574 related articles for article (PubMed ID: 19781438)
21. Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization.
Rücker FG; Bullinger L; Schwaenen C; Lipka DB; Wessendorf S; Fröhling S; Bentz M; Miller S; Scholl C; Schlenk RF; Radlwimmer B; Kestler HA; Pollack JR; Lichter P; Döhner K; Döhner H
J Clin Oncol; 2006 Aug; 24(24):3887-94. PubMed ID: 16864856
[TBL] [Abstract][Full Text] [Related]
22. Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia.
Ganly P; McDonald M; Spearing R; Morris CM
Cancer Genet Cytogenet; 2004 Mar; 149(2):125-30. PubMed ID: 15036888
[TBL] [Abstract][Full Text] [Related]
23. del(6)(p23) in two cases of de novo AML--a new recurrent primary chromosome abnormality.
Anwar Iqbal M; Al-Omar HM; Owaidah T; Al-Humaidan H; Bhuiyan ZA; Sahovic E
Eur J Haematol; 2006 Sep; 77(3):245-50. PubMed ID: 16856925
[TBL] [Abstract][Full Text] [Related]
24. A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes.
MacKinnon RN; Kannourakis G; Wall M; Campbell LJ
Cancer Genet; 2011 Apr; 204(4):187-94. PubMed ID: 21536236
[TBL] [Abstract][Full Text] [Related]
25. Array comparative genomic hybridization analysis of adult acute leukemia patients.
Yasar D; Karadogan I; Alanoglu G; Akkaya B; Luleci G; Salim O; Timuragaoglu A; Toruner GA; Berker-Karauzum S
Cancer Genet Cytogenet; 2010 Mar; 197(2):122-9. PubMed ID: 20193845
[TBL] [Abstract][Full Text] [Related]
26. Cytogenetic, spectral karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization characterization of two new secondary leukemia cell lines with 5q deletions, and MYC and MLL amplification.
Knutsen T; Pack S; Petropavlovskaja M; Padilla-Nash H; Knight C; Mickley LA; Ried T; Elwood PC; Roberts SJ
Genes Chromosomes Cancer; 2003 Jul; 37(3):270-81. PubMed ID: 12759925
[TBL] [Abstract][Full Text] [Related]
27. Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group.
Heerema NA; Nachman JB; Sather HN; La MK; Hutchinson R; Lange BJ; Bostrom B; Steinherz PG; Gaynon PS; Uckun FM;
Leukemia; 2004 May; 18(5):939-47. PubMed ID: 14999294
[TBL] [Abstract][Full Text] [Related]
28. Correlation between selected environmental exposures and karyotype in acute myelocytic leukemia.
Crane MM; Strom SS; Halabi S; Berman EL; Fueger JJ; Spitz MR; Keating MJ
Cancer Epidemiol Biomarkers Prev; 1996 Aug; 5(8):639-44. PubMed ID: 8824367
[TBL] [Abstract][Full Text] [Related]
29. Upregulation of c-myc gene accompanied by PU.1 deficiency in radiation-induced acute myeloid leukemia in mice.
Hirouchi T; Takabatake T; Yoshida K; Nitta Y; Nakamura M; Tanaka S; Ichinohe K; Oghiso Y; Tanaka K
Exp Hematol; 2008 Jul; 36(7):871-85. PubMed ID: 18375040
[TBL] [Abstract][Full Text] [Related]
30. Evaluation of chromosome 5 aberrations in complex karyotypes of patients with myeloid disorders reveals their contribution to dicentric and tricentric chromosomes, resulting in the loss of critical 5q regions.
Herry A; Douet-Guilbert N; Morel F; Le Bris MJ; Morice P; Abgrall JF; Berthou C; De Braekeleer M
Cancer Genet Cytogenet; 2007 Jun; 175(2):125-31. PubMed ID: 17556068
[TBL] [Abstract][Full Text] [Related]
31. Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome.
Asou H; Matsui H; Ozaki Y; Nagamachi A; Nakamura M; Aki D; Inaba T
Biochem Biophys Res Commun; 2009 May; 383(2):245-51. PubMed ID: 19358830
[TBL] [Abstract][Full Text] [Related]
32. [Cytogenetic marker del(12p) in a case of acute myeloid leukemia M4 with eosinophilia and inv(16)].
Cigudosa JC; Calasanz MJ; Gullón A; Cuesta B; Rifón J; Rocha E
Sangre (Barc); 1992 Apr; 37(2):125-7. PubMed ID: 1621181
[TBL] [Abstract][Full Text] [Related]
33. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype.
Gross M; Mkrtchyan H; Glaser M; Fricke HJ; Höffken K; Heller A; Weise A; Liehr T
Int J Oncol; 2009 Feb; 34(2):417-23. PubMed ID: 19148476
[TBL] [Abstract][Full Text] [Related]
34. Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation.
Liu TX; Becker MW; Jelinek J; Wu WS; Deng M; Mikhalkevich N; Hsu K; Bloomfield CD; Stone RM; DeAngelo DJ; Galinsky IA; Issa JP; Clarke MF; Look AT
Nat Med; 2007 Jan; 13(1):78-83. PubMed ID: 17159988
[TBL] [Abstract][Full Text] [Related]
35. Array comparative genomic hybridization analysis of PTCL-U reveals a distinct subgroup with genetic alterations similar to lymphoma-type adult T-cell leukemia/lymphoma.
Nakagawa M; Nakagawa-Oshiro A; Karnan S; Tagawa H; Utsunomiya A; Nakamura S; Takeuchi I; Ohshima K; Seto M
Clin Cancer Res; 2009 Jan; 15(1):30-8. PubMed ID: 19118030
[TBL] [Abstract][Full Text] [Related]
36. Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study.
Hasle H; Alonzo TA; Auvrignon A; Behar C; Chang M; Creutzig U; Fischer A; Forestier E; Fynn A; Haas OA; Harbott J; Harrison CJ; Heerema NA; van den Heuvel-Eibrink MM; Kaspers GJ; Locatelli F; Noellke P; Polychronopoulou S; Ravindranath Y; Razzouk B; Reinhardt D; Savva NN; Stark B; Suciu S; Tsukimoto I; Webb DK; Wojcik D; Woods WG; Zimmermann M; Niemeyer CM; Raimondi SC
Blood; 2007 Jun; 109(11):4641-7. PubMed ID: 17299091
[TBL] [Abstract][Full Text] [Related]
37. Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.
Lu CM; Murata-Collins JL; Wang E; Siddiqi I; Lawrence H
Am J Hematol; 2006 Dec; 81(12):963-8. PubMed ID: 16917916
[TBL] [Abstract][Full Text] [Related]
38. Trisomy 22 as the sole abnormality is an important marker for the diagnosis of acute myeloid leukemia with inversion 16.
Xu W; Zhou HF; Fan L; Qian SX; Chen LJ; Qiu HR; Zhang SJ; Li JY
Onkologie; 2008 Sep; 31(8-9):440-4. PubMed ID: 18787351
[TBL] [Abstract][Full Text] [Related]
39. The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies.
Chen Z; Pasquini M; Hong B; DeHart S; Heikens M; Tsai S
Cancer Genet Cytogenet; 2005 Oct; 162(2):95-8. PubMed ID: 16213355
[TBL] [Abstract][Full Text] [Related]
40. Deletion 15q as the sole abnormality in acute myeloid leukemia: report of three cases and review of the literature.
Lu G; Yin CC; Medeiros LJ; Abruzzo LV
Cancer Genet Cytogenet; 2009 Jan; 188(2):118-23. PubMed ID: 19100517
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
