-
1
-
-
80053385569
-
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)
-
Ostergaard P, Simpson MA, Connell FC, Steward CG, Brice G, Woollard WJ, et al. Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nat Genet. 2011;43(10):929-31.
-
(2011)
Nat Genet.
, vol.43
, Issue.10
, pp. 929-931
-
-
Ostergaard, P.1
Simpson, M.A.2
Connell, F.C.3
Steward, C.G.4
Brice, G.5
Woollard, W.J.6
-
2
-
-
80053383273
-
Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia
-
Hahn CN, Chong CE, Carmichael CL, Wilkins EJ, Brautigan PJ, Li XC, et al. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia. Nat Genet. 2011;43(10):1012-7.
-
(2011)
Nat Genet.
, vol.43
, Issue.10
, pp. 1012-1017
-
-
Hahn, C.N.1
Chong, C.E.2
Carmichael, C.L.3
Wilkins, E.J.4
Brautigan, P.J.5
Li, X.C.6
-
3
-
-
84862129223
-
Germ-line GATA2 p. THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival
-
Bodor C, Renneville A, Smith M, Charazac A, Iqbal S, Etancelin P, et al. Germ-line GATA2 p. THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival. Haematologica. 2012;97(6):890-4.
-
(2012)
Haematologica
, vol.97
, Issue.6
, pp. 890-894
-
-
Bodor, C.1
Renneville, A.2
Smith, M.3
Charazac, A.4
Iqbal, S.5
Etancelin, P.6
-
4
-
-
84863449106
-
Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia
-
Holme H, Hossain U, Kirwan M, Walne A, Vulliamy T, Dokal I. Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia. Br J Haematol. 2012;158(2):242-8.
-
(2012)
Br J Haematol.
, vol.158
, Issue.2
, pp. 242-248
-
-
Holme, H.1
Hossain, U.2
Kirwan, M.3
Walne, A.4
Vulliamy, T.5
Dokal, I.6
-
5
-
-
84880449489
-
GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
-
Hsu AP, Johnson KD, Falcone EL, Sanalkumar R, Sanchez L, Hickstein DD, et al. GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome. Blood. 2013;121(19):3830-7, S1-7.
-
(2013)
Blood
, vol.121
, Issue.19
, pp. 3830-3837
-
-
Hsu, A.P.1
Johnson, K.D.2
Falcone, E.L.3
Sanalkumar, R.4
Sanchez, L.5
Hickstein, D.D.6
-
6
-
-
84873530537
-
High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia
-
Pasquet M, Bellanne-Chantelot C, Tavitian S, Prade N, Beaupain B, Larochelle O, et al. High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia. Blood. 2013;121 (5):822-9.
-
(2013)
Blood
, vol.121
, Issue.5
, pp. 822-829
-
-
Pasquet, M.1
Bellanne-Chantelot, C.2
Tavitian, S.3
Prade, N.4
Beaupain, B.5
Larochelle, O.6
-
7
-
-
84893285755
-
GATA2 deficiency: A protean disorder of hematopoiesis, lymphatics and immunity
-
Nov 13. [Epub ahead of print]
-
Spinner MA, Sanchez LA, Hsu AP, Shaw PA, Zerbe CS, Calvo KR, et al. GATA2 deficiency: a protean disorder of hematopoiesis, lymphatics and immunity. Blood. 2013 Nov 13. [Epub ahead of print]
-
(2013)
Blood
-
-
Spinner, M.A.1
Sanchez, L.A.2
Hsu, A.P.3
Shaw, P.A.4
Zerbe, C.S.5
Calvo, K.R.6
-
8
-
-
84896732313
-
Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation
-
West RR, Hsu AP, Holland SM, Cuellar-Rodriguez J, Hickstein DD. Acquired ASXL1 mutations are common in patients with inherited GATA2 mutations and correlate with myeloid transformation. Haematologica. 2014;99(2):276-81.
-
(2014)
Haematologica
, vol.99
, Issue.2
, pp. 276-281
-
-
West, R.R.1
Hsu, A.P.2
Holland, S.M.3
Cuellar-Rodriguez, J.4
Hickstein, D.D.5
-
9
-
-
79961074298
-
Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
-
Hsu AP, Sampaio EP, Khan J, Calvo KR, Lemieux JE, Patel SY, et al. Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome. Blood. 2011;118(10):2653-5.
-
(2011)
Blood
, vol.118
, Issue.10
, pp. 2653-2655
-
-
Hsu, A.P.1
Sampaio, E.P.2
Khan, J.3
Calvo, K.R.4
Lemieux, J.E.5
Patel, S.Y.6
-
10
-
-
80052089944
-
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
-
Dickinson RE, Griffin H, Bigley V, Reynard LN, Hussain R, Haniffa M, et al. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency. Blood. 2011;118(10):2656-8.
