-
1
-
-
67349135808
-
Acute myeloid leukemia: The challenge of capturing disease variety
-
Lowenberg B. Acute myeloid leukemia: the challenge of capturing disease variety. Hematology Am Soc Hematol Educ Program 2008;1-11.
-
(2008)
Hematology Am Soc Hematol Educ Program
, pp. 1-11
-
-
Lowenberg, B.1
-
2
-
-
19944427850
-
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype
-
Falini B, Mecucci C, Tiacci E, Alcalay M, Rosati R, Pasqualucci L, et al. Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype. N Engl J Med. 2005;352(3):254-66.
-
(2005)
N Engl J Med
, vol.352
, Issue.3
, pp. 254-266
-
-
Falini, B.1
Mecucci, C.2
Tiacci, E.3
Alcalay, M.4
Rosati, R.5
Pasqualucci, L.6
-
3
-
-
23044459136
-
Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+ AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance
-
Alcalay M, Tiacci E, Bergomas R, Bigerna B, Venturini E, Minardi SP, et al. Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+ AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance. Blood. 2005;106(3):899-902.
-
(2005)
Blood
, vol.106
, Issue.3
, pp. 899-902
-
-
Alcalay, M.1
Tiacci, E.2
Bergomas, R.3
Bigerna, B.4
Venturini, E.5
Minardi, S.P.6
-
4
-
-
33846876123
-
Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): Bio- logic and clinical features
-
Falini B, Nicoletti I, Martelli MF, Mecucci C. Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): bio- logic and clinical features. Blood. 2007;109(3):874-85.
-
(2007)
Blood
, vol.109
, Issue.3
, pp. 874-885
-
-
Falini, B.1
Nicoletti, I.2
Martelli, M.F.3
Mecucci, C.4
-
5
-
-
41649119008
-
Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophos- min
-
Garzon R, Garofalo M, Martelli MP, Briesewitz R, Wang L, Fernandez-Cymering C, et al. Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophos- min. Proc Natl Acad Sci USA. 2008;105(10):3945-50.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.10
, pp. 3945-3950
-
-
Garzon, R.1
Garofalo, M.2
Martelli, M.P.3
Briesewitz, R.4
Wang, L.5
Fernandez-Cymering, C.6
-
6
-
-
42949142189
-
Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia
-
Schlenk RF, Dohner K, Krauter J, Frohling S, Corbacioglu A, Bullinger L, et al. Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia. N Engl J Med. 2008;358(18):1909-18.
-
(2008)
N Engl J Med
, vol.358
, Issue.18
, pp. 1909-1918
-
-
Schlenk, R.F.1
Dohner, K.2
Krauter, J.3
Frohling, S.4
Corbacioglu, A.5
Bullinger, L.6
-
7
-
-
62249168182
-
Acute myeloid leukaemia with recurrent genetic abnormalities
-
In: Swerdlow SH et al., International Agency for Research on Cancer (IARC), Lyon
-
Arber D, Brunning RD, Le Beau MM, et al. Acute myeloid leukaemia with recurrent genetic abnormalities. In: Swerdlow SH et al., Eds, WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. International Agency for Research on Cancer (IARC), Lyon, 2008, p.110-23.
-
(2008)
WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues
, pp. 110-123
-
-
Arber, D.1
Brunning, R.D.2
Le Beau, M.M.3
-
8
-
-
77449140390
-
Favorable prognostic impact of NPM1 mutations in older patients with cytogenetically normal de novo acute myeloid leukemia and associated gene- and microRNA-expression signatures: A cancer and leukemia group B study
-
Becker H, Marcucci G, Maharry K, Radmacher MD, Mrozek K, Margeson D, et al. Favorable prognostic impact of NPM1 mutations in older patients with cytogenetically normal de novo acute myeloid leukemia and associated gene- and microRNA-expression signatures: a cancer and leukemia group B study. J Clin Oncol. 2010;28(4):596-604.
