-
1
-
-
0030903602
-
Clinical features and treatment outcome of childhood T-lineage acute lymphoblastic leukemia according to the apparent maturational stage of T-lineage leukemic blasts: A Children's Cancer Group study
-
Uckun FM, Gaynon PS, Sensel MG, Nachman J, Trigg ME, Steinherz PG, et al. Clinical features and treatment outcome of childhood T-lineage acute lymphoblastic leukemia according to the apparent maturational stage of T-lineage leukemic blasts: a Children's Cancer Group study. J Clin Oncol. 1997;15(6):2214-2221.
-
(1997)
J Clin Oncol
, vol.15
, Issue.6
, pp. 2214-2221
-
-
Uckun, F.M.1
Gaynon, P.S.2
Sensel, M.G.3
Nachman, J.4
Trigg, M.E.5
Steinherz, P.G.6
-
2
-
-
78650305754
-
The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function
-
Kox C, Zimmermann M, Stanulla M, Leible S, Schrappe M, Ludwig WD, et al. The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function. Leukemia. 2010;24(12):2005-2013.
-
(2010)
Leukemia
, vol.24
, Issue.12
, pp. 2005-2013
-
-
Kox, C.1
Zimmermann, M.2
Stanulla, M.3
Leible, S.4
Schrappe, M.5
Ludwig, W.D.6
-
3
-
-
33747155025
-
Activating NOTCH1 mutations predict favorable early treatment response and long-term outcome in childhood precursor T-cell lymphoblastic leukemia
-
Breit S, Stanulla M, Flohr T, Schrappe M, Ludwig WD, Tolle G, et al. Activating NOTCH1 mutations predict favorable early treatment response and long-term outcome in childhood precursor T-cell lymphoblastic leukemia. Blood. 2006;108(4): 1151-1157.
-
(2006)
Blood
, vol.108
, Issue.4
, pp. 1151-1157
-
-
Breit, S.1
Stanulla, M.2
Flohr, T.3
Schrappe, M.4
Ludwig, W.D.5
Tolle, G.6
-
4
-
-
78650311120
-
NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951
-
Clappier E, Collette S, Grardel N, Girard S, Suarez L, Brunie G, et al. NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951. Leukemia. 2010;24(12):2023-2031.
-
(2010)
Leukemia
, vol.24
, Issue.12
, pp. 2023-2031
-
-
Clappier, E.1
Collette, S.2
Grardel, N.3
Girard, S.4
Suarez, L.5
Brunie, G.6
-
5
-
-
78650307928
-
NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols
-
Zuurbier L, Homminga I, Calvert V, te Winkel ML, Buijs-Gladdines JG, Kooi C, et al. NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols. Leukemia. 2010;24(12):2014-2022.
-
(2010)
Leukemia
, vol.24
, Issue.12
, pp. 2014-2022
-
-
Zuurbier, L.1
Homminga, I.2
Calvert, V.3
te Winkel, M.L.4
Buijs-Gladdines, J.G.5
Kooi, C.6
-
6
-
-
73949110789
-
T-cell acute lymphoblastic leukemia in adults: Clinical features, immunophenotype, cytogenetics, and outcome from the large randomized prospective trial (UKALL XII/ECOG 2993)
-
Marks DI, Paietta EM, Moorman AV, Richards SM, Buck G, DeWald G, et al. T-cell acute lymphoblastic leukemia in adults: clinical features, immunophenotype, cytogenetics, and outcome from the large randomized prospective trial (UKALL XII/ECOG 2993). Blood. 2009;114(25): 5136-5145.
-
(2009)
Blood
, vol.114
, Issue.25
, pp. 5136-5145
-
-
Marks, D.I.1
Paietta, E.M.2
Moorman, A.V.3
Richards, S.M.4
Buck, G.5
Dewald, G.6
-
7
-
-
0032932735
-
Alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia
-
Kawamura M, Ohnishi H, Guo SX, Sheng XM, Minegishi M, Hanada R, et al. Alterations of the p53, p21, p16, p15 and RAS genes in childhood T-cell acute lymphoblastic leukemia. Leuk Res. 1999; 23(2):115-126.
-
(1999)
Leuk Res
, vol.23
, Issue.2
, pp. 115-126
-
-
Kawamura, M.1
Ohnishi, H.2
Guo, S.X.3
Sheng, X.M.4
Minegishi, M.5
Hanada, R.6
-
8
-
-
3142512347
-
Activating FLT3 mutations in CD117/KIT(+) T-cell acute lymphoblastic leukemias
-
Paietta E, Ferrando AA, Neuberg D, Bennett JM, Racevskis J, Lazarus H, et al. Activating FLT3 mutations in CD117/KIT(+) T-cell acute lymphoblastic leukemias. Blood. 2004;104(2):558-560.
