-
1
-
-
0030894499
-
The TEL gene contributes to the pathogenesis of myeloid and lymphoid leukemias by diverse molecular genetic mechanisms
-
Golub TR, Barker GF, Stegmaier K, Gilliland DG. The TEL gene contributes to the pathogenesis of myeloid and lymphoid leukemias by diverse molecular genetic mechanisms. Curr Top Microbiol Immunol. 1997;220:67-79.
-
(1997)
Curr Top Microbiol Immunol.
, vol.220
, pp. 67-79
-
-
Golub, T.R.1
Barker, G.F.2
Stegmaier, K.3
Gilliland, D.G.4
-
2
-
-
0033570032
-
TEL is a sequence-specific transcriptional repressor
-
Lopez RG, Carron C, Oury C, Gardellin P, Bernard O, Ghysdael J. TEL is a sequence-specific transcriptional repressor. J Biol Chem. 1999;274(42):30132-8.
-
(1999)
J Biol Chem.
, vol.274
, Issue.42
, pp. 30132-30138
-
-
Lopez, R.G.1
Carron, C.2
Oury, C.3
Gardellin, P.4
Bernard, O.5
Ghysdael, J.6
-
3
-
-
17044429678
-
ETV6: A versatile player in leukemogenesis
-
Bohlander SK. ETV6: a versatile player in leukemogenesis. Semin Cancer Biol. 2005;15(3):162-74.
-
(2005)
Semin Cancer Biol.
, vol.15
, Issue.3
, pp. 162-174
-
-
Bohlander, S.K.1
-
4
-
-
4644274431
-
Tel/Etv6 is an essential and selective regulator of adult hematopoietic stem cell survival
-
Hock H, Meade E, Medeiros S, Schindler JW, Valk PJ, Fujiwara Y, et al. Tel/Etv6 is an essential and selective regulator of adult hematopoietic stem cell survival. Genes Dev. 2004;18(19):2336-41.
-
(2004)
Genes Dev.
, vol.18
, Issue.19
, pp. 2336-2341
-
-
Hock, H.1
Meade, E.2
Medeiros, S.3
Schindler, J.W.4
Valk, P.J.5
Fujiwara, Y.6
-
5
-
-
33847204694
-
Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia
-
Attarbaschi A, Mann G, Strehl S, Konig M, Steiner M, Jeitler V, et al. Deletion of 11q23 is a highly specific nonrandom secondary genetic abnormality of ETV6/RUNX1-rearranged childhood acute lymphoblastic leukemia. Leukemia. 2007;21(3):584-6.
-
(2007)
Leukemia.
, vol.21
, Issue.3
, pp. 584-586
-
-
Attarbaschi, A.1
Mann, G.2
Strehl, S.3
Konig, M.4
Steiner, M.5
Jeitler, V.6
-
6
-
-
84870465632
-
ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7
-
Wall M, Rayeroux KC, MacKinnon RN, Zordan A, Campbell LJ. ETV6 deletion is a common additional abnormality in patients with myelodysplastic syndromes or acute myeloid leukemia and monosomy 7. Haematologica. 2012;97(12):1933-6.
-
(2012)
Haematologica
, vol.97
, Issue.12
, pp. 1933-1936
-
-
Wall, M.1
Rayeroux, K.C.2
McKinnon, R.N.3
Zordan, A.4
Campbell, L.J.5
-
7
-
-
0035022501
-
Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping
-
Odero MD, Carlson K, Calasanz MJ, Lahortiga I, Chinwalla V, Rowley JD. Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping. Genes Chromosomes Cancer. 2001;31(2): 134-42.
-
(2001)
Genes Chromosomes Cancer.
, vol.31
, Issue.2
, pp. 134-142
-
-
Odero, M.D.1
Carlson, K.2
Calasanz, M.J.3
Lahortiga, I.4
Chinwalla, V.5
Rowley, J.D.6
-
8
-
-
0028224348
-
Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
-
Golub TR, Barker GF, Lovett M, Gilliland DG. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell. 1994;77(2):307-16.
-
(1994)
Cell.
