-
1
-
-
55949118684
-
PHD fingers in human diseases: Disorders arising from misinterpreting epigenetic marks
-
Baker LA, Allis CD, Wang GG. PHD fingers in human diseases: disorders arising from misinterpreting epigenetic marks. Mutat Res 2008;647: 3-12.
-
(2008)
Mutat Res
, vol.647
, pp. 3-12
-
-
Baker, L.A.1
Allis, C.D.2
Wang, G.G.3
-
2
-
-
33751328324
-
The Börjeson-Forssman-Lehman syndrome (BFLS, MIM #301900)
-
Gécz J, Turner G, Nelson J, et al. The Börjeson-Forssman- Lehman syndrome (BFLS, MIM #301900). Eur JHum Genet 2006;14: 1233-1237.
-
(2006)
Eur JHum Genet
, vol.14
, pp. 1233-1237
-
-
Gécz, J.1
Turner, G.2
Nelson, J.3
-
3
-
-
77950299929
-
PHF6 mutations in T-cell acute lymphoblastic leukemia
-
Van Vlierberghe P, Palomero T, Khiabanian H, et al. PHF6 mutations in T-cell acute lymphoblastic leukemia. Nat Genet 2010: 42: 338-342.
-
(2010)
Nat Genet
, vol.42
, pp. 338-342
-
-
Van Vlierberghe, P.1
Palomero, T.2
Khiabanian, H.3
-
4
-
-
82855168107
-
Mutation of PHF6 is associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia
-
Wang Q, Qiu H, Jiang H, et al. Mutation of PHF6 is associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia. Haematologica 2011: 96: 1808-1814.
-
(2011)
Haematologica
, vol.96
, pp. 1808-1814
-
-
Wang, Q.1
Qiu, H.2
Jiang, H.3
-
5
-
-
78651299314
-
PHF6 mutations in adult acute myeloid leukemia
-
Van Vlierberghe P, Patel J, Abdel-Wahab O, et al. PHF6 mutations in adult acute myeloid leukemia. Leukemia 2011: 25: 130-134.
-
(2011)
Leukemia
, vol.25
, pp. 130-134
-
-
Van Vlierberghe, P.1
Patel, J.2
Abdel-Wahab, O.3
-
6
-
-
84863393263
-
Prognostic relevance of integrated genetic prof ling in acute myeloid leukemia
-
Patel JP, Gönen M, Figueroa ME, et al. Prognostic relevance of integrated genetic prof ling in acute myeloid leukemia. N Engl J Med 2012;366: 1079-1089.
-
(2012)
N Engl J Med
, vol.366
, pp. 1079-1089
-
-
Patel, J.P.1
Gönen, M.2
Figueroa, M.E.3
-
8
-
-
0032241020
-
P53, p15INK4B, p16INK4A and p57KIP2 mutations during the progression of chronic myeloid leukemia
-
Güran S, Bahçe M, Beyan C, et al. P53, p15INK4B, p16INK4A and p57KIP2 mutations during the progression of chronic myeloid leukemia. Haematologia (Budap) 1998: 29: 181-193.
-
(1998)
Haematologia (Budap)
, vol.29
, pp. 181-193
-
-
Güran, S.1
Bahçe, M.2
Beyan, C.3
-
9
-
-
79952451556
-
A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76. 9% of cases
-
Grossmann V Kohlmann A, Zenger M, et al. A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76. 9% of cases. Leukemia 2011: 25: 557-560.
-
(2011)
Leukemia
, vol.25
, pp. 557-560
-
-
Grossmann, V.1
Kohlmann, A.2
Zenger, M.3
-
10
-
-
41149169150
-
Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia
-
Zhang SJ, Ma LY, Huang QH, et al. Gain-of-function mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia. Proc Natl Acad Sci USA 2008;105: 2076-2081.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 2076-2081
-
-
Zhang, S.J.1
Ma, L.Y.2
Huang, Q.H.3
-
11
-
-
79957593717
-
CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia
-
Makishima H, Jankowska AM, McDevitt MA, et al. CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia. Blood 2011;117: e198-e206.
-
(2011)
Blood
, vol.117
-
-
Makishima, H.1
Jankowska, A.M.2
McDevitt, M.A.3
|