-
0344577960
-
Analysis of p73 and p53 gene deletions in multiple myeloma
-
Schultheis, B., Kramer, A., Willer, A., Hegenbart, U., Goldschmidt, H., and Hehlmann, R. Analysis of p73 and p53 gene deletions in multiple myeloma. Leukemia (Baltimore), 13: 2099-2103, 1999.
-
(1999)
Leukemia (Baltimore)
, vol.13
, pp. 2099-2103
-
-
Schultheis, B.1
Kramer, A.2
Willer, A.3
Hegenbart, U.4
Goldschmidt, H.5
Hehlmann, R.6
-
138
-
-
0026508061
-
Mutations of the p53 gene in human myeloma cell lines
-
Mazars, G. R., Portier, M., Zhang, X. G., Jourdan, M., Bataille, R., Theillet, C., and Klein, B. Mutations of the p53 gene in human myeloma cell lines. Oncogene, 7: 1015-1018, 1992.
-
(1992)
Oncogene
, vol.7
, pp. 1015-1018
-
-
Mazars, G.R.1
Portier, M.2
Zhang, X.G.3
Jourdan, M.4
Bataille, R.5
Theillet, C.6
Klein, B.7
-
139
-
-
0028302085
-
Inactivation of tumor suppressor genes, p53 and Rbl, in plasma cell dyscrasias
-
Corradini, P., Inghirami, G., Astolfi, M., Ladetto, M., Voena, C., Ballerini, P., Gu, W., Nilsson, K., Knowles, D. M., Boccadoro, M., Pileri, A., and Dalla-Favera, R. Inactivation of tumor suppressor genes, p53 and Rbl, in plasma cell dyscrasias. Leukemia (Baltimore), 8: 758-767, 1994.
-
(1994)
Leukemia (Baltimore)
, vol.8
, pp. 758-767
-
-
Corradini, P.1
Inghirami, G.2
Astolfi, M.3
Ladetto, M.4
Voena, C.5
Ballerini, P.6
Gu, W.7
Nilsson, K.8
Knowles, D.M.9
Boccadoro, M.10
Pileri, A.11
Dalla-Favera, R.12
-
140
-
-
0027505575
-
p53 gene mutations in multiple myeloma are associated with advanced forms of malignancy
-
Neri, A., Baldini, L., Trecca, D., Cro, L., Polli, E., and Maiolo, A. T. p53 gene mutations in multiple myeloma are associated with advanced forms of malignancy. Blood, 81: 128-135, 1993.
-
(1993)
Blood
, vol.81
, pp. 128-135
-
-
Neri, A.1
Baldini, L.2
Trecca, D.3
Cro, L.4
Polli, E.5
Maiolo, A.T.6
-
141
-
-
0026780478
-
Rare occurrence of p53 gene mutations in multiple myeloma
-
Preudhomme, C., Facon, T., Zandecki, M., Vanrumbeke, M., Lai, J. L., Nataf, E., Loucheux, L. M. H., Kerckaert, J. P., and Fenaux, P. Rare occurrence of p53 gene mutations in multiple myeloma. Br. J. Haematol., 81: 440-443, 1992.
-
(1992)
Br. J. Haematol.
, vol.81
, pp. 440-443
-
-
Preudhomme, C.1
Facon, T.2
Zandecki, M.3
Vanrumbeke, M.4
Lai, J.L.5
Nataf, E.6
Loucheux, L.M.H.7
Kerckaert, J.P.8
Fenaux, P.9
-
142
-
-
0032428365
-
Absence of p53 deletions in bone marrow plasma cells of patients with monoclonal gammopathy of undetermined significance
-
Ackermann, J., Meidlinger, P., Zojer, N., Gisslinger, H., Ludwig, H., Huber, H., and Drach, J. Absence of p53 deletions in bone marrow plasma cells of patients with monoclonal gammopathy of undetermined significance. Br. J. Haematol., 103: 1161-1163, 1998.
-
(1998)
Br. J. Haematol.
