-
1
-
-
0028979666
-
Prognostic significance of karyotype in de novo adult acute myeloid leukemia
-
Dastugue N, Payen C, Lafage-Pochitaloff M, Bernard P, Leroux D, Huguet-Rigal F, Stoppa A-M, Marit G, Molina L, Michallet M, Maraninchi D, Attal M, Reiffers J. Prognostic significance of karyotype in de novo adult acute myeloid leukemia. Leukemia 1995; 9: 1491-1498.
-
(1995)
Leukemia
, vol.9
, pp. 1491-1498
-
-
Dastugue, N.1
Payen, C.2
Lafage-Pochitaloff, M.3
Bernard, P.4
Leroux, D.5
Huguet-Rigal, F.6
Stoppa, A.-M.7
Marit, G.8
Molina, L.9
Michallet, M.10
Maraninchi, D.11
Attal, M.12
Reiffers, J.13
-
2
-
-
0022135739
-
Proposed revised criteria for the classification of acute myeloid leukemia
-
Bennett JM, Catovsky D, Daniel MT, Flandrin G, Galton DAG, Gralnick HR, Sultan C. Proposed revised criteria for the classification of acute myeloid leukemia. Ann Intern Med 1985; 103: 626-629.
-
(1985)
Ann Intern Med
, vol.103
, pp. 626-629
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
Flandrin, G.4
Galton, D.A.G.5
Gralnick, H.R.6
Sultan, C.7
-
3
-
-
0023857049
-
Chromosome change at 16q22 in nonlymphocytic leukemia. Clinical implication on leukemia patients with inv(16) versus del(16)
-
Ohyashiki K, Ohyashiki JH, Kondo M, Toyama K. Chromosome change at 16q22 in nonlymphocytic leukemia. Clinical implication on leukemia patients with inv(16) versus del(16). Leukemia 1988; 2: 35-40.
-
(1988)
Leukemia
, vol.2
, pp. 35-40
-
-
Ohyashiki, K.1
Ohyashiki, J.H.2
Kondo, M.3
Toyama, K.4
-
4
-
-
0026728034
-
Quantitative acute leukemia cytogenetics
-
Mitelman F, Heim S. Quantitative acute leukemia cytogenetics. Genes Chromosom Cancer 1992; 5: 57-66.
-
(1992)
Genes Chromosom Cancer
, vol.5
, pp. 57-66
-
-
Mitelman, F.1
Heim, S.2
-
5
-
-
20244365471
-
Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias
-
Poirel H, Radford-Weiss I, Rack K, Troussard X, Veile A, Valensi F, Picard F, Guesnu M, Leboeuf D, Melle J. Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias. Blood 1995; 85: 1313-1322.
-
(1995)
Blood
, vol.85
, pp. 1313-1322
-
-
Poirel, H.1
Radford-Weiss, I.2
Rack, K.3
Troussard, X.4
Veile, A.5
Valensi, F.6
Picard, F.7
Guesnu, M.8
Leboeuf, D.9
Melle, J.10
-
7
-
-
0024424668
-
Acute nonlymphocytic leukemia with marrow eosinophilia and chromosome 16 abnormality: A report of 18 cases
-
Bernard P, Cachary D, Reiffers J, Marit G, Wen Z, Jonveaux P, David B, Lacombe F, Braustet A. Acute nonlymphocytic leukemia with marrow eosinophilia and chromosome 16 abnormality: a report of 18 cases. Leukemia 1989; 3: 740-745.
-
(1989)
Leukemia
, vol.3
, pp. 740-745
-
-
Bernard, P.1
Cachary, D.2
Reiffers, J.3
Marit, G.4
Wen, Z.5
Jonveaux, P.6
David, B.7
Lacombe, F.8
Braustet, A.9
-
8
-
-
0028221769
-
Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia
-
Claxton DF, Liu P, Hsu HB, Marlton P, Hester J, Collins F, Deisseroth AB, Rowley JD, Siciliano MJ. Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia. Blood 1994; 83: 1750-1756.