-
(2010)
J Clin Oncol
, vol.28
, Issue.4
, pp. 596-604
-
-
Becker, H.1
Marcucci, G.2
Maharry, K.3
Radmacher, M.D.4
Mrozek, K.5
Margeson, D.6
-
9
-
-
33744519686
-
Denaturing high-performance liquid chromatography: A valid approach for identifying NPM1 mutations in acute myeloid leukemia
-
Roti G, Rosati R, Bonasso R, Gorello P, Diverio D, Martelli MF, et al. Denaturing high-performance liquid chromatography: a valid approach for identifying NPM1 mutations in acute myeloid leukemia. J Mol Diagn. 2006;8(2):254-9.
-
(2006)
J Mol Diagn
, vol.8
, Issue.2
, pp. 254-259
-
-
Roti, G.1
Rosati, R.2
Bonasso, R.3
Gorello, P.4
Diverio, D.5
Martelli, M.F.6
-
10
-
-
47649107606
-
Rapid method for detection of mutations in the nucleophosmin gene in acute myeloid leukemia
-
Laughlin TS, Becker MW, Liesveld JL, Mulford DA, Abboud CN, Brown P, et al. Rapid method for detection of mutations in the nucleophosmin gene in acute myeloid leukemia. J Mol Diagn. 2008;10(4): 338-45.
-
(2008)
J Mol Diagn
, vol.10
, Issue.4
, pp. 338-345
-
-
Laughlin, T.S.1
Becker, M.W.2
Liesveld, J.L.3
Mulford, D.A.4
Abboud, C.N.5
Brown, P.6
-
11
-
-
43749104285
-
An allele-specific rt-PCR assay to detect type A mutation of the nucleophosmin-1 gene in acute myeloid leukemia
-
Ottone T, Ammatuna E, Lavorgna S, Noguera NI, Buccisano F, Venditti A, et al. An allele-specific rt-PCR assay to detect type A mutation of the nucleophosmin-1 gene in acute myeloid leukemia. J Mol Diagn. 2008;10(3):212-6.
-
(2008)
J Mol Diagn
, vol.10
, Issue.3
, pp. 212-216
-
-
Ottone, T.1
Ammatuna, E.2
Lavorgna, S.3
Noguera, N.I.4
Buccisano, F.5
Venditti, A.6
-
12
-
-
43749099253
-
A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electrophoresis
-
Szankasi P, Jama M, Bahler DW. A new DNA-based test for detection of nucleophosmin exon 12 mutations by capillary electrophoresis. J Mol Diagn. 2008;10(3):236-41.
-
(2008)
J Mol Diagn
, vol.10
, Issue.3
, pp. 236-241
-
-
Szankasi, P.1
Jama, M.2
Bahler, D.W.3
-
13
-
-
43749118762
-
Nucleophosmin (NPM1) mutations in acute myeloid leukemia: An ongoing (cytoplasmic) tale of dueling muta- tions and duality of molecular genetic testing methodologies
-
Wertheim G, Bagg A. Nucleophosmin (NPM1) mutations in acute myeloid leukemia: an ongoing (cytoplasmic) tale of dueling muta- tions and duality of molecular genetic testing methodologies. J Mol Diagn. 2008;10(3):198-202.
-
(2008)
J Mol Diagn
, vol.10
, Issue.3
, pp. 198-202
-
-
Wertheim, G.1
Bagg, A.2
-
14
-
-
46949098927
-
A rapid, one step assay for simultaneous detection of FLT3/ITD and NPM1 mutations in AML with normal cytogenetics
-
Huang Q, Chen W, Gaal KK, Slovak ML, Stein A, Weiss LM. A rapid, one step assay for simultaneous detection of FLT3/ITD and NPM1 mutations in AML with normal cytogenetics. Br J Haematol. 2008;142(3):489-92.