-
(2004)
Blood
, vol.104
, Issue.2
, pp. 558-560
-
-
Paietta, E.1
Ferrando, A.A.2
Neuberg, D.3
Bennett, J.M.4
Racevskis, J.5
Lazarus, H.6
-
9
-
-
33751168051
-
The cryptic chromosomal deletion del(11)(p12p13) as a new activation mechanism of LMO2 in pediatric T-cell acute lymphoblastic leukemia
-
Van Vlierberghe P, van Grotel M, Beverloo HB, Lee C, Helgason T, Buijs-Gladdines J, et al. The cryptic chromosomal deletion del(11)(p12p13) as a new activation mechanism of LMO2 in pediatric T-cell acute lymphoblastic leukemia. Blood. 2006;108 (10):3520-3529.
-
(2006)
Blood
, vol.108
, Issue.10
, pp. 3520-3529
-
-
van Vlierberghe, P.1
van Grotel, M.2
Beverloo, H.B.3
Lee, C.4
Helgason, T.5
Buijs-Gladdines, J.6
-
10
-
-
5044225888
-
Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia
-
Weng AP, Ferrando AA, Lee W, Morris JP 4th, Silverman LB, Sanchez-Irizarry C, et al. Activating mutations of NOTCH1 in human T cell acute lymphoblastic leukemia. Science. 2004;306(5694):269-271.
-
(2004)
Science
, vol.306
, Issue.5694
, pp. 269-271
-
-
Weng, A.P.1
Ferrando, A.A.2
Lee, W.3
Morris IV, J.P.4
Silverman, L.B.5
Sanchez-Irizarry, C.6
-
11
-
-
34548009617
-
The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children
-
Clappier E, Cuccuini W, Kalota A, Crinquette A, Cayuela JM, Dik WA, et al. The C-MYB locus is involved in chromosomal translocation and genomic duplications in human T-cell acute leukemia (T-ALL), the translocation defining a new T-ALL subtype in very young children. Blood. 2007;110(4):1251-1261.
-
(2007)
Blood
, vol.110
, Issue.4
, pp. 1251-1261
-
-
Clappier, E.1
Cuccuini, W.2
Kalota, A.3
Crinquette, A.4
Cayuela, J.M.5
Dik, W.A.6
-
12
-
-
34250837539
-
The tumor suppressor gene hCDC4 is frequently mutated in human T-cell acute lymphoblastic leukemia with functional consequences for Notch signaling
-
Malyukova A, Dohda T, von der Lehr N, Akhoondi S, Corcoran M, Heyman M, et al. The tumor suppressor gene hCDC4 is frequently mutated in human T-cell acute lymphoblastic leukemia with functional consequences for Notch signaling. Cancer Res. 2007;67(12):5611-5616.
-
(2007)
Cancer Res
, vol.67
, Issue.12
, pp. 5611-5616
-
-
Malyukova, A.1
Dohda, T.2
von der Lehr, N.3
Akhoondi, S.4
Corcoran, M.5
Heyman, M.6
-
13
-
-
42249091014
-
Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia
-
Flex E, Petrangeli V, Stella L, Chiaretti S, Hornakova T, Knoops L, et al. Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia. J Exp Med. 2008; 205(4):751-758.
-
(2008)
J Exp Med
, vol.205
, Issue.4
, pp. 751-758
-
-
Flex, E.1
Petrangeli, V.2
Stella, L.3
Chiaretti, S.4
Hornakova, T.5
Knoops, L.6
-
14
-
-
70349232830
-
WT1 mutations in T-ALL
-
Tosello V, Mansour MR, Barnes K, Paganin M, Sulis ML, Jenkinson S, et al. WT1 mutations in T-ALL. Blood. 2009;114(5):1038-1045.
-
(2009)
Blood
, vol.114
, Issue.5
, pp. 1038-1045
-
-
Tosello, V.1
Mansour, M.R.2
Barnes, K.3
Paganin, M.4
Sulis, M.L.5
Jenkinson, S.6
-
15
-
-
77952887619
-
Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia
-
Kleppe M, Lahortiga I, El Chaar T, De Keersmaecker K, Mentens N, Graux C, et al. Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia. Nat Genet. 2010; 42(6):530-535.
-
(2010)
Nat Genet
, vol.42
, Issue.6
, pp. 530-535
-
-
Kleppe, M.1
Lahortiga, I.2
El Chaar, T.3
de Keersmaecker, K.4
Mentens, N.5
Graux, C.6
-
16
-
-
77951015381
-
Inactivation of LEF1 in T-cell acute lymphoblastic leukemia
-
Gutierrez A, Sanda T, Ma W, Zhang J, Grebliunaite R, Dahlberg S, et al. Inactivation of LEF1 in T-cell acute lymphoblastic leukemia. Blood. 2010;115(14): 2845-2851.
-
(2010)
Blood
, vol.115
, Issue.14
, pp. 2845-2851
-
-
Gutierrez, A.1
Sanda, T.2
Ma, W.3
Zhang, J.4
Grebliunaite, R.5
Dahlberg, S.6
-
17
-
-
18744393073
-
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
-
Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK, et al. Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome. Nat Genet. 2002;32(4):661-665.
