-
1
-
-
0028326283
-
The balanced and the unbalanced chromosome aberrations of acute myeloid leukemia may develop in different ways and may contribute differently to malignant transformaton
-
Pedersen-Bjergaard J, Rowley JD. The balanced and the unbalanced chromosome aberrations of acute myeloid leukemia may develop in different ways and may contribute differently to malignant transformaton. Blood 83:2780-2786, 1994.
-
(1994)
Blood
, vol.83
, pp. 2780-2786
-
-
Pedersen-Bjergaard, J.1
Rowley, J.D.2
-
2
-
-
0030916736
-
The inv(II)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene. DDX10
-
Arai Y, Hosoda F, Kobayashi H, et al. The inv(II)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene. DDX10. Blood 89: 3936-3944, 1997.
-
(1997)
Blood
, vol.89
, pp. 3936-3944
-
-
Arai, Y.1
Hosoda, F.2
Kobayashi, H.3
-
3
-
-
0019952276
-
Proposals for the classification of the myelodysplastic syndromes
-
Bennett JM, Catovsky D, Daniel MT, et al. Proposals for the classification of the myelodysplastic syndromes. Br J Haematol 51: 189-199, 1982.
-
(1982)
Br J Haematol
, vol.51
, pp. 189-199
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
-
4
-
-
0025769346
-
Increased risk of myelodysplasia and leukaemia after etoposide, cisplatin, and bleomycin for germ-cell tumours
-
Pedersen-Bjergaard J, Daugaard G, Hansen SW, et al. Increased risk of myelodysplasia and leukaemia after etoposide, cisplatin, and bleomycin for germ-cell tumours. Lancet 338: 359-363, 1991.
-
(1991)
Lancet
, vol.338
, pp. 359-363
-
-
Pedersen-Bjergaard, J.1
Daugaard, G.2
Hansen, S.W.3
-
5
-
-
0025995996
-
Epipodophyllotoxin-related leukemia: Identification of a new subset of secondary leukemia
-
Whitlock JA, Greer JP, Lukens JN. Epipodophyllotoxin-related leukemia: Identification of a new subset of secondary leukemia. Cancer 68: 600-604, 1991.
-
(1991)
Cancer
, vol.68
, pp. 600-604
-
-
Whitlock, J.A.1
Greer, J.P.2
Lukens, J.N.3
-
6
-
-
0025222615
-
Chromosome aberrations induced by etoposide (VP-16) are not random
-
Maraschin J, Dutrillaux B, Aurias A. Chromosome aberrations induced by etoposide (VP-16) are not random. Int J Cancer 46: 808-812, 1990.
-
(1990)
Int J Cancer
, vol.46
, pp. 808-812
-
-
Maraschin, J.1
Dutrillaux, B.2
Aurias, A.3
-
7
-
-
0030976312
-
Inversion of chromosome 11, inv (11) (p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: Identification of a P1 clone spanning the 11q22 breakpoint
-
Kobayashi H, Arai Y, Hosoda F, et al. Inversion of chromosome 11, inv (11) (p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: Identification of a P1 clone spanning the 11q22 breakpoint. Genes Chromosom Cancer 19; 150-155, 1997.
-
(1997)
Genes Chromosom Cancer
, vol.19
, pp. 150-155
-
-
Kobayashi, H.1
Arai, Y.2
Hosoda, F.3
-
8
-
-
0028325337
-
A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities
-
Yamamoto K, Seto M, Iida S, et al. A reverse transcriptase-polymerase chain reaction detects heterogeneous chimeric mRNAs in leukemias with 11q23 abnormalities. Blood 83: 2912-2921, 1994.
-
(1994)
Blood
, vol.83
, pp. 2912-2921
-
-
Yamamoto, K.1
Seto, M.2
Iida, S.3
-
9
-
-
0029925097
-
A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23
-
Savitsky K, Ziv Y, Bar-Shira A, et al. A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23. Genomics 33: 199-206, 1996.
-
(1996)
Genomics
, vol.33
, pp. 199-206
-
-
Savitsky, K.1
Ziv, Y.2
Bar-Shira, A.3
-
10
-
-
0026569419
-
D-E-A-D protein family of putative RNA helicases
-
Schmid SR, Linder P. D-E-A-D protein family of putative RNA helicases. Mol Microbiol 6: 283-292, 1992.
-
(1992)
Mol Microbiol
, vol.6
, pp. 283-292
-
-
Schmid, S.R.1
Linder, P.2
-
11
-
-
9044241254
-
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t (7;11) (p15;p15) in human myeloid leukaemia
-
Nakamura T, Largaespada DA, Lee MP, et al. Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t (7;11) (p15;p15) in human myeloid leukaemia. Nature Genet 12: 154-158, 1996.
-
(1996)
Nature Genet
, vol.12
, pp. 154-158
-
-
Nakamura, T.1
Largaespada, D.A.2
Lee, M.P.3
-
12
-
-
9044249724
-
The t (7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9
-
Borrow J, Shearman AM, Stanton Jr VP, et al. The t (7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9. Nature Genet 12: 159-167, 1996.
-
(1996)
Nature Genet
, vol.12
, pp. 159-167
-
-
Borrow, J.1
Shearman, A.M.2
Stanton Jr., V.P.3
-
13
-
-
0029021567
-
The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex
-
Radu A, Moore MS, Blobel G. The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex. Cell 81: 215-222, 1995.
-
(1995)
Cell
, vol.81
, pp. 215-222
-
-
Radu, A.1
Moore, M.S.2
Blobel, G.3
|