, vol.103
, pp. 1161-1163
-
-
Ackermann, J.1
Meidlinger, P.2
Zojer, N.3
Gisslinger, H.4
Ludwig, H.5
Huber, H.6
Drach, J.7
-
143
-
-
0030921866
-
MDM2 protein overexpression promotes proliferation and survival of multiple myeloma cells
-
Teoh, G., Urashima, M., Ogata, A., Chauhan, D., DeCaprio, J. A., Treon, S. P., Schlossman, R. L., and Anderson, K. C. MDM2 protein overexpression promotes proliferation and survival of multiple myeloma cells. Blood, 90: 1982-1992, 1997.
-
(1997)
Blood
, vol.90
, pp. 1982-1992
-
-
Teoh, G.1
Urashima, M.2
Ogata, A.3
Chauhan, D.4
DeCaprio, J.A.5
Treon, S.P.6
Schlossman, R.L.7
Anderson, K.C.8
-
144
-
-
0026582025
-
Perspectives on the origins of multiple myeloma and plasmacytomas in mice
-
Potter, M. Perspectives on the origins of multiple myeloma and plasmacytomas in mice. Hematol. Oncol. Clin. North Am., 6: 211-223, 1992.
-
(1992)
Hematol. Oncol. Clin. North Am.
, vol.6
, pp. 211-223
-
-
Potter, M.1
-
145
-
-
0035072851
-
Mouse plasmacytoma: An experimental model of human multiple myeloma
-
Review
-
Gado, K., Silva, S., Paloczi, K., Domjan, G., and Falus, A. Mouse plasmacytoma: an experimental model of human multiple myeloma. [Review]. Haematologica, 86: 227-236, 2001.
-
(2001)
Haematologica
, vol.86
, pp. 227-236
-
-
Gado, K.1
Silva, S.2
Paloczi, K.3
Domjan, G.4
Falus, A.5
-
146
-
-
0034751091
-
Efficiency alleles of the Pctr1 modifier locus for plasmacytoma susceptibility
-
Zhang, S-L., DuBois, W., Ramsay, E. S., Bliskovski, V., Morse, H. C., III, Taddesse-Heath, L., Vass, W. C., DePinho, R. A., and Mock, B. A. Efficiency alleles of the Pctr1 modifier locus for plasmacytoma susceptibility. Mol. Cell. Biol., 21: 310-318, 2001.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 310-318
-
-
Zhang, S.-L.1
DuBois, W.2
Ramsay, E.S.3
Bliskovski, V.4
Morse III, H.C.5
Taddesse-Heath, L.6
Vass, W.C.7
DePinho, R.A.8
Mock, B.A.9
-
147
-
-
0034161312
-
Germline CDKN2A mutation implicated in predisposition to multiple myeloma
-
Dilworth, D., Liu, L., Stewart, A. K., Berenson, J. R., Lassam, N., and Hogg, D. Germline CDKN2A mutation implicated in predisposition to multiple myeloma. Blood, 95: 1869-1871, 2000.
-
(2000)
Blood
, vol.95
, pp. 1869-1871
-
-
Dilworth, D.1
Liu, L.2
Stewart, A.K.3
Berenson, J.R.4
Lassam, N.5
Hogg, D.6
-
148
-
-
0343048351
-
De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis
-
Gonzalez, M., Mateos, M. V., Garcia-Sanz, R., Balanzategui, A., Lopez-Perez, R., Chillon, M. C., Gonzalez, D., Alaejos, I., and San Miguel, J. F. De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis. Leukemia (Baltimore), 14: 183-187, 2000.
-
(2000)
Leukemia (Baltimore)
, vol.14
, pp. 183-187
-
-
Gonzalez, M.1
Mateos, M.V.2
Garcia-Sanz, R.3
Balanzategui, A.4
Lopez-Perez, R.5
Chillon, M.C.6
Gonzalez, D.7
Alaejos, I.8
San Miguel, J.F.9
-
149
-
-
0034746509
-
Hypermethylation of p16 INK4A gene promoter during the progression of plasma cell dyscrasia
-
Uchida, T., Kinoshita, T., Ohno, T., Ohashi, H., Nagai, H., and Saito, H. Hypermethylation of p16 INK4A gene promoter during the progression of plasma cell dyscrasia. Leukemia (Baltimore), 15: 157-165, 2001.