-
(2008)
Br J Haematol
, vol.142
, Issue.3
, pp. 489-492
-
-
Huang, Q.1
Chen, W.2
Gaal, K.K.3
Slovak, M.L.4
Stein, A.5
Weiss, L.M.6
-
15
-
-
64849105990
-
A novel quantitative assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPM1 (nucleophosmin) exon 12 mutations
-
Dvorakova D, Lengerova M, Pospisilova J, Palasek I, Mayer J. A novel quantitative assessment of minimal residual disease in patients with acute myeloid leukemia carrying NPM1 (nucleophosmin) exon 12 mutations. Leukemia. 2009;23(4):793-6.
-
(2009)
Leukemia
, vol.23
, Issue.4
, pp. 793-796
-
-
Dvorakova, D.1
Lengerova, M.2
Pospisilova, J.3
Palasek, I.4
Mayer, J.5
-
16
-
-
61449197851
-
Detection of nucleophosmin gene mutations in plasma from patients with acute myeloid leukemia: Clinical significance and implications
-
Ma W, Kantarjian H, Zhang X, Jilani I, Sheikholeslami MR, Donahue AC, et al. Detection of nucleophosmin gene mutations in plasma from patients with acute myeloid leukemia: clinical significance and implications. Cancer Biomark. 2009;5(1):51-8.
-
(2009)
Cancer Biomark
, vol.5
, Issue.1
, pp. 51-58
-
-
Ma, W.1
Kantarjian, H.2
Zhang, X.3
Jilani, I.4
Sheikholeslami, M.R.5
Donahue, A.C.6
-
17
-
-
34250721029
-
Cytoplasmic mutated nucleophosmin (NPM) defines the molecu- lar status of a significant fraction of myeloid sarcomas
-
Falini B, Lenze D, Hasserjian R, Coupland S, Jaehne D, Soupir C, et al. Cytoplasmic mutated nucleophosmin (NPM) defines the molecu- lar status of a significant fraction of myeloid sarcomas. Leukemia. 2007;21(7):1566-70.
-
(2007)
Leukemia
, vol.21
, Issue.7
, pp. 1566-1570
-
-
Falini, B.1
Lenze, D.2
Hasserjian, R.3
Coupland, S.4
Jaehne, D.5
Soupir, C.6
-
18
-
-
73349090569
-
Nucleophosmin (NPM1) mutations in adult and childhood acute myeloid leukaemia: Towards definition of a new leukaemia entity
-
Rau R, Brown P. Nucleophosmin (NPM1) mutations in adult and childhood acute myeloid leukaemia: towards definition of a new leukaemia entity. Hematol Oncol. 2009;27(4):171-81.
-
(2009)
Hematol Oncol
, vol.27
, Issue.4
, pp. 171-181
-
-
Rau, R.1
Brown, P.2
-
19
-
-
34247596501
-
Identification and functional characterization of a cytoplasmic nucle- ophosmin leukaemic mutant generated by a novel exon-11 NPM1 mutation
-
Albiero E, Madeo D, Bolli N, Giaretta I, Bona ED, Martelli MF, et al. Identification and functional characterization of a cytoplasmic nucle- ophosmin leukaemic mutant generated by a novel exon-11 NPM1 mutation. Leukemia. 2007;21(5):1099-103.
-
(2007)
Leukemia
, vol.21
, Issue.5
, pp. 1099-1103
-
-
Albiero, E.1
Madeo, D.2
Bolli, N.3
Giaretta, I.4
Bona, E.D.5
Martelli, M.F.6
-
20
-
-
23744479178
-
Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype
-
Cazzaniga G, Dell'Oro MG, Mecucci C, Giarin E, Masetti R, Rossi V, et al. Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype. Blood. 2005;106(4):1419-22.
-
(2005)
Blood
, vol.106
, Issue.4
, pp. 1419-1422
-
-
Cazzaniga, G.1
Dell'oro, M.G.2
Mecucci, C.3
Giarin, E.4
Masetti, R.5
Rossi, V.6
-
21
-
-
34547954572
-
The incidence and clinical significance of nucleophosmin mutations in childhood AML
-
Brown P, McIntyre E, Rau R, Meshinchi S, Lacayo N, Dahl G, et al. The incidence and clinical significance of nucleophosmin mutations in childhood AML. Blood. 2007;110(3):979-85.
