247 related articles for article (PubMed ID: 22103895)
21. Fusion of NUP98 and the SET binding protein 1 (SETBP1) gene in a paediatric acute T cell lymphoblastic leukaemia with t(11;18)(p15;q12).
Panagopoulos I; Kerndrup G; Carlsen N; Strömbeck B; Isaksson M; Johansson B
Br J Haematol; 2007 Jan; 136(2):294-6. PubMed ID: 17233820
[TBL] [Abstract][Full Text] [Related]
22. Molecular heterogeneity of the NUP98/HOXA9 fusion transcript in myelodysplastic syndromes associated with t(7;11)(p15;p15).
Hatano Y; Miura I; Nakamura T; Yamazaki Y; Takahashi N; Miura AB
Br J Haematol; 1999 Dec; 107(3):600-4. PubMed ID: 10583265
[TBL] [Abstract][Full Text] [Related]
23. NUP98-HOXA9 bearing therapy-related myeloid neoplasm involves myeloid-committed cell and induces HOXA5, EVI1, FLT3, and MEIS1 expression.
Burillo-Sanz S; Morales-Camacho RM; Caballero-Velázquez T; Vargas MT; García-Lozano JR; Falantes JF; Prats-Martín C; Bernal R; Pérez-Simón JA
Int J Lab Hematol; 2016 Feb; 38(1):64-71. PubMed ID: 26418229
[TBL] [Abstract][Full Text] [Related]
24. A t(11;20)(p15;q11) may identify a subset of nontherapy-related acute myelocytic leukemia.
Potenza L; Sinigaglia B; Luppi M; Morselli M; Saviola A; Ferrari A; Riva G; Zucchini P; Giacobbi F; Emilia G; Temperani P; Torelli G
Cancer Genet Cytogenet; 2004 Mar; 149(2):164-8. PubMed ID: 15036893
[TBL] [Abstract][Full Text] [Related]
25. Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene.
van Zutven LJ; Onen E; Velthuizen SC; van Drunen E; von Bergh AR; van den Heuvel-Eibrink MM; Veronese A; Mecucci C; Negrini M; de Greef GE; Beverloo HB
Genes Chromosomes Cancer; 2006 May; 45(5):437-46. PubMed ID: 16419055
[TBL] [Abstract][Full Text] [Related]
26. Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts.
La Starza R; Gorello P; Rosati R; Riezzo A; Veronese A; Ferrazzi E; Martelli MF; Negrini M; Mecucci C
Genes Chromosomes Cancer; 2004 Dec; 41(4):395-9. PubMed ID: 15382262
[TBL] [Abstract][Full Text] [Related]
27. t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia.
Gorello P; Brandimarte L; La Starza R; Pierini V; Bury L; Rosati R; Martelli MF; Vandenberghe P; Wlodarska I; Mecucci C
Haematologica; 2008 Sep; 93(9):1398-401. PubMed ID: 18603550
[TBL] [Abstract][Full Text] [Related]
28. Fusion of the NUP98 gene with the LEDGF/p52 gene defines a recurrent acute myeloid leukemia translocation.
Hussey DJ; Moore S; Nicola M; Dobrovic A
BMC Genet; 2001; 2():20. PubMed ID: 11737860
[TBL] [Abstract][Full Text] [Related]
29. NUP98 dysregulation in myeloid leukemogenesis.
Moore MA; Chung KY; Plasilova M; Schuringa JJ; Shieh JH; Zhou P; Morrone G
Ann N Y Acad Sci; 2007 Jun; 1106():114-42. PubMed ID: 17442773
[TBL] [Abstract][Full Text] [Related]
30. A novel t(5;11)(q31;p15) involving the NUP98 gene on 11p15 is associated with a loss of the EGR1 gene on 5q31 in a patient with acute myeloid leukemia.
Wang Y; Xue Y; Chen S; Wu Y; Pan J; Zhang J; Shen J
Cancer Genet Cytogenet; 2010 May; 199(1):9-14. PubMed ID: 20417862
[TBL] [Abstract][Full Text] [Related]
31. Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review.