-
(2001)
Leukemia (Baltimore)
, vol.15
, pp. 157-165
-
-
Uchida, T.1
Kinoshita, T.2
Ohno, T.3
Ohashi, H.4
Nagai, H.5
Saito, H.6
-
150
-
-
0032846413
-
DNA methylation changes and multiple myeloma
-
Review
-
Ng, M. H., Wong, I. H., and Lo, K. W. DNA methylation changes and multiple myeloma. [Review]. Leuk. Lymphoma, 34: 463-472, 1999.
-
(1999)
Leuk. Lymphoma
, vol.34
, pp. 463-472
-
-
Ng, M.H.1
Wong, I.H.2
Lo, K.W.3
-
151
-
-
0033566692
-
Quantitative analysis of aberrant p16 methylation using real-time quantitative methylation-specific polymerase chain reaction
-
Lo, Y. M., Wong, I. H., Zhang, J., Tein, M. S., Ng, M. H., and Hjelm, N. M. Quantitative analysis of aberrant p16 methylation using real-time quantitative methylation-specific polymerase chain reaction. Cancer Res., 59: 3899-3903, 1999.
-
(1999)
Cancer Res.
, vol.59
, pp. 3899-3903
-
-
Lo, Y.M.1
Wong, I.H.2
Zhang, J.3
Tein, M.S.4
Ng, M.H.5
Hjelm, N.M.6
-
152
-
-
0032496135
-
Differential myeloma cell responsiveness to interferon-α correlates with differential induction of p19(Ink4d) and cyclin D2 expression
-
Arora, T., and Jelinek, D. F. Differential myeloma cell responsiveness to interferon-α correlates with differential induction of p19(Ink4d) and cyclin D2 expression. J. Biol. Chem., 273: 11799-11805, 1998.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 11799-11805
-
-
Arora, T.1
Jelinek, D.F.2
-
153
-
-
18544379572
-
Methylation is an inactivating mechanism of the p16 gene in multiple myeloma associated with high plasma cell proliferation and short survival
-
Mateos, M. V., Garcia-Sanz, R., Lopez-Perez, R., Moro, M. J., Ocio, E., Hernandez, J., Megido, M., Caballero, M. D., Fernandez-Calvo, J., Barez, A., Almeida, J., Orfao, A., Gonzalez, M., and San Miguel, J. F. Methylation is an inactivating mechanism of the p16 gene in multiple myeloma associated with high plasma cell proliferation and short survival. Br. J. Haematol., 118: 1034-1040, 2002.
-
(2002)
Br. J. Haematol.
, vol.118
, pp. 1034-1040
-
-
Mateos, M.V.1
Garcia-Sanz, R.2
Lopez-Perez, R.3
Moro, M.J.4
Ocio, E.5
Hernandez, J.6
Megido, M.7
Caballero, M.D.8
Fernandez-Calvo, J.9
Barez, A.10
Almeida, J.11
Orfao, A.12
Gonzalez, M.13
San Miguel, J.F.14
-
154
-
-
0035412365
-
p16(INK4a) and p15(INK4b) gene methylations in plasma cells from monoclonal gammopathy of undetermined significance
-
Guillerm, G., Gyan, E., Wolowiec, D., Facon, T., Avet-Loiseau, H., Kuliczkowski, K., Bauters, F., Fenaux, P., and Quesnel, B. p16(INK4a) and p15(INK4b) gene methylations in plasma cells from monoclonal gammopathy of undetermined significance. Blood, 98: 244-246, 2001.