-
(2002)
Nat Genet
, vol.32
, Issue.4
, pp. 661-665
-
-
Lower, K.M.1
Turner, G.2
Kerr, B.A.3
Mathews, K.D.4
Shaw, M.A.5
Gedeon, A.K.6
-
18
-
-
77950299929
-
PHF6 mutations in T-cell acute lymphoblastic leukemia
-
Van Vlierberghe P, Palomero T, Khiabanian H, Van der Meulen J, Castillo M, Van Roy N, et al. PHF6 mutations in T-cell acute lymphoblastic leukemia. Nat Genet. 2010; 42(4):338-342.
-
(2010)
Nat Genet
, vol.42
, Issue.4
, pp. 338-342
-
-
van Vlierberghe, P.1
Palomero, T.2
Khiabanian, H.3
van der Meulen, J.4
Castillo, M.5
van Roy, N.6
-
19
-
-
78651299314
-
PHF6 mutations in adult acute myeloid leukemia
-
Van Vlierberghe P, Patel J, Abdel-Wahab O, Lobry C, Hedvat CV, Balbin M, et al. PHF6 mutations in adult acute myeloid leukemia. Leukemia. 2011;25(1):130-134.
-
(2011)
Leukemia
, vol.25
, Issue.1
, pp. 130-134
-
-
van Vlierberghe, P.1
Patel, J.2
Abdel-Wahab, O.3
Lobry, C.4
Hedvat, C.V.5
Balbin, M.6
-
20
-
-
34547820257
-
The SCFFBW7 ubiquitin ligase complex as a tumor suppressor in T cell leukemia
-
Thompson BJ, Buonamici S, Sulis ML, Palomero T, Vilimas T, Basso G, et al. The SCFFBW7 ubiquitin ligase complex as a tumor suppressor in T cell leukemia. J Exp Med. 2007;204(8):1825-1835.
-
(2007)
J Exp Med
, vol.204
, Issue.8
, pp. 1825-1835
-
-
Thompson, B.J.1
Buonamici, S.2
Sulis, M.L.3
Palomero, T.4
Vilimas, T.5
Basso, G.6
-
21
-
-
33744812702
-
NOTCH1 mutations in T-cell acute lymphoblastic leukemia: Prognostic significance and implication in multifactorial leukemogenesis
-
Zhu YM, Zhao WL, Fu JF, Shi JY, Pan Q, Hu J, et al. NOTCH1 mutations in T-cell acute lymphoblastic leukemia: prognostic significance and implication in multifactorial leukemogenesis. Clin Cancer Res. 2006; 12(10):3043-3049.
-
(2006)
Clin Cancer Res
, vol.12
, Issue.10
, pp. 3043-3049
-
-
Zhu, Y.M.1
Zhao, W.L.2
Fu, J.F.3
Shi, J.Y.4
Pan, Q.5
Hu, J.6
-
22
-
-
47149084727
-
The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia
-
Van Vlierberghe P, van Grotel M, Tchinda J, Lee C, Beverloo HB, van der Spek PJ, et al. The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia. Blood. 2008;111(9):4668-4680.
-
(2008)
Blood
, vol.111
, Issue.9
, pp. 4668-4680
-
-
van Vlierberghe, P.1
van Grotel, M.2
Tchinda, J.3
Lee, C.4
Beverloo, H.B.5
van der Spek, P.J.6
-
23
-
-
0041743184
-
CALM-AF10 is a common fusion transcript in T-ALL and is specific to the TCRgammadelta lineage
-
Asnafi V, Radford-Weiss I, Dastugue N, Bayle C, Leboeuf D, Charrin C, et al. CALM-AF10 is a common fusion transcript in T-ALL and is specific to the TCRgammadelta lineage. Blood. 2003; 102(3):1000-1006.
-
(2003)
Blood
, vol.102
, Issue.3
, pp. 1000-1006
-
-
Asnafi, V.1
Radford-Weiss, I.2
Dastugue, N.3
Bayle, C.4
Leboeuf, D.5
Charrin, C.6
-
24
-
-
77957078794
-
T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6
-
Chao MM, Todd MA, Kontny U, Neas K, Sullivan MJ, Hunter AG, et al. T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6. Pediatr Blood Cancer. 2010;55(4):722-724.
-
(2010)
Pediatr Blood Cancer
, vol.55
, Issue.4
, pp. 722-724
-
-
Chao, M.M.1
Todd, M.A.2
Kontny, U.3
Neas, K.4
Sullivan, M.J.5
Hunter, A.G.6
-
25
-
-
35248866342
-
Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman- Lehmann syndrome of intellectual disability and obesity
-
Voss AK, Gamble R, Collin C, Shoubridge C, Corbett M, Gecz J, et al. Protein and gene expression analysis of Phf6, the gene mutated in the Borjeson-Forssman- Lehmann syndrome of intellectual disability and obesity. Gene Expr Patterns. 2007;7 (8):858-871.
-
(2007)
Gene Expr Patterns
, vol.7
, Issue.8
, pp. 858-871
-
-
Voss, A.K.1
Gamble, R.2
Collin, C.3
Shoubridge, C.4
Corbett, M.5
Gecz, J.6
|