These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 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]
    of 8.