-
(2001)
Blood
, vol.98
, pp. 244-246
-
-
Guillerm, G.1
Gyan, E.2
Wolowiec, D.3
Facon, T.4
Avet-Loiseau, H.5
Kuliczkowski, K.6
Bauters, F.7
Fenaux, P.8
Quesnel, B.9
-
155
-
-
0030891628
-
Induction of cell cycle arrest and B cell terminal differentiation by CDK inhibitor p18(INK4c) and IL-6
-
Morse, L., Chen, D., Franklin, D., Xiong, Y., and Chen-Kiang, S. Induction of cell cycle arrest and B cell terminal differentiation by CDK inhibitor p18(INK4c) and IL-6. Immunity, 6: 47-56, 1997.
-
(1997)
Immunity
, vol.6
, pp. 47-56
-
-
Morse, L.1
Chen, D.2
Franklin, D.3
Xiong, Y.4
Chen-Kiang, S.5
-
156
-
-
85009921564
-
Frequent inactivation of the cyclin-dependent kinase inhibitor p18 by homozygous deletion in multiple myeloma cell lines: Ectopicp18 expression inhibits growth and induces apoptosis
-
Kulkarni, M. S., Daggett, J. L., Bender, T. P., Kuehl, W. M., Bergsagel, P. L., and Williams, M. E. Frequent inactivation of the cyclin-dependent kinase inhibitor p18 by homozygous deletion in multiple myeloma cell lines: ectopicp18 expression inhibits growth and induces apoptosis. Leukemia (Baltimore), 16: 127-134, 2002.
-
(2002)
Leukemia (Baltimore)
, vol.16
, pp. 127-134
-
-
Kulkarni, M.S.1
Daggett, J.L.2
Bender, T.P.3
Kuehl, W.M.4
Bergsagel, P.L.5
Williams, M.E.6
-
157
-
-
0029144829
-
The retinoblastoma gene (RB-1) status in multiple myeloma: A report on 35 cases
-
Zandecki, M., Facon, T., Preudhomme, C., Vanrumbeke, M., Vachee, A., Quesnel, B., Lai, J. L., Cosson, A., and Fenaux, P. The retinoblastoma gene (RB-1) status in multiple myeloma: a report on 35 cases. Leuk Lymphoma, 18: 497-503, 1995.
-
(1995)
Leuk. Lymphoma
, vol.18
, pp. 497-503
-
-
Zandecki, M.1
Facon, T.2
Preudhomme, C.3
Vanrumbeke, M.4
Vachee, A.5
Quesnel, B.6
Lai, J.L.7
Cosson, A.8
Fenaux, P.9
-
158
-
-
0031040365
-
The retinoblastoma susceptibility gene RB-1 in multiple myeloma
-
Juge-Morineau, N., Harousseau, J. L., Amiot, M., and Bataille, R. The retinoblastoma susceptibility gene RB-1 in multiple myeloma. [Review]. Leuk. Lymphoma, 24: 229-237, 1997.
-
(1997)
Leuk. Lymphoma
, vol.24
, pp. 229-237
-
-
Juge-Morineau, N.1
Harousseau, J.L.2
Amiot, M.3
Bataille, R.4
-
159
-
-
0034669945
-
Loss of PTEN expression leading to high Akt activation in human multiple myelomas
-
Hyun, T., Yam, A., Pece, S., Xie, X., Zhang, J., Miki, T., Gutkind, J. S., and Li, W. Loss of PTEN expression leading to high Akt activation in human multiple myelomas. Blood, 96: 3560-3568, 2000.
-
(2000)
Blood
, vol.96
, pp. 3560-3568
-
-
Hyun, T.1
Yam, A.2
Pece, S.3
Xie, X.4
Zhang, J.5
Miki, T.6
Gutkind, J.S.7
Li, W.8
-
160
-
-
0034710535
-
Expression of PTEN in PTEN-deficient multiple myeloma cells abolishes tumor growth in vivo
-
Ge, N., and Rudikoff, S. Expression of PTEN in PTEN-deficient multiple myeloma cells abolishes tumor growth in vivo. Oncogene, 19: 4091-4095, 2000.