-
(2007)
Blood
, vol.110
, Issue.3
, pp. 979-985
-
-
Brown, P.1
McIntyre, E.2
Rau, R.3
Meshinchi, S.4
Lacayo, N.5
Dahl, G.6
-
22
-
-
33846475525
-
Different types of NPM1 mutations in children and adults: Evidence for an effect of patient age on the prevalence of the TCTG-tandem duplica- tion in NPM1-exon 12
-
Thiede C, Creutzig E, Reinhardt D, Ehninger G, Creutzig U. Different types of NPM1 mutations in children and adults: evidence for an effect of patient age on the prevalence of the TCTG-tandem duplica- tion in NPM1-exon 12. Leukemia. 2007;21(2):366-7.
-
(2007)
Leukemia
, vol.21
, Issue.2
, pp. 366-367
-
-
Thiede, C.1
Creutzig, E.2
Reinhardt, D.3
Ehninger, G.4
Creutzig, U.5
-
23
-
-
43449096376
-
Cytoplasmic mutated nucleophosmin is stable in primary leukemic cells and in a xenotransplant model of NPMc+ acute myeloid leukemia in SCID mice
-
Falini B, Martelli MP, Mecucci C, Liso A, Bolli N, Bigerna B, et al. Cytoplasmic mutated nucleophosmin is stable in primary leukemic cells and in a xenotransplant model of NPMc+ acute myeloid leukemia in SCID mice. Haematologica 2008;93(5):775-9.
-
(2008)
Haematologica
, vol.93
, Issue.5
, pp. 775-779
-
-
Falini, B.1
Martelli, M.P.2
Mecucci, C.3
Liso, A.4
Bolli, N.5
Bigerna, B.6
-
24
-
-
33744464741
-
Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations
-
Gorello P, Cazzaniga G, Alberti F, Dell'Oro MG, Gottardi E, Specchia G, et al. Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations. Leukemia. 2006;20(6):1103-8.
-
(2006)
Leukemia
, vol.20
, Issue.6
, pp. 1103-1108
-
-
Gorello, P.1
Cazzaniga, G.2
Alberti, F.3
Dell'oro, M.G.4
Gottardi, E.5
Specchia, G.6
-
25
-
-
34247640052
-
Clinical implications of minimal residual disease monitoring by quantitative polymerase chain reaction in acute myeloid leukemia patients bear- ing nucleophosmin (NPM1) mutations
-
Chou WC, Tang JL, Wu SJ, Tsay W, Yao M, Huang SY, et al. Clinical implications of minimal residual disease monitoring by quantitative polymerase chain reaction in acute myeloid leukemia patients bear- ing nucleophosmin (NPM1) mutations. Leukemia. 2007;21(5):998-1004.
-
(2007)
Leukemia
, vol.21
, Issue.5
, pp. 998-1004
-
-
Chou, W.C.1
Tang, J.L.2
Wu, S.J.3
Tsay, W.4
Yao, M.5
Huang, S.Y.6
-
26
-
-
47649122245
-
Minimal residual disease detection in acute myeloid leukemia by mutant nucleophosmin (NPM1): Comparison with WT1 gene expression
-
Barragan E, Pajuelo JC, Ballester S, Fuster O, Cervera J, Moscardo F, et al. Minimal residual disease detection in acute myeloid leukemia by mutant nucleophosmin (NPM1): comparison with WT1 gene expression. Clin Chim Acta. 2008;395(1-2):120-3.