-
(2011)
Blood
, vol.118
, Issue.10
, pp. 2656-2658
-
-
Dickinson, R.E.1
Griffin, H.2
Bigley, V.3
Reynard, L.N.4
Hussain, R.5
Haniffa, M.6
-
11
-
-
84922336738
-
Prognostic score including gene mutations in chronic myelomonocytic leukemia
-
Itzykson R, Kosmider O, Renneville A, Gelsi-Boyer V, Meggendorfer M, Morabito M, et al. Prognostic score including gene mutations in chronic myelomonocytic leukemia. J Clin Oncol. 2013;31(19):2428-36.
-
(2013)
J Clin Oncol.
, vol.31
, Issue.19
, pp. 2428-2436
-
-
Itzykson, R.1
Kosmider, O.2
Renneville, A.3
Gelsi-Boyer, V.4
Meggendorfer, M.5
Morabito, M.6
-
12
-
-
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
-
13
-
-
84861813715
-
Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia
-
Beekman R, Valkhof MG, Sanders MA, van Strien PM, Haanstra JR, Broeders L, et al. Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia. Blood. 2012;119(22):5071-7.
-
(2012)
Blood
, vol.119
, Issue.22
, pp. 5071-5077
-
-
Beekman, R.1
Valkhof, M.G.2
Sanders, M.A.3
van Strien, P.M.4
Haanstra, J.R.5
Broeders, L.6
-
14
-
-
41149169150
-
Gain-offunction mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia
-
Zhang SJ, Ma LY, Huang QH, Li G, Gu BW, Gao XD, et al. Gain-offunction mutation of GATA-2 in acute myeloid transformation of chronic myeloid leukemia. Proc Natl Acad Sci USA. 2008;105 (6):2076-81.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.6
, pp. 2076-2081
-
-
Zhang, S.J.1
Ma, L.Y.2
Huang, Q.H.3
Li, G.4
Gu, B.W.5
Gao, X.D.6
-
15
-
-
84893317397
-
The role of different genetic subtypes of CEBPA mutated AML
-
Sep 13. [Epub ahead of print]
-
Fasan A, Haferlach C, Alpermann T, Jeromin S, Grossmann V, Eder C, et al. The role of different genetic subtypes of CEBPA mutated AML. Leukemia. 2013 Sep 13. [Epub ahead of print]
-
(2013)
Leukemia
-
-
Fasan, A.1
Haferlach, C.2
Alpermann, T.3
Jeromin, S.4
Grossmann, V.5
Eder, C.6
-
16
-
-
84865152223
-
ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression
-
Abdel-Wahab O, Adli M, LaFave LM, Gao J, Hricik T, Shih AH, et al. ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression. Cancer Cell. 2012;22(2):180-93.
-
(2012)
Cancer Cell.
, vol.22
, Issue.2
, pp. 180-193
-
-
Abdel-Wahab, O.1
Adli, M.2
LaFave, L.M.3
Gao, J.4
Hricik, T.5
Shih, A.H.6
-
17
-
-
77952429798
-
Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB
-
Scheuermann JC, de Ayala Alonso AG, Oktaba K, Ly-Hartig N, McGinty RK, Fraterman S, et al. Histone H2A deubiquitinase activity of the Polycomb repressive complex PR-DUB. Nature. 2010;465(7295):243-7.
-
(2010)
Nature.
, vol.465
, Issue.7295
, pp. 243-247
-
-
Scheuermann, J.C.1
de Ayala Alonso, A.G.2
Oktaba, K.3
Ly-Hartig, N.4
McGinty, R.K.5
Fraterman, S.6
-
18
-
-
84888116023
-
Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo
-
Abdel-Wahab O, Gao J, Adli M, Dey A, Trimarchi T, Chung YR, et al. Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo. J Exp Med. 2013;210(12):2641-59.
-
(2013)
J Exp Med.
, vol.210
, Issue.12
, pp. 2641-2659
-
-
Abdel-Wahab, O.1
Gao, J.2
Adli, M.3
Dey, A.4
Trimarchi, T.5
Chung, Y.R.6
-
19
-
-
84890129231
-
Dynamic analysis of gene expression and genome-wide transcription factor binding during lineage specification of multipotent progenitors
-
May G, Soneji S, Tipping AJ, Teles J, McGowan SJ, Wu M, et al. Dynamic analysis of gene expression and genome-wide transcription factor binding during lineage specification of multipotent progenitors. Cell Stem Cell. 2013;13(6):754-68.
-
(2013)
Cell Stem Cell
, vol.13
, Issue.6
, pp. 754-768
-
-
May, G.1
Soneji, S.2
Tipping, A.J.3
Teles, J.4
McGowan, S.J.5
Wu, M.6
-
20
-
-
84896700729
-
The evolution of cellular deficiency in GATA2 mutation
-
Dec 17. [Epub ahead of print]
-
Dickinson RE, Milne P, Jardine L, Zandi S, Swierczek SI, McGovern N, et al. The evolution of cellular deficiency in GATA2 mutation. Blood. 2013 Dec 17. [Epub ahead of print]
-
(2013)
Blood
-
-
Dickinson, R.E.1
Milne, P.2
Jardine, L.3
Zandi, S.4
Swierczek, S.I.5
McGovern, N.6
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