Tosić N; Stojiljković M; Colović N; Colović M; Pavlović S
Cancer Genet Cytogenet; 2009 Sep; 193(2):98-103. PubMed ID: 19665070
[TBL] [Abstract][Full Text] [Related]
32. The inv(11)(p15q22) chromosome translocation of therapy-related myelodysplasia with NUP98-DDX10 and DDX10-NUP98 fusion transcripts.
Ikeda T; Ikeda K; Sasaki K; Kawakami K; Takahara J
Int J Hematol; 1999 Apr; 69(3):160-4. PubMed ID: 10222653
[TBL] [Abstract][Full Text] [Related]
33. Inv(11)(p15q22)/NUP98-DDX10 fusion and isoforms in a new case of de novo acute myeloid leukemia.
Gorello P; Nofrini V; Brandimarte L; Pierini V; Crescenzi B; Nozza F; Daniele G; Storlazzi CT; Di Giacomo D; Matteucci C; La Starza R; Mecucci C
Cancer Genet; 2013 Mar; 206(3):92-6. PubMed ID: 23522748
[TBL] [Abstract][Full Text] [Related]
34. PRDX4, a member of the peroxiredoxin family, is fused to AML1 (RUNX1) in an acute myeloid leukemia patient with a t(X;21)(p22;q22).
Zhang Y; Emmanuel N; Kamboj G; Chen J; Shurafa M; Van Dyke DL; Wiktor A; Rowley JD
Genes Chromosomes Cancer; 2004 Aug; 40(4):365-70. PubMed ID: 15188461
[TBL] [Abstract][Full Text] [Related]
35. Deletion 6p23 and add(11)(p15) leading to NUP98 translocation in a case of therapy-related atypical chronic myelocytic leukemia transforming to acute myelocytic leukemia.
Takeshita A; Naito K; Shinjo K; Sahara N; Matsui H; Ohnishi K; Beppu H; Ohtsubo K; Horii T; Maekawa M; Inaba T; Ohno R
Cancer Genet Cytogenet; 2004 Jul; 152(1):56-60. PubMed ID: 15193442
[TBL] [Abstract][Full Text] [Related]
36. NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia.
Raza-Egilmez SZ; Jani-Sait SN; Grossi M; Higgins MJ; Shows TB; Aplan PD
Cancer Res; 1998 Oct; 58(19):4269-73. PubMed ID: 9766650
[TBL] [Abstract][Full Text] [Related]
37. The prognostic value of MLL-AF9 detection in patients with t(9;11)(p22;q23)-positive acute myeloid leukemia.
Scholl C; Schlenk RF; Eiwen K; Döhner H; Fröhling S; Döhner K;
Haematologica; 2005 Dec; 90(12):1626-34. PubMed ID: 16330435
[TBL] [Abstract][Full Text] [Related]
38. A new fusion gene NUP98-IQCG identified in an acute T-lymphoid/myeloid leukemia with a t(3;11)(q29q13;p15)del(3)(q29) translocation.
Pan Q; Zhu YJ; Gu BW; Cai X; Bai XT; Yun HY; Zhu J; Chen B; Weng L; Chen Z; Xue YQ; Chen SJ
Oncogene; 2008 May; 27(24):3414-23. PubMed ID: 18084320
[TBL] [Abstract][Full Text] [Related]
39. PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies.
Duhoux FP; Ameye G; Montano-Almendras CP; Bahloula K; Mozziconacci MJ; Laibe S; Wlodarska I; Michaux L; Talmant P; Richebourg S; Lippert E; Speleman F; Herens C; Struski S; Raynaud S; Auger N; Nadal N; Rack K; Mugneret F; Tigaud I; Lafage M; Taviaux S; Roche-Lestienne C; Latinne D; Libouton JM; Demoulin JB; Poirel HA; ;
Br J Haematol; 2012 Jan; 156(1):76-88. PubMed ID: 22050763
[TBL] [Abstract][Full Text] [Related]
40. A novel gene, MDS2, is fused to ETV6/TEL in a t(1;12)(p36.1;p13) in a patient with myelodysplastic syndrome.
Odero MD; Vizmanos JL; Román JP; Lahortiga I; Panizo C; Calasanz MJ; Zeleznik-Le NJ; Rowley JD; Novo FJ
Genes Chromosomes Cancer; 2002 Sep; 35(1):11-9. PubMed ID: 12203785
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]