-
(2008)
Clin Chim Acta
, vol.395
, Issue.1-2
, pp. 120-123
-
-
Barragan, E.1
Pajuelo, J.C.2
Ballester, S.3
Fuster, O.4
Cervera, J.5
Moscardo, F.6
-
27
-
-
57549101876
-
Quantitative monitoring of NPM1 mutations provides a valid mini- mal residual disease parameter following allogeneic stem cell trans- plantation
-
Bacher U, Badbaran A, Fehse B, Zabelina T, Zander AR, Kroger N. Quantitative monitoring of NPM1 mutations provides a valid mini- mal residual disease parameter following allogeneic stem cell trans- plantation. Exp Hematol. 2009;37(1):135-42.
-
(2009)
Exp Hematol
, vol.37
, Issue.1
, pp. 135-142
-
-
Bacher, U.1
Badbaran, A.2
Fehse, B.3
Zabelina, T.4
Zander, A.R.5
Kroger, N.6
-
28
-
-
70349579540
-
Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML
-
Schnittger S, Kern W, Tschulik C, Weiss T, Dicker F, Falini B, et al. Minimal residual disease levels assessed by NPM1 mutation-specific RQ-PCR provide important prognostic information in AML. Blood. 2009;114(11):2220-31.
-
(2009)
Blood
, vol.114
, Issue.11
, pp. 2220-2231
-
-
Schnittger, S.1
Kern, W.2
Tschulik, C.3
Weiss, T.4
Dicker, F.5
Falini, B.6
-
29
-
-
75649091203
-
Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1 and CBFB-MYH11 acute myeloid leukemias
-
Ommen HB, Schnittger S, Jovanovic JV, Ommen IB, Hasle H, Ostergaard M, et al. Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1 and CBFB-MYH11 acute myeloid leukemias. Blood. 2010;115(2):198-205.
-
(2010)
Blood
, vol.115
, Issue.2
, pp. 198-205
-
-
Ommen, H.B.1
Schnittger, S.2
Jovanovic, J.V.3
Ommen, I.B.4
Hasle, H.5
Ostergaard, M.6
-
30
-
-
57849131651
-
A western blot assay for detecting mutant nucle- ophosmin (NPM1) proteins in acute myeloid leukaemia
-
Martelli MP, Manes N, Liso A, Pettirossi V, Verducci Galletti B, Bigerna B, et al. A western blot assay for detecting mutant nucle- ophosmin (NPM1) proteins in acute myeloid leukaemia. Leukemia. 2008;22(12):2285-8.
-
(2008)
Leukemia
, vol.22
, Issue.12
, pp. 2285-2288
-
-
Martelli, M.P.1
Manes, N.2
Liso, A.3
Pettirossi, V.4
Verducci Galletti, B.5
Bigerna, B.6
-
31
-
-
0035060568
-
Realistic pathologic classification of acute myeloid leukemias
-
Arber DA. Realistic pathologic classification of acute myeloid leukemias. Am J Clin Pathol. 2001;115(4):552-60.
-
(2001)
Am J Clin Pathol
, vol.115
, Issue.4
, pp. 552-560
-
-
Arber, D.A.1
-
32
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman JW, Harris NL, Brunning RD. The World Health Organization (WHO) classification of the myeloid neoplasms. Blood. 2002;100(7):2292-302.
-
(2002)
Blood
, vol.100
, Issue.7
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
33
-
-
28444449081
-
Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype
-
Schnittger S, Schoch C, Kern W, Mecucci C, Tschulik C, Martelli MF, et al. Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. Blood. 2005;106(12):3733-9.
-
(2005)
Blood
, vol.106
, Issue.12
, pp. 3733-3739
-
-
Schnittger, S.1
Schoch, C.2
Kern, W.3
Mecucci, C.4
Tschulik, C.5
Martelli, M.F.6
-
34
-
-
0037344424
-
Acute myeloid leukemia with recurring chromosome abnormali- ties as defined by the WHO-classification: Incidence of subgroups, additional genetic abnormalities, FAB subtypes and age distribution in an unselected series of 1,897 patients with acute myeloid leukemia
-
Schoch C, Schnittger S, Kern W, Dugas M, Hiddemann W, Haferlach T. Acute myeloid leukemia with recurring chromosome abnormali- ties as defined by the WHO-classification: incidence of subgroups, additional genetic abnormalities, FAB subtypes and age distribution in an unselected series of 1,897 patients with acute myeloid leukemia. Haematologica. 2003;88(3):351-2.
