-
1
-
-
0343355828
-
High incidence of translocations t(11; 14)(q13;q32) and t(4;14)(p16;q32) in patients with plasma cell malignancies
-
Avet-Loiseau H, Li JY, Facon T, Brigaudeau C, Morineau N, Maloisel F, Rapp MJ, Talmant P, Trimoreau F, Jaccard A, Harousseau JL, Bataille R. 1998. High incidence of translocations t(11; 14)(q13;q32) and t(4;14)(p16;q32) in patients with plasma cell malignancies. Cancer Res 58:5640-5645.
-
(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
-
2
-
-
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, Laï JL, Daviet A, Li JY, Praloran V, Rapp MJ, Harousseau JL, Facon T, Bataille R. 1999. 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)
Genes Chromosomes Cancer
, vol.24
, pp. 9-15
-
-
Avet-Loiseau, H.1
Brigaudeau, C.2
Morineau, N.3
Talmant, P.4
Laï, 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
-
3
-
-
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 MJ, Harousseau JL, Minvielle S, Bataille R. for the Intergroupe Francophone du Myélome. 2002. 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)
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
-
4
-
-
0030464093
-
Promiscuous translocations into immunoglogulin heavy chain switch regions in multiple myeloma
-
Bergsagel PL, Chesi M, Nardini E, Brents LA, Kirby SL, Kuehl WM. 1996. Promiscuous translocations into immunoglogulin heavy chain switch regions in multiple myeloma. Proc Natl Acad Sci USA 93:13931-13936.
-
(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
-
5
-
-
0030922231
-
Frequent translocation t(4;14)(p16.3;q32) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3
-
Chesi M, Nardini E, Brents LA, Schrock E, Ried T, Kuehl WM, Bergsagel PL. 1997. Frequent translocation t(4;14)(p16.3;q32) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3. Nat Genet 16:260-265.
-
(1997)
Nat Genet
, vol.16
, pp. 260-265
-
-
Chesi, M.1
Nardini, E.2
Brents, L.A.3
Schrock, E.4
Ried, T.5
Kuehl, W.M.6
Bergsagel, P.L.7
-
6
-
-
0031839633
-
Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma
-
Chesi M, Bergsagel PL, Shonukan OO, Martelli ML, Brents LA, Chen T, Schröck E, Ried T, Kuehl WM. 1998. Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma. Blood 91:4457-4463.
-
(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
Schröck, E.7
Ried, T.8
Kuehl, W.M.9
-
7
-
-
0016804136
-
A clinical staging system for multiple myeloma: Correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival
-
Durie BGM, Salmon SE. 1975. A clinical staging system for multiple myeloma: correlation of measured myeloma cell mass with presenting clinical features, response to treatment, and survival. Cancer 36:842-854.
-
(1975)
Cancer
, vol.36
, pp. 842-854
-
-
Durie, B.G.M.1
Salmon, S.E.2
-
8
-
-
0033566346
-
Detection of t(4;14)(p16.3;q32) chromosomal translocation in multiple myeloma by double-color fluorescent in situ hybridization
-
Finelli P, Fabris S, Zagano S, Baldini L, Intini D, Nobili L, Lombardi L, Maiolo T, Neri A. 1999. Detection of t(4;14)(p16.3;q32) chromosomal translocation in multiple myeloma by double-color fluorescent in situ hybridization. Blood 94:724-732.
-
(1999)
Blood
, vol.94
, pp. 724-732
-
-
Finelli, P.1
Fabris, S.2
Zagano, S.3
Baldini, L.4
Intini, D.5
Nobili, L.6
Lombardi, L.7
Maiolo, T.8
Neri, A.9
-
9
-
-
0035883062
-
The t(4; 14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance
-
Fonseca R, Oken MM, Greipp PR, on behalf of the Eastern Cooperative Oncology Group Myeloma Group. 2001. The t(4; 14)(p16.3;q32) is strongly associated with chromosome 13 abnormalities in both multiple myeloma and monoclonal gammopathy of undetermined significance. Blood 98:1271-1272.
-
(2001)
Blood
, vol.98
, pp. 1271-1272
-
-
Fonseca, R.1
Oken, M.M.2
Greipp, P.R.3
-
10
-
-
0037092981
-
Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique subset of patients
-
Fonseca R, Blood EA, Oken MM, Kyle RA, Dewald GW, Bailey RJ, Van Wier SA, Henderson KJ, Hoyer JD, Harrington D, Kay NE, Van Ness B, Griep P. 2002. Myeloma and the t(11;14)(q13;q32); evidence for a biologically defined unique subset of patients. Blood 99:3735-3741.
-
(2002)
Blood
, vol.99
, pp. 3735-3741
-
-
Fonseca, R.1
Blood, E.A.2
Oken, M.M.3
Kyle, R.A.4
Dewald, G.W.5
Bailey, R.J.6
Van Wier, S.A.7
Henderson, K.J.8
Hoyer, J.D.9
Harrington, D.10
Kay, N.E.11
Van Ness, B.12
Griep, P.13
-
11
-
-
0031985198
-
Multiple myeloma: Increasing evidence for a multistep transformation process
-
Hallek M, Bergsagel PL, Anderson KC. 1998. Multiple myeloma: increasing evidence for a multistep transformation process. Blood 91:3-21.
