-
1
-
-
0031799784
-
Chromosome region 8p11-p21: Refined mapping and molecular alterations in breast cancer
-
Adélaïde J, Chaffanet M, Imbert A, Allione F, Geneix J, Popovici C, Van Alewijk D, Trapman J, Zeillinger R, Borresen-Dale A-L, Lidereau R, Birnbaum D, Pébusque M-J. 1998. Chromosome region 8p11-p21: refined mapping and molecular alterations in breast cancer. Genes Chromosomes Cancer 22:186-199.
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 186-199
-
-
Adélaïde, J.1
Chaffanet, M.2
Imbert, A.3
Allione, F.4
Geneix, J.5
Popovici, C.6
Van Alewijk, D.7
Trapman, J.8
Zeillinger, R.9
Borresen-Dale, A.-L.10
Lidereau, R.11
Birnbaum, D.12
Pébusque, M.-J.13
-
2
-
-
0030480969
-
The CBP co-activator is a histone acetyltransferase
-
Bannister AJ, Kouzarides T. 1996. The CBP co-activator is a histone acetyltransferase. Nature 384:641-643.
-
(1996)
Nature
, vol.384
, pp. 641-643
-
-
Bannister, A.J.1
Kouzarides, T.2
-
3
-
-
9544220768
-
The translocation t(8;16)(p11;p13) of acute myeloid leukemia fuses a putative acetyl transferase to the CREB-binding protein
-
Borrow J, Stanton VP Jr, Andressen JM, Becher R, Behm FG, Chaganti RSK, Civin CI, Disteche C, Dubé I, Frischauf AM, Hosman D, Mitelman F, Volinia S, Watmore AE, Housman DE. 1996. The translocation t(8;16)(p11;p13) of acute myeloid leukemia fuses a putative acetyl transferase to the CREB-binding protein. Nat Genet 14:33-41.
-
(1996)
Nat Genet
, vol.14
, pp. 33-41
-
-
Borrow, J.1
Stanton V.P., Jr.2
Andressen, J.M.3
Becher, R.4
Behm, F.G.5
Chaganti, R.S.K.6
Civin, C.I.7
Disteche, C.8
Dubé, I.9
Frischauf, A.M.10
Hosman, D.11
Mitelman, F.12
Volinia, S.13
Watmore, A.E.14
Housman, D.E.15
-
4
-
-
0032080173
-
A novel fusion between MOZ and the nuclear receptor coactivator TIF2 in acute myeloid leukemia
-
Carapeti M, Aguiar RCT, Goldman JM, Cross NCP. 1998. A novel fusion between MOZ and the nuclear receptor coactivator TIF2 in acute myeloid leukemia. Blood 91:3127-3133.
-
(1998)
Blood
, vol.91
, pp. 3127-3133
-
-
Carapeti, M.1
Aguiar, R.C.T.2
Goldman, J.M.3
Cross, N.C.P.4
-
5
-
-
0030057689
-
A 3.1 Mb YAC contig within the Werner syndrome region, on the short arm of chromosome 8
-
Chaffanet M, Imbert A, Adélaïde J, Le Paslier D, Wagner MJ, Wells DE, Birnbaum D, Pébusque M-J. 1996. A 3.1 Mb YAC contig within the Werner syndrome region, on the short arm of chromosome 8. Cytogenet Cell Genet 72:63-68.
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 63-68
-
-
Chaffanet, M.1
Imbert, A.2
Adélaïde, J.3
Le Paslier, D.4
Wagner, M.J.5
Wells, D.E.6
Birnbaum, D.7
Pébusque, M.-J.8
-
6
-
-
14444277275
-
t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12
-
Chaffanet M, Popovici C, Leroux D, Jacrot M, Adélaïde J, Dastugue N, Grégoire M-J, Hagemeijer A, Lafage-Potchitaloff M, Birnbaum D, Pébusque M-J. 1998. t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12. Oncogene 16:945-949.
-
(1998)
Oncogene
, vol.16
, pp. 945-949
-
-
Chaffanet, M.1
Popovici, C.2
Leroux, D.3
Jacrot, M.4
Adélaïde, J.5
Dastugue, N.6
Grégoire, M.-J.7
Hagemeijer, A.8
Lafage-Potchitaloff, M.9
Birnbaum, D.10
Pébusque, M.-J.11
-
7
-
-
0031811538
-
Two cases of inv(8)(p11q13) in AML with erythrophagocytosis: A new cytogenetic variant
-
Coulthard S, Chase A, Orchard K, Watmore A, Vora A, Goldman JM, Swirsky DM. 1998. Two cases of inv(8)(p11q13) in AML with erythrophagocytosis: a new cytogenetic variant. Br J Haematol 100:561-563.
