118 related articles for article (PubMed ID: 11908737)
1. Rearrangements of chromosome band 3q21 in myeloid leukemia.
Wieser R
Leuk Lymphoma; 2002 Jan; 43(1):59-65. PubMed ID: 11908737
[TBL] [Abstract][Full Text] [Related]
2. Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contig.
Wieser R; Volz A; Schnittger S; Jäger U; Grüner H; Meran JG; Wimmer K; Ziegler A; Fonatsch C
Br J Haematol; 2000 Aug; 110(2):343-50. PubMed ID: 10971391
[TBL] [Abstract][Full Text] [Related]
3. Interphase fluorescence in situ hybridization assay for the detection of 3q21 rearrangements in myeloid malignancies.
Wieser R; Schreiner U; Pirc-Danoewinata H; Aytekin M; Schmidt HH; Rieder H; Fonatsch C
Genes Chromosomes Cancer; 2001 Dec; 32(4):373-80. PubMed ID: 11746978
[TBL] [Abstract][Full Text] [Related]
4. Conventional cytogenetics and breakpoint distribution by fluorescent in situ hybridization in patients with malignant hemopathies associated with inv(3)(q21;q26) and t(3;3)(q21;q26).
De Braekeleer E; Douet-Guilbert N; Basinko A; Bovo C; Guéganic N; Le Bris MJ; Morel F; De Braekeleer M
Anticancer Res; 2011 Oct; 31(10):3441-8. PubMed ID: 21965759
[TBL] [Abstract][Full Text] [Related]
5. Identification of breakpoint cluster regions at 1p36.3 and 3q21 in hematologic malignancies with t(1;3)(p36;q21).
Shimizu S; Suzukawa K; Kodera T; Nagasawa T; Abe T; Taniwaki M; Yagasaki F; Tanaka H; Fujisawa S; Johansson B; Ahlgren T; Yokota J; Morishita K
Genes Chromosomes Cancer; 2000 Mar; 27(3):229-38. PubMed ID: 10679911
[TBL] [Abstract][Full Text] [Related]
6. Interphase fluorescence in situ hybridization assay for the detection of rearrangements of the EVI-1 locus in chromosome band 3q26 in myeloid malignancies.
Wieser R; Schreiner U; Rieder H; Pirc-Danoewinata H; Grüner H; Loncarevic IF; Fonatsch C
Haematologica; 2003 Jan; 88(1):25-30. PubMed ID: 12551823
[TBL] [Abstract][Full Text] [Related]
7. Identification of a breakpoint cluster region 3' of the ribophorin I gene at 3q21 associated with the transcriptional activation of the EVI1 gene in acute myelogenous leukemias with inv(3)(q21q26).
Suzukawa K; Parganas E; Gajjar A; Abe T; Takahashi S; Tani K; Asano S; Asou H; Kamada N; Yokota J
Blood; 1994 Oct; 84(8):2681-8. PubMed ID: 7919381
[TBL] [Abstract][Full Text] [Related]
8. Identification of translocational breakpoints within the intron region before the last coding exon (exon 12) of the EVI1 gene in two cases of CML-BC with inv(3)(q21q26).
Suzukawa K; Taki T; Abe T; Asoh H; Kamada N; Yokota J; Morishita K
Genomics; 1997 Jun; 42(2):356-60. PubMed ID: 9192861
[TBL] [Abstract][Full Text] [Related]
9. Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases.
Haferlach C; Bacher U; Grossmann V; Schindela S; Zenger M; Kohlmann A; Kern W; Haferlach T; Schnittger S
Genes Chromosomes Cancer; 2012 Dec; 51(12):1079-85. PubMed ID: 22887804
[TBL] [Abstract][Full Text] [Related]
10. Structural rearrangements of chromosome 3 in 57 patients with acute myeloid leukemia: clinical, hematological and cytogenetic features.