-
(2003)
Haematologica
, vol.88
, Issue.3
, pp. 351-352
-
-
Schoch, C.1
Schnittger, S.2
Kern, W.3
Dugas, M.4
Hiddemann, W.5
Haferlach, T.6
-
35
-
-
5644235305
-
PAX5 expression in acute leukemias: Higher B-lineage specificity than CD79a and selective association with t(8;21)-acute myelogenous leukemia
-
Tiacci E, Pileri S, Orleth A, Pacini R, Tabarrini A, Frenguelli F, et al. PAX5 expression in acute leukemias: higher B-lineage specificity than CD79a and selective association with t(8;21)-acute myelogenous leukemia. Cancer Res. 2004;64(20):7399-404.
-
(2004)
Cancer Res
, vol.64
, Issue.20
, pp. 7399-7404
-
-
Tiacci, E.1
Pileri, S.2
Orleth, A.3
Pacini, R.4
Tabarrini, A.5
Frenguelli, F.6
-
36
-
-
12944281159
-
Detection of acute leukemia cells with mixed lin- eage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1
-
Wuchter C, Harbott J, Schoch C, Schnittger S, Borkhardt A, Karawajew L, et al. Detection of acute leukemia cells with mixed lin- eage leukemia (MLL) gene rearrangements by flow cytometry using monoclonal antibody 7.1. Leukemia. 2000;14(7):1232-8.
-
(2000)
Leukemia
, vol.14
, Issue.7
, pp. 1232-1238
-
-
Wuchter, C.1
Harbott, J.2
Schoch, C.3
Schnittger, S.4
Borkhardt, A.5
Karawajew, L.6
-
37
-
-
33748703838
-
Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia
-
Falini B, Martelli MP, Bolli N, Bonasso R, Ghia E, Pallotta MT, et al. Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia. Blood. 2006;108(6):1999-2005.
-
(2006)
Blood
, vol.108
, Issue.6
, pp. 1999-2005
-
-
Falini, B.1
Martelli, M.P.2
Bolli, N.3
Bonasso, R.4
Ghia, E.5
Pallotta, M.T.6
-
38
-
-
70350724838
-
Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: Molecular basis and clinical implications
-
Falini B, Bolli N, Liso A, Martelli MP, Mannucci R, Pileri S, et al. Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: molecular basis and clinical implications. Leukemia. 2009;23(10):1731-43.
-
(2009)
Leukemia
, vol.23
, Issue.10
, pp. 1731-1743
-
-
Falini, B.1
Bolli, N.2
Liso, A.3
Martelli, M.P.4
Mannucci, R.5
Pileri, S.6
-
39
-
-
73949088393
-
Cytoplasmic expression of nucleophosmin accurately predicts muta- tion in the nucleophosmin gene in patients with acute myeloid leukemia and normal karyotype
-
Luo J, Qi C, Xu W, Kamel-Reid S, Brandwein J, Chang H. Cytoplasmic expression of nucleophosmin accurately predicts muta- tion in the nucleophosmin gene in patients with acute myeloid leukemia and normal karyotype. Am J Clin Pathol. 2010;133(1):34-40.
-
(2010)
Am J Clin Pathol
, vol.133
, Issue.1
, pp. 34-40
-
-
Luo, J.1
Qi, C.2
Xu, W.3
Kamel-Reid, S.4
Brandwein, J.5
Chang, H.6
-
40
-
-
70350091450
-
Cytoplasmic localization of nucleophosmin in bone mar- row blasts of acute myeloid leukemia patients is not completely con- cordant with NPM1 mutation and is not predictive of prognosis
-
Konoplev S, Huang X, Drabkin HA, Koeppen H, Jones D, Kantarjian HM, et al. Cytoplasmic localization of nucleophosmin in bone mar- row blasts of acute myeloid leukemia patients is not completely con- cordant with NPM1 mutation and is not predictive of prognosis. Cancer. 2009;115(20):4737-44.