-
(1998)
Br J Haematol
, vol.100
, pp. 561-563
-
-
Coulthard, S.1
Chase, A.2
Orchard, K.3
Watmore, A.4
Vora, A.5
Goldman, J.M.6
Swirsky, D.M.7
-
8
-
-
0026317492
-
Complex chromosomal translocations in the Philadelphia chromosome leukemias: Serial translocations or a concerted genomic rearrangement?
-
Fitzgerald P, Morris C. 1991. Complex chromosomal translocations in the Philadelphia chromosome leukemias: serial translocations or a concerted genomic rearrangement? Cancer Genet Cytogenet 57: 143-151.
-
(1991)
Cancer Genet Cytogenet
, vol.57
, pp. 143-151
-
-
Fitzgerald, P.1
Morris, C.2
-
9
-
-
0031570335
-
Construction of a 1.2-Mb contig surrounding, and molecular analysis of the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3
-
Giles RH, Petrij F, Dauwerse HG, den Hollander AI, Lushnikova T, van Ommen G-JB, Goodman RH, Deaven LL, Doggett NA, Peters DJM, Breuning MH. 1997. Construction of a 1.2-Mb contig surrounding, and molecular analysis of the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3. Genomics 42:96-114.
-
(1997)
Genomics
, vol.42
, pp. 96-114
-
-
Giles, R.H.1
Petrij, F.2
Dauwerse, H.G.3
Den Hollander, A.I.4
Lushnikova, T.5
Van Ommen, G.-J.B.6
Goodman, R.H.7
Deaven, L.L.8
Doggett, N.A.9
Peters, D.J.M.10
Breuning, M.H.11
-
13
-
-
0023245048
-
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia
-
Heim S, Avanzi GC, Billstrom R, Kristoffersson U, Mandahl N, Bekassy AN, Garwicz S, Wiebe T, Pegoraro L, Falda M, Resegotti L, Mitelman F. 1987. A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia. Br J Haematol 66:323-326.
-
(1987)
Br J Haematol
, vol.66
, pp. 323-326
-
-
Heim, S.1
Avanzi, G.C.2
Billstrom, R.3
Kristoffersson, U.4
Mandahl, N.5
Bekassy, A.N.6
Garwicz, S.7
Wiebe, T.8
Pegoraro, L.9
Falda, M.10
Resegotti, L.11
Mitelman, F.12
-
15
-
-
0023264187
-
Three cases of translocation (8;16)(p11;p13) observed in acute myelomonocytic leukemia: A new specific subgroup?
-
Lai JL, Zandecki M, Jouet JP, Savary JB, Lambiliotte A, Bauters F, Cosson A, Deminatti M. 1987. Three cases of translocation (8;16)(p11;p13) observed in acute myelomonocytic leukemia: a new specific subgroup? Cancer Genet Cytogenet 27:101-109.
-
(1987)
Cancer Genet Cytogenet
, vol.27
, pp. 101-109
-
-
Lai, J.L.1
Zandecki, M.2
Jouet, J.P.3
Savary, J.B.4
Lambiliotte, A.5
Bauters, F.6
Cosson, A.7
Deminatti, M.8
-
16
-
-
0026659823
-
Acute monocytic leukemia with (8;22)(p11;q13) translocation: Involvement of 8p11 as in classical t(8;16)(p11;p13)
-
Lai JL, Zandecki M, Fenaux P, Preudhomme C, Facon T, Deminatti M. 1992. Acute monocytic leukemia with (8;22)(p11;q13) translocation: involvement of 8p11 as in classical t(8;16)(p11;p13). Cancer Genet Cytogenet 60:180-182.
-
(1992)
Cancer Genet Cytogenet
, vol.60
, pp. 180-182
-
-
Lai, J.L.1
Zandecki, M.2
Fenaux, P.3
Preudhomme, C.4
Facon, T.5
Deminatti, M.6
-
17
-
-
0032530267
-
Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2
-
Liang J, Prouty L, Williams BJ, Dayton MA, Blanchard KL. 1998. Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2. Blood 92:2118-2122.
-
(1998)
Blood
, vol.92
, pp. 2118-2122
-
-
Liang, J.1
Prouty, L.2
Williams, B.J.3
Dayton, M.A.4
Blanchard, K.L.5
-
18
-
-
0028869005
-
A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: A review
-
Macdonald D, Aguiar RC, Mason PJ, Goldman JM, Cross NC. 1995. A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review. Leukemia 9:1628-1630.
-
(1995)
Leukemia
, vol.9
, pp. 1628-1630
-
-
Macdonald, D.1
Aguiar, R.C.2
Mason, P.J.3
Goldman, J.M.4
Cross, N.C.5
-
20
-
-
0030606239
-
The transcriptional coactivators p300 and CBP are histone acetyltransferases
-
Ogryzko VV, Schiltz RL, Russanova V, Howard BH, Nakatani Y. 1996. The transcriptional coactivators p300 and CBP are histone acetyltransferases. Cell 87:953-959.