-
(2000)
Oncogene
, vol.19
, pp. 4091-4095
-
-
Ge, N.1
Rudikoff, S.2
-
161
-
-
0020470134
-
Mouse c-myc oncogene is located on chromosome 15 and translocated to chromosome 12 in plasmacytomas
-
Crews, S., Barth, R., Hood, L., Prehn, J., and Calame, K. Mouse c-myc oncogene is located on chromosome 15 and translocated to chromosome 12 in plasmacytomas. Science (Wash. DC), 218: 1319-1321, 1982.
-
(1982)
Science (Wash. DC)
, vol.218
, pp. 1319-1321
-
-
Crews, S.1
Barth, R.2
Hood, L.3
Prehn, J.4
Calame, K.5
-
162
-
-
0020582671
-
Translocation, breakage and truncated transcripts of c-myc oncogene in murine plasmacytomas
-
Stanton, L. W., Watt, R., and Marcu, K. B. Translocation, breakage and truncated transcripts of c-myc oncogene in murine plasmacytomas. Nature (Lond.), 303: 401-406, 1983.
-
(1983)
Nature (Lond.)
, vol.303
, pp. 401-406
-
-
Stanton, L.W.1
Watt, R.2
Marcu, K.B.3
-
163
-
-
0021141444
-
Transcriptional activation of the translocated c-myc oncogene in mouse plasmacytomas: Similar RNA levels in tumor and proliferating normal cells
-
Keath, E. I., Kelekar, A., and Cole, M. D. Transcriptional activation of the translocated c-myc oncogene in mouse plasmacytomas: similar RNA levels in tumor and proliferating normal cells. Cell, 37: 521-528, 1984.
-
(1984)
Cell
, vol.37
, pp. 521-528
-
-
Keath, E.I.1
Kelekar, A.2
Cole, M.D.3
-
164
-
-
0021223739
-
A conserved sequence at c-myc oncogene chromosomal translocation breakpoints in plasmacytomas
-
Piccoli, S. P., Caimi, P. G., and Cole, M. D. A conserved sequence at c-myc oncogene chromosomal translocation breakpoints in plasmacytomas. Nature (Lond.), 310: 327-330, 1984.
-
(1984)
Nature (Lond.)
, vol.310
, pp. 327-330
-
-
Piccoli, S.P.1
Caimi, P.G.2
Cole, M.D.3
-
165
-
-
0021800641
-
The c-myc oncogene is translocated to the involved chromosome 12 in mouse plasmacytoma
-
Erikson, J., Miller, D. A., Miller, O. J., Abcarian, P. W., Skurla, R. M., Mushinski, J. F., and Croce, C. M. The c-myc oncogene is translocated to the involved chromosome 12 in mouse plasmacytoma. Proc. Natl. Acad. Sci. USA, 82: 4212-4216, 1985.
-
(1985)
Proc. Natl. Acad. Sci. USA
, vol.82
, pp. 4212-4216
-
-
Erikson, J.1
Miller, D.A.2
Miller, O.J.3
Abcarian, P.W.4
Skurla, R.M.5
Mushinski, J.F.6
Croce, C.M.7
-
166
-
-
0022380768
-
The c-myc oncogene driven by immunoglobulin enhancers induces lymphoid malignancy in transgenic mice
-
Adams, J. M., Harris, A. W., Pinkert, C. A., Corcoran, L. M., Alexander, W. S., Cory, S., Palmiter, R. D., and Brinster, R. L. The c-myc oncogene driven by immunoglobulin enhancers induces lymphoid malignancy in transgenic mice. Nature (Lond.), 318: 533-538, 1985.
-
(1985)
Nature (Lond.)
, vol.318
, pp. 533-538
-
-
Adams, J.M.1
Harris, A.W.2
Pinkert, C.A.3
Corcoran, L.M.4
Alexander, W.S.5
Cory, S.6
Palmiter, R.D.7
Brinster, R.L.8
|