146 related articles for article (PubMed ID: 20013897)
1. Focal 9p instability in hematologic neoplasias revealed by comparative genomic hybridization and single-nucleotide polymorphism microarray analyses.
Usvasalo A; Ninomiya S; Räty R; Hollmén J; Saarinen-Pihkala UM; Elonen E; Knuutila S
Genes Chromosomes Cancer; 2010 Apr; 49(4):309-18. PubMed ID: 20013897
[TBL] [Abstract][Full Text] [Related]
2. IKZF1 (Ikaros) deletions in BCR-ABL1-positive acute lymphoblastic leukemia are associated with short disease-free survival and high rate of cumulative incidence of relapse: a GIMEMA AL WP report.
Martinelli G; Iacobucci I; Storlazzi CT; Vignetti M; Paoloni F; Cilloni D; Soverini S; Vitale A; Chiaretti S; Cimino G; Papayannidis C; Paolini S; Elia L; Fazi P; Meloni G; Amadori S; Saglio G; Pane F; Baccarani M; Foà R
J Clin Oncol; 2009 Nov; 27(31):5202-7. PubMed ID: 19770381
[TBL] [Abstract][Full Text] [Related]
3. Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis.
Huh J; Tiu RV; Gondek LP; O'Keefe CL; Jasek M; Makishima H; Jankowska AM; Jiang Y; Verma A; Theil KS; McDevitt MA; Maciejewski JP
Genes Chromosomes Cancer; 2010 Apr; 49(4):390-9. PubMed ID: 20095039
[TBL] [Abstract][Full Text] [Related]
4. Integrated analysis of gene copy number, copy neutral LOH, and microRNA profiles in adult acute lymphoblastic leukemia.
Ninomiya S; Tyybäkinoja A; Borze I; Räty R; Saarinen-Pihkala UM; Usvasalo A; Elonen E; Knuutila S
Cytogenet Genome Res; 2012; 136(4):246-55. PubMed ID: 22456238
[TBL] [Abstract][Full Text] [Related]
5. Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung.
Kang JU; Koo SH; Kwon KC; Park JW
Int J Oncol; 2010 Aug; 37(2):327-35. PubMed ID: 20596660
[TBL] [Abstract][Full Text] [Related]
6. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.
Gaasenbeek M; Howarth K; Rowan AJ; Gorman PA; Jones A; Chaplin T; Liu Y; Bicknell D; Davison EJ; Fiegler H; Carter NP; Roylance RR; Tomlinson IP
Cancer Res; 2006 Apr; 66(7):3471-9. PubMed ID: 16585170
[TBL] [Abstract][Full Text] [Related]
7. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
8. Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization.
Strefford JC; Worley H; Barber K; Wright S; Stewart AR; Robinson HM; Bettney G; van Delft FW; Atherton MG; Davies T; Griffiths M; Hing S; Ross FM; Talley P; Saha V; Moorman AV; Harrison CJ
Oncogene; 2007 Jun; 26(29):4306-18. PubMed ID: 17237825
[TBL] [Abstract][Full Text] [Related]
9. Detection of copy number alterations in acute myeloid leukemia and myelodysplastic syndromes.
Jacoby MA; Walter MJ
Expert Rev Mol Diagn; 2012 Apr; 12(3):253-64. PubMed ID: 22468816
[TBL] [Abstract][Full Text] [Related]
10. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
11. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
[TBL] [Abstract][Full Text] [Related]
12. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D
Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
[TBL] [Abstract][Full Text] [Related]
13. High-resolution oligonucleotide array comparative genomic hybridization study and methylation status of the RPS14 gene in de novo myelodysplastic syndromes.
Borze I; Juvonen E; Ninomiya S; Jee KJ; Elonen E; Knuutila S
Cancer Genet Cytogenet; 2010 Mar; 197(2):166-73. PubMed ID: 20193850
[TBL] [Abstract][Full Text] [Related]
14. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
Svobodova K; Zemanova Z; Lhotska H; Novakova M; Podskalska L; Belickova M; Brezinova J; Sarova I; Izakova S; Lizcova L; Berkova A; Siskova M; Jonasova A; Cermak J; Michalova K
Leuk Res; 2016 Mar; 42():7-12. PubMed ID: 26851439
[TBL] [Abstract][Full Text] [Related]
15. Homozygous deletion of MTAP gene as a poor prognosticator in gastrointestinal stromal tumors.
Huang HY; Li SH; Yu SC; Chou FF; Tzeng CC; Hu TH; Uen YH; Tian YF; Wang YH; Fang FM; Huang WW; Wei YC; Wu JM; Li CF
Clin Cancer Res; 2009 Nov; 15(22):6963-72. PubMed ID: 19887491
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
Wang L; Fidler C; Nadig N; Giagounidis A; Della Porta MG; Malcovati L; Killick S; Gattermann N; Aul C; Boultwood J; Wainscoat JS
Haematologica; 2008 Jul; 93(7):994-1000. PubMed ID: 18508791
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Chromosomal aberrations in head and neck squamous cell carcinomas in Norwegian and Sudanese populations by array comparative genomic hybridization.
Roman E; Meza-Zepeda LA; Kresse SH; Myklebost O; Vasstrand EN; Ibrahim SO
Oncol Rep; 2008 Oct; 20(4):825-43. PubMed ID: 18813824
[TBL] [Abstract][Full Text] [Related]
19. Fine-mapping loss of gene architecture at the CDKN2B (p15INK4b), CDKN2A (p14ARF, p16INK4a), and MTAP genes in head and neck squamous cell carcinoma.
Worsham MJ; Chen KM; Tiwari N; Pals G; Schouten JP; Sethi S; Benninger MS
Arch Otolaryngol Head Neck Surg; 2006 Apr; 132(4):409-15. PubMed ID: 16618910
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-density single-nucleotide polymorphism arrays.
Stark M; Hayward N
Cancer Res; 2007 Mar; 67(6):2632-42. PubMed ID: 17363583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]