-
(1998)
Blood
, vol.91
, pp. 3-21
-
-
Hallek, M.1
Bergsagel, P.L.2
Anderson, K.C.3
-
12
-
-
0035863790
-
Illegitimate switch recombinations are present in approximately half of primary myeloma tumors, but do not relate to known prognostic indicators or survival
-
Ho PJ, Brown RD, Pelka GJ, Basten A, Gibson J, Joshua DE. 2001. Illegitimate switch recombinations are present in approximately half of primary myeloma tumors, but do not relate to known prognostic indicators or survival. Blood 97:490-495.
-
(2001)
Blood
, vol.97
, pp. 490-495
-
-
Ho, P.J.1
Brown, R.D.2
Pelka, G.J.3
Basten, A.4
Gibson, J.5
Joshua, D.E.6
-
13
-
-
84984756503
-
Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma
-
Ida S, Rao PH, Butler M, Corradini P, Boccadoro M, Klein B, Chaganti RSK, Dalla-Favera R. 1997. Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma. Nat Genet 17:226-230.
-
(1997)
Nat Genet
, vol.17
, pp. 226-230
-
-
Ida, S.1
Rao, P.H.2
Butler, M.3
Corradini, P.4
Boccadoro, M.5
Klein, B.6
Chaganti, R.S.K.7
Dalla-Favera, R.8
-
15
-
-
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 JL, Bataille R, Avet-Loiseau H, for the Intergroupe Francophone du Myélome. 2002. Recurrent 14q32 translocations determine the prognosis of multiple myeloma, especially in patients receiving intensive chemotherapy. Blood 100:1579-1583.
-
(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
-
16
-
-
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, Taniwaki M. 1997. 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)
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
-
17
-
-
0035123860
-
Insertional events as well as translocations may arise during aberrant immunoglobulin switch recombination in a patient with multiple myeloma
-
Pratt G, Fenton AL, Davies FE, Rawstron AC, Richards SJ, Collins JE, Owen RG, Jack AS, Smith GM, Morgan GJ. 2001. Insertional events as well as translocations may arise during aberrant immunoglobulin switch recombination in a patient with multiple myeloma. Br J Haematol 112:388-391.
-
(2001)
Br J Haematol
, vol.112
, pp. 388-391
-
-
Pratt, G.1
Fenton, A.L.2
Davies, F.E.3
Rawstron, A.C.4
Richards, S.J.5
Collins, J.E.6
Owen, R.G.7
Jack, A.S.8
Smith, G.M.9
Morgan, G.J.10
-
18
-
-
0032170964
-
Multicolor spectral karyotyping identifies new recurrent breakpoints and translocations in multiple myeloma
-
Rao PH, Cigudosa JC, Ning Y, Calasanz MJ, Lida S, Tagawa S, Michaeli J, Klein B, Dalla-Favera R, Jhanwar SC, Ried T, Chaganti RSK. 1998. Multicolor spectral karyotyping identifies new recurrent breakpoints and translocations in multiple myeloma. Blood 92:1743-1748.
-
(1998)
Blood
, vol.92
, pp. 1743-1748
-
-
Rao, P.H.1
Cigudosa, J.C.2
Ning, Y.3
Calasanz, M.J.4
Lida, 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.K.12
-
19
-
-
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 AT, Neri A. 1997. 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)
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
-
20
-
-
0029072506
-
Cytogenetic study in multiple myeloma at diagnosis: Comparison of two techniques
-
Smadja NV, Louvet C, Isnard F, Dutel JL, Grange MJ, Varette C, Krulik M. 1995. Cytogenetic study in multiple myeloma at diagnosis: comparison of two techniques. Br J Haematol 90:619-624.
-
(1995)
Br J Haematol
, vol.90
, pp. 619-624
-
-
Smadja, N.V.1
Louvet, C.2
Isnard, F.3
Dutel, J.L.4
Grange, M.J.5
Varette, C.6
Krulik, M.7
-
21
-
-
0031861960
-
Chromosomal analysis in multiple myeloma: Cytogenetic evidence of two different diseases
-
Smadja NV, Fruchart C, Isnard F, Louvet C, Dutel JL, Cheron N, Grange MJ, Monconduit M, Bastard C. 1998. Chromosomal analysis in multiple myeloma: cytogenetic evidence of two different diseases. Leukemia 12:960-969.
-
(1998)
Leukemia
, 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
-
22
-
-
0035496928
-
Hypodiploidy is a major prognostic factor in multiple myeloma
-
Smadja NV, Bastard C, Brigaudeau C, Leroux D, Fruchart C, on behalf of the groupe Français de Cytogénétique Hématologique. 2001. Hypodiploidy is a major prognostic factor in multiple myeloma. Blood 98:2229-2238.
-
(2001)
Blood
, vol.98
, pp. 2229-2238
-
-
Smadja, N.V.1
Bastard, C.2
Brigaudeau, C.3
Leroux, D.4
Fruchart, C.5
|