178 related articles for article (PubMed ID: 22468816)
1. 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]
2. 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]
3. 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]
4. 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]
5. Significance of genome-wide analysis of copy number alterations and UPD in myelodysplastic syndromes using combined CGH - SNP arrays.
Ahmad A; Iqbal MA
Curr Med Chem; 2012; 19(22):3739-47. PubMed ID: 22680919
[TBL] [Abstract][Full Text] [Related]
6. Array CGH in human leukemia: from somatics to genetics.
van der Veken LT; Buijs A
Cytogenet Genome Res; 2011; 135(3-4):260-70. PubMed ID: 21893961
[TBL] [Abstract][Full Text] [Related]
7. High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes.
Cheung KJ; Delaney A; Ben-Neriah S; Schein J; Lee T; Shah SP; Cheung D; Johnson NA; Mungall AJ; Telenius A; Lai B; Boyle M; Connors JM; Gascoyne RD; Marra MA; Horsman DE
Genes Chromosomes Cancer; 2010 Aug; 49(8):669-81. PubMed ID: 20544841
[TBL] [Abstract][Full Text] [Related]
8. Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype.
Akagi T; Ogawa S; Dugas M; Kawamata N; Yamamoto G; Nannya Y; Sanada M; Miller CW; Yung A; Schnittger S; Haferlach T; Haferlach C; Koeffler HP
Haematologica; 2009 Feb; 94(2):213-23. PubMed ID: 19144660
[TBL] [Abstract][Full Text] [Related]
9. Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes.
Barresi V; Romano A; Musso N; Capizzi C; Consoli C; Martelli MP; Palumbo G; Di Raimondo F; Condorelli DF
Genes Chromosomes Cancer; 2010 Nov; 49(11):1014-23. PubMed ID: 20725993
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Application of SNP genotype arrays to determine somatic changes in cancer.
Gupta M; Young BD
Methods Mol Biol; 2009; 538():179-206. PubMed ID: 19277572
[TBL] [Abstract][Full Text] [Related]
13. AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
Zatkova A; Merk S; Wendehack M; Bilban M; Muzik EM; Muradyan A; Haferlach C; Haferlach T; Wimmer K; Fonatsch C; Ullmann R
Genes Chromosomes Cancer; 2009 Jun; 48(6):510-20. PubMed ID: 19306356
[TBL] [Abstract][Full Text] [Related]
14. DNA profiling by arrayCGH in acute myeloid leukemia and myelodysplastic syndromes.
Suela J; Alvarez S; Cigudosa JC
Cytogenet Genome Res; 2007; 118(2-4):304-9. PubMed ID: 18000384
[TBL] [Abstract][Full Text] [Related]
15. Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes.
Starczynowski DT; Vercauteren S; Sung S; Brooks-Wilson A; Lam WL; Karsan A
Leuk Res; 2011 Apr; 35(4):444-7. PubMed ID: 20801506
[TBL] [Abstract][Full Text] [Related]
16. Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.
Huh J; Jung CW; Kim HJ; Kim YK; Moon JH; Sohn SK; Kim HJ; Min WS; Kim DH
Genes Chromosomes Cancer; 2013 Jan; 52(1):44-55. PubMed ID: 23023762
[TBL] [Abstract][Full Text] [Related]
17. SNP array analysis in hematologic malignancies: avoiding false discoveries.
Heinrichs S; Li C; Look AT
Blood; 2010 May; 115(21):4157-61. PubMed ID: 20304806
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Microarray-based comparative genomic hybridization of cancer targets reveals novel, recurrent genetic aberrations in the myelodysplastic syndromes.
Kolquist KA; Schultz RA; Furrow A; Brown TC; Han JY; Campbell LJ; Wall M; Slovak ML; Shaffer LG; Ballif BC
Cancer Genet; 2011 Nov; 204(11):603-28. PubMed ID: 22200086
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
