-
1
-
-
0024211470
-
Chromosomal aberrations in progressive and indolent chronic B-lymphocytic leukemia. A longitudinal study
-
Juliusson G., Friberg K., Gahrton G. Chromosomal aberrations in progressive and indolent chronic B-lymphocytic leukemia. A longitudinal study. Acta Oncol. 27:1988;473-477.
-
(1988)
Acta Oncol
, vol.27
, pp. 473-477
-
-
Juliusson, G.1
Friberg, K.2
Gahrton, G.3
-
2
-
-
0023485005
-
Role of chromosomal abnormalities in chronic lymphocytic leukemia
-
Gahrton G., Juliusson G., Robert K.H., Friberg K. Role of chromosomal abnormalities in chronic lymphocytic leukemia. Blood Rev. 1:1987;183-192.
-
(1987)
Blood Rev
, vol.1
, pp. 183-192
-
-
Gahrton, G.1
Juliusson, G.2
Robert, K.H.3
Friberg, K.4
-
3
-
-
0023432301
-
Prognostic significance of karyotypic abnormalities in B cell chronic lymphocytic leukemia: An update
-
Han T., Henderson E.S., Emrich L.J., Sandberg A.A. Prognostic significance of karyotypic abnormalities in B cell chronic lymphocytic leukemia. an update Semin Hematol. 24:1987;257-263.
-
(1987)
Semin Hematol
, vol.24
, pp. 257-263
-
-
Han, T.1
Henderson, E.S.2
Emrich, L.J.3
Sandberg, A.A.4
-
4
-
-
0030930177
-
Cytogenetic, fluorescence in situ hybridization, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia
-
Gardiner A.C., Corcoran M.M., Oscier D.G. Cytogenetic, fluorescence in situ hybridization, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia. Genes Chromosom Cancer. 20:1997;73-81.
-
(1997)
Genes Chromosom Cancer
, vol.20
, pp. 73-81
-
-
Gardiner, A.C.1
Corcoran, M.M.2
Oscier, D.G.3
-
5
-
-
0030915891
-
Cytogenetic and molecular cytogenetic analysis of B cell chronic lymphocytic leukemia: Specific chromosome aberrations identify prognostic subgroups of patients and point to loci of candidate genes
-
Dohner H., Stilgenbauer S., Fischer K., Bentz M., Lichter P. Cytogenetic and molecular cytogenetic analysis of B cell chronic lymphocytic leukemia. specific chromosome aberrations identify prognostic subgroups of patients and point to loci of candidate genes Leukemia. 11(Suppl 2):1997;S19-S24.
-
(1997)
Leukemia
, vol.11
, Issue.SUPPL. 2
-
-
Dohner, H.1
Stilgenbauer, S.2
Fischer, K.3
Bentz, M.4
Lichter, P.5
-
6
-
-
1842328565
-
11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis
-
Hunstein W., Lichter P. 11q deletions identify a new subset of B-cell chronic lymphocytic leukemia characterized by extensive nodal involvement and inferior prognosis. Blood. 89:1997;2516-2522.
-
(1997)
Blood
, vol.89
, pp. 2516-2522
-
-
Hunstein, W.1
Lichter, P.2
-
8
-
-
0027229604
-
Trisomy 12 in B-cell chronic lymphocytic leukemia: Interphase study by in situ hybridization in 75 patients
-
Coignet L., Bertheas M.F., Vasselon C., Jaubert J., Calmard Oriol P., Brizard C.P., Guyotat D. Trisomy 12 in B-cell chronic lymphocytic leukemia. interphase study by in situ hybridization in 75 patients Nouv Rev Fr Hematol. 35:1993;129-134.
-
(1993)
Nouv Rev Fr Hematol
, vol.35
, pp. 129-134
-
-
Coignet, L.1
Bertheas, M.F.2
Vasselon, C.3
Jaubert, J.4
Calmard Oriol, P.5
Brizard, C.P.6
Guyotat, D.7
-
10
-
-
0021829149
-
Clustering of breakpoints on chromosome 11 in human B-cell neoplasms with the t(11;14) chromosome translocation
-
Tsujimoto Y., Jaffe E., Cossman J., Gorham J., Nowell P.C., Croce C.M. Clustering of breakpoints on chromosome 11 in human B-cell neoplasms with the t(11;14) chromosome translocation. Nature. 315:1985;340-343.
-
(1985)
Nature
, vol.315
, pp. 340-343
-
-
Tsujimoto, Y.1
Jaffe, E.2
Cossman, J.3
Gorham, J.4
Nowell, P.C.5
Croce, C.M.6
-
11
-
-
0031908870
-
Translocation t(1;10)(q21;q26) in a case of acute nonlymphocytic leukemia
-
Terreros M.C., Qesada M., Slavutsky I.R. Translocation t(1;10)(q21;q26) in a case of acute nonlymphocytic leukemia. Acta Haematol. 99:1998;92-94.