Charrin C; Belhabri A; Treille-Ritouet D; Theuil G; Magaud JP; Fiere D; Thomas X
Hematol J; 2002; 3(1):21-31. PubMed ID: 11960392
[TBL] [Abstract][Full Text] [Related]
11. Transcription factor GATA-2 gene is located near 3q21 breakpoints in myeloid leukemia.
Wieser R; Volz A; Vinatzer U; Gardiner K; Jäger U; Mitterbauer M; Ziegler A; Fonatsch C
Biochem Biophys Res Commun; 2000 Jun; 273(1):239-45. PubMed ID: 10873593
[TBL] [Abstract][Full Text] [Related]
12. Leukemia breakpoint region in 3q21 is gene rich.
Rynditch A; Pekarsky Y; Schnittger S; Gardiner K
Gene; 1997 Jul; 193(1):49-57. PubMed ID: 9249066
[TBL] [Abstract][Full Text] [Related]
13. Development of a dual-color, double fusion FISH assay to detect RPN1/EVI1 gene fusion associated with inv(3), t(3;3), and ins(3;3) in patients with myelodysplasia and acute myeloid leukemia.
Shearer BM; Sukov WR; Flynn HC; Knudson RA; Ketterling RP
Am J Hematol; 2010 Aug; 85(8):569-74. PubMed ID: 20556821
[TBL] [Abstract][Full Text] [Related]
14. Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia.
Lugthart S; Gröschel S; Beverloo HB; Kayser S; Valk PJ; van Zelderen-Bhola SL; Jan Ossenkoppele G; Vellenga E; van den Berg-de Ruiter E; Schanz U; Verhoef G; Vandenberghe P; Ferrant A; Köhne CH; Pfreundschuh M; Horst HA; Koller E; von Lilienfeld-Toal M; Bentz M; Ganser A; Schlegelberger B; Jotterand M; Krauter J; Pabst T; Theobald M; Schlenk RF; Delwel R; Döhner K; Löwenberg B; Döhner H
J Clin Oncol; 2010 Aug; 28(24):3890-8. PubMed ID: 20660833
[TBL] [Abstract][Full Text] [Related]
15. An interphase fluorescence in situ hybridisation assay for the detection of 3q26.2/EVI1 rearrangements in myeloid malignancies.
Bobadilla D; Enriquez EL; Alvarez G; Gaytan P; Smith D; Slovak ML
Br J Haematol; 2007 Mar; 136(6):806-13. PubMed ID: 17341266
[TBL] [Abstract][Full Text] [Related]
16. Refined chromosomal localization of the human thrombopoietin gene to 3q27-q28 and exclusion as the responsible gene for thrombocytosis in patients with rearrangements of 3q21 and 3q26.
Schnittger S; de Sauvage FJ; Le Paslier D; Fonatsch C
Leukemia; 1996 Dec; 10(12):1891-6. PubMed ID: 8946927
[TBL] [Abstract][Full Text] [Related]
17. Breakpoints at 1p36.3 in three MDS/AML(M4) patients with t(1;3)(p36;q21) occur in the first intron and in the 5' region of MEL1.
Xinh PT; Tri NK; Nagao H; Nakazato H; Taketazu F; Fujisawa S; Yagasaki F; Chen YZ; Hayashi Y; Toyoda A; Hattori M; Sakaki Y; Tokunaga K; Sato Y
Genes Chromosomes Cancer; 2003 Mar; 36(3):313-6. PubMed ID: 12557231
[TBL] [Abstract][Full Text] [Related]
18. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
19. Double Inv(3)(q21q26), a rare but recurrent chromosomal abnormality in myeloid hemopathies.
De Braekeleer E; Douet-Guilbert N; Le Bris MJ; Ianotto JC; Berthou C; Gueganic N; Bovo C; Basinko A; Morel F; De Braekeleer M
Anticancer Res; 2013 Feb; 33(2):639-42. PubMed ID: 23393360
[TBL] [Abstract][Full Text] [Related]
20. Abnormalities of 3q21 and 3q26 in myeloid malignancy: a United Kingdom Cancer Cytogenetic Group study.
Secker-Walker LM; Mehta A; Bain B
Br J Haematol; 1995 Oct; 91(2):490-501. PubMed ID: 8547101
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]