, vol.77
, Issue.2
, pp. 307-316
-
-
Golub, T.R.1
Barker, G.F.2
Lovett, M.3
Gilliland, D.G.4
-
9
-
-
84862532344
-
ETV6 fusion genes in hematological malignancies: A review
-
De Braekeleer E, Douet-Guilbert N, Morel F, Le Bris MJ, Basinko A, De Braekeleer M. ETV6 fusion genes in hematological malignancies: a review. Leuk Res. 2012;36(8):945-61.
-
(2012)
Leuk Res.
, vol.36
, Issue.8
, pp. 945-961
-
-
De Braekeleer, E.1
Douet-Guilbert, N.2
Morel, F.3
Le Bris, M.J.4
Basinko, A.5
De Braekeleer, M.6
-
10
-
-
16944367034
-
ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia
-
Cave H, Cacheux V, Raynaud S, Brunie G, Bakkus M, Cochaux P, et al. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia. Leukemia. 1997;11(9):1459-64.
-
(1997)
Leukemia.
, vol.11
, Issue.9
, pp. 1459-1464
-
-
Cave, H.1
Cacheux, V.2
Raynaud, S.3
Brunie, G.4
Bakkus, M.5
Cochaux, P.6
-
11
-
-
79959794787
-
Clinical effect of point mutations in myelodysplastic syndromes
-
Bejar R, Stevenson K, Abdel-Wahab O, Galili N, Nilsson B, Garcia-Manero G, et al. Clinical effect of point mutations in myelodysplastic syndromes. N Engl J Med. 2011;364(26):2496-506.
-
(2011)
N Engl J Med.
, vol.364
, Issue.26
, pp. 2496-2506
-
-
Bejar, R.1
Stevenson, K.2
Abdel-Wahab, O.3
Galili, N.4
Nilsson, B.5
Garcia-Manero, G.6
-
12
-
-
84862907593
-
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
-
Zhang J, Ding L, Holmfeldt L, Wu G, Heatley SL, Payne-Turner D, et al. The genetic basis of early T-cell precursor acute lymphoblastic leukaemia. Nature. 2012;481(7380):157-63.
-
(2012)
Nature.
, vol.481
, Issue.7380
, pp. 157-163
-
-
Zhang, J.1
Ding, L.2
Holmfeldt, L.3
Wu, G.4
Heatley, S.L.5
Payne-Turner, D.6
-
13
-
-
84855508998
-
ETV6 mutations in early immature human T cell leukemias
-
Van Vlierberghe P, Ambesi-Impiombato A, Perez-Garcia A, Haydu JE, Rigo I, Hadler M, et al. ETV6 mutations in early immature human T cell leukemias. J Exp Med. 2011;208(13):2571-9.
-
(2011)
J Exp Med.
, vol.208
, Issue.13
, pp. 2571-2579
-
-
Van Vlierberghe, P.1
Ambesi-Impiombato, A.2
Perez-Garcia, A.3
Haydu, J.E.4
Rigo, I.5
Hadler, M.6
-
14
-
-
21344448655
-
Somatic heterozygous mutations in ETV6 (TEL) and frequent absence of ETV6 protein in acute myeloid leukemia
-
Barjesteh van Waalwijk van Doorn-Khosrovani S, Spensberger D, de Knegt Y, Tang M, Lowenberg B, Delwel R. Somatic heterozygous mutations in ETV6 (TEL) and frequent absence of ETV6 protein in acute myeloid leukemia. Oncogene. 2005;24(25):4129-37.
-
(2005)
Oncogene.
, vol.24
, Issue.25
, pp. 4129-4137
-
-
Barjesteh van Waalwijk van Doorn-Khosrovani, S.1
Spensberger, D.2
de Knegt, Y.3
Tang, M.4
Lowenberg, B.5
Delwel, R.6
-
15
-
-
6344289461
-
Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: An interphase FISH analysis
-
Attarbaschi A, Mann G, Konig M, Dworzak MN, Trebo MM, Muhlegger N, et al. Incidence and relevance of secondary chromosome abnormalities in childhood TEL/AML1+ acute lymphoblastic leukemia: an interphase FISH analysis. Leukemia. 2004;18(10): 1611-6.
-
(2004)
Leukemia.
, vol.18
, Issue.10
, pp. 1611-1616
-
-
Attarbaschi, A.1
Mann, G.2
Konig, M.3
Dworzak, M.N.4
Trebo, M.M.5
Muhlegger, N.6
|