-
(1998)
Acta Haematol
, vol.99
, pp. 92-94
-
-
Terreros, M.C.1
Qesada, M.2
Slavutsky, I.R.3
-
13
-
-
13344269022
-
Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features
-
Dierlamm J., Pittaluga S., Wlodarska I., Stul M., Thomas J., Boogaerts M., Michaux L., Driessen A., Mecucci C., Cassiman J.J., Wolf-Peeters C.D., Van den Berghe H. Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features. Blood. 87:1996;299-307.
-
(1996)
Blood
, vol.87
, pp. 299-307
-
-
Dierlamm, J.1
Pittaluga, S.2
Wlodarska, I.3
Stul, M.4
Thomas, J.5
Boogaerts, M.6
Michaux, L.7
Driessen, A.8
Mecucci, C.9
Cassiman, J.J.10
Wolf-Peeters, C.D.11
Van Den Berghe, H.12
-
14
-
-
0027976182
-
Primary central nervous system lymphomas. Immunophenotypic, virologic, and cytogenetic findings of three patients without immune defects
-
Itoyama T., Sadamori N., Tsutsimi K., Tokunaga Y., Soda H., Tomonaga M., Yamamori S., Masuda O., Oshima K., Kikuchi M. Primary central nervous system lymphomas. Immunophenotypic, virologic, and cytogenetic findings of three patients without immune defects. Cancer. 73:1994;455-463.
-
(1994)
Cancer
, vol.73
, pp. 455-463
-
-
Itoyama, T.1
Sadamori, N.2
Tsutsimi, K.3
Tokunaga, Y.4
Soda, H.5
Tomonaga, M.6
Yamamori, S.7
Masuda, O.8
Oshima, K.9
Kikuchi, M.10
-
15
-
-
0025949494
-
Clonal cytogenetic abnormalities in Hodgkin's disease
-
Ladanyi M., Parsa N.Z., Offit K., Wachtel M.S., Filippa D.A., Jhanwar S.C. Clonal cytogenetic abnormalities in Hodgkin's disease. Genes Chromosom Cancer. 3:1991;294-299.
-
(1991)
Genes Chromosom Cancer
, vol.3
, pp. 294-299
-
-
Ladanyi, M.1
Parsa, N.Z.2
Offit, K.3
Wachtel, M.S.4
Filippa, D.A.5
Jhanwar, S.C.6
-
16
-
-
0028802240
-
Non-random distribution of spontaneous chromosome aberrations in two Bloom Syndrome patients
-
Fundia A., Gorla N., Larripa I. Non-random distribution of spontaneous chromosome aberrations in two Bloom Syndrome patients. Hereditas. 122:1995;239-243.
-
(1995)
Hereditas
, vol.122
, pp. 239-243
-
-
Fundia, A.1
Gorla, N.2
Larripa, I.3
-
17
-
-
0028198465
-
Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints
-
Fundia A., Gorla N., Larripa I. Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints. Hereditas. 120:1994;47-50.
-
(1994)
Hereditas
, vol.120
, pp. 47-50
-
-
Fundia, A.1
Gorla, N.2
Larripa, I.3
-
18
-
-
0032520975
-
Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21
-
Willis T.G., Zalcberg I.R., Coignet L.J., Wlodarska I., Stul M., Jadayel D.M., Bastard C., Treleaven J.G., Catovsky D., Silva M.L., Dyer M.J. Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21. Blood. 91:1998;1873-1881.
-
(1998)
Blood
, vol.91
, pp. 1873-1881
-
-
Willis, T.G.1
Zalcberg, I.R.2
Coignet, L.J.3
Wlodarska, I.4
Stul, M.5
Jadayel, D.M.6
Bastard, C.7
Treleaven, J.G.8
Catovsky, D.9
Silva, M.L.10
Dyer, M.J.11
-
19
-
-
0027957089
-
Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL 1 maps to human chromosome 1q21,a region that is frequently altered in preneoplastic and neoplastic disease
-
Craig R.W., Jabs E.W., Zhou P., Kozopas K.M., Hawkins A.L., Rochelle J.M., Seldin M.F., Griffin C.A. Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene. MCL 1 maps to human chromosome 1q21,a region that is frequently altered in preneoplastic and neoplastic disease Genomics. 23:1994;457-463.
-
(1994)
Genomics
, vol.23
, pp. 457-463
-
-
Craig, R.W.1
Jabs, E.W.2
Zhou, P.3
Kozopas, K.M.4
Hawkins, A.L.5
Rochelle, J.M.6
Seldin, M.F.7
Griffin, C.A.8
-
20
-
-
0027535559
-
Toward an understanding of the molecular mechanisms of physiological cell death
-
Vaux D.L. Toward an understanding of the molecular mechanisms of physiological cell death. Proc Natl Acad Sci USA. 90:1993;786-789.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 786-789
-
-
Vaux, D.L.1
-
21
-
-
0028350579
-
PE-1, a novel ETS oncogene family member, localizes to chromosome 1q21-23
-
Klemsz M., Hromas R., Raskind W., Bruno E., Hoffman R. PE-1, a novel ETS oncogene family member, localizes to chromosome 1q21-23. Genomics. 20:1994;291-294.
-
(1994)
Genomics
, vol.20
, pp. 291-294
-
-
Klemsz, M.1
Hromas, R.2
Raskind, W.3
Bruno, E.4
Hoffman, R.5
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