-
(1996)
Cell
, vol.87
, pp. 953-959
-
-
Ogryzko, V.V.1
Schiltz, R.L.2
Russanova, V.3
Howard, B.H.4
Nakatani, Y.5
-
21
-
-
0032510791
-
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12)
-
Popovici C, Adélaïde J, Ollendorff V, Chaffanet M, Guasch G, Jacrot M, Leroux D, Birnbaum D, Pébusque M-J. 1998. Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13)(p12;q12). Proc Natl Acad Sci USA 95:5712-5717.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 5712-5717
-
-
Popovici, C.1
Adélaïde, J.2
Ollendorff, V.3
Chaffanet, M.4
Guasch, G.5
Jacrot, M.6
Leroux, D.7
Birnbaum, D.8
Pébusque, M.-J.9
-
22
-
-
0033558253
-
The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1
-
Popovici C, Zhang B, Grégoire M-J, Jonveaux P, Lafage-Pochitaloff M, Birnbaum D, Pébusque M-J. 1999. The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. Blood 93:1381-1389.
-
(1999)
Blood
, vol.93
, pp. 1381-1389
-
-
Popovici, C.1
Zhang, B.2
Grégoire, M.-J.3
Jonveaux, P.4
Lafage-Pochitaloff, M.5
Birnbaum, D.6
Pébusque, M.-J.7
-
23
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome
-
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Goncalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC. 1998. Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. Blood 92:1735-1742.
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
Chase, A.4
Macdonald, D.H.5
Aguiar, R.C.6
Goncalves, C.7
Hernandez, J.M.8
Jennings, B.A.9
Goldman, J.M.10
Cross, N.C.11
-
24
-
-
6844255886
-
The t(8;13)(p11; q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP
-
Smedley D, Hamoudi R, Clark J, Warren W, Abdul-Rauf M, Somers G, Venter D, Fagan K, Cooper C, Shipley J. 1998. The t(8;13)(p11; q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. Hum Mol Genet 7:637-642.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 637-642
-
-
Smedley, D.1
Hamoudi, R.2
Clark, J.3
Warren, W.4
Abdul-Rauf, M.5
Somers, G.6
Venter, D.7
Fagan, K.8
Cooper, C.9
Shipley, J.10
-
25
-
-
0029001261
-
A distinct subtype of M4/M5 acute myeloblastic leukemia (AML) associated with t(8;16)(p11;p13), in a patient with the variant t(8;19)(p11;q13): Case report and review of the literature
-
Stark B, Resnitzky P, Jeison M, Luria D, Blau O, Avigad S, Shaft D, Kodman Y, Gobuzov R, Ash S, Stein J, Yaniv I, Barak Y, Zaizov R. 1995. A distinct subtype of M4/M5 acute myeloblastic leukemia (AML) associated with t(8;16)(p11;p13), in a patient with the variant t(8;19)(p11;q13): case report and review of the literature. Leuk Res 19:367-379.
-
(1995)
Leuk Res
, vol.19
, pp. 367-379
-
-
Stark, B.1
Resnitzky, P.2
Jeison, M.3
Luria, D.4
Blau, O.5
Avigad, S.6
Shaft, D.7
Kodman, Y.8
Gobuzov, R.9
Ash, S.10
Stein, J.11
Yaniv, I.12
Barak, Y.13
Zaizov, R.14
-
26
-
-
0032518944
-
The coactivator TIF2 contains three nuclear receptor-binding motifs and mediates transactivation through CBP binding-dependent and -independent pathways
-
Voegel JJ, Heine MJ, Tini M, Vivat V, Chambon P, Gronemeyer H. 1998. The coactivator TIF2 contains three nuclear receptor-binding motifs and mediates transactivation through CBP binding-dependent and -independent pathways. EMBO J 17:507-519.
-
(1998)
EMBO J
, vol.17
, pp. 507-519
-
-
Voegel, J.J.1
Heine, M.J.2
Tini, M.3
Vivat, V.4
Chambon, P.5
Gronemeyer, H.6
-
27
-
-
17344373285
-
FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome
-
Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, Weissman SM, Hudson TJ, Fletcher JA. 1998. FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome. Nat Genet 18:84-87.
-
(1998)
Nat Genet
, vol.18
, pp. 84-87
-
-
Xiao, S.1
Nalabolu, S.R.2
Aster, J.C.3
Ma, J.4
Abruzzo, L.5
Jaffe, E.S.6
Stone, R.7
Weissman, S.M.8
Hudson, T.J.9
Fletcher, J.A.10
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