-
(2009)
Cancer
, vol.115
, Issue.20
, pp. 4737-4744
-
-
Konoplev, S.1
Huang, X.2
Drabkin, H.A.3
Koeppen, H.4
Jones, D.5
Kantarjian, H.M.6
-
41
-
-
0030733063
-
Immunocytochemical diagnosis of acute promyelocytic leukemia (M3) with the monoclonal antibody PG-M3 (anti-PML)
-
Falini B, Flenghi L, Fagioli M, Lo Coco F, Cordone I, Diverio D, et al. Immunocytochemical diagnosis of acute promyelocytic leukemia (M3) with the monoclonal antibody PG-M3 (anti-PML). Blood. 1997;90(10):4046-53.
-
(1997)
Blood
, vol.90
, Issue.10
, pp. 4046-4053
-
-
Falini, B.1
Flenghi, L.2
Fagioli, M.3
Lo Coco, F.4
Cordone, I.5
Diverio, D.6
-
42
-
-
77950688823
-
Improving the treatment outcome of acute promyelocytic leukemia in developing countries through International Cooperative Network. Report on the International Consortium on Acute Promyelocytic Leukemia Study Group
-
(ASH Annual Meeting Abstracts)
-
Rego EM, Kim HT, Ruiz-Arguelles GJ, Uriarte R, Jacomo RH, Gutierrez-Aguirre H, et al. Improving the treatment outcome of acute promyelocytic leukemia in developing countries through International Cooperative Network. Report on the International Consortium on Acute Promyelocytic Leukemia Study Group. Blood. (ASH Annual Meeting Abstracts) 2009;114, 6.
-
(2009)
Blood
, vol.114
, pp. 6
-
-
Rego, E.M.1
Kim, H.T.2
Ruiz-Arguelles, G.J.3
Uriarte, R.4
Jacomo, R.H.5
Gutierrez-Aguirre, H.6
-
43
-
-
77950685471
-
Can cytoplasmic nucleophosmin be detected by immunocy- tochemical staining of cell smears in acute myeloid leukemia?
-
Mattsson G, Turner SH, Cordell J, Ferguson DJ, Schuh A, Grimwade LF, et al. Can cytoplasmic nucleophosmin be detected by immunocy- tochemical staining of cell smears in acute myeloid leukemia? Haematologica. 2010;95(4):670-3.
-
(2010)
Haematologica
, vol.95
, Issue.4
, pp. 670-673
-
-
Mattsson, G.1
Turner, S.H.2
Cordell, J.3
Ferguson, D.J.4
Schuh, A.5
Grimwade, L.F.6
-
44
-
-
33845483445
-
Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification
-
Pasqualucci L, Liso A, Martelli MP, Bolli N, Pacini R, Tabarrini A, et al. Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification. Blood. 2006;108(13):4146-55.
-
(2006)
Blood
, vol.108
, Issue.13
, pp. 4146-4155
-
-
Pasqualucci, L.1
Liso, A.2
Martelli, M.P.3
Bolli, N.4
Pacini, R.5
Tabarrini, A.6
-
45
-
-
70449562580
-
A rapid flow cytometric method for the detection of NPM1 mutated patients with acute myeloid leukemia (AML)
-
(ASH Annual Meeting Abstracts)
-
Oelschlaegel U KS, Schaich M, Kroschinsky F, Parmentier S, Ehninger G, Thiede C. A rapid flow cytometric method for the detection of NPM1 mutated patients with acute myeloid leukemia (AML). Blood. (ASH Annual Meeting Abstracts) 2008;112:1490.
-
(2008)
Blood
, vol.112
, pp. 1490
-
-
Oelschlaegel, U.K.S.1
Schaich, M.2
Kroschinsky, F.3
Parmentier, S.4
Ehninger, G.5
Thiede, C.6
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