-
(1994)
Blood
, vol.83
, pp. 1750-1756
-
-
Claxton, D.F.1
Liu, P.2
Hsu, H.B.3
Marlton, P.4
Hester, J.5
Collins, F.6
Deisseroth, A.B.7
Rowley, J.D.8
Siciliano, M.J.9
-
9
-
-
0029097178
-
Detection of CBFB/MYH11 transcripts in patients with inversion and other abnormalities of chromosome 16 at presentation and remission
-
Tobal K, Johnson PR, Saunders MJ, Harrison CJ, Liu Yin JA. Detection of CBFB/MYH11 transcripts in patients with inversion and other abnormalities of chromosome 16 at presentation and remission. Br J Haematol 1995; 91: 104-108.
-
(1995)
Br J Haematol
, vol.91
, pp. 104-108
-
-
Tobal, K.1
Johnson, P.R.2
Saunders, M.J.3
Harrison, C.J.4
Liu Yin, J.A.5
-
10
-
-
0028979457
-
Heterogeneity in CBFb/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia
-
Shurtleff SA, Meyers S, Hiebert SW, Raimondi SC, Head DR, Willman CL, Wolman S, Slovak ML, Carroll AJ, Behm F, Hulshof MG, Motroni TA, Okuda T, Pu L, Collins FS, Downing JR. Heterogeneity in CBFb/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia. Blood 1995; 85: 3695-3703.
-
(1995)
Blood
, vol.85
, pp. 3695-3703
-
-
Shurtleff, S.A.1
Meyers, S.2
Hiebert, S.W.3
Raimondi, S.C.4
Head, D.R.5
Willman, C.L.6
Wolman, S.7
Slovak, M.L.8
Carroll, A.J.9
Behm, F.10
Hulshof, M.G.11
Motroni, T.A.12
Okuda, T.13
Pu, L.14
Collins, F.S.15
Downing, J.R.16
-
11
-
-
0029161440
-
Novel CBFb-MYH11 fusion transcripts and alternative splicing in acute myeloid leukemia with inversion of chromosome 16
-
Novak M, Laczika K, Mitterbauer M, Purtscher B, Scheidel-Petrovic A, Lechner K, Jaeger U. Novel CBFb-MYH11 fusion transcripts and alternative splicing in acute myeloid leukemia with inversion of chromosome 16. Blood 1995; 86: 2449-2450.
-
(1995)
Blood
, vol.86
, pp. 2449-2450
-
-
Novak, M.1
Laczika, K.2
Mitterbauer, M.3
Purtscher, B.4
Scheidel-Petrovic, A.5
Lechner, K.6
Jaeger, U.7
-
12
-
-
0027373893
-
Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia
-
Liu P, Tarie SA, Hajra A, Claxton DF, Marlton P, Freedman M, Siciliano MJ, Collins FS. Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia. Science 1993; 261: 1041-1044.
-
(1993)
Science
, vol.261
, pp. 1041-1044
-
-
Liu, P.1
Tarie, S.A.2
Hajra, A.3
Claxton, D.F.4
Marlton, P.5
Freedman, M.6
Siciliano, M.J.7
Collins, F.S.8
-
13
-
-
0029004047
-
Structure of the leukemia-associated human CBF/3 gene
-
Hajra A, Collins FS, Structure of the leukemia-associated human CBF/3 gene. Genomics 1995; 26: 571-579.
-
(1995)
Genomics
, vol.26
, pp. 571-579
-
-
Hajra, A.1
Collins, F.S.2
-
14
-
-
0027509732
-
Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12
-
Matsuoka R, Yoshida MC, Furutani Y, Imamura S, Kanda N, Yanagisawa M, Masaki T, Takao A. Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12. Am J Med Genet 1993; 46: 61-67.
-
(1993)
Am J Med Genet
, vol.46
, pp. 61-67
-
-
Matsuoka, R.1
Yoshida, M.C.2
Furutani, Y.3
Imamura, S.4
Kanda, N.5
Yanagisawa, M.6
Masaki, T.7
Takao, A.8
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